213 results about "Tridentate ligand" patented technology

The present invention relates to organic light emitting devices (OLEDs), and more specifically to phosphorescent organic materials used in such devices. More specifically, the present invention relates to emissive phosphorescent material which comprise at least one tridentate ligand bound to a metal center, wherein at least one of the bonds to the tridentate ligand is a carbon-metal bond.

The present invention relates to organic light emitting devices (OLEDs), and more specifically to phosphorescent organic materials used in such devices. More specifically, the present invention relates to emissive phosphorescent material which comprise at least one tridentate ligand bound to a metal center, wherein at least one of the bonds to the tridentate ligand is a carbon-metal bond.

Provided are an organic electroluminescence device whose wavelength of light emission is short and which can emit blue light having a high color purity, and a metal complex compound for realizing the device. The metal complex compound is of a specific structure having a partial structure including two tridentate ligands. The organic electroluminescence device includes: a pair of electrodes; and an organic thin film layer which has one layer or a plurality of layers including at least a light emitting layer and is disposed between the pair of electrodes. In the organic electroluminescence device, at least one layer of the organic thin film layer contains the metal complex compound. The organic electroluminescence device emits light by applying a voltage between both the electrodes.

The catalyst for polymerization and copolymerization of olefine is one novel kind of group III to group XIII transition metal complex of tridentate ligand.

Panchromatic photosensitizers having a Formula of ML₁L₂X were synthesized, wherein M comprises ruthenium atom; X is a monodentate anion; L₁ is heterocyclic bidentate ligand having one of formulae listed below:

The substituents R₁, R₂, R₃, R₄, R₅, R₆, R₇ of L₁ and L₂ are the same or different, and represent alkyl, alkoxy, alkylthio, alkylamino, halogenated alkyl, phenyl or substituted phenyl group, carboxylic acid or counter anion thereof, sulfonic acid or counter anion thereof, phosphoric acid or counter anion thereof, amino-group, halogens, or hydrogen. The above-mentioned photosensitizers are suitable to use as sensitizers for fabrication of high efficiency dye-sensitized solar cell.

Photosensitizers having a formula of RuL₁L₂ (1) are provided, wherein Ru is ruthenium; L₁ and L₂ are heterocyclic tridentate ligands. L₁ has a formula of (2), and L₂ has a formula of G₁G₂G₃ (3), wherein G₁ and G₃ are selected from the group consisting of formulae (4) to (7), and G₂ is selected from the group consisting of formulae (7) and (8). The above-mentioned photosensitizers are suitable to be used as sensitizers for fabrication of high efficiency dye-sensitized solar cells.

Disclosed is a 4,4′-dicarboxy-2,2′-bipyridine derived tridentate ligand represented by formula (I):

Also disclosed are a metal complex containing the aforesaid tridentate ligand and a dye-sensitized solar cell containing the metal complex.

Panchromatic photo sensitizers having a Formula of ML₁L₂X were synthesized, wherein M represents ruthenium atom; X represents a monodentate anion; L₁ is heterocyclic bidentate ligand having one of formulae listed below:

Substituents R₁, R₂, R₃ and R₄ of L₁ are the same or different and are selected from the group consisting of hydrogen, halogens, amino-group alkyl, alkoxy, alkylthio, alkylamino, halogenated alkyl, phenyl and substituted phenyl group. Substituents R₅, R₆ and R₇ of L₂ are the same or different and are selected from the group consisting of carboxylic acid and counter anion thereof, sulfonic acid and counter anion thereof, phosphoric acid and counter anion thereof. The above-mentioned photosensitizers are suitable to use as sensitizers for fabrication of high efficiency dye-sensitized solar cell.

The present invention relates to a ruthenium carbonyl complex that is represented by the following Formula (1):

RuXY(CO)(L)  (1)

• • (in the Formula (1), X and Y, which may be the same or different from each other, represent an anionic ligand and L represents a tridentate aminodiphosphine ligand which has two phosphino groups and a —NH— group), its production method, and a method for production of alcohols by hydrogenation-reduction of ketones, esters, and lactones using the complex as a catalyst.

The ruthenium carbonyl complex of the invention has a high catalytic activity and it can be easily prepared and handled.

A class of luminescent gold(III) compounds containing a tridentate ligand with one strong σ-donating group having the chemical structure depicted by generic formula (I):

The present invention provides 1) a complex comprising a mono-anionictridentate ligand, represented by the following general formula (I); 2) a polymerization catalyst composition, comprising the complex; and 3) a cis-1,4-isoprene polymer, a cis-1,4-butadiene polymer, a cis-1,4-isoprene-styrene copolymer, a cis-1,4-butadiene-styrene copolymer, a cis-1,4-butadiene-cis-1,4-isoprene copolymer, and a cis-1,4-butadiene-cis-1,4-isoprene-styrene copolymer, each of which has high-cis-1,4 content in a micro structure and a sharp molecular-weight distribution.

The present invention aims to provide organic EL elements etc., containing phosphorescent organometallic complexes, that can exhibit longer durability, higher emitting efficiency, superior thermal/electrical stability, significantly longer operating life. The organic EL elements comprise an organic thin layer interposed between a positive hole transport layer and a electron transport layer, the organic thin layer comprises an organometallic complex comprising at least a metal element, a tridentate ligand, and a monodentate ligand, wherein the tridentate ligand bonds with the metal atom through two nitrogen atoms and one carbon atom, and the carbon atom exists between the two nitrogen atoms, and a monodentate ligand bonds with the metal atom through a atom selected from the group consisting of C, N, O, P and S atoms.

The invention provides organometallic complexes comprising an extended π-conjugated tridentate ligand having a platinum center in which chemical and/or physical properties of the complexes may be modified by changing the structure of the ligands. The complex finds use in devices incorporated into electroluminescent devices, flat panel displays, organic light emitting devices, polymer light emitting devices, transistors, serrors, and lasers.

The present invention is directed to lubricating oils of improved antioxidancy comprising a base oil selected from the group consisting of mineral oils, synthetic oils and mixtures thereof containing an effective amount of one or more organometallic compound and/or coordination complex selected from the group consisting of (a) a metal or metal cation with more than one oxidation state, above the ground state, and two or more anions, (b) a metal or metal cation with more than one oxidation state above the ground state and one or more bidentate or tridentate ligands, (c) a metal or metal cation with more than one oxidation state above the ground slate, and one or more amines and one or more ligands, and (d) mixtures thereof, to a method for improving the antioxidancy of formulated lubricating oil compositions by the addition thereto of an effective amount of the aforementioned organometallic compound, and/or coordination complex, and to an additive concentrate containing the aforementioned organometallic compound and/or coordination complex.

An atomic layer deposition method which comprises forming a metal oxide thin film by using, as a group IV metal precursor, a complex of a formula M(L)2 in which M is a group IV metal ion having a charge of +4 and L is a tridentate ligand having a charge of -2, the ligand being represented by the following formula (I): wherein each of R1 and R2, independently, is a linear or branched C1-4 alkyl group; and R3 is a linear or branched C1-5 alkylene group. The group IV metal precursor exhibits excellent thermal and chemical stabilities under a carrier gas atmosphere, whereas it has high reactivity with a reaction gas.

The invention belongs to the technical field of asymmetric catalysis and specifically relates to a chiral nitrogen nitrogen phosphine tridentate ligand based on a ferrocene skeleton and an applicationthereof. A coordination compound is obtained by the disclosed chiral nitrogen nitrogen phosphine tridentate ligand base on the ferrocene skeleton complexed with a transition metal precursor, the complex is used as a precious metal catalyst, and is successfully applied to high efficiency asymmetric hydrogenation of aromatic ketone. Compared with other tridentate ligands, the ligand is simple to synthetize, is stable to water and air, and easy to prepare on a large scale, shows high activity and high enantioselectivity on carbon and oxygen double bond, and has greater implementation value and social and economic benefits.

The invention relates to a method for synthesizing chiral beta-acetenyl ketone by catalytic intermolecular decarboxylation from beta-ketonic acid and a propargyl compound. A chiral copper catalyst adopted in the invention is synthesized in stiu from a copper salt and a chiral P,N,N-tridentate ligand in various polar solvents and nonpolar solvents. According to the invention, various chiral beta-acetenyl ketone compounds with substituent groups can be synthesized conveniently, and can obtain a percent enantiomeric excess as high as 95%. The method in the invention is advantaged by operational simplicity, available raw materials, wide substrate application range, high enantioselectivity, and the like.

A ruthenium complex having a chemical formula of RuL₁L₂X is provided. The chemical formula includes a structural formula represented by the following Formula (I):

in which, X is a monodentate anion ligand, L₁ and L₂ respectively represent a heterocyclic tridentate ligand with a structure shown in the following structural formula (II):

and a bipyridine ligand derivative with a structure shown in the following structural formula (III):

in which R₁, R₂, R₄ and R₅ of L₁ and L₂ are the same or different substituents and represent alkyl, alkoxy, aminoalkyl, haloalkanes or substituted phenyl group, carboxylic acid group or acid radical salt thereof, sulfonic acid group or acid radical salt thereof, phosphoric acid group or acid radical salt thereof or hydrogen atom. R₃ represents perhalogenated alkyl group, alkoxy, alkyl, amino, halogens, or hydrogen atom. The ruthenium complexes are suitable for being used as dye-sensitizers for fabricating dye-sensitized solar cells.

A novel process of preparing tridentate ligands containing a diarylphosphine electron donating group are disclosed. Use of this process for preparing a combinatorial library of such tridentate ligands and of organometallic complexes containing same is also disclosed. Further disclosed are novel diarylphosphine-containing compounds that can serve as tridentate ligands (e.g., pincer ligands), combinatorial libraries of such tridentate ligands, organometallic complexes containing these ligands (e.g., pincer complexes), and combinatorial libraries of such complexes. Methods utilizing these libraries for screening for candidate organometallic catalysts are also disclosed.

The invention relates to PNHO tridentate ligands and application of related ligands in asymmetric hydrogenation and similar reactions. The novel tridentate nitrogen-phosphine-oxygen ligands are first tridentate nitrogen-phosphine-oxygen ligands containing ferrocenyl planar chiral phosphine, and are successfully applied to high-efficiency high-selectivity asymmetric hydrogenation and other similar reactions of simple aromatic ketone, alpha-hydroxyketone and beta-ketone ester. Compared with other dominant tridentate ligands, the ligands provided by the invention have the advantages of simple synthesis route and low cost, can easily implement large-scale synthesis, are stable in air, and have high activity and high selectivity in asymmetric hydrogenation reactions of carbon-oxygen double bonds.

The invention relates to an aluminum chemical polishing solution and a polishing method with the same, in particular to a chemical polishing solution used for polishing aluminum, aluminum alloys, aluminum oxide and aluminum alloy oxide. Each liter of polishing solution at least comprises 100-450 g of an alkali compound, 60-120 g of NaNO2, 0.5-20 g of a chelating agent, 0.5-20 g of cationic polymer and the balance water. The alkali compound is selected from at least one of NaOH, KOH and Ba(OH)2, tridentate ligand serves as the chelating agent, and ligating atoms are selected from N and/or O.

The present invention is directed to a coordinating catalyst system comprising at least one pre-catalyst selected from late transition metal bidentate or tridentate ligand containing compounds, at least one support-agglomerate having chromium immobilized thereto (e.g., spray dried silica/clay agglomerate), and optionally at least one organometallic compound in controlled amounts, and methods for preparing the same. The resulting catalyst system exhibits enhanced activity for polymerizing olefins and yields polymer products having very good morphology.