Herbicide / safener combinations based on safeners from the class of substituted [(1,5-diphenyl-1h-1,2,4-triazol-3-yl)oxy] acetic acids and herbicides from the class of substituted cyclic diones and the salts thereof

Abstract

The present invention relates to combinations comprising one or more components (A) active as safener and one or more herbicidally active compounds (component (B)), where component (A) represents one or more compounds of general formula (I) or agrochemically compatible salts thereof and component (B) represents one or more herbicides. The application further relates to a process and to the use of the herbicide / safener combinations of the invention for control of harmful plants or for growth regulation.

Description

[0001] Herbicide / safener combinations based on safeners from the class of substituted [(1,5-diphenyl-1H-1,2,4-triazol-3-yl)oxy]acetic acids and herbicides from the class of substituted cyclic diones and salts thereof Description The invention lies in the technical field of crop protection agents which can be used against undesired plant growth in cultivated land, for seed preparation or in plant crops and which contain a combination of at least one safener (A) and at least one herbicide (B), where the safener (A) corresponds to one or more substituted [(1,5-diphenyl-1H-1,2,4-triazol-3-yl)oxy]acetic acids of the general formula (I) and / or their agrochemically acceptable salts (hereinafter also component (A)).The effectiveness of known herbicides against weeds is at a high level, but generally depends on the application rate, the respective preparation form, the weed spectrum, the weeds to be controlled, the climatic and soil conditions, etc., but above all on crop compatibility. One possibility for improving the application profile of a herbicide can be to combine a safener with one or more herbicidal active ingredients that contribute the desired additional properties. However, phenomena of physical and biological incompatibility often occur when several active ingredients are used in combination, e.g. insufficient stability in a co-formulation, decomposition of an active ingredient orAntagonism of the active ingredients, or the safeners have a limited range of action, protecting the crop only against one herbicide but not against all components in the case of combined applications of several herbicides. Safeners, also called antidotes, with different chemical structures have been known for around 70 years. It is also known that they differ significantly in their protective functions, i.e., their use is limited to selected herbicides and / or the crops to be protected. In addition, it is required that a selected herbicide / safener combination does not negatively affect the herbicidal efficacy with respect to the weeds to be controlled. [(1,5-Diphenyl-1H-1,2,4-triazol-3-yl)oxy]acetic acid derivatives and their salts are known from the PCT application with the application number PCT / EP2020 / 083167 (WO2021 / 105101).Substituted cyclic diones and their salts are known, for example, from the PCT application with the application number WO2021009229. It has now been found that compounds from the class of substituted [(1,5-diphenyl-1H-1,2,4-triazol-3-yl)oxy]acetic acids can be used extremely effectively to protect various crops when applying one or more herbicides from the class of substituted cyclic diones (hereinafter referred to as component B). The herbicide / safener combinations according to the invention interact in a particularly advantageous manner, e.g., when used to combat unwanted plant growth in crops such as wheat (durum and soft wheat), maize, soybeans, sugar beet, sugar cane, cotton, rice, beans (such as, for example, bush beans and horse beans), flax, barley, oats, rye, triticale, potatoes, and sorghum.The present invention thus relates to combinations comprising one or more component(s) (A) acting as safeners and one or more herbicidally active compound(s) as component (B), where (A) is one or more compounds of the general formula (I) or their agrochemically acceptable salts, and where. (R a )p-Phenyl for groups Q-1.1 to Q-1.55

[0002] stands, R c stands for hydrogen, and R dfür Wasserstoff, Methyl, Ethyl, n-Propyl, i-Propyl, n-Butyl, n-Pentyl, Phenyl, Benzyl, CH2(4-Cl-Ph), CH2(4-F-Ph), CH2(4-OMe-Ph), 2-Methoxyethyl, Tetrahydrofuran-2-yl- methyl, Tetrahydrofuran-3-yl-methyl, Tetrahydropyran-2-yl-methyl, Tetrahydropyran-3-yl- methyl, Tetrahydropyran-4-yl-methyl, Methylpropionat-3-yl, Ethylpropionat-3-yl, Methylacetat-2-yl, Ethylacetat-2-yl, Methylpivalat-2-yl, Ethylpivalat-3-yl, Methyl-2- methylpropanoat-3-yl, Methyl-2,2-dimethylpropanoat-3-yl, Ethyl-2-methylpropanoat-3-yl, Methyl-2-propanoat-2-yl, Ethyl-2-propanoat-2-yl, Methyl-acetat-2yl, Ethyl-acetat-2yl, Methyl-1-methylcyclopropancarboxylat-2yl, Ethyl-1-methylcyclopropan-carboxylat-2yl, 2-(Dimethylamino)ethyl, Oxetan-3-yl, (3-Methyloxetan-3-yl)methyl, 2,2,2-Trifluorethyl, 2,2-Difluorethyl, 2-Fluorethyl, 2,2,3,3,3-Pentafluorpropyl, Cyclopropylmethyl, 1- Cyclopropyl-ethyl, (1-Methyl-cyclopropyl)-methyl, (2,2-Dichlorcyclopropyl)-methyl, (2,2- Dimethyl-cyclopropyl)-methyl, Allyl, Propargyl (Prop-2-in-1-yl),2-Chloroprop-2-en-1-yl, 3-Phenylprop-2-yn-1-yl, 3,3-Dichloroprop-2-en-1-yl, 3,3-Dichloro-2-fluoro-prop-2-en-1-yl, Methylprop-2-yn-1-yl, 2-Methylprop-2-en-1-yl, But-2-en-1-yl, But-3-en-1-yl, But-2-yn-1-yl, but-3-yn-1-yl, 4-chloro-but-2-yn-1-yl, 3-methyl-but-2-en-1-yl, 3-methyl-but-1-en-1-yl, 1-(2E)-1-methylbut-2-en-1-yl, (E)-pent-3-en-2-yl or (Z)-Pent-3-en-2-yl, cyclobutylmethyl, Cyclopentylmethyl, cyclohexylmethyl, heptan-2-yl, iso-butyl, 1,3-dioxolan-2-ylmethyl or 1-ethyl-5-methyl-1-pyrazol-4-methyl, and (B) represents one or more compounds of the general formula (II) or their agrochemically acceptable salts, wherein Q is selected from a group consisting of Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-11, Q-12, Q-13, Q-14, Q-15, Q-16, Q-17, Q-18, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-27, Q-28, Q-29, Q-30, Q-31 and Q-32:

[0003] where the arrow indicates the bond of the carbon atom to the residue Z and the dashed line indicates the bond of the carbon atom to the residue W; R 1 represents methyl, ethynyl, 1-propynyl, phenyl or a five- or six-membered heteroaryl ring containing one or two nitrogen atoms, where the phenyl ring and the heteroaryl ring are connected by one or two radicals R 9 can be substituted, R 2 represents chlorine, (C1-C3)-alkoxy, (C1-C2)-alkoxy-(C1-C3)-alkoxy, (C1-C2)-fluoroalkoxy, methyl, ethyl, n-propyl, n-butyl, cyclopropyl or ethynyl, R 3 represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, cyclopropyl, vinyl, ethynyl, (C1-C3)-alkoxy, (C1-C3)-fluoroalkyl, (C1-C2)-fluoroalkoxy, (C1-C2)-alkoxy-(C1-C3)-alkoxy or C1-fluoroalkoxy-(C1-C3)-alkoxy, W represents a bond, CR 4 R 5 , O, NH or N-CH3, Z represents a bond, CR 6 R 7, O, NH or N-CH3, provided that W and Z do not both represent a bond, Y represents O or NR 8 n1 and n2 independently represent 0, 1, 2 or 3, provided that n1 + n2 is equal to 2, 3, 4, 5 or 6, R 1Q3 represents hydrogen, (C1-C6)-alkyl, (C1-C6)-haloalkyl, (C1-C6)-alkoxy-(C1-C3)-alkyl or (C1-C6)-haloalkoxy-(C1-C3)-alkyl, R 2Q3 for -(CH2) k -R 3Q3 where R 3Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and - S(O)2NR 16N R 17N , and k is 0, 1 or 2, or R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 independently represent 1 or 2, R 4Q3 represents hydrogen, (C1-C6)-alkyl, hydroxy, methoxy or halogen, R 5Q3 is selected from a group consisting of -C(O)NR5N R 6N , -NR 5N R 6N and -S(O)2NR 16N R 17N , or R 4Q3 and R 5Q3 together for -(CH2) nq3 -N(R 8 )-(CH2) nq4 - where nq3 and nq4 independently represent 1 or 2, R 1Q10 and R 2Q10 are independently selected from a group consisting of hydrogen, halogen, (C1-C3)-alkyl, (C1-C3)-haloalkyl and (C1-C3)-alkoxy, Y p is selected from a group consisting of O, CR Y1 R Y2 and NR Y3 , where R Y1 represents hydrogen or (C1-C4)-alkyl, R Y2 represents hydrogen or (C1-C4)-alkyl and R Y3 is selected from a group consisting of hydrogen, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-haloalkyl, -(CO)(C1-C4)-alkyl and -(CO)(C1-C4)-haloalkyl; Y q stands for N or CH, R 4 , R 5 , R 6 and R 7independently of one another represent hydrogen, (C1-C5)-alkyl, (C2-C4)-alkenyl, (C2-C4)-alkynyl, (C1-C2)-fluoroalkyl, (C1-C3)-alkoxy-(C1-C3)-alkyl, (C1-C3)-alkylthio-(C1-C3)-alkyl, (C1-C3)-alkylsulfinyl-(C1-C3)-alkyl, (C1-C3)-alkylsulfonyl-(C1-C3)-alkyl, (C3-C4)-cycloalkyl or represent an unsubstituted 4, 5 or 6-membered monocyclic heterocyclyl ring which carries a ring heteroatom selected from the group consisting of oxygen, sulfur or nitrogen and which is attached within the heterocyclyl group to a ring carbon atom, with the proviso that not more than one of the radicals from the group R 4 , R 5 , R 6 and R 7 represents alkenyl, alkynyl, alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, cycloalkyl or heterocyclyl, or R 4 and R 5 together a group -(CH2) n3 - or -(CH2) n4 -X 1 -(CH2) n5 - form and R 6 and R 7as defined above, or R 6 and R 7 together a group -(CH2) n3 - or -(CH2) n4 -X 1 -(CH2) n5 - form and R 4 and R 5 as defined above, where X 1 for O (oxygen), S (sulfur), S(O), S(O)2, N(R 8 ), C(H)((C1-C2)-alkyl), C((C1-C2)-alkyl)2or C(H)((C1-C2)-alkoxy); n3 is 2, 3, 4 or 5, n4 and n5 independently of one another are 1, 2 or 3, provided that n4 + n5 is equal to 2, 3 or 4, or R 5 and R 6 together a group -(CH2) n6 - or -(CH2) n7 -C(R 10a )(R 10b )-(CH2) n8 - or - C(R 10c )=C(R 10d )-, where R 10a represents (C1-C2)-alkyl or (C1-C2)-alkoxy; and R 10b represents hydrogen or (C1-C2)-alkyl, provided that R 10b represents hydrogen when R 10arepresents (C1-C2)-alkoxy and wherein n6 represents 1, 2 or 3 and n7 and n8 independently represent 0, 1 or 2, with the proviso that n7 + n8 is equal to 0, 1 or 2 and wherein R 10c and R 10d independently of one another represent hydrogen or (C1-C2)-alkyl, R 8 for hydrogen, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-haloalkyl, -C(O)(C1-C4)-alkyl, -C(O)(C1-C4)-haloalkyl, -S(O) n (C1-C6)-alkyl, -S(O) n (C1-C6)-haloalkyl, -S(O) n -(CH2) n -(C3-C6)-cycloalkyl, -S(O)nC(R 11N )R 12N R 13N , -C(O)H, -C(O)-(CH2) n -(C3-C6)-cycloalkyl, -C(O)C(R 11N )R 12N R 13N , -C(O)(C2-C4)-alkenyl, -C(O)(CR 9N R 10N )CN, -C(O)(CR 9N R 10N )(CR 9N R 10N )CN, -C(O)CH2C(O)-(C1-C6)-alkyl, -C(O)CH2OC(O)-(C1-C6)-alkyl, -C(O)O(C1-C6)-alkyl, -C(O)O(C1-C6)-haloalkyl, - C(O)(CH2)nS(O) n(C1-C6)-Alkyl, -C(O)(C1-C3)-Alkoxy-(C1-C6)-alkyl, -C(O)(C1-C3)-Alkoxy-(C2- C6)-alkenyl, -C(O)(C1-C3)-Alkoxy-(C2-C6)-alkinyl, -C(O)(C1-C3)-Alkoxy-(C1-C6)-haloalkyl, - C(O)(C1-C3)-Alkoxy-(C3-C6)-cycloalkyl, -C(O)O(C1-C3)-Alkoxy-(C1-C6)-alkyl, -C(O)(C1-C3)- Alkoxy-(C1-C3)-alkoxy-(C1-C6)-alkyl, -C(O)(CH2) n NR 5N R 6N , -C(O)-(CH2) n -NR 7N C(O)R 8N , -C(O)- (CH2) n -O-N=CR 5N R 5N , -CN, -S(O)2NR 16N R 17N , -S(O)(=NR 18N )R 19N , -C(O)C(O)R 20N , - C(O)C(R 23N )=N-O-R 24N , -C(O)C(R 23N )=N-NR 25N R 26N , -(CH2) n -Phenyl, -C(O)-(CH2) n -Phenyl, - S(O) n -(CH2) n -Phenyl, Heterocyclyl, -C(O)-(CH2) n -Heterocyclyl, -C(O)(CH2) n -O-(CH2) n - Heterocyclyl, -S(O) n -(CH2) n-Heterocyclyl, wherein each heterocyclyl radical is a five- or six-membered heterocyclyl ring which may be aromatic, saturated or partially saturated and which may contain one to four heteroatoms, wherein each heteroatom is independently selected from a group consisting of oxygen, nitrogen and sulfur, and wherein heterocyclyl or phenyl rings are optionally substituted by one, two or three substituents which are independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; R 9 represents substituents which are independently selected from a group consisting of (C1-C4)alkyl, (C1-C4)haloalkyl, cyano and halogen; R 5N represents substituents which are independently selected from a group consisting of hydrogen and (C1-C6)-alkyl, R 6Nrepresents substituents which are independently selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C2-C6)-alkenyl, (C2-C6)-alkynyl, (C1-C6)-haloalkyl, hydroxy, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, -(C1-C4)-alkoxy-(C1-C6)-alkyl, -(C1-C3)-alkoxy-(C1-C6)-haloalkyl, -(CR 9N R 10N )-(C1-C6)-haloalkyl, -(CR 9N R 10N )C(O)NR 5N R 5N , -C(O)H, -C(O)-(CH2) n -(C3-C6)-cycloalkyl, -C(O)-(CH2) n -C(R 11N )R 12N R 13N , phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; or R 5N and R 6N together form -CH2CH2OCH2CH2-; and R 7Nis selected from a group consisting of hydrogen and (C1-C6)-alkyl; R 8N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 9N represents hydrogen or methyl; R 10N represents hydrogen or methyl; or R 9N and R 10N together form -CH2CH2-; and R 11N represents hydrogen or methyl; R 12N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, hydroxy and (C1-C6)-alkoxy; R 13N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, hydroxy and (C1-C6)-alkoxy; or R 12N and R 13Ntogether form -CH2-X-CH2-; and X is selected from a group consisting of O, S and NR 14N ; R 14N is selected from a group consisting of hydrogen, (C1-C3)-alkyl and (C1-C3)-alkoxy; R 16N represents hydrogen or (C1-C6)-alkyl; and R 17N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C3-C6)-cycloalkyl, (C1-C6)-alkoxy-(C1-C3)-alkyl, -C(O)(C1-C6)-alkyl, -C(O)O(C1-C6)-alkyl and CH2CN; or R 16N and R 17N together form -CH2CH2OCH2CH2-, -CH2CH2S(O)2CH2CH2-; R 18N represents hydrogen or (C1-C6)-alkyl; R 19Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 20N is selected from a group consisting of (C1-C6)alkyl, (C1-C6)haloalkyl, (C1-C6)alkoxy, (C1-C6)haloalkoxy, -NR 21N R 22N , phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; R 21Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C1-C6)-alkoxy-(C1-C3)-alkyl, (C3-C6)-cycloalkyl, (C1-C6)-haloalkyl and (C1-C6)-haloalkoxy, - C(O)(C1-C6)-alkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 22N represents hydrogen or (C1-C6)-alkyl; or R 21N and R 22N together form -CH2CH2OCH2CH2-; R 23N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-haloalkyl, (C1-C6)-alkoxy-, (C1-C6)-haloalkoxy; R 24Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy-(C1-C3)-alkyl, (C3-C6)-cycloalkyl, -CH2CN, tetrahydropyranyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 25N represents hydrogen or (C1-C6)-alkyl; R 26N represents hydrogen or (C1-C6)-alkyl; n independently represents 0, 1 or 2; G represents hydrogen, an agronomically acceptable metal, an agronomically acceptable sulfonium group, an agronomically acceptable ammonium group, a group C(X 3 )-R 14 , -C(X 4 )-X 5 -R 15 , -C(X 6 )- N(R 16 )-R 17 , -SO2-R 18 , -P(X 7 )(R 19 )-R 20 , -CH2-X8 -R 21 , (C1-C6)-alkoxy-C(O)-CH2-, (C1-C6)-alkoxy- C(O)-CH=CH-, (C2-C7)-alken-1-yl-CH2-, (C2-C7)-alken-1-yl-CH[(C1-C2)-alkyl]-, (C2-C4)-fluoroalken-1-yl-CH2-, (C2-C7)-alkyn-1-yl-CH2-, (C2-C7)-alkyn-1-yl-CH[(C1-C2)-alkyl]-, heteroaryl-CH2-, heteroaryl-CH[(C1-C2)-alkyl]-, phenyl-CH2-, phenyl-CH[(C1-C2)-alkyl]-, phenyl-C(O)-CH2- stands, whereby the phenyl or heteroaryl group optionally continues is independently substituted by 1, 2 or 3 groups selected from (C1-C2)-alkyl, C1-fluoroalkyl, (C1-C2)-alkoxy, C1-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, X 3 , X 4 , X 5 , X 6 , X 7 and X 8 independently represent O (oxygen) and S (sulfur), R 14 for hydrogen, (C1-C 21 )-alkyl, (C2-C 21 )-alkenyl, (C2-C 18 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1- C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)- alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio- (C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, R, 15 for (C1-C 18 )-alkyl, (C3-C 18 )-alkenyl, (C3-C 18 )-alkynyl, (C2-C 10 )-fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C10 )-Nitroalkyl, (C2-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, R, 16 and R 17 independently of each other for hydrogen, (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )- alkynyl, (C2-C10 )-Fluoralkyl, (C1-C 10 )-Cyanoalkyl, (C1-C 10 )-Nitroalkyl, (C1-C 10)-Aminoalkyl, (C1- C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)- alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1- C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)- Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)-Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1- C5)-alkyl, (C1-C5)-Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylaminocarbonyl-(C1-C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylcarbonylamino-(C1-C5)-alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1-C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)- FluoralkyI, (C1-C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1- C3)-Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl,(C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, Diphenylamino or diphenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, (C3-C7)-cycloalkylamino, di-[(C3-C7)-cycloalkyl]amino, (C3-C7)-cycloalkoxy; or R, 16 and R 17, together with the nitrogen atom to which they are attached, form an unsubstituted 4- to 7-membered ring, which optionally comprises a heteroatom from the group O (oxygen) and S (sulfur), R 18 for (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl,(C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diphenylamino or diphenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, (C3-C7)-cycloalkylamino, di-[(C3-C7)-cycloalkyl]amino, (C3-C7)-cycloalkoxy, (C1-C, 10 )-alkoxy, (C1-C 10)-fluoroalkoxy, (C3-C7)-alkylamino, di-[(C3-C7)-alkyl]amino; R 19 and R 20 independently for (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )-alkynyl, (C1-C 10 )- fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)- Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)- alkyl, (C1-C5)-Alkylthio-(C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)- Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)-Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1- C5)-alkyl, (C1-C5)-Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylaminocarbonyl-(C1-C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylcarbonylamino-(C1-C5)-alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1-C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)- FluoralkyI, (C1-C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1- C3)-Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl,(C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, Diphenylamino or diphenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, benzyloxy and phenyloxy, wherein the respective phenyl group is optionally further substituted independently by 1,2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, and R, 21 for (C1-C 10 )-alkyl, (C3-C 10 )-alkenyl, (C3-C 10 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C2-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, phenoxy-(C1-C5)-alkyl, wherein the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, heteroaryloxy-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro,Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenyl-C(=O), where the phenyl group is optionally further independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro. Surprisingly, it has been shown that although the aforementioned herbicide structures are significantly more potent in their herbicidal activity than other herbicides,Nevertheless, a high protective effect is achieved through the use of the safeners according to the invention. In this respect, the herbicide structures according to the invention are highly effective and also break resistance in certain weeds, yet are safe for use on crop plants. With regard to the compounds according to the invention, the designations used above and below are explained. These are familiar to the person skilled in the art and have, in particular, the meanings explained below: If the above-mentioned variables "W" or "Z" represent a bond, this means that in the general formula (II) or in the formula (II-1) derived therefrom, the structural element Q is directly bonded to the carbon atom that is connected to Q via "W" or "Z". In general, the designation of chemical groups means that the bond to the backbone or the remainder of the molecule is via the last-mentioned structural element of the chemical group in question.i.e., for example, in the case of (C2-C8)-alkenyloxy, the bond is formed via the oxygen atom, and in the case of heterocyclyl-(C1-C8)-alkyl or (C1-C6)-alkoxy-(C1-C6)-alkoxy-(C1-C6)-alkyl, the bond is formed via the C atom of the alkyl group. In the case of bonds to the rest of the molecule marked with a "-", the bond is not formed via the last-mentioned structural element but via the structural motif directly adjacent to the bond symbol "-". Example: In the case of -(CO)(C1-C6)-alkoxy-(C1-C6)-alkyl, the bond is formed via the carbonyl group and not via the (C1-C6)-alkyl group, hence the bond line. According to the invention, “alkylthio” - alone or as part of a chemical group - stands for straight-chain or branched S-alkyl, preferably having 1 to 8, or having 1 to 6 carbon atoms, such as (C1-C, 10)-, (C1-C6)- oder (C1-C4)-Alkylthio, z.B. (aber nicht beschränkt auf) (C1- C6)-Alkylthio wie Methylthio, Ethylthio, Propylthio, 1-Methylethylthio, Butylthio, 1-Methylpropylthio, 2-Methylpropylthio, 1,1-Dimethylethylthio, Pentylthio, 1-Methylbutylthio, 2-Methylbutylthio, 3- Methylbutylthio, 1,1-Dimethylpropylthio, 1,2-Dimethylpropylthio, 2,2-Dimethylpropylthio, 1- Ethylpropylthio, Hexylthio, 1-Methylpentylthio, 2-Methylpentylthio, 3-Methylpentylthio, 4-Methyl- pentylthio, 1,1-Dimethylbutylthio, 1,2-Dimethylbutylthio, 1,3-Dimethylbutylthio, 2,2-Dimethylbutyl- thio, 2,3-Dimethylbutylthio, 3,3-Dimethylbutylthio, 1-Ethylbutylthio, 2-Ethylbutylthio, 1,1,2-Tri- methylpropylthio, 1,2,2-Trimethylpropylthio, 1-Ethyl-1-methylpropylthio und 1-Ethyl-2-methyl- propylthio. „Alkoxy“ bedeutet ein über ein Sauerstoffatom gebundenen Alkylrest, z. B.(but not limited to) (C1-C6) alkoxy such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1,1-dimethylethoxy, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-Trimethylpropoxy, 1,2,2-Trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy. Alkenyloxy means an alkenyl radical bonded via an oxygen atom, alkynyloxy means an alkynyl radical bonded via an oxygen atom such as (C2-C6). 10 )-, (C2-C6)- or (C2-C4)-alkenoxy or (C3-C 10)-, (C3-C6)- or (C3-C4)-alkynoxy. “Alkylcarbonyl” (alkyl-C(=O)-), unless defined otherwise elsewhere, represents alkyl radicals which are bonded to the skeleton via -C(=O)-, such as (C1-C 10 ), (C1-C6) or (C1-C4) alkylcarbonyl. The number of C atoms refers to the alkyl radical in the alkylcarbonyl group. “Alkoxycarbonyl (alkyl-OC(=O)-)”, unless defined otherwise elsewhere: Alkyl radicals that are bonded to the skeleton via -OC(=O)-, such as (C1-C 10 )-, (C1-C6)- or (C1-C4)-alkoxycarbonyl. The number of C atoms refers to the alkyl radical in the alkoxycarbonyl group. Analogously, "alkenyloxycarbonyl" and "alkynyloxycarbonyl", unless defined otherwise elsewhere, represent alkenyl or alkynyl radicals, respectively, which are bonded to the skeleton via -OC(=O)-, such as (C2-C 10 )-, (C2-C6)- or (C2-C4)-alkenyloxycarbonyl or (C3-C 10), (C3-C6) or (C3-C4) alkynyloxycarbonyl. The number of C atoms refers to the alkenyl or alkynyl radical in the alkene or alkynyloxycarbonyl group. The term "alkylcarbonyloxy" (alkyl-C(=O)-O-) stands for alkyl radicals which are bonded to the skeleton via a carbonyloxy group (-C(=O)-O-), such as (C1-C 10 )-, (C1-C6)- or (C1-C4)-alkylcarbonyloxy. The number of C atoms refers to the alkyl radical in the alkylcarbonyloxy group. In abbreviations such as C(O)R 13 , C(O)OR 13 , OC(O)NR 11 R 12 , or C(O)NR 11 R 12 The abbreviation O in parentheses stands for an oxygen atom bonded to the adjacent carbon atom via a double bond. In abbreviations such as OC(S)OR 13 , OC(S)SR 14 , OC(S)NR 11 R 12, the abbreviation S in parentheses stands for a sulfur atom bonded to the adjacent carbon atom via a double bond. The term “aryl” means an optionally substituted mono-, bi- or polycyclic aromatic system having preferably 6 to 14, in particular 6 to 10 ring C atoms, for example phenyl, naphthyl, anthryl, phenanthrenyl, and the like, preferably phenyl. The term “optionally substituted aryl” also includes multicyclic systems such as tetrahydronaphthyl, indenyl, indanyl, fluorenyl, biphenylyl, where the bonding site is on the aromatic system. From a systematic point of view, “aryl” is generally also included in the term “optionally substituted phenyl”. Preferred aryl substituents here are, for example, hydrogen, halogen, alkyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, halocycloalkyl, alkenyl, alkynyl, aryl, arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heterocyclyl, heterocyclylalkyl, alkoxyalkyl,Alkylthio, Haloalkylthio, Haloalkyl, Alkoxy, Haloalkoxy, Cycloalkoxy, Cycloalkylalkoxy, Aryloxy, Heteroraryloxy, Alkoxyalkoxy, Alkinylalkoxy, Alkenyloxy, Bis-alkylaminoalkoxy, Tris- [alkyl]silyl, Bis-[alkyl]arylsilyl, Bis-[alkyl]alkylsilyl, Tris-[alkyl]silylalkinyl, Arylalkinyl, Heteroarylalkinyl, Alkylalkinyl, Cycloalkylalkinyl, Haloalkylalkinyl, Heterocyclyl-N-alkoxy, Nitro, Cyano, Amino, Alkylamino, Bis-alkylamino, Alkylcarbonylamino, Cycloalkylcarbonylamino, Arylcarbonylamino, Alkoxycarbonylamino, Alkoxycarbonylalkylamino, Arylalkoxycarbonylalkylamino, Hydroxycarbonyl, Alkoxycarbonyl, Aminocarbonyl, Alkylaminocarbonyl, Cycloalkylaminocarbonyl, Bis-Alkylaminocarbonyl, Heteroarylalkoxy, Arylalkoxy. Ein heterocyclischer Rest (Heterocyclyl) enthält mindestens einen heterocyclischen Ring (=carbocyclischer Ring, in dem mindestens ein C-Atom durch ein Heteroatom ersetzt ist, vorzugsweise durch ein Heteroatom aus der Gruppe N, O, S, P) der gesättigt, ungesättigt,is partially saturated or heteroaromatic and may be unsubstituted or substituted, where the bonding site is located on a ring atom. If the heterocyclyl radical or the heterocyclic ring is optionally substituted, it may be fused with other carbocyclic or heterocyclic rings. In the case of optionally substituted heterocyclyl, polycyclic systems are also included, such as, for example, 8-aza-bicyclo[3.2.1]octanyl, 8-aza-bicyclo[2.2.2]octanyl or 1-aza-bicyclo[2.2.1]heptyl. In the case of optionally substituted heterocyclyl, spirocyclic systems are also included, such as, for example, 1-oxa-5-aza-spiro[2.3]hexyl. Unless otherwise defined, the heterocyclic ring preferably contains 3 to 9 ring atoms, in particular 3 to 6 ring atoms, and one or more, preferably 1 to 4, in particular 1, 2 or 3 heteroatoms in the heterocyclic ring, preferably from the group N, O, and S,however, two oxygen atoms should not be directly adjacent, such as, for example, with a heteroatom from the group N, O and S 1- or 2- or 3-pyrrolidinyl, 3,4-dihydro-2H-pyrrol-2- or 3-yl, 2,3-dihydro-1H-pyrrol- 1- or 2- or 3- or 4- or 5-yl; 2,5-dihydro-1H-pyrrol-1- or 2- or 3-yl, 1- or 2- or 3- or 4-piperidinyl; 2,3,4,5-tetrahydropyridin-2- or 3- or 4- or 5-yl or 6-yl; 1,2,3,6-tetrahydropyridin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,2,3,4-Tetrahydropyridin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,4-Dihydropyridin-1- or 2- or 3- or 4-yl; 2,3-Dihydropyridin- 2- or 3- or 4- or 5- or 6-yl; 2,5-Dihydropyridin-2- or 3- or 4- or 5- or 6-yl, 1- or 2- or 3- or 4-azepanyl; 2,3,4,5-Tetrahydro-1H-azepin-1- or 2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-Tetrahydro-1H-azepin-1- or 2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-Tetrahydro-1H-azepin-1- or 2- or 3- or 4-yl; 3,4,5,6-Tetrahydro-2H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5-Dihydro-1H-azepin-1- or 2- or 3- or 4-yl; 2,5-Dihydro-1H-azepin- 1- or -2- or 3- or 4- or 5- or 6- or 7-yl; 2,7-Dihydro-1H-azepin-1- or -2- or 3- or 4- yl; 2,3-Dihydro-1H-azepin-1- or -2- or 3- or 4- or 5- or 6- or 7-yl; 3,4-Dihydro-2H-azepin- 2- or 3- or 4- or 5- or 6- or 7-yl; 3,6-Dihydro-2H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 5,6-Dihydro-2H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5-Dihydro-3H-azepin- 2- or 3- or 4- or 5- or 6- or 7-yl; 1H-azepin-1- or -2- or 3- or 4- or 5- or 6- or 7-yl; 2H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 3H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4H-azepine-2- or 3- or 4- or 5- or 6- or 7-yl, 2- or 3-oxolanyl (= 2- or 3-tetrahydrofuranyl); 2,3-dihydrofuran-2- or 3- or 4- or 5-yl; 2,5-dihydrofuran-2- or 3-yl,2- or 3- or 4-oxanyl (= 2- or 3- or 4-tetrahydropyranyl); 3,4-dihydro-2H-pyran-2- or 3- or 4- or 5- or 6-yl; 3,6-dihydro-2H-pyran-2- or 3- or 4- or 5- or 6-yl; 2H-pyran-2- or 3- or 4- or 5- or 6-yl; 4H-pyran-2- or 3- or 4-yl, 2- or 3- or 4-oxepanyl; 2,3,4,5-tetrahydrooxepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-Tetrahydrooxepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-Tetrahydrooxepin-2- or 3- or 4-yl; 2,3-Dihydrooxepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5-Dihydrooxepin-2- or 3- or 4-yl; 2,5-Dihydrooxepin-2- or 3- or 4- or 5- or 6- or 7-yl; Oxepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2- or 3-Tetrahydrothiophenyl; 2,3-Dihydrothiophene-2- or 3- or 4- or 5-yl; 2,5-Dihydrothiophen-2- or 3-yl; tetrahydro-2H-thiopyran-2- or 3- or 4-yl; 3,4-Dihydro-2H-thiopyran-2- or 3- or 4- or 5- or 6-yl; 3,6-Dihydro-2H-thiopyran-2- or 3- or 4- or 5- or 6-yl; 2H-thiopyran-2- or 3- or 4- or 5- or 6-yl; 4H-thiopyran-2- or 3- or 4-yl. Preferred 3-membered and 4-membered ring heterocycles are, for example, 1- or 2-aziridinyl, oxiranyl, thiiranyl, 1- or 2- or 3-azetidinyl, 2- or 3-oxetanyl, 2- or 3-thietanyl, and 1,3-dioxetan-2-yl. Further examples of “heterocyclyl” are a partially or fully hydrogenated heterocyclic radical having two heteroatoms from the group consisting of N, O, and S, such as, for example, 1- or 2- or 3- or 4-pyrazolidinyl; 4,5-Dihydro-3H-pyrazol- 3- or 4- or 5-yl; 4,5-Dihydro-1H-pyrazol-1- or 3- or 4- or 5-yl; 2,3-Dihydro-1H-pyrazol-1- or 2- or 3- or 4- or 5-yl; 1- or 2- or 3- or 4- imidazolidinyl; 2,3-Dihydro-1H-imidazol-1- or 2- or 3- or 4-yl; 2,5-Dihydro-1H-imidazol-1- or 2- or 4- or 5-yl; 4,5-Dihydro-1H-imidazol-1- or 2- or 4- or 5-yl; Hexahydropyridazin-1- or 2- or 3- or 4-yl; 1,2,3,4-Tetrahydropyridazin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,2,3,6-Tetrahydropyridazin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,4,5,6-Tetrahydropyridazin-1- or 3- or 4- or 5- or 6-yl; 3,4,5,6-Tetrahydropyridazin-3- or 4- or 5-yl; 4,5-Dihydropyridazin-3- or 4-yl; 3,4-Dihydropyridazin-3- or 4- or 5- or 6-yl; 3,6-Dihydropyridazin-3- or 4-yl; 1,6-Dihydropyriazin-1- or 3- or 4- or 5- or 6-yl; Hexahydropyrimidin-1- or 2- or 3- or 4-yl; 1,4,5,6-Tetrahydropyrimidin-1- or 2- or 4- or 5- or 6-yl; 1,2,5,6-Tetrahydropyrimidin-1- or 2- or 4- or 5- or 6-yl; 1,2,3,4-Tetrahydropyrimidin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,6-Dihydropyrimidin-1- or 2- or 4- or 5- or 6-yl; 1,2-Dihydropyrimidin-1- or 2- or 4- or 5- or 6-yl; 2,5-Dihydropyrimidin- 2- or 4- or 5-yl; 4,5-Dihydropyrimidin- 4- or 5- or 6-yl; 1,4-Dihydropyrimidin-1- or 2- or 4- or 5- or 6-yl; 1- or 2- or 3-Piperazinyl; 1,2,3,6-Tetrahydropyrazin-1- or 2- or 3- or 5- or 6-yl; 1,2,3,4-Tetrahydropyrazin-1- or 2- or 3- or 4- or 5- or 6-yl; 1,2-Dihydropyrazin-1- or 2- or 3- or 5- or 6-yl; 1,4-Dihydropyrazin-1- or 2- or 3-yl; 2,3-Dihydropyrazin-2- or 3- or 5- or 6-yl; 2,5-Dihydropyrazin-2- or 3-yl; 1,3-Dioxolan-2- or 4- or 5-yl; 1,3-Dioxol-2- or 4-yl; 1,3-Dioxan-2- or 4- or 5-yl; 4H-1,3-dioxin-2- or 4- or 5- or 6-yl; 1,4-dioxan-2- or 3- or 5- or 6-yl; 2,3-dihydro-1,4-dioxin-2- or 3- or 5- or 6-yl; 1,4-dioxin-2- or 3-yl; 1,2-dithiolan-3- or 4-yl; 3H-1,2-dithiol-3- or 4- or 5-yl; 1,3-dithiolan-2- or 4-yl; 1,3-dithiol- 2- or 4-yl; 1,2-dithian-3- or 4-yl; 3,4-dihydro-1,2-dithiin-3- or 4- or 5- or 6-yl; 3,6-Dihydro- 1,2-dithiin-3- or 4-yl; 1,2-dithiin-3- or 4-yl; 1,3-dithian-2- or 4- or 5-yl; 4H-1,3-dithiin-2- or 4- or 5- or 6-yl; isoxazolidin-2- or 3- or 4- or 5-yl; 2,3-Dihydroisoxazol-2- or 3- or 4- or 5-yl; 2,5-Dihydroisoxazol-2- or 3- or 4- or 5-yl; 4,5-Dihydroisoxazol-3- or 4- or 5-yl; 1,3-Oxazolidin-2- or 3- or 4- or 5-yl; 2,3-Dihydro-1,3-oxazol-2- or 3- or 4- or 5-yl; 2,5-Dihydro-1,3-oxazol-2- or 4- or 5-yl; 4,5-Dihydro-1,3-oxazol-2- or 4- or 5-yl; 1,2-Oxazinan-2- or 3- or 4- or 5- or 6-yl; 3,4-Dihydro-2H-1,2-oxazin-2- or 3- or 4- or 5- or 6-yl; 3,6-Dihydro-2H-1,2-oxazin-2- or 3- or 4- or 5- or 6-yl; 5,6-Dihydro-2H-1,2-oxazin-2- or 3- or 4- or 5- or 6-yl; 5,6-Dihydro-4H-1,2-oxazin-3- or 4- or 5- or 6-yl; 2H-1,2-oxazin-2- or 3- or 4- or 5- or 6-yl; 6H-1,2-oxazin-3- or 4- or 5- or 6-yl; 4H-1,2-oxazin-3- or 4- or 5- or 6-yl; 1,3-Oxazinan-2- or 3- or 4- or 5- or 6-yl; 3,4-Dihydro-2H-1,3-oxazin-2- or 3- or 4- or 5- or 6-yl; 3,6-Dihydro-2H-1,3-oxazin-2- or 3- or 4- or 5- or 6-yl; 5,6-Dihydro-2H-1,3-oxazin-2- or 4- or 5- or 6-yl; 5,6-dihydro-4H-1,3-oxazin-2- or 4- or 5- or 6-yl; 2H-1,3-oxazin-2- or 4- or 5- or 6-yl; 6H-1,3-oxazin-2- or 4- or 5- or 6-yl; 4H-1,3-oxazin-2- or 4- or 5- or 6-yl; morpholin-2- or 3- or 4-yl; 3,4-dihydro-2H-1,4-oxazin-2- or 3- or 4- or 5- or 6-yl; 3,6-dihydro-2H-1,4-oxazin-2- or 3- or 5- or 6-yl; 2H-1,4-oxazin-2- or 3- or 5- or 6-yl; 4H-1,4-oxazin-2- or 3-yl; 1,2-oxazepan-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,5-tetrahydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-tetrahydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-tetrahydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5,6,7-Tetrahydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5,6,7-Tetrahydro-1,2-oxazepin-3- or 4- or 5- or 6- or 7-yl; 2,3-Dihydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5-Dihydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,7-dihydro-1,2-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5-dihydro-1,2-oxazepin-3- or 4- or 5- or 6- or 7-yl; 4,7-dihydro-1,2-oxazepin-3- or 4- or 5- or 6- or 7-yl; 6,7-dihydro-1,2-oxazepin-3- or 4- or 5- or 6- or 7-yl; 1,2-oxazepin-3- or 4- or 5- or 6- or 7-yl; 1,3-Oxazepan-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,5-Tetrahydro-1,3-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-Tetrahydro-1,3-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-Tetrahydro-1,3-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5,6,7-Tetrahydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 4,5,6,7-Tetrahydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 2,3-Dihydro-1,3-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5-Dihydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 2,7-Dihydro-1,3-oxazepin- 2- or 4- or 5- or 6- or 7-yl; 4,5-dihydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 4,7-dihydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 6,7-dihydro-1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 1,3-oxazepin-2- or 4- or 5- or 6- or 7-yl; 1,4-oxazepan-2- or 3- or 5- or 6- or 7-yl; 2,3,4,5-Tetrahydro-1,4-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-Tetrahydro-1,4-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-Tetrahydro-1,4-oxazepin- 2- or 3- or 5- or 6- or 7-yl; 2,5,6,7-Tetrahydro-1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; 4,5,6,7-Tetrahydro-1,4-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3-Dihydro-1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; 2,5-Dihydro-1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; 2,7-Dihydro-1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; 4,5-Dihydro-1,4-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 4,7-Dihydro-1,4-oxazepin-2- or 3- or 4- or 5- or 6- or 7-yl; 6,7-dihydro-1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; 1,4-oxazepin-2- or 3- or 5- or 6- or 7-yl; isothiazolidin-2- or 3- or 4- or 5-yl; 2,3-dihydroisothiazol-2- or 3- or 4- or 5-yl; 2,5-dihydroisothiazol-2- or 3- or 4- or 5-yl; 4,5-dihydroisothiazol-3- or 4- or 5-yl; 1,3-thiazolidin-2- or 3- or 4- or 5-yl; 2,3-Dihydro-1,3-thiazol-2- or 3- or 4- or 5-yl; 2,5-Dihydro-1,3-thiazol-2- or 4- or 5-yl; 4,5-Dihydro-1,3-thiazol-2- or 4- or 5-yl; 1,3-Thiazinan-2- or 3- or 4- or 5- or 6-yl; 3,4-Dihydro-2H-1,3-thiazin-2- or 3- or 4- or 5- or 6-yl; 3,6-Dihydro-2H-1,3-thiazin-2- or 3- or 4- or 5- or 6-yl; 5,6-Dihydro-2H-1,3-thiazin-2- or 4- or 5- or 6-yl; 5,6-Dihydro-4H-1,3-thiazin-2- or 4- or 5- or 6-yl; 2H-1,3-thiazin-2- or 4- or 5- or 6-yl; 6H-1,3-thiazin-2- or 4- or 5- or 6-yl; 4H-1,3-Thiazin-2- or 4- or 5- or 6-yl. Further examples of “heterocyclyl” are a partially or fully hydrogenated heterocyclic radical with 3 heteroatoms from the group N, O and S, such as, for example, 1,4,2-dioxazolidin-2- or 3- or 5-yl; 1,4,2-dioxazol-3- or 5-yl; 1,4,2-dioxazinan-2- or -3- or 5- or 6-yl; 5,6-dihydro-1,4,2-dioxazin-3- or 5- or 6-yl; 1,4,2-dioxazin-3- or 5- or 6-yl; 1,4,2-dioxazepan-2- or 3- or 5- or 6- or 7-yl; 6,7-Dihydro-5H-1,4,2-dioxazepin-3- or 5- or 6- or 7-yl; 2,3-Dihydro-7H-1,4,2-dioxazepin-2- or 3- or 5- or 6- or 7-yl; 2,3-Dihydro-5H-1,4,2-dioxazepin-2- or 3- or 5- or 6- or 7-yl; 5H-1,4,2-dioxazepin-3- or 5- or 6- or 7-yl; 7H-1,4,2-dioxazepin-3- or 5- or 6- or 7-yl. Structural examples of optionally further substituted heterocycles are also listed below:

[0004] Die oben aufgeführten Heterocyclen sind bevorzugt beispielsweise durch Wasserstoff, Halogen, Alkyl, Haloalkyl, Hydroxy, Alkoxy, Cycloalkoxy, Aryloxy, Alkoxyalkyl, Alkoxyalkoxy, Cycloalkyl, Halocycloalkyl, Aryl, Arylalkyl, Heteroaryl, Heterocyclyl, Alkenyl, Alkylcarbonyl, Cycloalkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, Alkoxycarbonyl, Hydroxycarbonyl, Cycloalkoxycarbonyl, Cycloalkylalkoxycarbonyl, Alkoxycarbonylalkyl, Arylalkoxycarbonyl, Arylalkoxycarbonylalkyl, Alkinyl, Alkinylalkyl, Alkylalkinyl, Tris-alkylsilylalkinyl, Nitro, Amino, Cyano, Haloalkoxy, Haloalkylthio, Alkylthio, Hydrothio, Hydroxyalkyl, Oxo, Heteroarylalkoxy, Arylalkoxy, Heterocyclylalkoxy, Heterocyclylalkylthio, Heterocyclyloxy, Heterocyclylthio, Heteroaryloxy, Bis- alkylamino, Alkylamino, Cycloalkylamino, Hydroxycarbonylalkylamino, Alkoxycarbonylalkylamino, Arylalkoxycarbonylalkylamino, Alkoxycarbonylalkyl(alkyl)amino, Aminocarbonyl, Alkylaminocarbonyl, Bis-alkylaminocarbonyl, Cycloalkylaminocarbonyl,Hydroxycarbonylalkylaminocarbonyl, alkoxycarbonylalkylaminocarbonyl, arylalkoxycarbonylalkylaminocarbonyl. If a basic structure is substituted "by one or more residues" from a list of residues (= group) or a generically defined group of residues, this includes simultaneous substitution by several identical and / or structurally different residues. If it is a partially or fully saturated nitrogen heterocycle, it can be linked to the rest of the molecule via both the carbon and the nitrogen atom. Possible substituents for a substituted heterocyclic residue are the substituents listed below:Additionally, oxo and thioxo are also included. The oxo group as a substituent on a ring C atom then means, for example, a carbonyl group in the heterocyclic ring. This preferably also includes lactones and lactams. The oxo group can also occur on the hetero ring atoms, which can exist in different oxidation states, e.g., N and S, and then forms, for example, the divalent groups N(O), S(O) (also abbreviated to SO) and S(O)2 (also abbreviated to SO2) in the heterocyclic ring. In the case of -N(O)- and -S(O)- groups, both enantiomers are included. According to the invention, the term "heteroaryl" stands for heteroaromatic compounds, i.e., fully unsaturated aromatic heterocyclic compounds, preferably 5- to 7-membered rings with 1 to 4, preferably 1 or 2 identical or different heteroatoms, preferably O,S oder N. Erfindungsgemäße Heteroaryle sind beispielsweise 1H-Pyrrol-1-yl; 1H-Pyrrol-2-yl; 1H-Pyrrol- 3-yl; Furan-2-yl; Furan-3-yl; Thien-2-yl; Thien-3-yl, 1H-Imidazol-1-yl; 1H-Imidazol-2-yl; 1H-Imidazol- 4-yl; 1H-Imidazol-5-yl; 1H-Pyrazol-1-yl; 1H-Pyrazol-3-yl; 1H-Pyrazol-4-yl; 1H-Pyrazol-5-yl, 1H-1,2,3- Triazol-1-yl, 1H-1,2,3-Triazol-4-yl, 1H-1,2,3-Triazol-5-yl, 2H-1,2,3-Triazol-2-yl, 2H-1,2,3-Triazol-4-yl, 1H-1,2,4-Triazol-1-yl, 1H-1,2,4-Triazol-3-yl, 4H-1,2,4-Triazol-4-yl, 1,2,4-Oxadiazol-3-yl, 1,2,4- Oxadiazol-5-yl, 1,3,4-Oxadiazol-2-yl, 1,2,3-Oxadiazol-4-yl, 1,2,3-Oxadiazol-5-yl, 1,2,5-Oxadiazol-3-yl, Azepinyl, Pyridin-2-yl, Pyridin-3-yl, Pyridin-4-yl, Pyrazin-2-yl, Pyrazin-3-yl, Pyrimidin-2-yl, Pyrimidin-4-yl, Pyrimidin-5-yl, Pyridazin-3-yl, Pyridazin-4-yl, 1,3,5-Triazin-2-yl, 1,2,4-Triazin-3-yl, 1,2,4-Triazin-5-yl, 1,2,4-Triazin-6-yl, 1,2,3-Triazin-4-yl, 1,2,3-Triazin-5-yl, 1,2,4-, 1,3,2-, 1,3,6- und 1,2,6-Oxazinyl, Isoxazol-3-yl, Isoxazol-4-yl, Isoxazol-5-yl, 1,3-Oxazol-2-yl,1,3-oxazol-4-yl, 1,3-oxazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl, 1,3-thiazol-2-yl, 1,3-thiazol-4-yl, 1,3-thiazol-5-yl, oxepinyl, thiepinyl, 1,2,4-triazolonyl and 1,2,4-diazepinyl, 2H-1,2,3,4-tetrazol-5-yl, 1H-1,2,3,4-tetrazol-5-yl, 1,2,3,4-oxatriazol-5-yl, 1,2,3,4-thiatriazol-5-yl, 1,2,3,5-oxatriazol-4-yl, 1,2,3,5-Thiatriazol-4-yl. The heteroaryl groups according to the invention can further be substituted by one or more identical or different radicals. If two adjacent carbon atoms are part of another aromatic ring, these are fused heteroaromatic systems, such as benzofused or multiply fused heteroaromatics. Preferred examples are quinolines (e.g., quinolin-2-yl, quinolin-3-yl, quinolin-4-yl, quinolin-5-yl, quinolin-6-yl, quinolin-7-yl, quinolin-8-yl); isoquinolines (e.g., isoquinolin-1-yl, isoquinolin-3-yl, isoquinolin-4-yl, isoquinolin-5-yl, isoquinolin-6-yl, isoquinolin-7-yl,Isochinolin-8-yl); Chinoxalin; Chinazolin; Cinnolin; 1,5-Naphthyridin; 1,6-Naphthyridin; 1,7-Naphthyridin; 1,8-Naphthyridin; 2,6- Naphthyridin; 2,7-Naphthyridin; Phthalazin; Pyridopyrazine; Pyridopyrimidine; Pyridopyridazine; Pteridine; Pyrimidopyrimidine. Beispiele für Heteroaryl sind auch 5- oder 6-gliedrige benzokondensierte Ringe aus der Gruppe 1H-Indol-1-yl, 1H-Indol-2-yl, 1H-Indol-3-yl, 1H-Indol-4-yl, 1H-Indol-5-yl, 1H- Indol-6-yl, 1H-Indol-7-yl, 1-Benzofuran-2-yl, 1-Benzofuran-3-yl, 1-Benzofuran-4-yl, 1-Benzofuran-5- yl, 1-Benzofuran-6-yl, 1-Benzofuran-7-yl, 1-Benzothiophen-2-yl, 1-Benzothiophen-3-yl, 1-Benzo- thiophen-4-yl, 1-Benzothiophen-5-yl, 1-Benzothiophen-6-yl, 1-Benzothiophen-7-yl, 1H-Indazol-1-yl, 1H-Indazol-3-yl, 1H-Indazol-4-yl, 1H-Indazol-5-yl, 1H-Indazol-6-yl, 1H-Indazol-7-yl, 2H-Indazol-2-yl, 2H-Indazol-3-yl, 2H-Indazol-4-yl, 2H-Indazol-5-yl, 2H-Indazol-6-yl, 2H-Indazol-7-yl, 2H-Isoindol-2- yl, 2H-Isoindol-1-yl, 2H-Isoindol-3-yl, 2H-Isoindol-4-yl, 2H-Isoindol-5-yl,2H-isoindol-6-yl; 2H-Isoindol-7-yl, 1H-Benzimidazol-1-yl, 1H-Benzimidazol-2-yl, 1H-Benzimidazol-4-yl, 1H-Benzimidazol-5-yl, 1H-Benzimidazol-6-yl, 1H-Benzimidazol-7-yl, 1,3-Benzoxazol-2-yl, 1,3-Benzoxazol-4-yl, 1,3-Benzoxazol-5-yl, 1,3-Benzoxazol-6-yl, 1,3-Benzoxazol-7-yl, 1,3-Benzthiazol-2-yl, 1,3-Benzthiazol-4-yl, 1,3-Benzthiazol-5-yl, 1,3-Benzthiazol-6-yl, 1,3-Benzthiazol-7-yl, 1,2-Benzisoxazol-3-yl, 1,2- Benzisoxazol-4-yl, 1,2-benzisoxazol-5-yl, 1,2-benzisoxazol-6-yl, 1,2-benzisoxazol-7-yl, 1,2-benzisothiazol-3-yl, 1,2-benzisothiazol-4-yl, 1,2-benzisothiazol-5-yl, 1,2-benzisothiazol-6-yl, 1,2-benzisothiazol-7-yl. The term "halogen" means, for example, fluorine, chlorine, bromine, or iodine. If the term is used for a radical, then "halogen" means, for example, a fluorine, chlorine, bromine, or iodine atom. According to the invention, "alkyl" means a straight-chain or branched, open-chain, saturated hydrocarbon radical,which is optionally mono- or polysubstituted and in the latter case is referred to as “substituted alkyl”. Preferred substituents are halogen atoms, alkoxy, haloalkoxy, cyano, alkylthio, haloalkylthio, amino or nitro groups, particular preference being given to methoxy, methyl, fluoroalkyl, cyano, nitro, fluorine, chlorine, bromine or iodine. The prefix “bis” also includes the combination of different alkyl radicals, e.g. methyl(ethyl) or ethyl(methyl). “Haloalkyl”, “-alkenyl” and “-alkynyl” mean alkyl, alkenyl or alkynyl which is partially or fully substituted by identical or different halogen atoms, e.g. monohaloalkyl (= monohaloalkyl) such as, for example, CH2CH2Cl, CH2CH2Br, CHClCH3, CH2Cl, CH2F; perhaloalkyl such as, for example, B. CCl3, CClF2, CFCl2, CF2CClF2, CF2CClFCF3; Polyhaloalkyl such as B. CH2CHFCl, CF2CClFH, CF2CBrFH,CH2CF3; The term "haloalkyl" also includes the term "fluoroalkyl." The term "perhaloalkyl" also includes the term "perfluoroalkyl." "Haloalkoxy" is, for example, OCF3, OCHF2, OCH2F, OCF2CF3, OCH2CF3, and OCH2CH2Cl; the same applies to haloalkenyl and other halogen-substituted radicals. The term "(C1-C5)-alkyl" used here as an example is a shorthand notation for straight-chain or branched alkyl with one to five carbon atoms, corresponding to the range specified for C atoms, i.e., it includes, for example, the radicals methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methylpropyl, tert-butyl, 1-pentyl, 2-methylbut-1-yl, 3-methylbut-1-yl, and 2,2-dimethylprop-1-yl. General alkyl radicals with a larger specified range of C atoms, e.g., "(C1-C6)-alkyl," correspondingly also include straight-chain or branched alkyl radicals with a larger number of C atoms, i.e., according to the example, also the alkyl radicals with 5 and 6 C atoms. Unless specifically stated,For hydrocarbon radicals such as alkyl, alkenyl, and alkynyl radicals, even in compound radicals, lower carbon skeletons, e.g., those with 1 to 6 C atoms, or for unsaturated groups with 2 to 6 C atoms, are preferred. Alkyl radicals, even in compound radicals such as alkoxy, haloalkyl, etc., are, for example, methyl, ethyl, n- or i-propyl, n-, i-, t-, or 2-butyl, pentyls, hexyls, such as n-hexyl, i-hexyl, and 1,3-dimethylbutyl, and heptyls, such as n-heptyl, 1-methylhexyl, and 1,4-dimethylpentyl. Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals, containing at least one double bond or triple bond. Preferred are radicals with one double bond or triple bond. The term "alkenyl" includes, in particular, straight-chain or branched open-chain hydrocarbon radicals with more than one double bond, such as 1,3-butadienyl and 1,4-pentadienyl.but also allenyl or cumulenyl residues with one or more cumulated double bonds, such as allenyl (1,2-propadienyl), 1,2-butadienyl and 1,2,3-pentatrienyl. Alkenyl means, for example, vinyl, which may optionally be substituted by further alkyl radicals, for example (but not limited to) (C2-C6)-alkenyl such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-Methyl-2-butenyl, 1-Methyl-3-butenyl, 2-Methyl-3-butenyl, 3-Methyl-3-butenyl, 1,1-Dimethyl-2-propenyl, 1,2-Dimethyl-1-propenyl, 1,2-Dimethyl-2-propenyl, 1-Ethyl-1-propenyl, 1-Ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl,2-Methyl-2-pentenyl, 3-Methyl-2-pentenyl, 4-Methyl-2-pentenyl, 1-Methyl-3- pentenyl, 2-Methyl-3-pentenyl, 3-Methyl-3-pentenyl, 4-Methyl-3-pentenyl, 1-Methyl-4-pentenyl, 2- Methyl-4-pentenyl, 3-Methyl-4-pentenyl, 4-Methyl-4-pentenyl, 1,1-Dimethyl-2-butenyl, 1,1-Dimethyl- 3-butenyl, 1,2-Dimethyl-1-butenyl, 1,2-Dimethyl-2-butenyl, 1,2-Dimethyl-3-butenyl, 1,3-Dimethyl-1- butenyl, 1,3-Dimethyl-2-butenyl, 1,3-Dimethyl-3-butenyl, 2,2-Dimethyl-3-butenyl, 2,3-Dimethyl-1- butenyl, 2,3-Dimethyl-2-butenyl, 2,3-Dimethyl-3-butenyl, 3,3-Dimethyl-1-butenyl, 3,3-Dimethyl-2- butenyl, 1-Ethyl-1-butenyl, 1-Ethyl-2-butenyl, 1-Ethyl-3-butenyl, 2-Ethyl-1-butenyl, 2-Ethyl-2-butenyl, 2-Ethyl-3-butenyl, 1,1,2-Trimethyl-2-propenyl, 1-Ethyl-1-methyl-2-propenyl,1-Ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl. The term "alkynyl" also includes, in particular, straight-chain or branched open-chain hydrocarbon radicals with more than one triple bond or with one or more triple bonds and one or more double bonds, such as 1,3-butatrienyl or 3-penten-1-yn-1-yl. (C2-C6)-alkynyl means, for example, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-Methyl-3-pentynyl, 1-Methyl-4-pentynyl, 2-Methyl-3-pentynyl, 2-Methyl-4-pentynyl, 3-Methyl-1-pentynyl, 3-Methyl-4-pentynyl, 4-Methyl-1-pentynyl, 4-Methyl-2-pentynyl, 1,1-Di-methyl-2-butynyl, 1,1-Dimethyl-3-butynyl, 1,2-Dimethyl-3-butynyl, 2,2-Dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl, and 1-ethyl-1-methyl-2-propynyl. The term "cycloalkyl" means a carbocyclic, saturated ring system with preferably 3-8 ring carbon atoms, e.g., cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, which is optionally further substituted, preferably by hydrogen, alkyl, alkoxy, cyano, nitro, alkylthio, haloalkylthio, halogen, alkenyl, alkynyl, haloalkyl, amino, alkylamino, bisalkylamino, alkoxycarbonyl, hydroxycarbonyl, arylalkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, or cycloalkylaminocarbonyl. In the case of optionally substituted cycloalkyl, cyclic systems with substituents are included, including substituents with a double bond on the cycloalkyl radical, e.g., an alkylidene group such as methylidene. In the case of optionally substituted cycloalkyl, polycyclic aliphatic systems are also included.such as bicyclo[1.1.0]butan-1-yl, bicyclo[1.1.0]butan-2-yl, bicyclo[2.1.0]pentan-1-yl, bicyclo[1.1.1]pentan-1-yl, bicyclo[2.1.0]pentan-2-yl, bicyclo[2.1.0]pentan-5-yl, bicyclo[2.1.1]hexyl, Bicyclo[2.2.1]hept-2-yl, bicyclo[2.2.2]octan-2-yl, bicyclo[3.2.1]octan-2-yl, bicyclo[3.2.2]nonan-2-yl, adamantan-1-yl and adamantan-2-yl, but also systems such as. B.1,1'-Bi(cyclopropyl)-1-yl, 1,1'-Bi(cyclopropyl)-2-yl. The term "(C3-C7)-cycloalkyl" is a shorthand notation for cycloalkyl with three to seven carbon atoms, corresponding to the range for C atoms. "Cycloalkenyl" means a carbocyclic, non-aromatic, partially unsaturated ring system with preferably 4-8 C atoms, e.g., 1-cyclobutenyl, 2-cyclobutenyl, 1-cyclopentenyl, 2-cyclopentenyl, 3-cyclopentenyl, or 1-cyclohexenyl, 2-cyclohexenyl, 3-cyclohexenyl, 1,3-cyclohexadienyl, or 1,4-cyclohexadienyl, where substituents with a double bond on the cycloalkenyl radical,e.g., an alkylidene group such as methylidene. In the case of optionally substituted cycloalkenyl, the explanations for substituted cycloalkyl apply accordingly. The term "alkylidene", e.g., also in the form (C1-C, 10 )-Alkylidene, means the residue of a straight-chain or branched open-chain hydrocarbon residue that is bonded via a double bond. Naturally, only positions on the parent structure where two H atoms can be replaced by the double bond are possible as bonding sites for alkylidene; examples of residues are, for example, =CH2, =CH-CH3, =C(CH3)-CH3, =C(CH3)-C2H5, or =C(C2H5)-C2H 5.Cycloalkylidene means a carbocyclic radical bonded via a double bond. The term "alkylene", e.g. also in the form (C1-C8)-alkylene, means the radical of a straight-chain or branched open-chain hydrocarbon radical bonded to other groups at two positions. "Alkoxyalkyl" stands for an alkoxy radical bonded via an alkyl group, and "alkoxyalkoxy" means an alkoxyalkyl radical bonded via an oxygen atom, e.g. (but not limited to) methoxymethoxy, methoxyethoxy, ethoxyethoxy, methoxy-n-propyloxy. "Arylalkyl" stands for an aryl radical bonded via an alkyl group, "heteroarylalkyl" means a heteroaryl radical bonded via an alkyl group, and "heterocyclylalkyl" means a heterocyclyl radical bonded via an alkyl group. "Cycloalkylalkyl" stands for a cycloalkyl radical bonded via an alkyl group, e.g.(but not limited to) Cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 1-cyclopropyleth-1-yl, 2-cyclopropyleth-1-yl, 1-cyclopropylprop-1-yl, 3-cyclopropylprop-1-yl. "Arylalkenyl" means an aryl radical attached via an alkenyl group, "heteroarylalkenyl" means a heteroaryl radical attached via an alkenyl group, and "heterocyclylalkenyl" means a heterocyclyl radical attached via an alkenyl group. "Arylalkynyl" means an aryl radical attached via an alkynyl group, "heteroarylalkynyl" means a heteroaryl radical attached via an alkynyl group, and "heterocyclylalkynyl" means a heterocyclyl radical attached via an alkynyl group. According to the invention, "haloalkylthio" - alone or as part of a chemical group - stands for straight-chain or branched S-haloalkyl, preferably with 1 to 8, or with 1 to 6 carbon atoms, such as (C1-C8)-, (C1-C6)- or (C1-C4)-haloalkylthio, e.g.(but not limited to) trifluoromethylthio, pentafluoroethylthio, difluoromethyl, 2,2-difluoroeth-1-ylthio, 2,2,2-difluoroeth-1-ylthio, 3,3,3-prop-1-ylthio. “Halocycloalkyl” and “halocycloalkenyl” mean radicals substituted by the same or different halogen atoms, such as F, Cl and Br, or by haloalkyl, such as B. Trifluoromethyl or difluoromethyl partially or fully substituted cycloalkyl or cycloalkenyl, e.g. 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocyclobut-1-yl, 1-trifluoromethylcycloprop-1-yl, 2-trifluoromethylcycloprop-1-yl, 1-chloro-cycloprop-1-yl, 2-chlorocycloprop-1-yl, 2,2-dichlorocycloprop-1-yl, 3,3-difluorocyclobutyl. In the following, only the neutral compound is mentioned and thus includes all existing forms as listed, unless a specific form of the active ingredient is relevant in a certain context, such as in the table examples below for biological activity.The herbicide / safener combinations according to the invention may contain further components, e.g., other active ingredients against harmful organisms such as harmful plants, plant-harming animals, or plant-harming fungi, in particular active ingredients from the group of herbicides other than the herbicides listed under B, fungicides, insecticides, acaricides, nematicides, and miticides and related substances, or also other types of crop protection active ingredients (e.g., resistance inducers), crop-protective active ingredients (safeners, antidotes, other than component (A)), plant growth regulators, and / or additives and / or formulation aids commonly used in crop protection. The components can be formulated and applied together (ready-to-use formulation), or they can be formulated separately and applied together, e.g., in a tank mix or in sequential application.The individual safeners of the general formula (I) contained as component (A) are also referred to below as compounds (A), active ingredients (A), components (A) or safeners (A). Accordingly, the individual herbicidal active ingredients contained as component (B) are also referred to below as compounds (B), active ingredients (B), components (B), herbicides (B) or compounds of the formula (II). An advantageous property of the inventive combination of safeners (A) and herbicides (B) is that safeners (A) and herbicides (B) are compatible with one another, i.e. they can be used together without significant chemical incompatibilities between the safener (A) and / or the herbizuids (B) occurring, which could lead to decomposition of the safener (A) or the herbicide(s) (B). This favorable compatibility also extends to the biological properties of the active ingredients when used in combination.Thus, antagonistic effects are generally not observed in the control of weeds with the herbicide / safener combinations according to the invention. The following definitions apply in formula (I) for compounds of the safener (A) and in formula (II) for compounds of the herbicide (B) and all subsequent formulas: The compounds of formula (I) or (II) can exist as stereoisomers depending on the nature and linkage of the substituents. If, for example, one or more asymmetrically substituted carbon and / or sulfur atoms are present, enantiomers and diastereomers can occur. Stereoisomers can be obtained from the mixtures obtained during production by customary separation methods, for example by chromatographic separation processes. Stereoisomers can also be selectively produced by using stereoselective reactions using optically active starting materials and / or auxiliaries.The invention also relates to all stereoisomers and mixtures thereof which are encompassed by the formula (I) or (II) but are not specifically defined. For the sake of simplicity, however, reference will always be made below to compounds of the formula (I) or (II), although this includes both the pure compounds and, where appropriate, mixtures with varying proportions of isomeric compounds. Depending on the nature of the substituents defined above, the compounds of the formula (I) or (II) have acidic properties and can form salts, optionally also internal salts or adducts, with inorganic or organic bases or with metal ions. If the compounds of the formula (I) or (II) carry hydroxyl, carboxyl or other groups which induce acidic properties, these compounds can be reacted with bases to form salts.Suitable bases include, for example, hydroxides, carbonates, bicarbonates of alkali and alkaline earth metals, particularly those of sodium, potassium, magnesium, and calcium, as well as ammonia, primary, secondary, and tertiary amines with (C1-C4) alkyl groups, mono-, di-, and trialkanolamines of (C1-C4) alkanols, choline, and chlorocholine, as well as organic amines such as trialkylamines, morpholine, piperidine, or pyridine. These salts are compounds in which the acidic hydrogen is replaced by a cation suitable for agriculture, for example, metal salts, particularly alkali metal salts or alkaline earth metal salts, particularly sodium and potassium salts, or ammonium salts, salts with organic amines, or quaternary ammonium salts, for example with cations of the formula [NRR´R´´R´´´]. +, wherein R to R''' each independently represent an organic radical, in particular alkyl, aryl, aralkyl or alkylaryl. Also suitable are alkylsulfonium and alkylsulfoxonium salts, such as (C1-C4)-trialkylsulfonium and (C1-C4)-trialkylsulfoxonium salts. In particular, G in compounds of the formula (II) can be an agronomically acceptable metal such as copper, iron, lithium, sodium, potassium, magnesium or calcium (in particular an alkali or alkaline earth metal). The compounds of the formula (I) or (II) can be obtained by addition of a suitable inorganic or organic acid, for example mineral acids, such as HCl, HBr, H2SO4, H3PO4 or HNO3, or organic acids, e.g. B. carboxylic acids, such as formic acid, acetic acid, propionic acid, oxalic acid, lactic acid or salicylic acid or sulfonic acids, such as p-toluenesulfonic acid, form salts with a basic group, such as amino, alkylamino, dialkylamino, piperidino, morpholino or pyridino.These salts then contain the conjugate base of the acid as an anion. Suitable substituents, which are present in deprotonated form, such as sulfonic acids or carboxylic acids, can form internal salts with protonatable groups, such as amino groups. If a group is polysubstituted by radicals, this means that this group is substituted by one or more of the same or different radicals mentioned. Preferred, particularly preferred, and very particularly preferred meanings are described below for the individual safeners (A) and the herbicides (B). If the compounds can form tautomers by hydrogen shift which would not be structurally covered by the general formula (A), these tautomers are nevertheless encompassed by the definition of the compounds of the general formula (A) according to the invention, unless a specific tautomer is the subject of consideration.For example, many carbonyl compounds can exist in both the keto and the enol form, both forms being encompassed by the definition of a compound of general formula (A). The compounds of general formula (I) can exist as stereoisomers depending on the type and linkage of the substituents. The possible stereoisomers defined by their specific spatial form, such as enantiomers, diastereomers, Z and E isomers, are all encompassed by general formula (I). If, for example, one or more alkenyl groups are present, diastereomers (Z and E isomers) can occur. If, for example, one or more asymmetric carbon atoms are present, enantiomers and diastereomers can occur. Stereoisomers can be obtained from the mixtures obtained during production using conventional separation methods. Chromatographic separation can be carried out on an analytical scale to determine the enantiomeric excess or the enantiomeric concentration.of the diastereomeric excess, as well as on a preparative scale for the production of test samples for biological testing. Stereoisomers can also be prepared selectively by using stereoselective reactions using optically active starting materials and / or auxiliaries. The invention thus also relates to all stereoisomers encompassed by the general formula (I) but not indicated with their specific stereoform, as well as mixtures thereof. If the compounds are obtained as solids, purification can also be carried out by recrystallization or digestion. If individual compounds of the general formula (I) cannot be satisfactorily obtained by the routes described below, they can be prepared by derivatization of other compounds of the general formula (I).Suitable methods for the isolation, purification, and stereoisomer separation of compounds of general formula (I) include methods generally known to the person skilled in the art from analogous cases, e.g., physical processes such as crystallization, chromatography, especially column chromatography and HPLC (high-pressure liquid chromatography), distillation, optionally under reduced pressure, extraction, and other processes. Any remaining mixtures can generally be separated by chromatographic separation, e.g., on chiral solid phases. For preparative quantities or on an industrial scale, processes such as crystallization, e.g., of diastereomeric salts, which can be obtained from the diastereomer mixtures with optically active acids and, if acidic groups are present, with optically active bases, are suitable.In one embodiment of the present invention, the herbicide / safener combination according to the invention contains, in addition to at least one component (B) as defined above, preferably a component (A) (safener (A)) of the general formula (I) or their agronomically acceptable salts according to Table 1. Table 1: IUPAC names and the structural formulas of the preferred compounds of the formula (I) (safener (A)).

[0005]

[0006] The compounds of formula (I) are known from the international application with application number PCT / EP2020 / 083167 (WO2021 / 105101) and can be prepared by the processes described therein. Particularly preferred safeners (A) within the meaning of the present invention are the compounds with the numbers A1, A3, A5, A7 and A9, according to Table 1 above. Compounds of the formula (II) are known from the international applications WO2021009229, WO2015197468, WO202109048, WO2021009232, WO2019158666, WO2020169648, WO2020165233, WO2020165102, WO2020074489, WO2019175117, WO2019170745 and WO202118826 and can be prepared by the processes described therein. Preference is given to herbicides of the general formula (II) in which Q is the radical Q-1, R 1 represents methyl, 1-propynyl or a six-membered heteroaryl ring containing one or two nitrogen atoms, where the heteroaryl ring is represented by a radical R 9 can be substituted, R 2represents chlorine, methoxy, methyl or ethyl, R 3 stands for chlorine, methyl or ethyl, W stands for CH2, O, NH or N-CH3, Y stands for O or NR 8 Z represents a bond or CH2, n1 and n2 independently represent 1 or 2, provided that n1 + n2 is equal to 2, 3 or 4, R 8 for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl, -C(O)O(C1-C6)-alkyl, - S(O)2NHR 17N , -S(O)(=NH)R 19N , -C(O)C(O)R 20N , -C(O)C(R 23N )=NOR 24N stands; R 9 represents cyano or halogen; R 17N represents methyl or ethyl; R 19N represents methyl or ethyl; R 20N for methyl, ethyl or -NHR 22N stands; R 22N represents methyl or ethyl; R 23N represents methyl or ethyl; R 24N represents methyl or ethyl; G represents hydrogen, an agronomically acceptable metal, C(O)-R 14 or for -C(O)-OR 15 stands, R 14represents (C1-C6)alkyl, R 15 represents (C1-C6)-alkyl. Preferred herbicides are those of the general formula (II) in which Q represents the radical Q-2, R 1 represents 1-propynyl, R 2 represents chlorine, methoxy, methyl or ethyl, R 3 stands for chlorine, methyl or ethyl, W stands for CH2, O, NH or N-CH3, Y stands for NR 8 stands for, Z stands for a bond or for CH2, n1 stands for 2, R 8 for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl or -S(O)2C(R 11N )R 12N R 13N stands; R 11N stands for hydrogen; R 12N stands for hydrogen; R 13N stands for methyl; G stands for hydrogen, an agronomically acceptable metal, for C(O)-R 14 or for -C(O)-OR 15 stands, R 14 represents (C1-C6)alkyl, R 15 represents (C1-C6)-alkyl. Preferred herbicides are those of the general formula (II) in which Q represents the radical Q-3, R 1 represents 1-propynyl, R 2represents chlorine, methoxy, methyl or ethyl, R 3 represents chlorine, methyl or ethyl, W represents CH2, O, NH or N-CH3, Z represents a bond or CH2, R 1Q3 represents hydrogen or (C1-C6)-alkyl, R 2Q3 for -(CH2) k -R 3Q3 where R 3Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and - S(O)2NR 16N R 17N , and k means 0, or R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 independently represent 1 or 2, R 4Q3 represents hydrogen or (C1-C6)-alkyl, R 5Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and -S(O)2NR 16N R 17N , or R 4Q3 and R 5Q3 together for -(CH2)-N(R 8 )-(CH2)-, R 8for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl or -S(O)2C(R 11N )R 12N R 13N stands; R 5N represents substituents which are independently selected from a group consisting of hydrogen and (C1-C6)-alkyl, R 6N represents substituents which are independently selected from a group consisting of hydrogen, (C1-C6)-alkyl and -C(O)-C(R 11N )R 12N R 13N , R 11N stands for hydrogen; R 12N stands for hydrogen; R 13N represents hydrogen or methyl; R 16N represents hydrogen or (C1-C6)-alkyl; R 17N represents hydrogen or (C1-C6)-alkyl; G represents hydrogen, an agronomically acceptable metal, C(O)-R 14 or for -C(O)-OR 15 stands, R 14 represents (C1-C6)-alkyl, R 15represents (C1-C6)-alkyl. In a further embodiment of the present invention, the herbicide / safener combination according to the invention preferably comprises a compound A1, A3, A5, A7 and A9 according to Table 1 above or their agronomically acceptable salts [safener (A)] and preferably a compound from the group of herbicidally active ingredients of the formula (II-1) listed in Table 2 below [herbicide (B)], wherein Q represents Q-1 and R 1 , R 2 , R 3 , W, Y, Z and G as well as n1 and n2 have the meanings below. Table 2:

[0007] In a further embodiment of the present invention, the herbicide / safener combination according to the invention preferably contains a compound A1, A3, A5, A7 and A9 according to Table 1 above or their agronomically acceptable salts [safener (A)] and preferably a compound from the group of the herbicidally active compounds of the formula (II-2) listed in Table 3 below [herbicide (B)], in which Q is Q-2 and Y and G have the meanings below and in which R 1 for 1-propynyl, R 2 and R 3 each represents methyl, W and Z each represents CH2, and n1 represents 2. Table 3: In a further embodiment of the present invention, the herbicide / safener combination according to the invention preferably contains a compound A1, A3, A5, A7 and A9 according to Table 1 above or their agronomically acceptable salts [safener (A)] and preferably a compound from the group of the herbicidally active compounds of the formula (II-3) listed in Table 4 below [herbicide (B)], in which Q is Q-3 and G has the meanings below and in which R 1 for 1-propynyl, R 2 and R 3 each for methyl, W and Z each for CH2 and R 1Q3 for hydrogen and R 2Q3 for -C(O)NR 5N R 6N where R 5N and R 6N both represent a methyl group. Table 4: In a further embodiment of the present invention, the herbicide / safener combination according to the invention preferably contains a compound A1, A3, A5, A7 and A9 according to Table 1 above or their agronomically acceptable salts [safener (A)] and preferably a compound from the group of the herbicidally active ingredients of the formula (II-4) listed in Table 5 below [herbicide (B)], in which Q is Q-3 and R 5Q3 and G have the meanings below and wherein R 1 for 1-propynyl, R 2 and R 3 each represent methyl and W and Z each represent CH2 and where the radicals R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 both stand for 2 and R 4Q3 Hydrogen means. Table 5: In a further embodiment of the present invention, the herbicide / safener combination according to the invention preferably contains a compound A1, A3, A5, A7 and A9 according to Table 1 above or their agronomically acceptable salts [safener (A)] and preferably a compound from the group of the herbicidally active compounds of the formula (II-5) listed in Table 6 below [herbicide (B)], in which Q is Q-3 and G has the meanings below and in which R 1 for 1-propynyl, R 2 and R 3 each represent methyl and W and Z each represent CH2 and where the radicals R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 both stand for 1, the residues R 4Q3 and R 5Q3 together for -(CH2)-N(R 8 )-(CH2)- and where R 8 -(CO)CH3. Table 6: Within the scope of the present invention, it is possible to combine the individual preferred and particularly preferred compounds with one another as desired. This means that herbicidal compositions comprising safeners (A), one or more compounds of the general formula (I) or their agrochemically acceptable salts [component (A)], and (B) one or more herbicides [component (B)] are encompassed by the present invention, in which any disclosed, preferred, and particularly preferred embodiments as listed above can be combined with one another. Some binary combinations comprising a compound (A) of the general formula (I) acting as a safener or its agrochemically acceptable salts [safener (A)], and a herbicide (B) have surprisingly proven particularly advantageous at the time of application. These are listed in Table 7 below. Table 7: Preferred Combinations

[0008] In a further embodiment, the following combinations according to Table 8 below are preferred: Table 8: Further preferred combinations Furthermore, the herbicide / safener combinations according to the invention can be used together with other active ingredients such as fungicides, insecticides, acaricides, etc. and / or plant growth regulators or adjuvants from the group of additives commonly used in crop protection, such as adjuvants and formulation aids. Their application forms, such as formulations or tank mixes, represent herbicidal compositions (compositions). The invention therefore also relates to the herbicide / safener combinations admixed with additives commonly used in crop protection, such as adjuvants and formulation aids, and optionally other crop protection active ingredients. The invention also relates to the use of, or the application method using, the herbicide / safener combinations according to the invention as herbicides and plant growth regulators.preferably as herbicides and plant growth regulators with a synergistically effective content of the respective herbicide combination contained. For the active ingredients from group (B), the application rate is preferably in the range from 5 to 400 g ai / ha, in particular in the range from 8 to 200 g / ha, and most preferably in the range from 10 to 90 g ai / ha. The quantity ratios (A):(B) based on the weight are, depending on the effective application rates, generally in the range from 1:400 to 500:1, preferably in the range from 1:100 to 100:1, particularly preferably in the range from 1:40 to 20:1. The quantities stated are application rates (g ai / ha = grams of active substance per hectare) and thus also define the quantity ratios in a co-formulation, a premix, a tank mix or a sequential application of the combined active ingredients. The herbicide / safener combinations according to the invention may contain further components,e.g. other active substances against harmful organisms such as harmful plants, plant-harming animals or plant-harming fungi, in particular active substances from the group of fungicides, insecticides, acaricides, nematicides, miticides and related substances. Fungicidally active compounds which can be used in conjunction with the herbicide / safener combinations according to the invention are preferably commercially available active ingredients, for example (analogous to the herbicides, the compounds are generally referred to by their common names, here in the usual English notation): 1) Inhibitors of ergosterol biosynthesis, for example cyproconazole, difenoconazole, epoxiconazole, fenhexamid, fenpropidin, fenpropimorph, fenpyrazamine, fluquinconazole, flutriafol, imazalil, imazalil sulfate, ipconazole, metconazole, myclobutanil, paclobutrazol, prochloraz, propiconazole, prothioconazole, pyrisoxazole, spiroxamine, tebuconazole, tetraconazole, triadimenol, tridemorph, triticonazole, (1R,2S,5S)-5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclo-pentanol, (1S,2R,5R)-5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (2R)-2-(1-Chlorcyclopropyl)-4-[(1R)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (2R)- 2-(1-Chlorcyclopropyl)-4-[(1S)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (2R)-2-[4- (4-Chlorphenoxy)-2-(trifluormethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (2S)-2-(1-Chlorcyclo- propyl)-4-[(1R)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (2S)-2-(1-Chlorcyclo- propyl)-4-[(1S)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (2S)-2-[4-(4-Chlorphen- oxy)-2-(trifluormethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (R)-[3-(4-Chlor-2-fluorphenyl)-5- (2,4-difluorphenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, (S)-[3-(4-Chlor-2-fluorphenyl)-5-(2,4- difluorphenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, [3-(4-Chlor-2-fluorphenyl)-5-(2,4-difluor- phenyl)-1,2-oxazol-4-yl](pyridin-3-yl)methanol, 1-({(2R,4S)-2-[2-Chlor-4-(4-chlorphenoxy)phenyl]-4- methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazol, 1-({(2S,4S)-2-[2-Chlor-4-(4-chlorphenoxy)phenyl]- 4-methyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazol, 1-{[3-(2-Chlorphenyl)-2-(2,4-difluor- phenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl-thiocyanat, 1-{[rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4- difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl-thiocyanat, 1-{[rel(2R,3S)-3-(2-Chlorphenyl)- 2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol-5-yl-thiocyanat, 2-[(2R,4R,5R)-1-(2,4- Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol-3-thion, 2- [(2R,4R,5S)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol- 3-thion, 2-[(2R,4S,5R)-1-(2,4-Dichlorophenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H- 1,2,4-triazol-3-thion, 2-[(2R,4S,5S)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4- dihydro-3H-1,2,4-triazol-3-thion, 2-[(2S,4R,5R)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6- trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol-3-thion, 2-[(2S,4R,5S)-1-(2,4-Dichlorphenyl)-5- hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol-3-thion, 2-[(2S,4S,5R)-1-(2,4- Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol-3-thion, 2- [(2S,4S,5S)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol- 3-thion, 2-[1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol- 3-thion, 2-[2-Chlor-4-(2,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, 2-[2-Chlor-4- (4-chlorphenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)- phenyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl]-1-(1H- 1,2,4-triazol-1-yl)pentan-2-ol, 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl]-1-(1H-1,2,4-triazol-1- yl)propan-2-ol, 2-{[3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-1,2,4- triazol-3-thion, 2-{[rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-2,4- dihydro-3H-1,2,4-triazol-3-thion, 2-{[rel(2R,3S)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2- yl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-thion, 5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol, 5-(Allylsulfanyl)-1-{[3-(2-chlorphenyl)-2-(2,4- difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol, 5-(Allylsulfanyl)-1-{[rel(2R,3R)-3-(2-chlorphenyl)- 2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol, 5-(Allylsulfanyl)-1-{[rel(2R,3S)-3-(2- chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazol, N'-(2,5-Dimethyl-4-{[3- (1,1,2,2-tetrafluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, N'-(2,5-Dimethyl- 4-{[3-(2,2,2-trifluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, N'-(2,5- Dimethyl-4-{[3-(2,2,3,3-tetrafluorpropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, N'-(2,5-Dimethyl-4-{[3-(pentafluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, N'-(2,5-Dimethyl-4-{3-[(1,1,2,2-tetrafluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N- methylimidoformamid, N'-(2,5-Dimethyl-4-{3-[(2,2,2-trifluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl- N-methylimidoformamid, N'-(2,5-Dimethyl-4-{3-[(2,2,3,3-tetrafluorpropyl)sulfanyl]phenoxy}phenyl)- N-ethyl-N-methylimidoformamid, N'-(2,5-Dimethyl-4-{3-[(pentafluorethyl)sulfanyl]phenoxy}phenyl)- N-ethyl-N-methylimidoformamid, N'-(2,5-Dimethyl-4-phenoxyphenyl)-N-ethyl-N- methylimidoformamid, N'-(4-{[3-(Difluormethoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N- methylimidoformamid, N'-(4-{3-[(Difluormethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N- methylimidoformamid, N'-[5-Brom-6-(2,3-dihydro-1H-inden-2-yloxy)-2-methylpyridin-3-yl]-N-ethyl- N-methylimidoformamid, N'-{4-[(4,5-Dichlor-1,3-thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl-N- methylimidoformamid, N'-{5-Brom-6-[(1R)-1-(3,5-difluorophenyl)ethoxy]-2-methylpyridin-3-yl}-N- ethyl-N-methylimidoformamid, N'-{5-Brom-6-[(1S)-1-(3,5-difluorphenyl)ethoxy]-2-methylpyridin-3- yl}-N-ethyl-N-methylimidoformamid, N'-{5-Brom-6-[(cis-4-isopropylcyclohexyl)oxy]-2- methylpyridin-3-yl}-N-ethyl-N-methylimidoformamid, N'-{5-Brom-6-[(trans-4- isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamid, N'-{5-Bromo-6-[1- (3,5-difluorphenyl)ethoxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamid, Mefentrifluconazole, Ipfentrifluconazole. 2) Inhibitoren der Atmungskette am Komplex I oder II beispielsweise Benzovindiflupyr, Bixafen, Boscalid, Carboxin, Fluopyram, Flutolanil, Fluxapyroxad, Furametpyr, Isofetamid, Isopyrazam (anti- epimeres Enantiomer 1R,4S,9S), Isopyrazam (anti-epimeres Enantiomer 1S,4R,9R), Isopyrazam (anti- epimeres Racemat 1RS,4SR,9SR), Isopyrazam (Mischung des syn-epimeren Razemates 1RS,4SR,9RS und des anti-epimeren Razemates 1RS,4SR,9SR), Isopyrazam (syn-epimeres Enantiomer 1R,4S,9R), (2.015) Isopyrazam (syn-epimeres Enantiomer 1S,4R,9S), Isopyrazam (syn-epimeres Racemat 1RS,4SR,9RS), Penflufen, Penthiopyrad, Pydiflumetofen, Pyraziflumid, Sedaxane, 1,3-Dimethyl-N- (1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazol-4-carboxamid, 1,3-Dimethyl-N-[(3R)-1,1,3- trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid, 1,3-Dimethyl-N-[(3S)-1,1,3-trimethyl- 2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid, 1-Methyl-3-(trifluormethyl)-N-[2'- (trifluormethyl)biphenyl-2-yl]-1H-pyrazol-4-carboxamid, 2-Fluor-6-(trifluoromethyl)-N-(1,1,3- trimethyl-2,3-dihydro-1H-inden-4-yl)benzamid, 3-(Difluormethyl)-1-methyl-N-(1,1,3-trimethyl-2,3- dihydro-1H-inden-4-yl)-1H-pyrazol-4-carboxamid, 3-(Difluormethyl)-1-methyl-N-[(3R)-1,1,3- trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid, 3-(Difluormethyl)-1-methyl-N-[(3S)- 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid, (2.030) 3-(Difluormethyl)-N-(7- fluor-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazol-4-carboxamid, 3-(Difluor- methyl)-N-[(3R)-7-fluor-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazol-4- carboxamid, 3-(Difluoromethyl)-N-[(3S)-7-fluor-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1-methyl- 1H-pyrazol-4-carboxamid, 5,8-Difluor-N-[2-(2-fluor-4-{[4-(trifluormethyl)pyridin-2- yl]oxy}phenyl)ethyl]quinazolin-4-amin, N-(2-Cyclopentyl-5-fluorbenzyl)-N-cyclopropyl-3- (difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, N-(2-tert-Butyl-5-methylbenzyl)-N- cyclopropyl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, N-(2-tert-Butylbenzyl)-N- cyclopropyl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, N-(5-Chlor-2-ethylbenzyl)- N-cyclopropyl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid,N-(5-Chlor-2- isopropylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, (2.039) N-[(1R,4S)-9-(Dichlormethylen)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluormethyl)-1- methyl-1H-pyrazol-4-carboxamid, N-[(1S,4R)-9-(Dichlormethylen)-1,2,3,4-tetrahydro-1,4- methanonaphthalen-5-yl]-3-(difluormethyl)-1-methyl-1H-pyrazol-4-carboxamid, N-[1-(2,4- Dichlorphenyl)-1-methoxypropan-2-yl]-3-(difluormethyl)-1-methyl-1H-pyrazol-4-carboxamid, N-[2- Chlor-6-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4- carboxamid, N-[3-Chlor-2-fluor-6-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5-fluor-1- methyl-1H-pyrazol-4-carboxamid, N-[5-Chlor-2-(trifluormethyl)benzyl]-N-cyclopropyl-3- (difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, N-Cyclopropyl-3-(difluormethyl)-5-fluor- 1-methyl-N-[5-methyl-2-(trifluormethyl)benzyl]-1H-pyrazol-4-carboxamid,N-Cyclopropyl-3- (difluormethyl)-5-fluor-N-(2-fluor-6-isopropylbenzyl)-1-methyl-1H-pyrazol-4-carboxamid, N- Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazol-4- carboxamid, N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazol-4- carbothioamid, N-Cyclopropyl-3-(difluoromethyl)-5-fluor-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazol- 4-carboxamid, N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(5-fluor-2-isopropylbenzyl)-1-methyl-1H- pyrazol-4-carboxamid, N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5-fluor-1- methyl-1H-pyrazol-4-carboxamid, N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-5-fluorbenzyl)-5-fluor- 1-methyl-1H-pyrazol-4-carboxamid, N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-5-methylbenzyl)-5- fluor-1-methyl-1H-pyrazole-4-carboxamid, N-Cyclopropyl-N-(2-cyclopropyl-5-fluorbenzyl)-3- (difluormethyl)-5-fluor-1-methyl-1H-pyrazole-4-carboxamid,N-Cyclopropyl-N-(2-cyclopropyl-5- methylbenzyl)-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazole-4-carboxamid, N-Cyclopropyl-N-(2- cyclopropylbenzyl)-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazole-4-carboxamid. 3) Inhibitoren der Atmungskette am Komplex III, beispielsweise Ametoctradin, Amisulbrom, Azoxystrobin, Coumethoxystrobin, Coumoxystrobin, Cyazofamid, Dimoxystrobin, Enoxastrobin, Famoxadon, Fenamidon, Flufenoxystrobin, Fluoxastrobin, Kresoxim-Methyl, Metominostrobin, Orysastrobin, Picoxystrobin, Pyraclostrobin, Pyrametostrobin, Pyraoxystrobin, Trifloxystrobin (3.021) (2E)-2-{2-[({[(1E)-1-(3-{[(E)-1-Fluor-2-phenylvinyl]oxy}phenyl)ethyliden]amino}oxy)methyl]- phenyl}-2-(methoxyimino)-N-methylacetamid, (2E,3Z)-5-{[1-(4-Chlorphenyl)-1H-pyrazol-3-yl]oxy}-2- (methoxyimino)-N,3-dimethylpent-3-enamid, (2R)-2-{2-[(2,5-Dimethylphenoxy)methyl]phenyl}-2- methoxy-N-methylacetamid, (2S)-2-{2-[(2,5-Dimethylphenoxy)methyl]phenyl}-2-methoxy-N- methylacetamid, (3S,6S,7R,8R)-8-Benzyl-3-[({3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2- yl}carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl-2-methylpropanoat, 2-{2-[(2,5- Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, N-(3-Ethyl-3,5,5- trimethylcyclohexyl)-3-formamido-2-hydroxybenzamid, (2E,3Z)-5-{[1-(4-Chlor-2-fluorphenyl)-1H- pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamid, Methyl {5-[3-(2,4-dimethylphenyl)- 1H-pyrazol-1-yl]-2-methylbenzyl}carbamate. 4) Inhibitoren der Mitose und Zellteilung, beispielsweise Carbendazim, Diethofencarb, Ethaboxam, Fluopicolid, Pencycuron, Thiabendazol, Thiophanat-Methyl, Zoxamid, 3-Chlor-4-(2,6-difluorphenyl)-6- methyl-5-phenylpyridazin, 3-Chlor-5-(4-chlorphenyl)-4-(2,6-difluorphenyl)-6-methylpyridazin, 3- Chlor-5-(6-chlorpyridin-3-yl)-6-methyl-4-(2,4,6-trifluorphenyl)pyridazin, 4-(2-Brom-4-fluorphenyl)-N- (2,6-difluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Brom-4-fluorphenyl)-N-(2-brom-6- fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin,4-(2-Brom-4-fluorphenyl)-N-(2-bromphenyl)-1,3- dimethyl-1H-pyrazol-5-amin, 4-(2-Brom-4-fluorphenyl)-N-(2-chlor-6-fluorphenyl)-1,3-dimethyl-1H- pyrazol-5-amin, (4.016) 4-(2-Brom-4-fluorphenyl)-N-(2-chlorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Brom-4-fluorphenyl)-N-(2-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Chlor-4- fluorphenyl)-N-(2,6-difluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Chlor-4-fluorphenyl)-N-(2- chlor-6-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Chlor-4-fluorphenyl)-N-(2-chlorphenyl)- 1,3-dimethyl-1H-pyrazol-5-amin, 4-(2-Chlor-4-fluorphenyl)-N-(2-fluorphenyl)-1,3-dimethyl-1H- pyrazol-5-amin, 4-(4-Chlorphenyl)-5-(2,6-difluorphenyl)-3,6-dimethylpyridazin, N-(2-Brom-6- fluorphenyl)-4-(2-chlor-4-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, N-(2-Bromphenyl)-4-(2-chlor- 4-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, N-(4-Chlor-2,6-difluorphenyl)-4-(2-chlor-4-fluor- phenyl)-1,3-dimethyl-1H-pyrazol-5-amine. 5) Compounds capable of multisite activity, for example Bordeaux mixture, captafol, captan, chlorothalonil, copper hydroxide, copper naphthenate, copper oxide, copper oxychloride, copper(2+) sulfate, dithianone, dodine, folpet, mancozeb, maneb, metiram, zinc metiram, copper oxine, propineb, sulfur and sulfur preparations including calcium polysulfide, thiram, zineb, ziram, 6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3',4':5,6][1,4]dithiino[2,3-c][1,2]thiazole-3-carbonitrile. 6) Compounds capable of triggering host defenses, for example, acibenzolar-S-methyl, isotianil, probenazole, tiadinil. 7) Inhibitors of amino acid and / or protein biosynthesis, for example, cyprodinil, kasugamycin, kasugamycin hydrochloride hydrate, oxytetracycline, pyrimethanil, 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline. (8) Inhibitors of ATP production, for example, silthiofam. 9) Inhibitors of cell wall synthesis.for example, benthiavalicarb, dimethomorph, flumorph, iprovalicarb, mandipropamid, pyrimorph, valifenalate, (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (2Z)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one. 10) Inhibitors of lipid and membrane synthesis, for example, propamocarb, propamocarb hydrochloride, tolclofos-methyl. 11) Inhibitors of melanin biosynthesis, for example, tricyclazole, 2,2,2-trifluoroethyl-{3-methyl-1-[(4-methylbenzoyl)amino]butan-2-yl}carbamate. 12) Nucleic acid synthesis inhibitors, for example, benalaxyl, benalaxyl-M (kiralaxyl), metalaxyl, metalaxyl-M (mefenoxam). 13) Signal transduction inhibitors, for example, fludioxonil, iprodione, procymidone, proquinazid, quinoxyfen, vinclozolin. 14) Compounds that can act as uncouplers, for example, fluazinam, meptyldinocap. 15) Other compounds, for example, abscisic acid, benthiazole, bethoxazine, capsimycin.Carvon, Chinomethionat, Cufraneb, Cyflufenamid, Cymoxanil, Cyprosulfamid, Flutianil, Fosetyl-Aluminium, Fosetyl-Calcium, Fosetyl-Natrium, Methylisothiocyanat, Metrafenon, Mildiomycin, Natamycin, Nickel- Dimethyldithiocarbamat, Nitrothal-Isopropyl, Oxamocarb, Oxathiapiprolin, Oxyfenthiin, Pentachlorphenol und Salze, Phosphonsäure und deren Salze, Propamocarb-fosetylat, Pyriofenone (Chlazafenone), Tebufloquin, Tecloftalam, Tolnifanide, 1-(4-{4-[(5R)-5-(2,6-Difluorphenyl)-4,5- dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluormethyl)-1H-pyrazol-1- yl]ethanon, 1-(4-{4-[(5S)-5-(2,6-Difluorphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2- yl}piperidin-1-yl)-2-[5-methyl-3-(trifluormethyl)-1H-pyrazol-1-yl]ethanon, 2-(6-Benzylpyridin-2- yl)quinazolin, 2,6-Dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c']dipyrrol-1,3,5,7(2H,6H)-tetron, 2-[3,5- Bis(difluormethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-in-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol- 3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanon, 2-[3,5-Bis(difluormethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2- chlor-6-(prop-2-in-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1- yl]ethanon, 2-[3,5-Bis(difluormethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-fluor-6-(prop-2-in-1- yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanon, 2-[6-(3-Fluor-4- methoxyphenyl)-5-methylpyridin-2-yl]quinazolin, 2-{(5R)-3-[2-(1-{[3,5-Bis(difluormethyl)-1H- pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorphenyl methanesulfonat, 2-{(5S)-3-[2-(1-{[3,5-Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3- thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorphenyl methanesulfonat, 2-{2-[(7,8-Difluor-2- methylquinolin-3-yl)oxy]-6-fluorphenyl}propan-2-ol, 2-{2-Fluor-6-[(8-fluor-2-methylquinolin-3- yl)oxy]phenyl}propan-2-ol, 2-{3-[2-(1-{[3,5-Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)- 1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorphenyl-methansulfonat, 2-{3-[2-(1-{[3,5- Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5- yl}phenyl methanesulfonat, 2-Phenylphenol und deren Salze, 3-(4,4,5-Trifluor-3,3-dimethyl-3,4- dihydroisoquinolin-1-yl)quinolin, 3-(4,4-Difluor-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolin, 4- Amino-5-fluorpyrimidin-2-ol (Tautomere Form: 4-Amino-5-fluorpyrimidin-2(1H)-on), 4-Oxo-4-[(2- phenylethyl)amino]buttersäure, 5-Amino-1,3,4-thiadiazol-2-thiol, 5-Chlor-N'-phenyl-N'-(prop-2-yn-1- yl)thiophen-2-sulfonohydrazid, 5-Fluor-2-[(4-fluorbenzyl)oxy]pyrimidin-4-amin, 5-Fluor-2-[(4- methylbenzyl)oxy]pyrimidin-4-amin, 9-Fluor-2,2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4- benzoxazepin, But-3-yn-1-yl-{6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylen]amino}oxy)- methyl]pyridin-2-yl}carbamat, Ethyl-(2Z)-3-amino-2-cyano-3-phenylacrylat, Phenazin-1-carbonsäure, Propyl 3,4,5-trihydroxybenzoat, Quinolin-8-ol,Quinolin-8-ol sulfate (2:1), tert-Butyl {6-[({[(1-methyl- 1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, 5-fluoro-4-imino-3-methyl-1)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one. Preferred fungicides are selected from the group consisting of benalaxyl, bitertanol, bromuconazole, captafol, carbendazim, carpropamid, cyazofamid, cyproconazole, diethofencarb, edifenphos, fenpropimorph, fentine, fluquinconazole, fosetyl, fluoroimide, folpet, iminoctadine, iprodionem, iprovalicarb, kasugamycin, maneb, nabam, pencycuron, prochloraz, propamocarb, propineb, pyrimethanil, sprioxamine, quintozene, tebuconazole, tolylfluanid, triadimefon, triadimenol, trifloxystrobin, zineb. Insecticides, acaricides, nematicides, miticides and related active substances are, for example (analogous to herbicides and fungicides, the compounds are referred to by their common names where possible, here in the usual English spelling): (1) Acetylcholinesterase (AChE) inhibitors,vorzugsweise Carbamate ausgewählt aus Alanycarb, Aldicarb, Bendiocarb, Benfuracarb, Butocarboxim, Butoxycarboxim, Carbaryl, Carbofuran, Carbosulfan, Ethiofencarb, Fenobucarb, Formetanate, Furathiocarb, Isoprocarb, Methiocarb, Methomyl, Metolcarb, Oxamyl, Pirimicarb, Propoxur, Thiodicarb, Thiofanox, Triazamate, Trimethacarb, XMC und Xylylcarb, oder Organophosphate ausgewählt aus Acephat, Azamethiphos, Azinphos-ethyl, Azinphos- methyl, Cadusafos, Chlorethoxyfos, Chlorfenvinphos, Chlormephos, Chlorpyrifos-methyl, Coumaphos, Cyanophos, Demeton-S-methyl, Diazinon, Dichlorvos / DDVP, Dicrotophos, Dimethoat, Dimethylvinphos, Disulfoton, EPN, Ethion, Ethoprophos, Famphur, Fenamiphos, Fenitrothion, Fenthion, Fosthiazat, Heptenophos, Imicyafos, Isofenphos, Isopropyl-O-(methoxyaminothio- phosphoryl)salicylat, Isoxathion, Malathion, Mecarbam, Methamidophos, Methidathion, Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion-methyl, Phenthoat, Phorat, Phosalon, Phosmet,Phosphamidone, Phoxim, Pirimiphos-methyl, Profenofos, Propetamphos, Prothiofos, Pyraclofos, Pyridaphenthion, Quinalphos, Sulfotep, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon, and Vamidothion. (2) GABA-gated chloride channel blockers, preferably cyclodiene organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fiprols) selected from ethiprol and fipronil. (3) sodium channel modulators, preferably pyrethroids selected from acrinathrin, allethrin, d-cis-trans-allethrin, d-trans-allethrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, Cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(1R)-trans isomer], deltamethrin, empenthrin [(EZ)-(1R) isomer], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin,Tau-fluvalinate, halfenprox, imiprothrin, kadethrin, momfluorothrin, permethrin, phenothrin [(1R)-trans isomer], prallethrin, pyrethrins (pyrethrum), resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin [(1R)-isomer], tralomethrin, and transfluthrin, or DDT or methoxychlor. (4) Competitive modulators of the nicotinic acetylcholine receptor (nAChR), preferably neonicotinoids selected from acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid, and thiamethoxam, or nicotine, or sufoximines selected from sulfoxaflor, or butenolides selected from flupyradifurone. (5) Allosteric modulators of the nicotinic acetylcholine receptor (nAChR), preferably spinosyns selected from spinetoram and spinosad. (6) Allosteric modulators of the glutamate-dependent chloride channel (GluCl), preferably avermectins / milbemycins selected from abamectin, emamectin benzoate, lepimectin, and milbemectin. (7) Juvenile hormone mimetics,preferably juvenile hormone analogues selected from hydroprene, kinoprene and methoprene, or fenoxycarb or pyriproxyfen. (8) Various non-specific (multi-site) inhibitors, preferably alkyl halides selected from methyl bromide and other alkyl halides, or chloropicrin or sulfuryl fluoride or borax or tartar emetic or methyl isocyanate generators selected from diazomet and metam. (9) TRPV channel modulators of chordotonal organs selected from pymetrozine and pyrifluquinazone. (10) Mite growth inhibitors selected from clofentezine, hexythiazox, diflovidazine and etoxazole. (11) Microbial disruptors of the insect intestinal membrane selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis and Bt plant proteins selected from Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105, Cry2Ab, VIP3A, mCry3A, Cry3Ab,Cry3Bb and Cry34Ab1 / 35Ab1. (12) Inhibitors of mitochondrial ATP synthase, preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotin, cyhexatin, and fenbutatin oxide, or propargite or tetradifon. (13) Uncouplers of oxidative phosphorylation by disrupting the proton gradient selected from chlorfenapyr, DNOC, and sulfluramide. (14) Blockers of the nicotinic acetylcholine receptor channel selected from bensultap, cartap hydrochloride, thiocyclam, and thiosultap sodium. (15) Chitin biosynthesis inhibitors, type 0, selected from bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron, and triflumuron. (16) Chitin biosynthesis inhibitors, type 1, selected from buprofezin. (17) Moulting disruptor (particularly in dipterans, i.e., flies) selected from cyromazine. (18) Ecdysone receptor agonists selected from chromafenozide, halofenozide,Methoxyfenozide and tebufenozide. (19) Octopamine receptor agonists selected from amitraz. (20) Mitochondrial complex III electron transport inhibitors selected from hydramethylnon, acequinocyl, and fluacrypyrim. (21) Mitochondrial complex I electron transport inhibitors, preferably METI acaricides selected from fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, and tolfenpyrad, or rotenone (Derris). (22) Voltage-gated sodium channel blockers selected from indoxacarb and metaflumizone. (23) Acetyl-CoA carboxylase inhibitors, preferably tetronic and tetramic acid derivatives selected from spirodiclofen, spiromesifen, and spirotetramat. (24) Inhibitors of mitochondrial complex IV electron transport, preferably phosphines selected from aluminum phosphide, calcium phosphide, phosphine, and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide, and sodium cyanide. (25) Inhibitors of mitochondrial complex II electron transport,preferably beta-ketonitrile derivatives selected from cyenopyrafen and cyflumetofen, or carboxanilides selected from pyflubumide. (28) Ryanodine receptor modulators, preferably diamides selected from chlorantraniliprole, cyantraniliprole, and flubendiamide. (29) Modulators of chordotonal organs (with undefined target structure) selected from flonicamid. (30) further active ingredients selected from Acynonapyr, Afidopyropen, Afoxolaner, Azadirachtin, Benclothiaz, Benzoximate, Benzpyrimoxane, Bifenazate, Broflanilide, Bromopropylate, Quinomethionate, Chloroprallethrin, Cryolite, Cyclaniliprol, Cycloxapride, Cyhalodiamide, Dicloromezotiaz, Dicofol, epsilon-Metofluthrin, epsilon-Momfluthrin, Flometoquin, Fluazaindolizine, Fluensulfone, Flufenerim, Flufenoxystrobin, Flufiprol, Fluhexafon, Fluopyram, Flupyrimine, Fluralaner, Fluxametamide, Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione, kappa-Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin, Oxazosulfyl, Paichongding, Pyridalyl, Pyrifluquinazone,Pyriminostrobin, spirobudiclovir, spiropidione, tetramethylfluthrin, tetraniliprol, tetrachloroantraniliprole, tigolaner, tioxazafen, thiofluoximate, triflumezopyrim and iodomethane; Furthermore, preparations based on Bacillus firmus (I-1582, BioNeem, Votivo), as well as the following compounds: 1-{2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazol-5-amine (known from WO2006 / 043635) (CAS 885026-50-6), {1'-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]-5-fluorospiro[indol-3,4'-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methanone (known from WO2003 / 106457) (CAS 637360-23-7), 2-Chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide (known from WO2006 / 003494) (CAS 872999-66-1), 3-(4-chloro- 2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2-one (known from WO 2010052161) (CAS 1225292-17-0), 3-(4-chloro-2, 6-dimethylphenyl)-8-methoxy-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-ethyl carbonate (known from EP 2647626) (CAS-1440516-42-6), 4-(But-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine (known from WO2004 / 099160) (CAS 792914-58-0), PF1364 (known from JP2010 / 018586) (CAS-Reg.No.1204776-60-2), (3E)-3-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoropropan-2-one (known from WO2013 / 144213) (CAS 1461743-15-6), N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide (known from WO2010 / 051926) (CAS 1226889-14-0), 5- Bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide (known from CN103232431) (CAS 1449220-44-3), 4-[5-(3,5-dichlorophenyl)-4,5-dihydro- and 4-[(5S)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluormethyl)-3-isoxazolyl]-2- methyl-N-(cis-1-oxido-3-thietanyl)benzamid (bekannt aus WO 2013 / 050317 A1) (CAS 1332628-83-7), N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid, (+)- N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid und (-)-N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid (bekannt aus WO 2013 / 162715 A2, WO 2013 / 162716 A2, US 2014 / 0213448 A1) (CAS 1477923-37-7), 5-[[(2E)-3-Chlor-2-propen-1-yl]amino]-1-[2,6-dichlor-4-(trifluormethyl)phenyl]-4- [(trifluormethyl)sulfinyl]-1H-pyrazol-3-carbonitrile (bekannt aus CN 101337937 A) (CAS 1105672-77- 2), 3-Brom-N-[4-chlor-2-methyl-6-[(methylamino)thioxomethyl]phenyl]-1-(3-chlor-2-pyridinyl)-1H- pyrazol-5-carboxamid, (Liudaibenjiaxuanan, bekannt aus CN 103109816 A) (CAS 1232543-85-9); N- [4-Chlor-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chlor-2-pyridinyl)-3- (fluormethoxy)-1H-pyrazol-5-carboxamid (bekannt aus WO 2012 / 034403 A1) (CAS 1268277-22-0), N- [2-(5-Amino-1,3,4-thiadiazol-2-yl)-4-chlor-6-methylphenyl]-3-brom-1-(3-chlor-2-pyridinyl)-1H- pyrazol-5-carboxamid (bekannt aus WO 2011 / 085575 A1) (CAS 1233882-22-8), 4-[3-[2,6-Dichlor-4- [(3,3-dichlor-2-propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluormethyl)pyrimidin (bekannt aus CN 101337940 A) (CAS 1108184-52-6); (2E)- und 2(Z)-2-[2-(4-Cyanophenyl)-1-[3- (trifluormethyl)phenyl]ethyliden]-N-[4-(difluormethoxy)phenyl]hydrazincarboxamid (bekannt aus CN 101715774 A) (CAS 1232543-85-9); Cyclopropancarbonsäure-3-(2,2-dichlorethenyl)-2,2-dimethyl-4- (1H-benzimidazol-2-yl)phenylester (bekannt aus CN 103524422 A) (CAS 1542271-46-4); (4aS)-7- Chlor-2,5-dihydro-2-[[(methoxycarbonyl)[4-[(trifluormethyl)thio]phenyl]amino]carbonyl]indeno[1,2- e][1,3,4]oxadiazin-4a(3H)-carbonsäuremethylester (bekannt aus CN 102391261 A) (CAS 1370358-69- 2); 6-Desoxy-3-O-ethyl-2,4-di-O-methyl-1-[N-[4-[1-[4-(1,1,2,2,2-pentafluorethoxy)phenyl]-1H-1,2,4- triazol-3-yl]phenyl]carbamat]-α-L-mannopyranose (bekannt aus US 2014 / 0275503 A1) (CAS 1181213- 14-8); 8-(2-Cyclopropylmethoxy-4-trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (CAS 1253850-56-4), (8-anti)-8-(2-Cyclopropylmethoxy-4- trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3-azabicyclo[3.2.1]octan (CAS 933798-27- 7), (8-syn)-8-(2-Cyclopropylmethoxy-4-trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (bekannt aus WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8), N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluorpropyl)thio]-propanamid (bekannt aus WO 2015 / 058021 A1,WO 2015 / 058028 A1) (CAS 1477919-27-9) and N-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide (known from CN 103265527 A) (CAS 1452877-50-7), 5-(1,3-Dioxan-2-yl)-4-[[4-(trifluoromethyl)phenyl]methoxy]-pyrimidine (known from WO 2013 / 115391 A1) (CAS 1449021-97-9), 3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione (known from WO 2014 / 187846 A1) (CAS 1638765-58-8), 3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl- 2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carboxylic acid ethyl ester (known from WO 2010 / 066780 A1, WO 2011151146 A1) (CAS 1229023-00-0), 4-[(5S)-5-(3,5-Dichloro-4-fluorophenyl)-4,5-dihydro-5- (trifluoromethyl)-3-isoxazolyl]-N-[(4R)-2-ethyl-3-oxo-4-isoxazolidinyl]-2-methylbenzamide (known from WO 2011 / 067272, WO2013 / 050302) (CAS 1309959-62-3). Insecticides that can preferably be used together with the herbicide / safener combinations according to the invention are:are, for example, the following: Acetamiprid, Acrinathrin, Aldicarb, Amitraz, Acinphos-methyl, Cyfluthrin, Carbaryl, Cypermethrin, Deltamethrin, Endosulfan, Ethoprophos, Fenamiphos, Fenthion, Fipronil, Imidacloprid, Methamidophos, Methiocarb, Niclosamide, Oxydemeton-methyl, Prothiophos, Silafluofen, Thiacloprid, Thiodicarb, Tralomethrin, Triazophos, Trichlorfon, Triflumuron, Terbufos, Fonofos, Phorate, Chlorpyriphos, Carbofuran, Tefluthrin. The herbicide / safener combinations according to the invention are preferably suitable for controlling undesirable plant growth in economically important crops such as wheat (durum and soft wheat), maize, soybeans, sugar beet, sugar cane, cotton, rice, beans (such as, for example, bush beans and horse beans), flax, barley, oats, rye, triticale,Potato and millet (sorghum). The herbicide / safener combinations according to the invention can be applied jointly or separately to the plants (e.g., harmful plants such as monocotyledonous or dicotyledonous weeds or undesirable crops), the seeds (e.g., grains, seeds, or vegetative propagating organs such as tubers or shoots with buds), or the area on which the plants grow (e.g., the cultivated area). The herbicide / safener combinations can be applied pre-sowing (if necessary, also by incorporation into the soil), pre-emergence, or post-emergence. Application is preferred in the early post-sowing pre-emergence or post-emergence methods against weeds that have not yet emerged or have already emerged. Application can also be carried out in weed management systems with divided multiple applications (sequence applications,"sequentials"). Some examples of representatives of the monocotyledonous and dicotyledonous weed flora that can be controlled by the herbicide / safener combinations according to the invention are mentioned, without implying a restriction to specific species. On the side of the monocotyledonous weed species, for example Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachicaria, Bromus, Cynodon, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Imperata, Ischaemum, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum, Sphenoclea and Cyperus species are included in the annual group. For dicotyledonous weed species, the spectrum of activity extends to species such as Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia,Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erodium, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Geranium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium. If the herbicide / safener combinations according to the invention are applied to the soil surface before germination, either the emergence of weed seedlings is completely prevented or the weeds grow to the cotyledon stage,However, they then cease growth and finally die completely after three to four weeks. When the herbicide / safener combinations are applied post-emergence to the green parts of the plants, growth stops after treatment, and the weeds remain in the growth stage present at the time of application or die completely after a certain period of time, thus eliminating weed competition that is harmful to the crop plants very early and sustainably. The crop plants, on the other hand, are not or only slightly affected in their development by the application of the herbicide / safener combination. The herbicide / safener combinations according to the invention are characterized by a rapid onset and long-lasting herbicidal action. The rainfastness of the active ingredients in the combinations according to the invention is generally favorable. A particular advantage isthat the effective dosages of components (A) and (B) used in the herbicide / safener combinations can be set so low that their soil effect is optimally low. This not only makes their use in sensitive crops possible, but also virtually prevents groundwater contamination. Economically important crops for the application of the herbicide / safener combinations according to the invention include, for example, dicotyledonous crops of the genera Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia, or monocotyledonous crops of the genera Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale, Triticum and Zea. Preferably, the herbicide / safener combinations according to the invention can also be used in transgenic crops which are resistant to growth factors or to herbicides,which inhibit essential plant enzymes, e.g., acetolactate synthases (ALS), EPSP synthases, glutamine synthases (GS), protoporphyrinogen IX oxidase (PPO), or hydroxyphenylpyruvate dioxygenases (HPPD), or are resistant to herbicides from the group of sulfonylureas, glyphosates, glufosinates, or benzoyl isoxazoles and analogous active ingredients. The herbicide / safener combinations according to the invention can be present either as mixed formulations of components (A) and (B), optionally with other active ingredients, additives, and / or conventional formulation auxiliaries, which are then diluted with water in the usual way for application, or as so-called tank mixes by jointly diluting the separately formulated or partially separately formulated components with water. The herbicide / safener combinations according to the invention can be formulated in various ways,Depending on the biological and / or chemical-physical parameters specified. General formulation options include, for example: wettable powders (WP), water-soluble powders (SP), emulsifiable concentrates (EC), water-soluble concentrates, aqueous solutions (SL), emulsions (EW) such as oil-in-water and water-in-oil emulsions, sprayable solutions or emulsions, oil- or water-based dispersions, oil dispersions (OD), suspoemulsions, suspension concentrates (SC), oil-miscible solutions, capsule suspensions (CS), dusts (DP), seed dressings, granules for soil or broadcast application, granules (GR) in the form of microgranules, spray granules, and adsorption granules, water-dispersible granules (WG), water-soluble granules (SG), ULV formulations, microcapsules, or waxes. The invention therefore also relates to herbicidal and plant growth regulating agents.which contain the herbicide / safener combinations according to the invention. The individual formulation types are known in principle and are described, for example, in: Winnacker-Küchler, "Chemische Technologie," Volume 7, C. Hanser Verlag, Munich, 4th ed., 1986; van Valkenburg, "Pesticides Formulations," Marcel Dekker, NY, 1973; K. Martens, "Spray Drying Handbook," 3rd ed., 1979, G. Goodwin Ltd., London. The necessary formulation aids such as inert materials, surfactants, solvents, and other additives are also known and are described, for example, in: Watkins, "Handbook of Insecticide Dust Diluents and Carriers," 2nd ed., Darland Books, Caldwell, NJ; Hv. Olphen, "Introduction to Clay Colloid Chemistry," 2nd ed., J. Wiley & Sons, NY; Marsden, "Solvents Guide," 2nd ed., Interscience, NY, 1963; McCutcheon's, "Detergents and Emulsifiers Annual," MC Publ. Corp., Ridegewood NJ; Sisley and Wood, “Encyclopedia of Surface Active Agents,” Chem. Publ. Co. Inc.,NY1964; Schönfeldt, "Grenzflächenaktive Äthylenoxidaddukte", Wiss. Verlagsgesellschaft, Stuttgart 1976, Winnacker-Küchler, "Chemische Technologie", Volume 7, C. Hanser Verlag Munich, 4th edition 1986. These formulations can also be used to produce combinations with other pesticidally active substances, such as other herbicides, fungicides, insecticides, or other pesticides (e.g., acaricides, nematicides, molluscicides, rodenticides, aphicides, avicides, larvicides, ovicides, bactericides, virucides, etc.), as well as other safeners, fertilizers, and / or growth regulators, e.g., in the form of a ready-to-use formulation or as a tank mix. Wettable powders are preparations which are evenly dispersible in water and which, in addition to the active ingredient, contain a diluent or inert substance as well as ionic and / or non-ionic surfactants (wetting agents, dispersants), e.g. polyoxyethylated alkylphenols, polyoxyethylated fatty alcohols, polyoxyethylated fatty amines,Fatty alcohol polyglycol ether sulfates, alkanesulfonates, alkylbenzenesulfonates, sodium ligninsulfonate, sodium 2,2'-dinaphthylmethane-6,6'-disulfonate, sodium dibutylnaphthalenesulfonate, or sodium oleoylmethyltaurine. To produce the wettable powders, the herbicidal active ingredients are finely ground in conventional equipment such as hammer mills, fan mills, and air jet mills and mixed simultaneously or subsequently with the formulation auxiliaries. Emulsifiable concentrates are prepared by dissolving the active ingredient in an organic solvent, e.g., butanol, cyclohexanone, dimethylformamide,Xylene or higher-boiling aromatics or hydrocarbons or mixtures of organic solvents with the addition of one or more ionic and / or non-ionic surfactants (emulsifiers). Examples of emulsifiers that can be used are: calcium salts of alkylarylsulfonic acid such as calcium dodecylbenzenesulfonate or non-ionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan esters such as sorbitan fatty acid esters or polyoxyethylene sorbitan fatty acid esters. Dusts are obtained by grinding the active ingredient with finely divided solid substances, e.g. talc, natural clays such as kaolin, bentonite and pyrophyllite, or diatomaceous earth. Suspension concentrates can be water- or oil-based. They can be obtained, for example, by wet grinding using commercially available bead mills and, if necessary, adding surfactants,as already listed above for the other formulation types. Emulsions, e.g. oil-in-water emulsions (EW), can be produced using stirrers, colloid mills and / or static mixers using aqueous organic solvents and, if appropriate, surfactants, as already listed above for the other formulation types. Granules can be produced either by spraying the active ingredient onto adsorptive, granulated inert material or by applying active ingredient concentrates using adhesives, e.g. polyvinyl alcohol, sodium polyacrylate or mineral oils, to the surface of carrier materials such as sand,Kaolinite or granulated inert material. Suitable active ingredients can also be granulated in the manner customary for the production of fertilizer granules – if desired, in a mixture with fertilizers. Water-dispersible granules are generally produced by processes such as spray drying, fluidized-bed granulation, disc granulation, mixing with high-speed mixers, and extrusion without solid inert material. The agrochemical preparations generally contain 0.1 to 99% by weight, in particular 0.2 to 95% by weight, of active ingredients of components (A) and / or (B). Depending on the type of formulation, the following concentrations are usual: In wettable powders, the active ingredient concentration is, for example, about 10 to 95% by weight, the remainder to 100% by weight consisting of customary formulation components. In emulsifiable concentrates, the active ingredient concentration can be about 1 to 90% by weight.preferably 5 to 80% by weight. Dust-like formulations usually contain 5 to 20% by weight of active ingredient, sprayable solutions contain approximately 0.05 to 80, preferably 2 to 50% by weight (wt. %) of active ingredient. In granules such as dispersible granules, the active ingredient content depends partly on whether the active compound is liquid or solid and which granulation aids and fillers are used. As a rule, the content for water-dispersible granules is between 1 and 95% by weight, preferably between 10 and 80% by weight. In addition, the above-mentioned active ingredient formulations may contain the usual adhesives, wetting agents, dispersants, emulsifiers, penetration agents, preservatives, antifreeze agents, solvents, fillers, dyes, carriers, defoamers, evaporation inhibitors, and agents,which influence the pH or viscosity. For application, the formulations available in commercial form are diluted, if necessary, in the usual way, e.g., with water in the case of wettable powders, emulsifiable concentrates, dispersions, and water-dispersible granules. Dust-like preparations, soil or broadcast granules, and sprayable solutions are not usually diluted with other inert substances before application. The herbicide / safener combinations according to the invention can be applied to the plants, plant parts, plant seeds, or the cultivated area (arable soil), preferably to the green plants and plant parts and, if appropriate, additionally to the arable soil. One possible application is the joint application of the herbicide / safener combinations in the form of tank mixtures.wherein the optimally formulated concentrated formulations of the individual active ingredients are mixed together with water in a tank, and the resulting spray mixture is applied. A joint formulation of the herbicide / safener combinations according to the invention has the advantage of being easier to use because the amounts of the components are already adjusted in the correct ratio to one another. Furthermore, the auxiliaries in the formulation can be optimally matched to one another, whereas a tank mix of different formulations can result in undesirable combinations of auxiliaries. General formulation examples a)-f): a) A dust is obtained by mixing 10 parts by weight (= parts by weight) of a component (A) or (B) or a component mixture (A) + (B) (and optionally further components) and / or their salts and 90 parts by weight of talc as an inert substance and comminuting in a hammer mill. b) A readily water-dispersible,A wettable powder is obtained by mixing 25 parts by weight of a component or a component mixture, 64 parts by weight of kaolin-containing quartz as an inert material, 10 parts by weight of potassium ligninsulfonate, and 1 part by weight of sodium oleoylmethyltaurine as a wetting and dispersing agent, and grinding the mixture in a pin-type mill. c) A dispersion concentrate that is easily dispersible in water is obtained by mixing 20 parts by weight of a component or a component mixture with 6 parts by weight of alkylphenol polyglycol ether (®Triton X 207), 3 parts by weight of isotridecanol polyglycol ether (8 EO), and 71 parts by weight of paraffinic mineral oil (boiling range, for example, approx. 255 to 277 °C) and grinding the mixture in a ball mill to a fineness of less than 5 microns. d) An emulsifiable concentrate is obtained from 15 parts by weight of a component or a mixture of components,75 parts by weight of cyclohexanone as solvent and 10 parts by weight of ethoxylated nonylphenol as emulsifier. e) Water-dispersible granules are obtained by mixing 75 parts by weight of one component of a component mixture, 10 parts by weight of calcium ligninsulfonate, 5 parts by weight of sodium lauryl sulfate, 3 parts by weight of polyvinyl alcohol, and 7 parts by weight of kaolin, grinding the mixture in a pin mill, and granulating the powder in a fluidized bed by spraying water as the granulating liquid. f) A water-dispersible granulate is also obtained by homogenising and pre-crushing 25 parts by weight of one component of a component mixture, 5 parts by weight of 2,2'-dinaphthylmethane-6,6'-disulfonic acid sodium, 2 parts by weight of oleoylmethyltauric acid sodium, 1 part by weight of polyvinyl alcohol, 17 parts by weight of calcium carbonate and 50 parts by weight of water on a colloid mill,subsequently ground in a bead mill, and the resulting suspension is atomized and dried in a spray tower using a single-component nozzle. BIOLOGICAL EXAMPLES Effect of selected herbicide / safener combinations according to the invention: The seeds of the crops to be treated were placed in soil in plastic pots (diameter ~7 cm), covered with soil, and grown in a greenhouse under favorable conditions for germination and growth. The test plants were treated in the early leaf stage (BBCH12). The safeners used (inventive safener according to compound A3, as well as mefenpyr diethyl and cloquintocet as comparison safeners) were sprayed as wettable powders (WP) at a dose of 100 g / ha with a water application rate corresponding to 300 l / ha, with the addition of the safener. The herbicide was then applied (component B, selected from: B1-6, B1-38, B1-42, B1-46, B1-66,B1-68). The herbicides used were formulated as wettable powders (WP), emulsifiable concentrates (EC), and / or water-soluble concentrates (SL), mixed according to the respective dosage, and sprayed onto the above-ground parts of the plants at a water application rate corresponding to 300 l / ha with the addition of formulation aids (Mero, 1.5 l / ha and diammonium phosphate (DAP), 1 g / ha). The herbicide dosage was selected such thatthat in the control treatment (herbicide without safener), a damage level of between 98 and 45% is achieved. Experience has shown that this allows for the best possible visual assessment of the safener effect under greenhouse conditions. After application, the plants were cultivated in a greenhouse under favorable growth conditions. 21 days after application, a visual assessment of the herbicide damage was carried out. The damage was visually assessed on a scale of 0-100% in comparison to untreated control plants and averaged across two replicates per treatment. Examples: 0% = no discernible effect compared to the untreated plant; 20% = the treated plant population is 20% damaged compared to the untreated control population (e.g., growth height, leaf damage, etc.); 100% = treated plants completely damaged or dead. The experiments show,that damage to the crop barley (HORVS; approx. Accordine) caused by the respective herbicide (component (B)) (= herbicide damage without safener by adding a safener (component (A)) is significantly reduced. The safeners were each applied at an application rate of 100 g / ha. In particular, compared to the known safeners mefenpyr-diethyl and cloquintocet, a significantly stronger safener effect was observed when compound A3 was used as the safener component (see Tables 9 and 10).

Claims

1. Herbicide / safener combination comprising one or more compounds (A) acting as safeners and one or more herbicidally active compounds (B), where (A) is one or more compounds of the general formula (I) or their agrochemically acceptable salts, and where (R a ) p -Phenyl for groups Q-1.1 to Q-1.55 stands, and (R b )q-Phenyl for the groups Q-2.1 to Q-2.55 stands, R c stands for hydrogen, and R dfür Wasserstoff, Methyl, Ethyl, n-Propyl, i-Propyl, n-Butyl, n-Pentyl, Phenyl, Benzyl, CH2(4-Cl-Ph), CH2(4-F-Ph), CH2(4-OMe-Ph), 2-Methoxyethyl, Tetrahydrofuran-2-yl- methyl, Tetrahydrofuran-3-yl-methyl, Tetrahydropyran-2-yl-methyl, Tetrahydropyran-3-yl- methyl, Tetrahydropyran-4-yl-methyl, Methylpropionat-3-yl, Ethylpropionat-3-yl, Methylacetat-2-yl, Ethylacetat-2-yl, Methylpivalat-2-yl, Ethylpivalat-3-yl, Methyl-2- methylpropanoat-3-yl, Methyl-2,2-dimethylpropanoat-3-yl, Ethyl-2-methylpropanoat-3-yl, Methyl-2-propanoat-2-yl, Ethyl-2-propanoat-2-yl, Methyl-acetat-2yl, Ethyl-acetat-2yl, Methyl-1-methylcyclopropancarboxylat-2yl, Ethyl-1-methylcyclopropan-carboxylat-2yl, 2-(Dimethylamino)ethyl, Oxetan-3-yl, (3-Methyloxetan-3-yl)methyl, 2,2,2-Trifluorethyl, 2,2-Difluoroethyl, 2-Fluoroethyl, 2,2,3,3,3-Pentafluoropropyl, Cyclopropylmethyl, 1-Cyclopropyl-ethyl, (1-Methyl-cyclopropyl)-methyl, (2,2-Dichlorocyclopropyl)-methyl, (2,2-Dimethyl-cyclopropyl)-methyl, Allyl, Propargyl (Prop-2-yn-1-yl), 2-Chloroprop-2-en-1-yl, 3-Phenylprop-2-yn-1-yl, 3,3-Dichloroprop-2-en-1-yl, 3,3-Dichloro-2-fluoro-prop-2-en-1-yl, Methylprop-2-yn-1-yl, 2-Methylprop-2-en-1-yl, But-2-en-1-yl, But-3-en-1-yl, But-2-yn-1-yl, but-3-yn-1-yl, 4-chloro-but-2-yn-1-yl, 3-methyl-but-2-en-1-yl, 3-methyl-but-1-en-1-yl, 1-(2E)-1-methylbut-2-en-1-yl, (E)-pent-3-en-2-yl or (Z)-pent-3-en-2-yl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, heptan-2-yl, iso-butyl, 1,3-dioxolan-2-ylmethyl or 1-ethyl-5-methyl-1-pyrazol-4-methyl, and (B) represents one or more compounds of the general formula (II) or their agrochemically acceptable salts, wherein Q is selected from a group consisting of Q-1, Q-2, Q-3, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-11, Q-12, Q-13, Q-14, Q-15, Q-16, Q-17, Q-18, Q-19, Q-20, Q-21, Q-22, Q-23, Q-24, Q-25, Q-26, Q-27, Q-28, Q-29, Q-30, Q-31 and Q-32: where the arrow X indicates the bond of the carbon atom to the residue Z and the dashed line indicates the bond of the carbon atom to the residue W; R 1 represents methyl, ethynyl, 1-propynyl, phenyl or a five- or six-membered heteroaryl ring containing one or two nitrogen atoms, where the phenyl ring and the heteroaryl ring are connected by one or two radicals R 9 can be substituted, R 2 represents chlorine, (C1-C3)-alkoxy, (C1-C2)-alkoxy-(C1-C3)-alkoxy, (C1-C2)-fluoroalkoxy, methyl, ethyl, n-propyl, n-butyl, cyclopropyl or ethynyl, R 3represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, cyclopropyl, vinyl, ethynyl, (C1-C3)-alkoxy, (C1-C3)-fluoroalkyl, (C1-C2)-fluoroalkoxy, (C1-C2)-alkoxy-(C1-C3)-alkoxy or C1-fluoroalkoxy-(C1-C3)-alkoxy, W represents a bond, CR 4 R 5 , O, NH or N-CH3, Z represents a bond, CR 6 R 7 , O, NH or N-CH3, provided that W and Z do not both represent a bond, Y represents O or NR 8 n1 and n2 independently represent 0, 1, 2 or 3, provided that n1 + n2 is equal to 2, 3, 4, 5 or 6, R 1Q3 represents hydrogen, (C1-C6)-alkyl, (C1-C6)-haloalkyl, (C1-C6)-alkoxy-(C1-C3)-alkyl or (C1-C6)-haloalkoxy-(C1-C3)-alkyl, R 2Q3 for -(CH2) k -R 3Q3 where R 3Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and - S(O)2NR 16N R 17N, and k is 0, 1 or 2, or R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 independently represent 1 or 2, R 4Q3 represents hydrogen, (C1-C6)-alkyl, hydroxy, methoxy or halogen, R 5Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and -S(O)2NR 16N R 17N , or R 4Q3 and R 5Q3 together for -(CH2) nq3 -N(R 8 )-(CH2) nq4 - where nq3 and nq4 independently represent 1 or 2, R 1Q10 and R 2Q10 are independently selected from a group consisting of hydrogen, halogen, (C1-C3)-alkyl, (C1-C3)-haloalkyl and (C1-C3)-alkoxy, Y p is selected from a group consisting of O, CR Y1 R Y2 and NR Y3 , where R Y1represents hydrogen or (C1-C4)-alkyl, R Y2 represents hydrogen or (C1-C4)-alkyl and R Y3 is selected from a group consisting of hydrogen, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-haloalkyl, -(CO)(C1-C4)-alkyl and -(CO)(C1-C4)-haloalkyl; Y q stands for N or CH, R 4 , R 5 , R 6 and R 7 independently of one another represent hydrogen, (C1-C5)-alkyl, (C2-C4)-alkenyl, (C2-C4)-alkynyl, (C1-C2)-fluoroalkyl, (C1-C3)-alkoxy-(C1-C3)-alkyl, (C1-C3)-alkylthio-(C1-C3)-alkyl, (C1-C3)-alkylsulfinyl-(C1-C3)-alkyl, (C1-C3)-alkylsulfonyl-(C1-C3)-alkyl, (C3-C4)-cycloalkyl or represent an unsubstituted 4, 5 or 6-membered monocyclic heterocyclyl ring which carries a ring heteroatom selected from the group consisting of oxygen, sulfur or nitrogen and which is attached within the heterocyclyl group to a ring carbon atom, with the proviso that not more than one of the radicals from the group R4 , R 5 , R 6 and R 7 represents alkenyl, alkynyl, alkoxyalkyl, alkylthioalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, cycloalkyl or heterocyclyl, or R 4 and R 5 together a group -(CH2) n3 - or -(CH2) n4 -X 1 -(CH2) n5 - form and R 6 and R 7 as defined above, or R 6 and R 7 together a group -(CH2) n3 - or -(CH2) n4 -X 1 -(CH2) n5 - form and R 4 and R 5 as defined above, where X 1 for O (oxygen), S (sulfur), S(O), S(O)2, N(R 8 ), C(H)((C1-C2)-alkyl), C((C1-C2)-alkyl)2or C(H)((C1-C2)-alkoxy); n3 is 2, 3, 4 or 5, n4 and n5 independently of one another are 1, 2 or 3, provided that n4 + n5 is equal to 2, 3 or 4, or R 5 and R 6 together a group -(CH2) n6 - or -(CH2)n7 -C(R 10a )(R 10b )-(CH2) n8 - or - C(R 10c )=C(R 10d )-, where R 10a represents (C1-C2)-alkyl or (C1-C2)-alkoxy; and R 10b represents hydrogen or (C1-C2)-alkyl, provided that R 10b stands for hydrogen, if R 10a represents (C1-C2)-alkoxy and wherein n6 represents 1, 2 or 3 and n7 and n8 independently represent 0, 1 or 2, with the proviso that n7 + n8 is equal to 0, 1 or 2 and wherein R 10c and R 10d independently of one another represent hydrogen or (C1-C2)-alkyl, R 8 for hydrogen, (C1-C4)-alkyl, (C1-C4)-alkoxy, (C1-C4)-haloalkyl, -C(O)(C1-C4)-alkyl, -C(O)(C1-C4)-haloalkyl, -S(O) n (C1-C6)-alkyl, -S(O) n (C1-C6)-haloalkyl, -S(O) n -(CH2) n -(C3-C6)-cycloalkyl, -S(O) n C(R 11N )R 12N R 13N , -C(O)H, -C(O)-(CH2) n-(C3-C6)-Cycloalkyl, -C(O)C(R 11N )R 12N R 13N , - C(O)(C2-C4)-Alkenyl, -C(O)(CR 9N R 10N )CN, -C(O)(CR 9N R 10N )(CR 9N R 10N )CN, -C(O)CH2C(O)-(C1- C6)-Alkyl, -C(O)CH2OC(O)-(C1-C6)-Alkyl, -C(O)O(C1-C6)-Alkyl, -C(O)O(C1-C6)-Haloalkyl, - C(O)(CH2)nS(O) n (C1-C6)-Alkyl, -C(O)(C1-C3)-Alkoxy-(C1-C6)-alkyl, -C(O)(C1-C3)-Alkoxy-(C2- C6)-alkenyl, -C(O)(C1-C3)-Alkoxy-(C2-C6)-alkinyl, -C(O)(C1-C3)-Alkoxy-(C1-C6)-haloalkyl, - C(O)(C1-C3)-Alkoxy-(C3-C6)-cycloalkyl, -C(O)O(C1-C3)-Alkoxy-(C1-C6)-alkyl, -C(O)(C1-C3)- Alkoxy-(C1-C3)-alkoxy-(C1-C6)-alkyl, -C(O)(CH2)nNR 5N R 6N , -C(O)-(CH2) n -NR 7N C(O)R 8N , -C(O)- (CH2) n -O-N=CR 5N R 5N , -CN, -S(O)2NR 16N R 17N , -S(O)(=NR 18N )R 19N , -C(O)C(O)R 20N , - C(O)C(R 23N )=N-O-R 24N , -C(O)C(R 23N )=N-NR 25N R 26N, -(CH2) n -Phenyl, -C(O)-(CH2) n -phenyl, -S(O) n -(CH2) n -Phenyl, Heterocyclyl, -C(O)-(CH2) n -Heterocyclyl, -C(O)(CH2) n -O-(CH2) n - Heterocyclyl, -S(O) n -(CH2) n -Heterocyclyl, wherein each heterocyclyl radical is a five- or six-membered heterocyclyl ring which may be aromatic, saturated or partially saturated and which may contain one to four heteroatoms, wherein each heteroatom is independently selected from a group consisting of oxygen, nitrogen and sulfur, and wherein heterocyclyl or phenyl rings are optionally substituted by one, two or three substituents which are independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; R 9represents substituents which are independently selected from a group consisting of (C1-C4)alkyl, (C1-C4)haloalkyl, cyano and halogen; R 5N represents substituents which are independently selected from a group consisting of hydrogen and (C1-C6)-alkyl, R 6N represents substituents which are independently selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C2-C6)-alkenyl, (C2-C6)-alkynyl, (C1-C6)-haloalkyl, hydroxy, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, -(C1-C4)-alkoxy-(C1-C6)-alkyl, -(C1-C3)-alkoxy-(C1-C6)-haloalkyl, -(CR 9N R 10N )-(C1-C6)-haloalkyl, -(CR 9N R 10N )C(O)NR 5N R 5N , -C(O)H, -C(O)-(CH2) n -(C3-C6)-cycloalkyl, -C(O)-(CH2) n -C(R 11N )R 12N R 13N , phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents which are independently are selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; or R 5N and R 6N together form -CH2CH2OCH2CH2-; and R 7N is selected from a group consisting of hydrogen and (C1-C6)-alkyl; R 8N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 9N represents hydrogen or methyl; R 10N represents hydrogen or methyl; or R 9N and R 10N together form -CH2CH2-; and R 11N represents hydrogen or methyl; R 12Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, hydroxy and (C1-C6)-alkoxy; R 13N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, hydroxy and (C1-C6)-alkoxy; or R 12N and R 13N together form -CH2-X-CH2-; and X is selected from a group consisting of O, S and NR 14N ; R 14N is selected from a group consisting of hydrogen, (C1-C3)-alkyl and (C1-C3)-alkoxy; R 16N represents hydrogen or (C1-C6)-alkyl; and R 17N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C3-C6)-cycloalkyl, (C1-C6)-alkoxy-(C1-C3)-alkyl, -C(O)(C1-C6)-alkyl, -C(O)O(C1-C6)-alkyl and CH2CN; or R 16N and R 17N together form -CH2CH2OCH2CH2-, -CH2CH2S(O)2CH2CH2-; R 18N represents hydrogen or (C1-C6)-alkyl; R 19Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C3-C6)-cycloalkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 20N is selected from a group consisting of (C1-C6)alkyl, (C1-C6)haloalkyl, (C1-C6)alkoxy, (C1-C6)haloalkoxy, -NR 21N R 22N , phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; R 21Nis selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-alkoxy, (C1-C6)-alkoxy-(C1-C3)-alkyl, (C3-C6)-cycloalkyl, (C1-C6)-haloalkyl and (C1-C6)-haloalkoxy, - C(O)(C1-C6)-alkyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)-alkyl, (C1-C3)-haloalkyl, (C1-C3)-alkoxy, (C2-C3)-alkenyl, (C2-C3)-alkynyl, halogen, cyano and nitro; R 22N represents hydrogen or (C1-C6)-alkyl; or R 21N and R 22N together form -CH2CH2OCH2CH2-; R 23N is selected from a group consisting of hydrogen, (C1-C6)-alkyl, (C1-C6)-haloalkyl, (C1-C6)-alkoxy-, (C1-C6)-haloalkoxy; R 24Nis selected from a group consisting of hydrogen, (C1-C6)alkyl, (C1-C6)alkoxy-(C1-C3)alkyl, (C3-C6)cycloalkyl, -CH2CN, tetrahydropyranyl, phenyl, pyridyl, wherein the phenyl and pyridyl rings are optionally substituted by one, two or three substituents independently selected from a group consisting of (C1-C3)alkyl, (C1-C3)haloalkyl, (C1-C3)alkoxy, (C2-C3)alkenyl, (C2-C3)alkynyl, halogen, cyano and nitro; R 25N represents hydrogen or (C1-C6)-alkyl; R 26N represents hydrogen or (C1-C6)-alkyl; n independently represents 0, 1 or 2; G represents hydrogen, an agronomically acceptable metal, an agronomically acceptable sulfonium group, an agronomically acceptable ammonium group, a group C(X 3 )-R 14 , -C(X 4 )-X 5 -R 15 , -C(X 6 )- N(R 16 )-R 17 , -SO2-R 18 , -P(X 7 )(R 19 )-R 20, -CH2-X 8 -R 21 , (C1-C6)-alkoxy-C(O)-CH2-, (C1-C6)-alkoxy- C(O)-CH=CH-, (C2-C7)-alken-1-yl-CH2-, (C2-C7)-alken-1-yl-CH[(C1-C2)-alkyl]-, (C2-C4)-fluoroalken-1-yl-CH2-, (C2-C7)-alkyn-1-yl-CH2-, (C2-C7)-alkyn-1-yl-CH[(C1-C2)-alkyl]-, heteroaryl-CH2-, heteroaryl-CH[(C1-C2)-alkyl]-, phenyl-CH2-, phenyl-CH[(C1-C2)-alkyl]-, phenyl-C(O)-CH2- stands, whereby the phenyl or heteroaryl group optionally continues is independently substituted by 1, 2 or 3 groups selected from (C1-C2)-alkyl, C1-fluoroalkyl, (C1-C2)-alkoxy, C1-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, X 3 , X 4 , X 5 , X 6 , X 7 and X 8 independently represent O (oxygen) and S (sulfur), R 14 represents hydrogen, (C1-C21)-alkyl, (C2-C21)-alkenyl, (C2-C 18 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1- C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)- alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio- (C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)alkyl, (C1-C3)fluoroalkyl, (C1-C2)alkoxy, (C1-C3)fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl, or which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, R 15 for (C1-C 18 )-alkyl, (C3-C 18 )-alkenyl, (C3-C 18 )-alkynyl, (C2-C 10 )-fluoroalkyl, (C1-C 10)-Cyanoalkyl, (C1-C 10 )-Nitroalkyl, (C2-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls weiter unabhänig voneinander durch 1, 2 oder 3 Gruppen ausgewählt aus (C1-C3)-Alkyl, (C1-C3)-FluoralkyI, (C1- C2)-Alkoxy, (C1-C3)-Fluoralkoxy, (C1-C3)-Alkylthio, (C1-C3)-Alkylsulfinyl, (C1-C3)- Alkylsulfonyl, Fluor, Chlor, Brom, Cyano,Nitro is substituted, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; Phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, R, 16 and R 17 independently of each other for hydrogen, (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )- alkynyl, (C2-C10 )-Fluoralkyl, (C1-C 10 )-Cyanoalkyl, (C1-C 10 )-Nitroalkyl, (C1-C 10 )-Aminoalkyl, (C1- C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)- alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1- C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)- Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)-Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1- C5)-alkyl, (C1-C5)-Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylaminocarbonyl-(C1-C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylcarbonylamino-(C1-C5)-alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1-C5)-alkyl, Phenyl-(C1-C5)-alkyl, wobei die Phenylgruppe gegebenenfalls further independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, heteroaryl-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy,(C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino in which the each phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diphenylamino or diphenylamino, in which the each phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl,(C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro is substituted, (C3-C7)-cycloalkylamino, di-[(C3-C7)-cycloalkyl]amino, (C3-C7)-cycloalkoxy; or R, 16 and R 17 , together with the nitrogen atom to which they are attached, form an unsubstituted 4- to 7-membered ring, which optionally comprises a heteroatom from the group O (oxygen) and S (sulfur), R 18 for (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-trialkylsilyl-(C1-C5)-alkyl, phenyl-(C1-C5)-alkyl, where the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, heteroaryl-(C1-C5)-alkyl, where the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano,Nitro is substituted, Heteroaryl or heteroaryl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, Heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, Diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano,Nitro is substituted, diphenylamino or diphenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, (C3-C7)-cycloalkylamino, di-[(C3-C7)-cycloalkyl]amino, (C3-C7)-cycloalkoxy, (C1-C, 10 )-alkoxy, (C1-C 10 )-fluoroalkoxy, (C3-C7)-alkylamino, di-[(C3-C7)-alkyl]amino; R 19 and R 20 independently for (C1-C 10 )-alkyl, (C2-C 10 )-alkenyl, (C2-C 10 )-alkynyl, (C1-C 10 )- fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C1-C 10)-Aminoalkyl, (C1-C5)- Alkylamino(C1-C5)-alkyl, (C2-C8)-Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3-C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)- alkyl, (C1-C5)-Alkylthio-(C1-C5)-alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)- Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)-Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1- C5)-alkyl, (C1-C5)-Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylaminocarbonyl-(C1-C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkylcarbonylamino-(C1-C5)-alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-trialkylsilyl-(C1-C5)-alkyl, phenyl-(C1-C5)-alkyl, where the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, heteroaryl-(C1-C5)-alkyl, where the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, (C2-C5)-fluoroalkenyl, (C3-C8)-cycloalkyl; phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently substituted by 1,2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroarylamino or heteroarylamino in which the heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diheteroarylamino or diheteroarylamino in which the respective heteroaryl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenylamino or phenylamino, in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, diphenylamino or diphenylamino,in which the respective phenyl group is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, benzyloxy and phenyloxy, wherein the respective phenyl group is optionally further independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, and R, 21 for (C1-C 10 )-alkyl, (C3-C 10 )-alkenyl, (C3-C 10 )-alkynyl, (C1-C 10 )-fluoroalkyl, (C1-C 10 )-cyanoalkyl, (C1-C 10 )-nitroalkyl, (C2-C 10)-Aminoalkyl, (C1-C5)-Alkylamino(C1-C5)-alkyl, (C2-C8)- Dialkylamino(C1-C5)-alkyl, (C3-C7)-Cycloalkyl-(C1-C5)-alkyl, (C1-C5)-Alkoxy-(C1-C5)-alkyl, (C3- C5)-Alkenyloxy-(C1-C5)-alkyl, (C3-C5)-Alkinyloxy-(C1-C5)-alkyl, (C1-C5)-Alkylthio-(C1-C5)- alkyl, (C1-C5)-Alkylsulfinyl-(C1-C5)-alkyl, (C1-C5)-Alkylsulfonyl-(C1-C5)-alkyl, (C2-C8)- Alkylidenaminoxy(C1-C5)-alkyl, (C1-C5)-Alkylcarbonyl-(C1-C5)-alkyl, (C1-C5)- Alkoxycarbonyl(C1-C5)-alkyl, Aminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylaminocarbonyl-(C1- C5)-alkyl, (C2-C8)-Dialkylaminocarbonyl-(C1-C5)-alkyl, (C1-C5)-Alkylcarbonylamino-(C1-C5)- alkyl, N-(C1-C5)-Alkylcarbonyl-N-(C1-C5)-alkylamino(C1-C5)-alkyl, (C3-C6)-Trialkylsilyl-(C1- C5)-alkyl, phenyl-(C1-C5)-alkyl, where the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, heteroaryl-(C1-C5)-alkyl, where the heteroaryl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)- Alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, phenoxy-(C1-C5)-alkyl, wherein the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro,Heteroaryloxy-(C1-C5)-alkyl, wherein the heteroaryl group is optionally further substituted independently by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, (C1-C3)-alkylthio, (C1-C3)-alkylsulfinyl, (C1-C3)-alkylsulfonyl, fluorine, chlorine, bromine, cyano, nitro, phenyl or phenyl which is independently substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, heteroaryl or heteroaryl which is independently is substituted by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano, nitro, phenyl-C(=O), where the phenyl group is optionally further substituted independently of one another by 1, 2 or 3 groups selected from (C1-C3)-alkyl, (C1-C3)-fluoroalkyl, (C1-C2)-alkoxy, (C1-C3)-fluoroalkoxy, fluorine, chlorine, bromine, cyano,2. The herbicide / safener combination according to claim 1, comprising as compound (A) one or more safeners selected from the group consisting of compounds A1, A2, A3, A4, A5, A6, A7, A8, A9, and A10, where A1 = methyl {[1,5-bis(4-chloro-2-fluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate, A2 = {[1,5-Bis(4-chloro-2-fluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetic acid A3 = Methyl {[5-(4-chloro-2-fluorophenyl)-1-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate A4 = {[5-(4-chloro-2-fluorophenyl)-1-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetic acid A5 = Methyl {[1-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate A6 = {[1-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetic acid A7 = Methyl {[5-(4-bromo-2-fluorophenyl)-1-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate A8 = {[5-(4-bromo-2-fluorophenyl)-1-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetic acid A9 = Methoxyethyl {[1-(4-bromo-2-fluorophenyl)-5-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate A10 = {[1-(4-bromo-2-fluorophenyl)-5-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetic acid 3. Herbicide / safener combination according to claim 2, wherein (A) is selected from A1, A3, A5, A7 and A9.

4. Herbicide / safener combination according to any one of claims 1 to 3, wherein (B) represents one or more compounds of the general formula (II) or their agrochemically acceptable salts, wherein: Q represents the radical Q-1, R 1 represents methyl, 1-propynyl or a six-membered heteroaryl ring containing one or two nitrogen atoms, where the heteroaryl ring is represented by a radical R 9 can be substituted, R 2represents chlorine, methoxy, methyl or ethyl, R 3 stands for chlorine, methyl or ethyl, W stands for CH2, O, NH or N-CH3, Y stands for O or NR 8 Z represents a bond or CH2, n1 and n2 independently represent 1 or 2, provided that n1 + n2 is equal to 2, 3 or 4, R 8 for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl, -C(O)O(C1-C6)-alkyl, - S(O)2NHR 17N , -S(O)(=NH)R 19N , -C(O)C(O)R 20N , -C(O)C(R 23N )=NOR 24N stands; R 9 represents cyano or halogen; R 17N represents methyl or ethyl; R 19N represents methyl or ethyl; R 20N for methyl, ethyl or -NHR 22N stands; R 22N represents methyl or ethyl; R 23N represents methyl or ethyl; R 24N represents methyl or ethyl; G represents hydrogen, an agronomically acceptable metal, C(O)-R 14 or for -C(O)-OR 15 stands, R 14represents (C1-C6)alkyl, R 15 represents (C1-C6)-alkyl.

5. The herbicide / safener combination according to claim 4, wherein Q represents Q-1 and R 1 , R 2 , R 3 , W, Y, Z and G as well as n1 and n2 have the following meanings:

6. Herbicide / safener combination according to one of claims 1 to 3, wherein (B) represents one or more compounds of the general formula (II) or their agrochemically acceptable salts, wherein: Q represents the radical Q-2, R 1 represents 1-propynyl, R 2 represents chlorine, methoxy, methyl or ethyl, R 3 stands for chlorine, methyl or ethyl, W stands for CH2, O, NH or N-CH3, Y stands for NR 8 stands for, Z stands for a bond or for CH2, n1 stands for 2, R 8for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl or - S(O)2C(R 11N )R 12N R 13N stands; R 11N stands for hydrogen; R 12N stands for hydrogen; R 13N stands for methyl; G stands for hydrogen, an agronomically acceptable metal, for C(O)-R 14 or for -C(O)-OR 15 stands, R 14 represents (C1-C6)alkyl, R 15 stands for (C1-C6)-alkyl.

7. Herbicide / safener combination according to claim 6, wherein Q is Q-2 and Y and G have the meanings below and wherein R 1 for 1-propynyl, R 2 and R 3 each represents methyl and W and Z each represents CH2 and n1 represents 2:

8. Herbicide / safener combination according to any one of claims 1 to 3, wherein (B) represents one or more compounds of the general formula (II) or their agrochemically acceptable salts, wherein: Q represents the radical Q-3, R 1 represents 1-propynyl, R2 represents chlorine, methoxy, methyl or ethyl, R 3 represents chlorine, methyl or ethyl, W represents CH2, O, NH or N-CH3, Z represents a bond or CH2, R 1Q3 represents hydrogen or (C1-C6)-alkyl, R 2Q3 for -(CH2) k -R 3Q3 where R 3Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and - S(O)2NR 16N R 17N , and k means 0, or R 1Q3 and R 2Q3 together for -(CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 independently represent 1 or 2, R 4Q3 represents hydrogen or (C1-C6)-alkyl, R 5Q3 is selected from a group consisting of -C(O)NR 5N R 6N , -NR 5N R 6N and - S(O)2NR 16N R 17N , or R 4Q3 and R 5Q3 together for -(CH2)-N(R 8)-(CH2)-, R 8 for (C1-C4)-alkoxy, -C(O)(C1-C4)-alkyl, -C(O)-(C3-C6)-cycloalkyl or -S(O)2C(R 11N )R 12N R 13N stands; R 5N represents substituents which are independently selected from a group consisting of hydrogen and (C1-C6)-alkyl, R 6N represents substituents which are independently selected from a group consisting of hydrogen, (C1-C6)-alkyl and -C(O)-C(R 11N )R 12N R 13N , R 11N stands for hydrogen; R 12N stands for hydrogen; R 13N represents hydrogen or methyl; R 16N represents hydrogen or (C1-C6)-alkyl; R 17N represents hydrogen or (C1-C6)-alkyl; G represents hydrogen, an agronomically acceptable metal, C(O)-R 14 or for -C(O)-OR 15 stands, R 14 represents (C1-C6)alkyl, R 15represents (C1-C6)-alkyl.

9. The herbicide / safener combination according to claim 8, wherein Q represents Q-3 and G has the meanings given below, and wherein R 1 for 1-propynyl, R 2 and R 3 each represents methyl, W and Z each represents CH2 and R 1Q3 for hydrogen and R 2Q3 for -C(O)NR 5N R 6N where R 5N and R 6N both represent a methyl group:

10. Herbicide / safener combination according to claim 8, wherein Q is Q-3 and R 5Q3 and G have the meanings below and wherein R 1 for 1-propynyl, R 2 and R 3 each represent methyl and W and Z each represent CH2 and where the radicals R 1Q3 and R 2Q3 together for - (CH2) nq1 -C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 both stand for 2 and R 4Q3 Hydrogen means:

11. Herbicide / safener combination according to claim 8, wherein Q is Q-3 and G has the meanings below and wherein R 1 for 1-propynyl, R 2 and R 3 each represent methyl and W and Z each represent CH2 and where the radicals R 1Q3 and R 2Q3 together for -(CH2) nq1 - C(R 4Q3 ) R 5Q3 -(CH2) nq2 - where nq1 and nq2 both stand for 1, the residues R 4Q3 and R 5Q3 together for -(CH2)-N(R 8 )-(CH2)- and where R 8 -(CO)CH3 means:

12. The herbicide / safener combination according to claim 5, wherein (A) represents A3=methyl {[5-(4-chloro-2-fluorophenyl)-1-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate, and (B) is selected from B1-6, B1-38, B1-42, B1-46, B1-66, and B1-68.

13. The herbicide / safener combination according to any one of claims 1 to 12, further comprising one or more additives customary in crop protection. 14.A method for protecting crop plants from phytotoxic side effects of a herbicide (B), characterized in that an effective amount of a safener (A) is applied before, after or simultaneously with the herbicide (B) to the plants, plant parts, plant seeds or the cultivated area, wherein the combination of herbicide (B) and safener (A) is defined according to any one of claims 1 to 12, preferably wherein the crop plants are cereal plants, and / or preferably the herbicides (B) are applied at an application rate of up to 40 to 200 g / ha of active ingredient and in a weight ratio of safener (A) to herbicide (B) of 1:400 to 500:

1.

15. Use of the herbicide / safener combination according to any one of claims 1 to 13 for controlling weeds or regulating plant growth.

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