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39 results about "Pincer ligand" patented technology

In chemistry, a transition metal pincer complex is a type of coordination complex with a pincer ligand. Pincer ligands are chelating agents that binds tightly to three adjacent coplanar sites in a meridional configuration. The inflexibility of the pincer-metal interaction confers high thermal stability to the resulting complexes. This stability is in part ascribed to the constrained geometry of the pincer, which inhibits cyclometallation of the organic substituents on the donor sites at each end. In the absence of this effect, cyclometallation is often a significant deactivation process for complexes, in particular limiting their ability to effect C-H bond activation. The organic substituents also define a hydrophobic pocket around the reactive coordination site. Stoichiometric and catalytic applications of pincer complexes have been studied at an accelerating pace since the mid-1970s. Most pincer ligands contain phosphines. Reactions of metal-pincer complexes are localized at three sites perpendicular to the plane of the pincer ligand, although in some cases one arm is hemi-labile and an additional coordination site is generated transiently. Early examples of pincer ligands (not called such originally) were anionic with a carbanion as the central donor site and flanking phosphine donors; these compounds are referred to as PCP pincers.

Alkane and alkane group dehydrogenation with organometallic catalysts

Novel polynuclear organometallic complexes useful as catalysts for the reversible deshydrogenation of alkanes and alkane group are disclosed. The novel compounds comprise a first transition, a second transition metal p-bonded to an ?5-aromatic ligand, and a pincer ligand. The pincer ligand comprises a 6p-electron aromatic ring having at least 2 ring atoms in an 1, 3 relationship bonded each to a neutral Lewis base through a bridge, the bridge being a diradical. The pincer ligand binds the first transition metal through each of the Lewis bases and through the ring atom adjacent to both Lewis bases and p-coordinates the second transition metal through all aromatic ring atoms. The first transition metal may also bond to 2 or 4 hydrogen atoms.
Owner:POWERNOVA TECH

Air-stable, blue light emitting chemical compounds

We report the synthesis and characterization of four novel CCC—NHC pincer platinum(II) and palladium(II) complexes, which adopt a distorted square planar configuration. These complexes emit bright blue light in the solid state under UV irradiation with emissions that are stable in ambient atmosphere (O2 and H2O) for extended periods. We also report the synthesis and characterization of CCC—NHC pincer ligand nickel complexes, and solid state fluorescence spectra have been collected for two of the complexes reported. X-ray structural analysis of a representative compound exhibits a distorted square planar geometry. Finally, we report the synthesis and characterization of CCC—NHC pincer ligand complexes for abnormal carbens, triazole, and BIA.
Owner:UNIVERSITY OF MISSISSIPPI

Novel diarylphosphine-containing compounds, processes of preparing same and uses thereof as tridentate ligands

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.
Owner:TECHNION RES & DEV FOUND LTD

Process for preparing gamma-valerolactone by utilizing iridium-pincer ligand complex catalyst

The invention relates to a process for preparing gamma-valerolactone by utilizing an iridium-pincer ligand complex catalyst, particularly to the process for preparing the gamma-valerolactone by catalyzing levulinic acid for hydrogenation reduction and and lactonization. The process for preparing the gamma-valerolactone by utilizing the iridium-pincer ligand complex catalyst is characterized in that 1-5 MPa hydrogen is used as a reducing agent at a temperature between 50 DEG C and 100 DEG C, the gamma-valerolactone is prepared by catalyzing the levulinic acid for hydrogenation reduction and lactonization under the action of iridium catalyst which accounts for 0.01 to 0.1 mol% of quantity of levulinic acid. The process for preparing the gamma-valerolactone by utilizing the iridium-pincer ligand complex catalyst eliminates the disadvantage that a high temperature and high pressure reaction condition is required for gamma-valerolactone production so that economy and security of the production system are improved. Dosage of the catalyst is small, productivity is high and selectivity is good.
Owner:NANKAI UNIV

Tridentate pincer ligand supported metal-alkylidyne and metallacycloalkylene complexes for alkyne polymerization

Tridentate pincer ligand supported metal complexes are formed where the complex is a trianionic pincer ligand supported metal-alkylidyne complex or a tetra-anionic pincer-ligand supported metallacycloalkylene complex formed by addition of an alkyne to the trianionic pincer ligand supported metal-alkylidyne complex. The tridentate pincer ligand supported metal complex that includes a group 5-7 transition metal and an OCO trianionic pincer ligand or an alkyne adduct thereof and methods of preparing the complexes are disclosed. The use of the tridentate pincer ligand supported metal complex for the polymerization of alkynes is disclosed, where high molecular weight poly(alkyne)s can be formed in high yield. The poly(alkyne) can be a macrocyclic polymer.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Homogeneous Hydrogenation of Esters Employing a Complex of Iron as Catalyst

The homogeneous hydrogenation of organic carbonyls, especially esters, under relatively mild conditions using iron hydrido-borohydride catalyst complexes having amino-phosphine pincer ligands. The catalyst and process are well-suited for catalyzing the hydrogenation of a wide variety of organic carbonyls, such as hydrogenation of fatty acid esters to alcohols. In particular embodiments, the process can be carried out in the absence of solvent.
Owner:THE PROCTER & GAMBLE COMPANY

Process for preparing amines from alcohols and ammonia

The present invention provides novel ruthenium based catalysts, and a process for preparing amines, by reacting a primary alcohol and ammonia in the presence of such catalysts, to generate the amine and water. According to the process of the invention, primary alcohols react directly with ammonia to produce primary amines and water in high yields and high turnover numbers. This reaction is catalyzed by novel ruthenium complexes, which are preferably composed of quinolinyl or acridinyl based pincer ligands.
Owner:YEDA RES & DEV CO LTD

Tridentate pincer ligand supported metal-alkylidyne and metallacycloalkylene complexes for alkyne polymerization

ActiveUS9206266B2AlkyneAdduct
Tridentate pincer ligand supported metal complexes are formed where the complex is a trianionic pincer ligand supported metal-alkylidyne complex or a tetra-anionic pincer-ligand supported metallacycloalkylene complex formed by addition of an alkyne to the trianionic pincer ligand supported metal-alkylidyne complex. The tridentate pincer ligand supported metal complex that includes a group 5-7 transition metal and an OCO trianionic pincer ligand or an alkyne adduct thereof and methods of preparing the complexes are disclosed. The use of the tridentate pincer ligand supported metal complex for the polymerization of alkynes is disclosed, where high molecular weight poly(alkyne)s can be formed in high yield. The poly(alkyne) can be a macrocyclic polymer.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Process for preparing amines from alcohols and ammonia

The present invention provides novel ruthenium based catalysts, and a process for preparing amines, by reacting a primary alcohol and ammonia in the presence of such catalysts, to generate the amine and water. According to the process of the invention, primary alcohols react directly with ammonia to produce primary amines and water in high yields and high turnover numbers. This reaction is catalyzed by novel ruthenium complexes, which are preferably composed of quinolinyl or acridinyl based pincer ligands.
Owner:YEDA RES & DEV CO LTD

Homogeneous hydrogenation of esters employing a complex of iron as catalyst

The homogeneous hydrogenation of organic carbonyls, especially esters, under relatively mild conditions using iron hydrido-borohydride catalyst complexes having amino-phosphine pincer ligands. The catalyst and process are well-suited for catalyzing the hydrogenation of a wide variety of organic carbonyls, such as hydrogenation of fatty acid esters to alcohols. In particular embodiments, the process can be carried out in the absence of solvent.
Owner:PROCTER & GAMBLE CO +1

Ferrocenyl pyrimidine pincer ligand and preparation method thereof

The invention discloses a ferrocenyl pyrimidine pincer ligand and a preparation method thereof and belongs to the technical field of organic synthesis. The ferrocenyl pyrimidine pincer ligand has the general formula shown in the specification, wherein X and Y are atom C or N; R1 and R2 are C1-C6 linear alkyl, -C6H5, -COCH3, -COOCH3, -CHO, -OCH3, -N(CH3)2, -CN or -COOH; R1 is connected to the ortho-position, meta-position or para-position of X; and R2 is connected to ortho-position, meta-position or para-position of Y. According to the corresponding preparation method, 2,4,6-trichloro pyrimidine, ferrocene mercuric chloride, aryl or heterocyclic aryl boric acid serve as raw materials, and the ferrocenyl pyrimidine pincer ligand of a rich structure is prepared through a stepped coupling method. The preparation method is mild in reaction conditions, wide in substrate range and high in yield. The selected raw material ferrocene mercuric chloride has high stability and high stereoselectivity in air and water, the compound can be prepared by directly mercurating ferrocene, and the operation is easy and readily available. Meanwhile, multiple asymmetric pincer structures can be conveniently obtained by utilizing the preparation method, and the ligand has wide application prospect.
Owner:LUOYANG NORMAL UNIV

Homogeneous iron catalysts for the conversion of methanol to methyl formate and hydrogen

Iron-based homogeneous catalysts, supported by pincer ligands, are employed in the catalytic dehydrocoupling of methanol to produce methyl formate and hydrogen. As both methanol and methyl formate are volatile materials, they can be readily separated from the catalyst by applying vacuum at room temperature. The hydrogen by-product of the reaction may be isolated and utilized as a feedstock in other chemical transformations.
Owner:EASTMAN CHEM CO

Trianionic pincer ligands, a CR(III)/CR(v) catalytic system and its use for catalytic aerobic oxidation of organic substrates

An embodiment of the invention is a novel Cr(V) OCO3- trianionic pincer ligand complex. Another embodiment of the invention is a catalytic method for oxidation of a substrate aerobically in the presence of a source of oxygen, where the novel Cr(V) OCO3- trianionic pincer ligand complex acts as the catalyst. The substrate can be a phosphine, amine, sulfide, alkene, alkane or a second metal complex. Another embodiment of the invention is directed to NCN pincer ligands that can form trianionic pincer ligand complexes.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Method for transferring n-atoms from metal complexes to organic and inorganic substrates

A complex for transference of a nitrogen atom to an electrophilic reagent comprises a hard-hard-hard pincer ligand and an early transition metal bound to a nitride. The pincer ligand can be an OCO ligand and the transition metal can be Mo. The complex can be used to transfer the nitrogen atom bound to the metal to an electrophile in a method to produce a nitrogen containing molecule. In one novel nitrogen transfer reaction, a Mo—N triple bond is broken where the nitrogen transfers to the sp2 hybridized carbon of an acid chloride to form a nitrile.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

ONO pincer ligands and ONO pincer ligand comprising metal complexes

Embodiments of the invention are directed to ONO pincer ligands that can be in a trianionic, protonated or protonated equivalent form. The ONO pincer ligand can be combined with a transition metal comprising compound to form an ONO pincer ligand comprising transition metal complex. By choice of the ONO pincer ligand structure, the steric and electronic properties of the transition metal complexes therefrom can be controlled. The ONO pincer ligands comprise a central nitrogen atom that is disubstituted with a pair of three atom comprising bridges where the three atoms are three sp2 hybridized carbons or the three atoms are a pair of sp2 hybridized carbons and an sp3 hybridized carbon or silicon.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Novel diarylphosphine- and dialkylphosphine-containing compounds, processes of preparing same and uses thereof as tridentate ligands

A novel process of preparing tridentate ligands containing one or more of a diarylphosphine and / or dialkylphosphine electron donating groups 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 and dialkylphosphine-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. Novel precursor molecules useful for preparing the tridentate ligands and processes of preparing same are also disclosed.
Owner:TECHNION RES & DEV FOUND LTD

Platinum (II) complexes containing n-heterocyclic carbene ligand and pincer ligands, synthesis, and their applications in cancer treatment

Provided herein is a method of synthesis of Pt(II) complexes, a pharmaceutical composition comprises thereof. Also provided herein are the methods for the treatment and prevention of cancer / tumor in patients in need thereof by the administration of the Pt(II) complexes. Also provided is a method of detecting the Pt(II) complex in a biological system. Also provided is a method of making the Pt(II) complex The Pt(II) complexes possess anticancer activity such as the induction of cell death, inhibition of cellular proliferation, and inhibition of tumor growth in vivo.
Owner:VERSITECH LTD

Ferrocenyl pyrimidine pincer ligand and preparation method thereof

The invention discloses a ferrocenyl pyrimidine pincer ligand and a preparation method thereof and belongs to the technical field of organic synthesis. The ferrocenyl pyrimidine pincer ligand has the general formula shown in the specification, wherein X and Y are atom C or N; R1 and R2 are C1-C6 linear alkyl, -C6H5, -COCH3, -COOCH3, -CHO, -OCH3, -N(CH3)2, -CN or -COOH; R1 is connected to the ortho-position, meta-position or para-position of X; and R2 is connected to ortho-position, meta-position or para-position of Y. According to the corresponding preparation method, 2,4,6-trichloro pyrimidine, ferrocene mercuric chloride, aryl or heterocyclic aryl boric acid serve as raw materials, and the ferrocenyl pyrimidine pincer ligand of a rich structure is prepared through a stepped coupling method. The preparation method is mild in reaction conditions, wide in substrate range and high in yield. The selected raw material ferrocene mercuric chloride has high stability and high stereoselectivity in air and water, the compound can be prepared by directly mercurating ferrocene, and the operation is easy and readily available. Meanwhile, multiple asymmetric pincer structures can be conveniently obtained by utilizing the preparation method, and the ligand has wide application prospect.
Owner:LUOYANG NORMAL UNIV

A kind of porphyrin conjugated polymer of pincer complex bridge, synthesis method and application

The invention discloses a clamp complex bridged porphyrin conjugated polymer, a synthesis method and an application. The present invention adopts Schiff base condensation reaction to combine 5,10,15,20-tetrakis(4-formylphenyl)porphyrin or its corresponding copper complex (i.e. CuPor) with pincer ligand 2,6-bis(5 ‑Amino‑1H‑benzimidazolyl)pyridine or its corresponding ruthenium pincer complex (i.e. RuN 3 ) to form conjugated polymers. Among them, CuPor‑RuN 3 The ruthenium / copper bimetallic center and conjugated structure of CP improve the intrinsic conductivity of the polymer and the adsorption of water molecules, and accelerate the electron transfer between copper and ruthenium metal centers, thus improving its electrocatalytic hydrogen evolution performance. The conjugated polymer has a promising application prospect as a general hydrogen evolution electrocatalyst in the whole pH range.
Owner:WUHAN UNIV

Method for the preparation of symmetrical pincer ligands of the m-terphenyl compound type

The present invention relates to a process for the preparation of symmetrical pincer ligands of the m-terphenyl compound type. In particular, the present invention relates to a process for the preparation of a compound of formula ABA by reacting a compound of formula (A) with a compound of formula (B), wherein X=-OR' or -NHR'; and R'=H or protecting group functional group, and R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are independently selected from hydrogen, (C 1 -C 12 )‑Alkyl, O‑(C 1 -C 12 )-Alkyl, (C 6 -C 20 )‑aryl, O‑(C 6 -C 20 )-aryl, wherein the group R 1 to R 4 Two of can also be linked by covalent bonds, and halogen, characterized in that the reaction is carried out electrochemically.
Owner:EVONIK OPERATIONS GMBH

Ono pincer ligands and ono pincer ligand comprising metal complexes

Embodiments of the invention are directed to ONO pincer ligands that can be in a trianionic, protonated or protonated equivalent form. The ONO pincer ligand can be combined with a transition metal comprising compound to form an ONO pincer ligand comprising transition metal complex. By choice of the ONO pincer ligand structure, the steric and electronic properties of the transition metal complexes therefrom can be controlled. The ONO pincer ligands comprise a central nitrogen atom that is disubstituted with a pair of three atom comprising bridges where the three atoms are three sp2 hybridized carbons or the three atoms are a pair of sp2 hybridized carbons and an sp3 hybridized carbon or silicon.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Iron-catalyzed cross-coupling of methanol with secondary or tertiary alcohols to produce formate esters

A process for preparing a variety of secondary and tertiary alkyl formate esters via the coupling of methanol and secondary (or tertiary) alcohols. Iron-based catalysts, supported by pincer ligands, are employed to produce these formate esters in high yields and unprecedentedly high selectivities (>99%). Remarkably, the coupling strategy is also applicable to bulkier tertiary alcohols, which afford corresponding tertiary formate esters in moderately high yields and high selectivities.
Owner:EASTMAN CHEM CO

Platinum (II) complexes containing N-heterocyclic carbene ligand and pincer ligands, synthesis, and their applications in cancer treatment

Provided herein is a method of synthesis of Pt(II) complexes, a pharmaceutical composition comprises thereof. Also provided herein are the methods for the treatment and prevention of cancer / tumor in patients in need thereof by the administration of the Pt(II) complexes. Also provided is a method of detecting the Pt(II) complex in a biological system. Also provided is a method of making the Pt(II) complex The Pt(II) complexes possess anticancer activity such as the induction of cell death, inhibition of cellular proliferation, and inhibition of tumor growth in vivo.
Owner:VERSITECH LTD

Iron-catalyzed cross-coupling of methanol with secondary or tertiary alcohols to produce formate esters

A process for preparing a variety of secondary and tertiary alkyl formate esters via the coupling of methanol and secondary (or tertiary) alcohols. Iron-based catalysts, supported by pincer ligands, are employed to produce these formate esters in high yields and unprecedentedly high selectivities (>99%). Remarkably, the coupling strategy is also applicable to bulkier tertiary alcohols, which afford corresponding tertiary formate esters in moderately high yields and high selectivities.
Owner:EASTMAN CHEM CO

Iron-catalyzed transfer hydrogenation of esters to alcohols

Iron-based homogeneous catalysts, supported by pincer ligands, are employed in the transfer hydrogenation of esters using C2-C12 alcohols as sacrificial hydrogen donors to produce corresponding alcohols from the esters. No external H2 pressure is required. The reaction can be carried out under ambient pressure.
Owner:EASTMAN CHEM CO

Method for transferring N-atoms from metal complexes to organic and inorganic substrates

A complex for transference of a nitrogen atom to an electrophilic reagent comprises a hard-hard-hard pincer ligand and an early transition metal bound to a nitride. The pincer ligand can be an OCO ligand and the transition metal can be Mo. The complex can be used to transfer the nitrogen atom bound to the metal to an electrophile in a method to produce a nitrogen containing molecule. In one novel nitrogen transfer reaction, a Mo—N triple bond is broken where the nitrogen transfers to the sp2 hybridized carbon of an acid chloride to form a nitrile.
Owner:UNIV OF FLORIDA RES FOUNDATION INC

Iron-catalyzed transfer hydrogenation of esters to alcohols

Iron-based homogeneous catalysts, supported by pincer ligands, are employed in the transfer hydrogenation of esters using C2-C12 alcohols as sacrificial hydrogen donors to produce corresponding alcohols from the esters. No external H2 pressure is required. The reaction can be carried out under ambient pressure.
Owner:EASTMAN CHEM CO
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