共 18 条
Facile and highly efficient light-induced PR3/CO ligand exchange:: A novel approach to the synthesis of [(μ-SCH2NnPrCH2S)Fe2(CO)4(PR3)2]
被引:24
作者:

Gao, Weiming
论文数: 0 引用数: 0
h-index: 0
机构: Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China

Liu, Jianhui
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h-index: 0
机构: Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China

Akermark, Bjoern
论文数: 0 引用数: 0
h-index: 0
机构: Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China

Sun, Licheng
论文数: 0 引用数: 0
h-index: 0
机构: Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China
机构:
[1] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China
[2] Stockholm Univ, Arrhenius Lab, Dept Organ Chem, S-10691 Stockholm, Sweden
[3] Royal Inst Technol, KTH Chem Organ Chem, S-10044 Stockholm, Sweden
基金:
中国国家自然科学基金;
关键词:
Fe-hydrogenases;
phosphine ligands;
bioinorganic chemistry;
hydrogen production;
D O I:
10.1016/j.jorganchem.2006.12.009
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
A straightforward and efficient transformation of the Fe-S complex [(mu-SCH2N"PrCH2S)Fe-2(CO)(6)] to its double phosphine coordinated analogues [(mu-(SCH2NPrCH2S)-Pr-n)Fe-2(CO)(4)(PR3)(2)] (R = Ph, Me) is described. The single crystal structure of the PPh3-disubstituted Complex [(mu-(SCH2NPrCH2S)-Pr-n)Fe-2(CO)(4)(Ph3P)(2)] (3) showed that both of the phosphine ligands take an apical/apical instead of a basal/ basal or an apical/basal configuration. (c) 2006 Elsevier B.V. All rights reserved.
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页码:1579 / 1583
页数:5
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