Structural and functional models related to the nickel hydrogenases

被引：125

作者：

Bouwman, E ^{[1
]}

Reedijk, J ^{[1
]}

机构：

[1] Leiden Univ, Leiden Inst Chem, POB 9502, NL-2300 RA Leiden, Netherlands

来源：

COORDINATION CHEMISTRY REVIEWS | 2005年 / 249卷 / 15-16期

关键词：

NiFe] hydrogenase; model systems; nickel; iron; structures; biomimetic;

D O I：

10.1016/j.ccr.2004.10.010

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

In this review a historic overview is given of the biomimetic models synthesised since the presence of nickel in hydrogenases was first reported in 1981. The crystal structure of the [NiFe] hydrogenase isolated from Desulvofibrio gigas unexpectedly revealed a heterodinuclear active site, including a nickel ion and an iron centre. This report in 1995 gave an impetus to the development of new structural models for these enzymes. This review is focussed on the synthesis, spectroscopic features, and reactivity of the complexes that have been designed and synthesised as model systems for [NiFe] hydrogenases, with special attention for the heterodimetallic complexes that have been reported in the past decade. The complexes are classified according to the various ligand types, including sulfur, oxygen, nitrogen, and phosphorus donor atoms. (c) 2004 Elsevier B.V. All rights reserved.

引用

页码：1555 / 1581

页数：27

共 185 条

[31] Synthesis and structure of a thiolate-ligated Ni cluster which contains an unusual thiolate bridging mode and an exposed Ni site [J].

Cha, M ;

Sletten, J ;

Critchlow, S ;

Kovacs, JA .

INORGANICA CHIMICA ACTA, 1997, 263 (1-2) :153-159

[32] NICKEL-PROMOTED REDUCTIVE C-S BOND-CLEAVAGE - A MODEL FOR THE 1ST STEP IN THE REACTION PROMOTED BY METHYL COENZYME-M REDUCTASE [J].

CHA, MY ;

SHONER, SC ;

KOVACS, JA .

INORGANIC CHEMISTRY, 1993, 32 (09) :1860-1863

[33] PROBING THE INFLUENCE OF LOCAL COORDINATION ENVIRONMENT LIGAND-BINDING IN NICKEL HYDROGENASE MODEL COMPLEXES [J].

CHA, MY ;

CATLIN, CL ;

CRITCHLOW, SC ;

KOVACS, JA .

INORGANIC CHEMISTRY, 1993, 32 (25) :5868-5877

[34]

Chalbot MU, 2003, EUR J INORG CHEM, P453

[35] Preparative and structural studies on iron(II)-thiolate cyanocarbonyls: relevance to the [NiFe]/[Fe]-hydrogenases [J].

Chen, CH ;

Chang, YS ;

Yang, CY ;

Chen, TN ;

Lee, CM ;

Liaw, WF .

DALTON TRANSACTIONS, 2004, (01) :137-143

[36] Pyrazolyl[(methylthio)methyl]borates: hybrid ligands providing nitrogen and sulfur donors [J].

Chiou, SJ ;

Ge, PH ;

Riordan, CG ;

Liable-Sands, LM ;

Rheingold, AL .

CHEMICAL COMMUNICATIONS, 1999, (02) :159-160

[37] STRUCTURE AND REDOX CHEMISTRY OF ANALOGOUS NICKEL THIOLATO AND SELENOLATO COMPLEXES - IMPLICATIONS FOR THE NICKEL SITES IN HYDROGENASES [J].

CHOUDHURY, SB ;

PRESSLER, MA ;

MIRZA, SA ;

DAY, RO ;

MARONEY, MJ .

INORGANIC CHEMISTRY, 1994, 33 (22) :4831-4839

[38] Kinetic evidence for intramolecular proton transfer between nickel and coordinated thiolate [J].

Clegg, W ;

Henderson, RA .

INORGANIC CHEMISTRY, 2002, 41 (05) :1128-1135

[39] X-RAY SPECTROSCOPIC STUDIES OF NICKEL-COMPLEXES, WITH APPLICATION TO THE STRUCTURE OF NICKEL SITES IN HYDROGENASES [J].

COLPAS, GJ ;

MARONEY, MJ ;

BAGYINKA, C ;

KUMAR, M ;

WILLIS, WS ;

SUIB, SL ;

BAIDYA, N ;

MASCHARAK, PK .

INORGANIC CHEMISTRY, 1991, 30 (05) :920-928

[40] STRUCTURAL INVESTIGATIONS OF NICKEL-COMPLEXES WITH NITROGEN AND SULFUR DONOR LIGANDS [J].

COLPAS, GJ ;

KUMAR, M ;

DAY, RO ;

MARONEY, MJ .

INORGANIC CHEMISTRY, 1990, 29 (23) :4779-4788

← 1 2 3 4 5 6 7 8 9 10 →