Synthesis of the ruthenaboratranes [Ru(CS)(PPh3){B(mt) 3}](Ru→B)8 and [Ru(CO)(CNR){B(mt)3}] (Ru→B)8 (mt = methimazolyl, R = tBu, C 6H3Me2-2,6, C6H2Me 3-2,4,6)

Ian R. Crossley, Mark R.St J. Foreman, Anthony F. Hill*, Gareth R. Owen, Andrew J.P. White, David J. Williams, Anthony C. Willis

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    75 Citations (Scopus)

    Abstract

    The reaction of [Ru(CH=CH2)Cl(CS)(PPh3)2] with Na[HB(mt)3] (mt = methimazolyl) provides the ruthenaboratrane [Ru(CS)(PPh3){B(mt)3}]. The reaction of [Ru(CO)(PPh 3){B(mt)3}] with CO to provide [Ru(CO)2{B(mt) 3}] is reversible, while the phosphine-free ruthenaboratranes [Ru(CO)(CNR){B(mt)3}] (R = tBu, C6H 3Me2-2,6, C6H2Me3-2,4,6) form irreversibly upon addition of isonitriles (CNR) to [Ru(CO)(PPh 3){B(mt)3}]. The crystal structures of the ruthenaboratranes [Ru(CS)(PPh3){B(mt)3}J, [Ru(CO)(CN tBu)({B(mt)3)], and [Ru(CO)(CNC6H 2Me3-2,4,6){B(mt)3}] are reported.

    Original languageEnglish
    Pages (from-to)381-386
    Number of pages6
    JournalOrganometallics
    Volume27
    Issue number3
    DOIs
    Publication statusPublished - 11 Feb 2008

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