Novel carbon monochalcogenide coordination mode: [Rh 2{μ- SeCMo(CO) 2(Tp*)} 24-cod) 2] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate; Cod = cyclo-octa-1,5-diene)

Anthony F. Hill*, Caitlin M.A. McQueen

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    24 Citations (Scopus)

    Abstract

    The reaction of [Et 4N][Mo(CSe)(CO) 2(Tp*)] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate) with [Rh 2(μ-Cl) 24-cod) 2] (cod = cyclo-octa-1,5-diene) results in the formation of the tetrametallic complex [Rh 2{SeCMo(CO) 2(Tp*)} 24- cod) 2] in which the CSe ligand adopts a crystallographically confirmed and unprecedented μ 3:σ,σ′(Se), σ″(C) coordination mode.

    Original languageEnglish
    Pages (from-to)2482-2485
    Number of pages4
    JournalOrganometallics
    Volume31
    Issue number6
    DOIs
    Publication statusPublished - 26 Mar 2012

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