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Please use this identifier to cite or link to this item: http://ir.ncue.edu.tw/ir/handle/987654321/18942

Title: Robust and Electron-Rich cis-Palladium(II) Complexes with Phosphine and Carbene Ligands as Catalytic Precursors in Suzuki Coupling Reactions
Authors: Liao, Chuang-Yi;Chan, Kai-Ting;Tu, Cheng-Yi;Chang, Yu-Wei;Hu, Ching-Han;Lee, Hon Man
Contributors: 化學系
Keywords: Aryl chlorides;Carbene ligands;Cross-coupling;Palladium;Phosphine ligands
Date: 2009
Issue Date: 2014-08-14T04:29:32Z
Publisher: John Wiley & Sons, Inc.
Abstract: A new imidazolinium ligand precursor [L(2)H]Cl (2) was prepared in 86 % yield. Compared with its imidazolium counterpart, [L(1)H]Cl (1), 2 is very sensitive to moisture and can undergo ring-opening reactions very readily. Palladium complexes with the ring-opened products from imidazolinium salts were isolated and characterized by X-ray crystallography. Theoretical studies confirmed that the imidazolinium salt has a higher propensity for the ring-opening reaction than the imidazolium counterpart. New mixed phosphine/carbene palladium complexes, cis-[PdCl(2)(L)(PR(3))] (L=L(1) and L(2); R=Ph, Cy), were successfully prepared. These complexes are highly robust as revealed by variable-temperature NMR spectroscopic studies and thermal gravimetric analysis. The structural and electronic properties of the new complexes on varying the carbene group (imidazol-2-ylidene group (unsaturated carbene) vs. imidazolin-2-ylidene (saturated carbene)) and the phosphine group (PPh(3) vs. PCy(3)) were studied in detail by X-ray crystallography, X-ray photoelectron spectroscopy, and theoretical calculations. The catalytic study reveals that cis-[PdCl(2)(L(2))(PCy(3))] is a competent Pd(II) precatalyst for Suzuki coupling reactions, in which unreactive aryl chlorides can be applied as substrates.
Relation: Chemistry - A European Journal, 15(2): 405-417
Appears in Collections:[化學系] 期刊論文

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