Oxidation states and photoinduced metastable states in [Fe(CO)2(NO)2]

被引:17
作者
Klein, Axel [1 ]
von Mering, Yvonne [1 ]
Uthe, Andre [1 ]
Butsch, Katharina [1 ]
Schaniel, Dominik [2 ,3 ]
Mockus, Nicholas [2 ]
Woike, Theo [2 ]
机构
[1] Univ Cologne, Inst Anorgan Chem, D-50939 Cologne, Germany
[2] Univ Koln 1, Inst Phys, D-50937 Cologne, Germany
[3] Nancy Univ, CNRS, CRM2, F-54506 Nancy, France
关键词
Iron; Nitrosyl; Carbonyl; Electrochemistry; Spectroelectrochemistry; Linkage isomers; TRANSITION-METAL NITROSYL; NO-CENTER-DOT; NITRIC-OXIDE; INFRARED-SPECTRA; REDOX STATES; EPR-SPECTRUM; COMPLEXES; IRON; DIFFRACTION; CHEMISTRY;
D O I
10.1016/j.poly.2010.05.028
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The electrochemistry of the complex [Fe(CO)(2)(NO)(2)] and the IR and EPR spectra of the one-electron reduced [Fe(CO)(2)(NO)(2)](center dot-) and one-electron oxidised species [Fe(CO)(2)(NO)(2)](center dot+) reveal mainly NO-centred spin density for the unpaired electron. The results are discussed in term of oxidation states. Furthermore, the parent complex was investigated for light-induced linkage isomerisation using IR spectroscopy. Thermally and optically reversible generation of a new species identified by new vibrational bands is interpreted in terms of photoinduced nitrosyl linkage isomers. (C) 2010 Elsevier Ltd. All rights reserved.
引用
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页码:2553 / 2559
页数:7
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