| Literature DB >> 17263395 |
Mikhail V Barybin1, William W Brennessel, Benjamin E Kucera, Mikhail E Minyaev, Victor J Sussman, Victor G Young, John E Ellis.
Abstract
Treatment of [M(CO)(6)](-), M = Nb, Ta, with Ag(+), I(2) or NO(+) in the presence of CNXyl provided [M(CNXyl)(7)](+), M(CNXyl)(6)I, or cis-[M(CNXyl)(4)(NO)(2)](+), which are isocyanide analogues of the unknown carbonyl complexes [M(CO)(7)](+), M(CO)(6)I, or cis-[M(CO)(4)(NO)(2)](+), respectively. Reduction of M(CNXyl)(6)I by cesium graphite gave the respective Cs[M(CNXyl)(6)], which have been structurally characterized and represent the first isolable homoleptic isocyanidemetalates for second or third row transition metals. Nitrosylation of [Ta(CNXyl)(6)](-) affords a rare example of a mononitrosyl tantalum complex, Ta(CNXyl)(5)NO, which is an isocyanide analogue of the unknown Ta(CO)(5)NO. This study emphasizes, inter alia, the remarkable versatility of the CNXyl ligand compared to CO in stabilizing various electronic environments at heavier group 5 metal centers.Entities:
Year: 2007 PMID: 17263395 DOI: 10.1021/ja065964q
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419