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带冠醚的反式螯合双(N-杂环卡宾)配体:合成、结构与催化作用

Canopied trans-chelating bis(N-heterocyclic carbene) ligand: synthesis, structure and catalysis.

作者信息

Morgan Brad P, Galdamez Gabriela A, Gilliard Robert J, Smith Rhett C

机构信息

Department of Chemistry and Center for Optical Materials Science and Engineering Technologies (COMSET), Clemson University, Clemson, SC 29634, USA.

出版信息

Dalton Trans. 2009 Mar 21(11):2020-8. doi: 10.1039/b815739a. Epub 2009 Jan 30.

Abstract

The terphspan scaffold was employed to support a bis(N-heterocyclic carbene) ligand () that provides a m-terphenyl canopy over one side of its metal complexes. Single-crystal X-ray diffraction studies on a silver complex of {[Ag()]AgBr(2)}(2) revealed an unusual tetranuclear silver core with a Ag-Ag bond distance of 3.0241(8) A with as a trans-chelating ligand (C-Ag-C = 171 degrees ). A preliminary X-ray structure of pseudo-square planar [PdCl(2)()] showed a similar binding mode of (C-Pd-C = 177 degrees ). High yields were obtained in Suzuki-Miyaura coupling reactions utilizing [PdCl(2)()] as the procatalyst and the results were compared with analogous complexes of trans-spanning diphosphine () and diphosphinite () complexes. The diphosphinite complex, [PdCl(2)()], decomposes to mu-ClPd(PPh(2)OH)(PPh(2)O) at room temperature.

摘要

采用三联苯支架来支撑双(N-杂环卡宾)配体(),该配体在其金属配合物的一侧提供一个间三联苯冠层。对{[Ag()]AgBr(2)}(2)的银配合物进行的单晶X射线衍射研究揭示了一种不寻常的四核银核,其Ag-Ag键长为3.0241(8)Å,作为反式螯合配体(C-Ag-C = 171°)。伪方形平面[PdCl(2)()]的初步X射线结构显示出类似的结合模式(C-Pd-C = 177°)。以[PdCl(2)()]作为前催化剂进行铃木-宫浦偶联反应时获得了高产率,并将结果与跨式双膦()和双亚膦酸酯()配合物的类似配合物进行了比较。双亚膦酸酯配合物[PdCl(2)()]在室温下分解为[μ-ClPd(PPh(2)OH)(PPh(2)O)](2)。

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