The first bimetallic metallaboratrane: [Rh2{B(mt) 3}22-S,S′-HB(mt)3}]Cl and its synthesis from the fluxional rhodaboratrane Salt [Rh{B(mt) 3}(η4-C8H12)]Cl, (Rh→B, mt = Methimazolyl)

Ian R. Crossley, Anthony F. Hill*, Elizabeth R. Humphrey, Anthony C. Willis

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    93 Citations (Scopus)

    Abstract

    The prolonged reaction of [Rh{B(mt)3}(η4C 8H12)]Cl, prepared from [Rh(η4-C 8H12)Cl]2 and 2 equiv of Na[HB(mt) 3], with a further excess of Na[HB(mt)3] leads to formation of the first binuclear metallaboratrane salt, [Rh2[B(mt) 3]22-S,S′-HB(mt)3}]Cl. This compound, which is also observed as a decomposition product of rhodium tris(methimazolyl)borane complexes, affords the first evidence for bridging of transition metals by the methimazolyl sulfur donors.

    Original languageEnglish
    Pages (from-to)4083-4086
    Number of pages4
    JournalOrganometallics
    Volume24
    Issue number16
    DOIs
    Publication statusPublished - 1 Aug 2005

    Fingerprint

    Dive into the research topics of 'The first bimetallic metallaboratrane: [Rh2{B(mt) 3}22-S,S′-HB(mt)3}]Cl and its synthesis from the fluxional rhodaboratrane Salt [Rh{B(mt) 3}(η4-C8H12)]Cl, (Rh→B, mt = Methimazolyl)'. Together they form a unique fingerprint.

    Cite this