67 results about "Tridentate ligand" patented technology

The invention provides a polyurethane epoxy polymer network as well as a preparation method and application thereof, and belongs to the technical field of woven polymer networks, the preparation method comprises the following steps: (1) carrying out reaction on polyalcohol, a small molecule chain extender, diisocyanate and a tridentate ligand to obtain polyurethane; (2) dissolving the obtained polyurethane in an organic solvent, and adding a bivalent palladium compound and a monodentate ligand to carry out a coordination reaction; and (3) adding epoxy resin and a curing agent into the reaction liquid obtained in the step (2), mixing, removing the solvent, and curing to obtain the polyurethane epoxy polymer network. Linear polyurethane and epoxy resin penetrate through each other through palladium coordinated weaving nodes, the mechanical performance and energy absorption capacity of polyurethane and epoxy resin are enhanced through a weaving network, the phase separation trend between two polymers is weakened, the material can bear a higher stress level, the toughness of the material is improved, and the service life of the material is prolonged. And the original strength of the polymer is maintained, and meanwhile, the maximum extensibility and the plastic deformation capacity of the polymer are improved.

The invention belongs to the technical field of asymmetric catalysis, and discloses a chiral phosphine nitrogen-nitrogen tridentate ligand based on a ferrocene skeleton as well as a preparation method and application of the chiral phosphine nitrogen-nitrogen tridentate ligand. The structural formula of the ligand is shown as (I) or an enantiomer (II) of the ligand. The preparation method comprises the steps of acylation reaction, oxazoline ring construction, aldehyde group introduction, reductive amination and the like, and application in asymmetric hydrogenation reaction, such as asymmetric hydrogenation of aryl ketone. The ligand has a plurality of chiral factors, simultaneously has a potential hydrogen bond donor, forms secondary interaction with a substrate in an asymmetric catalytic reaction, can further stabilize a reaction transition state, is an efficient novel chiral P, N, N-ligand, has the advantages of high reaction activity, good stereoselectivity, wide substrate range and the like, and has a wide application prospect. # imgabs0 #

The present invention provides a polyurethane epoxy polymer network and its preparation method and application. The present invention belongs to the technical field of braided polymer networks. The preparation method comprises: (1) reacting a polyol, a small molecule chain extender, a diisocyanate and a tridentate ligand to obtain a polyurethane; (2) dissolving the obtained polyurethane in an organic solvent, adding a divalent palladium compound and a monodentate ligand to carry out a coordination reaction; (3) adding an epoxy resin and a curing agent to the reaction solution obtained in step (2), removing the solvent after mixing, and curing to obtain a polyurethane epoxy polymer network. In the present invention, linear polyurethane and epoxy resin are interpenetrated through palladium-coordinated braided nodes, and the braided network is used to enhance the mechanical properties and energy absorption capacity of the polyurethane and epoxy resin, reduce the phase separation tendency between the two polymers, enable the material to withstand higher stress levels, improve its toughness, and improve its maximum elongation and plastic deformation capacity while maintaining the original strength of the polymer.

The invention provides a solid electrolyte coated positive electrode material and a preparation method thereof. The material takes a positive electrode active material as a core layer, and a shell layer contains a glassy-state MOF material, a solid electrolyte and a conductive material. The preparation method comprises the steps of pretreatment of positive electrode particles, preparation of a precursor solution, in-situ MOF coating and the like, wherein parameters such as temperature, pressure, ligand proportion and the like are strictly controlled in each stage of a gradient reaction. Glass MOF is compounded with a conductive material, the crystalline structure stability of the MOF positive electrode material is improved by utilizing a bidentate ligand and a tridentate ligand, and the capacity retention ratio of the positive electrode material is greater than 90% after 1000 times of circulation under 5C multiplying power by virtue of collaborative innovation of gradient defect design and a gradient solvothermal reaction system.

A novel class of gold (III) compounds with thermally stimulated delayed phosphorescence (TSDP) properties, methods of making and use thereof are disclosed. The gold (III) compound includes a triazine-containing cyclometalating tridentate ligand and one auxiliary ligand, both coordinated to a gold (III) metal center. The gold (III) compounds can be used as light-emitting material for fabrication of OLEDs. A novel concept of TSDP to harvest light emission from the higher energy triplet excited state via the up-conversion from the lowest-energy triplet excited state by efficient spin-allowed reverse internal conversion is also disclosed.

A method of promoting growth in a photosynthetic organism comprising treating the photosynthetic organism with a metal complex or a precursor thereof, wherein the metal complex comprises a metal selected from the group consisting of zinc (Zn), cobalt (Co), copper (Cu), nickel (Ni) and iron (Fe), and a ligand, which is a bidentate or tridentate ligand. Metal complexes and their ligands are also describe.

Disclosed are an organometallic compound, an organic light emitting device including the same, and an electronic device including the organic light emitting device. The organometallic compound is represented by Formula 1, in which M is a transition metal; L1 is a ligand represented by Formula 2 as disclosed herein; L2 is a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand; n1 is 1, 2, or 3, wherein, when n1 is 2 or more, two or more ligands L1 are the same as or different from each other; n2 is 0, 1, 2, 3, or 4, wherein, when n2 is 2 or more, two or more ligands L2 are the same as or different from each other; and L1 and L2 are different from each other. Formula 1 M(L1) n1 (L2) n2 .

The invention relates to the technical field of DNA intercalating agents, in particular to a near-infrared luminous ruthenium (II) complex, a preparation method thereof and application of the complex as a DNA intercalating agent. The preparation method comprises the following steps: firstly, preparing a precursor 4 '-(1H-benzimidazole-2-yl)-2, 2': 6 ', 2' '-terpyridyl; then, preparing a target precursor, namely, 2-(4-(anthracene-10-yl)-6-(pyrazine-2-yl) pyridine-2-yl) pyrazine as a ligand; and finally, synthesizing a complex [Ru (An-di (2-Pz) Py) (Bitpy)]. The complex is inserted into a DNA base pair as an intercalating agent, has very strong interaction with DNA, and provides basic research for researching the interaction mode of the ruthenium (II) polypyridine complex of the tridentate ligand and DNA and taking the ruthenium (II) polypyridine complex as a diagnosis and treatment reagent.

The application discloses a bisoxazoline pyridine functionalized porous organic polymer and preparation and application thereof; firstly, a styryl functionalized PyBox monomer (VPyBox) is designed and synthesized, and VPyBox, styrene and divinylbenzene are subjected to free radical polymerization under initiation of azobisisobutyronitrile in a certain proportion to obtain a series of porous organic polymers (POP-PyBox); the POP-PyBox can be used as a solid N , N , N tridentate ligand for Co-catalyzed hydrosilylation of arylalkynes with diphenylsilane; the heterogeneous catalyst system developed by the application has a catalytic activity comparable to that of a homogeneous catalyst reported in the literature, and the catalyst is easy to separate and recover; the recovered catalyst can be recycled for more than 6 times, which can not only greatly reduce the preparation cost of vinylsilane, but also simplify the post-treatment process and reduce the three wastes, and has a good practical application prospect.

Described herein are a novel concept of thermally stimulated delayed phosphorescence (TSDP) to harvest light emission from the higher energy triplet excited state via the up-conversion from the lowest-energy triplet excited state by efficient spin-allowed reverse internal conversion as well as the development of TSDP emitters, as exemplified by a novel class of gold(III) compounds with TSDP properties and methods of making and using said compounds. The gold(III) compound includes a triazine-containing cyclometalating tridentate ligand and one auxiliary ligand, both coordinated to a gold(III) metal center. The gold(III) compounds disclosed herein can be used as light-emitting material for fabrication of OLEDs.

The invention discloses a rhenium complex catalyst and a preparation method and application thereof, and belongs to the technical field of carbonyl derivative hydrogenation catalysts, the rhenium complex catalyst comprises a complex catalyst, the complex catalyst is coordinated with a bidentate ligand, a tridentate ligand and a tetradentate ligand, and the bidentate ligand, the tridentate ligand and the tetradentate ligand respectively correspond to a general formula I, a general formula II and a general formula III. Aiming at the defects that a reported complex catalyst for catalyzing hydrogenation of carbonyl derivative molecules is high in price and the like, the invention provides a rhenium complex catalyst which has the characteristics of high reaction activity and good selectivity of a noble metal catalyst, low-price metal, environment friendliness, low cost and the like, and the rhenium complex catalyst is simple in preparation process, low in cost and the like. The catalyst can efficiently catalyze hydrogenation of carbonyl derivative molecules to prepare alcohol, meets the development requirements of green chemistry, and has good popularization and application prospects.

The invention discloses a chiral P, N, N-tridentate ligand based on a ferrocene skeleton as shown in a formula I, a preparation method of an iridium catalyst containing the ligand and application of the ligand in preparation of a carbon-nitrogen axial chiral compound and a diltiazem intermediate. According to the present invention, the chiral P, N, N-tridentate ligand based on the ferrocene skeleton and the metal iridium precursor [Ir (COD) Cl] 2 are subjected to complexation to obtain the complex as the iridium catalyst, and the catalyst can be used as the iridium catalyst with characteristics of high yield (up to 99%), high enantioselectivity (up to gt; 99% ee) and high diastereoselectivity (up to gt; according to the method, N-aryl indolal or N-aryl indolone is subjected to asymmetric hydrogenation by using N-aryl indolal or N-aryl indolone (R1, R2, R3, R4, R5, R6, R7, R7, R8, R9, R9, R9, the catalyst can also be applied to asymmetric synthesis of diltiazem intermediate (2R, 3S)-3-(4-methoxyphenyl)-2, 3-epoxidized propionate, has the advantages of short synthesis route, high yield, good stereoselectivity (as high as 99% ee, 97 / 3dr) and the like, and has better economic and social benefits.

Tridentate platinum, palladium, and gold complexes of Formulas A-I and A-II and tridentate iridium and rhodium compounds of Formulas B-I, B-II, and B-III suitable for delayed fluorescent and phosphorescent or phosphorescent emitters in display and lighting applications.

The present invention discloses a dibromo-1,3-bis(1-butylimidazole-3-yl)benzene ligand modified with an nitrogen heteroaromatic ring and a preparation method thereof, an iridium complex and an organic electroluminescent device. The dibromo-1,3-bis(1-butylimidazole-3-yl)benzene ligand modified with an nitrogen heteroaromatic ring has the following structure: wherein R is an nitrogen heteroaromatic ring group or a derivative thereof. The present invention introduces an nitrogen heteroaromatic ring group or a derivative thereof at position 5 of dibromo-1,3-bis(1-butylimidazole-3-yl)benzene to obtain a dibromo-1,3-bis(1-butylimidazole-3-yl)benzene ligand modified with an nitrogen heteroaromatic ring, which can be used as a tridentate ligand of an iridium complex, increases the rigidity of the ligand and the complex, regulates the luminescent color and efficiency of the complex, increases steric hindrance, reduces molecular stacking, thereby suppressing the non-radiative transition process of the molecule and improving the luminous efficiency of an organic electroluminescent device using an iridium complex.

The application belongs to the technical field of polymer material recycling and catalytic chemistry, and discloses a composite catalyst for PET waste bottle alcoholysis and a preparation method thereof. The composite catalyst is based on biomimetic enzyme engineering and dynamic covalent chemistry strategy, and comprises a binuclear metal cluster active center, a limited microenvironment shell layer and a dynamic covalent network skeleton. The binuclear metal cluster is constructed by zinc / cobalt / manganese ions and a tridentate ligand C9H8N2O4, the shell layer is a polydopamine derived functional polymer, and the skeleton is formed by cross-linking aromatic and aliphatic monomers through borate ester bonds. The application solves the performance degradation problem caused by the instability of the active center of the existing enzyme-like catalyst in industrial circulation application. The catalyst not only has the enzyme-like catalytic characteristics of high activity and high selectivity, but also realizes self-repairing after damage through the built-in multiple dynamic chemical mechanism, thereby providing a new catalytic material with performance and durability for efficient and sustainable chemical recycling of PET waste bottles.

The application discloses a kind of big steric hindrance C-C coupling palladium ligand and synthesis method, ligand is used naphthyl as the main group of stable ligand, this group provides big plane rigid configuration during ligand use, simultaneously, it provides big π electron for complex molecule to stabilize complex;In addition, the configuration of pyridofuran is used, the N coordination point of traditional N-P bidentate ligand is introduced O by furan this functional group in ortho position to adjust the chemical environment of intramolecular N coordination point, so as to modify the traditional N-P bidentate ligand to tridentate ligand, this change can effectively increase the penetration ability of Pd active center in actual ligand use to improve catalytic activity.

The present invention provides a degradable polyurethane material, a preparation method thereof, and an application thereof. The present invention belongs to the field of polymer chemistry. The preparation method comprises the following steps: (1) reacting a polyol, a small molecule chain extender, a diisocyanate, and a tridentate ligand to obtain a linear polyurethane; 2) performing a coordination reaction between the linear polyurethane obtained in step (1) and a divalent palladium compound and a monodentate ligand; (3) performing a coordination reaction between an o-phenanthroline ligand and a monovalent copper compound; and (4) mixing the solution obtained in step (3) with a diprimary amine compound and the solution obtained in step (2), removing the solvent, and hot pressing to obtain the degradable polyurethane material. The polyurethane material of the present invention has good tensile strength and toughness and has degradability.

The invention discloses a preparation method and application of a semi-sandwich type iridium complex containing a tridentate ligand. The structural formula of the complex is shown as a formula (I), a ligand and a dimer react under the reaction condition, sodium bicarbonate is continuously added into a reaction system, proton H on coumarin unit carbon in the ligand can be selectively removed, and therefore the semi-sandwich type iridium complex (I) of the CNS tridentate ligand is obtained. Wherein a coordination carbon atom (C, blue) in the tridentate chelate ligand is derived from a coumarin unit, a nitrogen atom (N, red) is derived from a Schiff base structure, a sulfur atom (S, pink) is derived from thiosemicarbazide, the obtained iridium complex shows good anticancer activity, the performance of the iridium complex is close to or even superior to that of commercial cis-platinum, and the iridium complex is a very potential anticancer drug.

The invention relates to the technical field of research and development of tumor photodynamic therapy photosensitizers, photothermal therapy photothermal reagents and sonodynamic therapy sonosensitizers, and provides a preparation method and application of a binuclear metal complex of a polythiophene bridging ligand. The invention relates to a ruthenium complex TBLRu3a-TBLRu6a and a ruthenium complex TBLRu3b-TBLRu6b of a polythiophene bridged tri-bidentate ligand, a ruthenium complex TTLRu1-TTLRu12 of a polythiophene bridged bis-tridentate ligand, and an osmium complex TTLOs1-TTLOs6 of a polythiophene bridged bis-tridentate ligand, which are respectively designed and invented by the invention. The invention further relates to a preparation method of the ruthenium complex TBLRu3a-TBLRu6a and the ruthenium complex TBLRu3b-TBLRu6b of the polythiophene bridged tri-bidentate ligand and a preparation method of the ruthenium complex TTLRu1-TTLRu12 of the polythiophene bridged bis-tridentate ligand. The polythiophene bridged metal complex has extremely high stability and excellent two-photon absorption characteristic, has excellent biotoxicity and photothermal conversion capability under the action of infrared exciting light, and can induce A549R cell apoptosis. The polythiophene bridged metal complex provided by the invention is a potential novel two-photon absorption photodynamic therapy photosensitizer, a photothermal therapy photothermal reagent and a sonodynamic therapy sonosensitizer, and has a wide application prospect in photodynamic therapy, photothermal therapy and sonodynamic therapy of tumors.

The present invention relates to a preparation method for and an application of a chiral spirocyclic phosphine-nitrogen-phosphine tridentate ligand SpiroPNP and an iridium catalyst Ir-SpiroPNP thereof. The chiral spirocyclic phosphine-nitrogen-phosphine tridentate ligand is a compound represented by formula I, or a racemate or optical isomer thereof or a catalytically acceptable salt thereof; and the main structural feature is a phosphine ligand having a chiral spiro indene skeleton and a large sterically hindered substituent. The chiral spirocyclic phosphine-nitrogen-phosphine tridentate ligand can be synthesized into a chiral starting material from a 7-diaryl / alkylphosphino-7′-amino-1,1′-spirodihydroindenyl compound having a spiro ring skeleton. The iridium catalyst of the chiral spirocyclic phosphino-7′-amino-1,1′-spirodihydroindenyl compound having a spiro ring skeleton. The iridium catalyst of the chiral spirocyclic phosphine-nitrogen-phosphine tridentate ligand is a compound represented by formula II, or a racemate or optical isomer thereof, or a catalytically acceptable salt thereof. The iridium catalyst can be used to catalyze the asymmetric catalytic hydrogenation of carbonyl compounds, and especially in the asymmetric catalytic hydrogenation of simple dialkyl ketones. Said catalyst exhibits high yield (>99%) and enantioselectivity (up to 99.8% ee), thus having practical value.

The application discloses a synthesis method of a deuterated aryl compound promoted by a tridentate ligand. An aryl compound shown in formula I is subjected to a deuterium substitution reaction with a deuterium source reagent in an organic solvent reaction medium under catalysis of a complex formed by a palladium catalyst and a tridentate ligand, and a silver salt is used as a reaction aid. The reaction product is separated and purified to obtain a deuterated aryl compound shown in formula II. The tridentate ligand has high reactivity in a Pd-catalyzed HIE reaction and can form a stable catalyst.

According to the invention, three [3 + 2 + 1] coordination mode red light iridium (III) complexes are synthesized: Ir (diqzb) (CF3PhCF3py) Cl, Ir (diqzb) (CF3ppy) Cl and Ir (diqzb) (ppy) Cl. A rigid tridentate ligand diqzb is coordinated with bidentate ligands CF3PhCF3py, CF3ppy and ppy, so that the ligand is synthesized. The emission wavelength of the OLED device is 616 to 649 nm, the current efficiency is 8.6 to 25.6 cd.A <-1 >, and the EQE is 21 to 28%. When the EQEmax of Ir (diqzb) (CF3ppy) Cl reaches 28%, the same type of records are refreshed; and the CIE coordinate (0.703, 0.292) of the Ir (diqzb) (ppy) Cl is close to the standard red coordinate of ITU-R BT.2020. The invention discloses a complex structure, synthesis and a device manufacturing method.

The invention provides a chiral ferrocenyl P, N, N tridentate ligand containing large steric hindrance aryl substitution, a preparation method of the chiral ferrocenyl P, N, N tridentate ligand and application of the chiral ferrocenyl P, N, N tridentate ligand in asymmetric hydrogenation reaction. The chiral ligand is novel in structure, simple and convenient to prepare and stable in property, and has good tolerance to air and humidity. The chiral ligand is obtained by condensation and reduction of chiral ferrocenyl ethylamine and pyridine aldehyde. A catalyst formed by the chiral ligand and metal precursors such as Mn, Ir and Ru has excellent catalyst activity and stereoselectivity on catalytic asymmetric hydrogenation reaction of C = C, C = N and C = O double bonds, enantioselectivity reaches up to 99% ee, and TON reaches up to 10000.

A catalyst system for preparing terephthalic acid includes a first complex of a manganese salt and a first multidentate ligand; and a second complex of a cobalt salt and a second polydentate ligand wherein the first polydentate ligand is a tridentate ligand, a tetradentate ligand, a pentadentate ligand or a hexadentate ligand and the second polydentate ligand is a tridentate ligand, a tetradentate ligand, a pentadentate ligand or a hexadentate ligand.

The invention discloses an indazole europium complex and application thereof, and particularly relates to the field of rare earth complexes and luminescent materials. The general structural formula of the europium complex is Eu (IZ) xAyLm, IZ is an indazole-3-formic acid anion ligand, A is other anion ligands except IZ, and L is a neutral ligand; x is selected from 1 or 2 or 3 or 4, y is selected from 0 or 1 or 2, x + y = 3 or x + y = 4, and m is selected from 0 or 1 or 2; and the neutral ligand L is selected from a bidentate ligand containing pyridine, a tridentate ligand containing pyridine or a monodentate ligand containing phosphine. The europium complex provided by the invention has efficient photoluminescence efficiency, relatively high thermal stability and low cost, and effectively solves the problems existing in the prior art.

An organometallic compound represented by Formula 1:M(L1)n1(L2)n2  Formula 1wherein M is a transition metal, L1 is a ligand represented by Formula 2 as provided herein, n1 is 1, 2, or 3, wherein, when n1 is 2, two L1 groups are identical to or different from each other, and when n1 is 3, two or more of three L1 groups are different from each other, L2 is a monodentate ligand, a bidentate ligand, a tridentate ligand, or a tetradentate ligand, and n2 is 0, 1, 2, 3, or 4, wherein, when n2 is 2 or greater, two or more L2 groups are identical to or different from each other, and L1 and L2 are different from each other.

The invention discloses a chiral bisoxazoline phosphine tridentate ligand compound as well as a preparation method and application thereof. The invention provides a compound as shown in a formula I. The chiral bisoxazoline phosphine tridentate ligand of the compound shown in the formula I can be used as a catalyst for asymmetric reaction catalyzed by transition metal, the catalytic effect is remarkable, the product yield is high, and the product er value is high. # imgabs0 #

The invention belongs to the technical field of high polymer material recovery and catalytic chemistry, and discloses a composite catalyst for alcoholysis of a PET waste bottle and a preparation method of the composite catalyst. The composite catalyst is based on bionic enzyme engineering and a dynamic covalent chemical strategy and comprises a binuclear metal cluster active center, a confinement microenvironment shell layer and a dynamic covalent network framework, a binuclear metal cluster is constructed by zinc / cobalt / manganese ions and a tridentate ligand C9H8N2O4, the shell layer is a functional polymer derived from polydopamine, and the dynamic covalent network framework is constructed by zinc / cobalt / manganese ions and a tridentate ligand C9H8N2O4. And the skeleton is formed by cross-linking aromatic and aliphatic monomers with boric acid ester bonds. According to the invention, the problem of performance degradation caused by active center instability of the existing enzyme-like catalyst in industrial cyclic application is solved. The catalyst not only has high-activity and high-selectivity enzyme-like catalytic characteristics, but also realizes self-repair after damage through built-in multiple dynamic chemical mechanisms, and provides a novel catalytic material with both performance and durability for efficient and sustainable chemical recovery of PET waste bottles.

A porous coordination network is represented by the following formulas (I) to (VIII), in which M2+ is a divalent metal ion, M3+ is a trivalent metal ion, L1a and L1b are tridentate ligands having hexaazaphenalenyl, L2a and L2b are bidentate or tridentate ligands containing a carboxy group, L3− is a tertiary ligand ion that is an anion of triazole or a triazole derivative, and Y is a cation.

The present invention relates to a method for preparing chiral dihydropyrano[3,2-c]coumarin compounds. The chiral copper catalyst used in this method is generated in situ from a copper salt and a chiral P,N,N-tridentate ligand in a reaction medium. Through an asymmetric [3+3] cycloaddition reaction, a series of chiral dihydropyrano[3,2-c]coumarin compounds are synthesized with high yields and high enantioselectivities. The present invention has the characteristics of simple operation, readily available raw materials, a wide range of substrate applicability, and high enantioselectivity.