The Lewis acidic pincer with a labile triflate ligand, viz. [Pd(OTf)(PCP)] (PCP = (-)CH(CH(2)CH(2)PPh(2))(2)) was prepared from [PdCl(PCP)] with AgOTf. It reacts readily with neutral bidentate ligands [L = 4,4'-bipyridine (4,4'-bpy) and 1,1'-bis(diphenylphosphino)ferrocene (dppf)] to give dinuclear PCP pincers [{Pd(PCP)}(2)(micro-L)][OTf](2) (L = 4,4'-bpy, 2; dppf,3). [PdCl(PCP)] also reacts with 4-mercaptopyridine in the presence of KOH to give a Lewis basic pincer with a free pyridine functional group [Pd(4-Spy)(PCP)]4. Its metalloligand character is exemplified by the isolation of an asymmetric dinuclear double-pincer complex [{Pd(PCP)}(2)(micro-4-Spy)][PF(6)] 6 bridged by an ambidentate pyridinethiolato ligand. Complexes 1, 2, 3, 4 and 6 have been characterized by single-crystal X-ray diffraction analyses.
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http://dx.doi.org/10.1039/b710752h | DOI Listing |
Chem Commun (Camb)
November 2024
Institute für Anorganische Chemie und Kristallographie, Universität Bremen, Leobener Str. 7, 28359 Bremen, Germany.
The facile synthesis of the cationic dinuclear group 10 complexes [M(PCP)-Cl] (M = Ni, Pd, Pt) by transmetallation from a simple Ga precursor is reported (PCP = 2,6-(PhP)CH). Their use for the catalysed dehydrogenation of MeNHBH shows that Ni has a higher reactivity than Pt, whereas Pd is inactive.
View Article and Find Full Text PDFInorg Chem
October 2021
Departamento Química Inorgánica-Instituto Síntesis Química y Catálisis Homogénea (ISQCH), Universidad de Zaragoza-CSIC, C/Pedro Cerbuna 12, 50009 Zaragoza, Spain.
The catalysts [Ir(COD)(κ-,,-PCP)]BF and [Ir(COD)(κ--PCO)]BF proved to be active in the solventless dehydrogenation of formic acid. The impact of various cosolvents on the activity was evaluated, showing an outstanding improvement of the catalytic performance of [Ir(COD)(κ--PCO)]BF] in "green" organic carbonates: namely, dimethyl carbonate (DMC) and propylene carbonate (PC). The TOF value for [Ir(COD)(κ--PCO)]BF increases from 61 to 988 h upon changing from solventless conditions to a 1/1 (v/v) DMC/HCOOH mixture.
View Article and Find Full Text PDFMolecules
September 2020
Department of Chemistry and Science, Materials Sciences Center, Philipps University of Marburg, 35043 Marburg, Germany.
A series of dinuclear copper(I) and carbodiphosphorane (CDP) complexes using multidentate ligands CDP(Py) () and (CDP(CHPPh) () have been isolated and characterized. Detailed structural information was gained by single-crystal XRD analyses of nine representative examples. The common structural motive is the central double ylidic carbon atom with its characteristic two lone pairs involved in the binding of two geminal L-Cu(I) fragments at Cu-Cu distances in the range 2.
View Article and Find Full Text PDFDalton Trans
August 2020
Guangxi Key laboratory of Chemistry and Engineering of Forest Products, Guangxi University for Nationalities, Nanning, 530006, P.R. China.
Coordination polymers [Cd(1,4-bpeb)(L1)] (1), [Zn2(1,4-bpeb)2(L2)2(SO42-)2] (2) and [Cd(1,4-bpeb)(L3)] (H2O) (3) (H2L1, 3-[2-(3-hydroxy-phenoxymethyl)-benzyloxy]-benzoic acid; HL2, 1H-Indazole-3-carboxylic acid; H3L3, benzene-1,2,3-tricarboxylic acid; 1,4-bpeb, 1,4-bis[2-(4-pyridyl)vinyl]benzene have been synthesized under solvothermal conditions. Complexes 1-3 underwent photodimerization in the solid-state to give quantitative yields of single isomeric products. The choice of carboxyl ligands L and metal center determined the arrangement of 1,4-bpeb ligands, which in turn directed the regiochemistry of the final photoproducts.
View Article and Find Full Text PDFInorg Chem
November 2016
State Key Laboratory of Materials-Oriented Chemical Engineering and College of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 210009, P. R. China.
A Zn-based metal-organic framework (MOF)/porous coordination polymer (PCP), (EMIM)[Zn(SIP)] (1) (SIP = 5-sulfoisophthalate, EMIM = 1-ethyl-3-methylimidazolium), was synthesized using the ionothermal reaction. The Zn ion adopts distorted square pyramid coordination geometry with five oxygen atoms from three carboxylates and one sulfo group. One of two carboxylates in SIP serves as a μ-bridge ligand to link two Zn ions and form the dinuclear SBU, and such SBUs are connected by SIP ligands to build the three-dimensional framework with rutile (rtl) topology.
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