Dinitrosyl iron adducts of (N2S2)M(NO) complexes (M = Fe, Co) as metallodithiolate ligands

doi:10.1016/j.poly.2012.09.047

淡江大學機構典藏 > 理學院 > 化學學系暨研究所 > 期刊論文 > Item 987654321/97541

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题名:	Dinitrosyl iron adducts of (N2S2)M(NO) complexes (M = Fe, Co) as metallodithiolate ligands
作者:	Hsieh, Chung-Hung;Chupik, Rachel B.;Pinder, Tiffany A.;Darensbourg, Marcetta Y.
贡献者:	淡江大學化學學系
关键词:	Dinitrosyl iron complex (DNIC);Trinitrosyl iron complex (TNIC);NO trapping agent;Heterobimetallic;Metallodithiolate ligand
日期:	2013-07
上传时间:	2014-03-26 14:26:02 (UTC+8)
出版者:	Kidlington: Pergamon
摘要:	Adducts of the dinitrosyl iron unit and mono-nitrosyl bis-mercaptoethanediazacycloheptane (bme-dach) iron and cobalt are described in terms of the (bme-dach)M(NO) as metallodithiolate ligands. With M = Fe, a diamagnetic (N2S2)Fe(NO)·Fe(NO)2 diiron complex, in which the (N2S2)Fe(NO) unit serves as a bidentate ligand to the Fe(NO)2 unit is derived by use of a trinitrosyliron cation as precursor to the DNIC unit as well as a NO source to cleave the [(bme-dach)Fe]2 dimer (J. Am. Chem. Soc., 2010, 132, 14118). By a similar approach of [(bme-dach)Co]2 dimer cleavage, the Co–Fe bimetallic contains (N2S2)Co(NO) as a monodentate metallothiolate ligand to Fe(NO)2L, L = I-Mes, 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene. Characterization of this paramagnetic cation includes infrared and EPR spectroscopies, and X-ray diffraction analysis. The latter finds a Co⋯Fe distance of 3.697 Å in contrast to the Fe–Fe bond distance of 2.7857(8) Å in the homobimetallic complex.
關聯:	Polyhedron 58, pp.151–155
DOI:	10.1016/j.poly.2012.09.047
显示于类别:	[化學學系暨研究所] 期刊論文

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