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论文类型：期刊论文

发表时间：2008-04-01

发表刊物：JOURNAL OF INORGANIC BIOCHEMISTRY

收录刊物：SCIE、PubMed

卷号：102

期号：4

页面范围：952-959

ISSN号：0162-0134

关键字：bioinorganic chemistry; diiron complex; electrochemistry; [FeFe]-hydrogenase; rigid bridge

摘要：Three diiron dithiolate complexes containing rigid and conjugated bridges, [mu-SC(6)H(4)-2-(CO)S-mu]Fe(2)(CO)(6) (1), [2-mu-SC(5)H(3)N-3-(CO)S-mu]Fe(2)(CO)(6) (2). and the PPh(3)-monosubstituted complex [mu-SC(6)H(4)-2-(CO)S-mu]Fe(2)(CO)(5)(PPh(3)) (1-P), were prepared as biomimetic models for the [FeFe]-hydrogenase active site. The structures of complexes 1 and 2 were determined by single crystal X-ray analysis, which shows that each complex features a rigid coplanar dithiolate bridge with a 2-3 degrees deviation from the bisect plane of the molecule. The influence of the rigid bridge on the reduction potentials of complexes 1, 2 and 1-P was investigated by electrochemistry. The cyclic voltammograms of complexes 1 and 2 display large positive shifts for the primary reduction potentials, that is, 380-480 mV in comparison to that of the pdt-bridged (pdt = propane-1,3-dithiolato) complex (mu-pdt)Fe(2)(CO)(6) and 160-260 mV to that of the bdt-bridged (bdt = benzene- 1,2-dithiolato) analogue ([mu-bdt)Fe(2)(CO)(6). (C) 2008 Elsevier Inc. All rights reserved.