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A facile synthesis of a binuclear Ag complex of a bis(carbone) ligand and its application as a carbone-transfer agent for the generation of other transition-metal complexes of Au (), Ni (), and Pd () is presented. Complex was synthesized through multiple synthetic routes under mild reaction conditions using the tetracationic [H][OTf·Cl] precursor salt, the dicationic [H][OTf] ylide salt, and the free ligand . The first two synthesis routes require no prior isolation of the air-, moisture-, and temperature-sensitive free ligand , thus affording complex with high yield and purity. Multinuclear NMR techniques, high-resolution mass spectrometry, and single-crystal X-ray diffraction analysis confirmed the identity of complex as a binuclear Ag complex of with a molecular formula of [Ag][OTf] and a 16-membered-ring metallomacrocyclic structure. During the transmetalation reaction with Au, the binuclear nature of complex remains intact to give analogous complex ([Au][OTf]). However, the dimeric structure was disrupted upon the carbone-transfer reaction with Ni and Pd, yielding mononuclear C-N-C pincer-type complexes ([NiCl][OTf]) and ([PdCl][OTf]), respectively. These results demonstrated the versatile use of complex as a carbone-transfer agent to other transition metals regardless of the type or size of the metals or the geometry they prefer.
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http://dx.doi.org/10.1021/acs.inorgchem.3c00765 | DOI Listing |
Inorg Chem
August 2023
Institute of Chemistry, Academia Sinica, Taipei 11529, Taiwan.
A facile synthesis of a binuclear Ag complex of a bis(carbone) ligand and its application as a carbone-transfer agent for the generation of other transition-metal complexes of Au (), Ni (), and Pd () is presented. Complex was synthesized through multiple synthetic routes under mild reaction conditions using the tetracationic [H][OTf·Cl] precursor salt, the dicationic [H][OTf] ylide salt, and the free ligand . The first two synthesis routes require no prior isolation of the air-, moisture-, and temperature-sensitive free ligand , thus affording complex with high yield and purity.
View Article and Find Full Text PDFChemistry
June 2017
Department of Applied Molecular Chemistry, College of Industrial Technology, Nihon University, Chiba, 275-8575, Japan.
Bis(sulfane)carbon(0) (BSC; Ph S→C←SPh (1)) is successfully synthesized by deprotonation of the corresponding protonated salt 1⋅HTfO. The diprotonated salt 1⋅(HTfO) as the starting material can be also easily accessed by the deimination of iminosulfane(sulfane)carbon(0) (iSSC)⋅HBF . Density functional theory calculations revealed the peculiar electronic structure of 1, which has two lone pairs of electrons at the central carbon atom.
View Article and Find Full Text PDFChemistry
October 2015
Department of Applied Molecular Chemistry, College of Industrial Technology, Nihon University, Chiba 275-8575 (Japan).
Iminosulfane(phosphane)carbon(0) derivatives (iSPCs; Ar3 P→C←SPh2 (NMe); Ar=Ph (1), 4-MeOC6 H4 (2), 4-(Me2 N)C6 H4 (3)) have been successfully synthesized and the molecular structure of 3 characterized. Carbone 3 is the first thermally and hydrolytically stable carbone stabilized by phosphorus and sulfur ligands. DFT calculations reveal the electronic structures of 1-3, which have two lone pairs of electrons at the carbon center.
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