کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1334558 | 1500281 | 2013 | 5 صفحه PDF | دانلود رایگان |
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.
Release of nitric oxide from an N-heterocyclic carbene-trinitrosyl iron complex (TNIC) and transfer to [(N2S2)M]2, M = Fe, Co. Herein we report the synthesis and characterization of binuclear, paramagnetic Co–Fe complex 1 which is comprised of a {Fe(NO)2}9 unit and S-bound (N2S2)Co(NO) which serves as a mono-dentate metallothiolate ligand.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 58, 13 July 2013, Pages 151–155