Reactivity of three-coordinate iron-NHC complexes towards phenylselenol and lithium phenylselenide.
نویسندگان
چکیده
The three-coordinate iron(II) NHC complexes [(IPr)Fe(N'')2] (1) and [(I(t)Bu)Fe(N'')2] (3) (N'' = N(SiMe3)2) react with PhSeH or LiSePh to give the iron(II) selenolates [(IPr)Fe(N'')(SePh)] (6) and [I(t)Bu(H)][(aI(t)Bu)Fe(SePh)3], [I(t)Bu(H)][7], with complex 7 containing an abnormal NHC ligand.
منابع مشابه
A combined magnetic circular dichroism and density functional theory approach for the elucidation of electronic structure and bonding in three- and four-coordinate iron(ii)–N-heterocyclic carbene complexes† †Electronic supplementary information (ESI) available: Supplemental MCD and Mössbauer data; MO diagrams, TD-DFT, optimized geometry coordinates and X-ray crystallographic details. CCDC 1023546–1023548. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4sc02791d Click here for additional data file. Click here for additional data file.
The combination of iron salts and N-heterocyclic carbene (NHC) ligands is a highly effective combination in catalysis, with observed catalytic activities being highly dependent on the nature of the NHC ligand. Detailed spectroscopic and electronic structure studies have been performed on both three- and four-coordinate iron(II)-NHC complexes using a combined magnetic circular dichroism (MCD) an...
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ورودعنوان ژورنال:
- Dalton transactions
دوره 43 11 شماره
صفحات -
تاریخ انتشار 2014