Flexible Platinum(0) Coordination to a Ditungsten Ethanediylidyne

Benjamin J. Frogley, Anthony F. Hill*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    22 Citations (Scopus)

    Abstract

    The lithiocarbyne [W(≡CLi)(CO)2(Tp*)] (Tp*=hydrotris(3,5-dimethylpyrazol-1-yl)borate) reacts with [PtCl2(L2)] (L2=1,5-cyclo-octadiene, norbornadiene) to furnish ditungsten ethanediylidyne complexes, [W2{μ-C2Pt(L2)}(CO)4(Tp*)2], wherein a trigonal platinum(0) center unsymmetrically ligates one W≡C bond in the solid state but rapidly shimmies between the two W≡C bonds in solution. The η4-dienes are displaced by monodentate CO or isocyanide ligands to provide derivatives where both W≡C bonds coordinate to a single Pt0 center, attended by significant distortion of the WCCW spine.

    Original languageEnglish
    Pages (from-to)8044-8048
    Number of pages5
    JournalAngewandte Chemie - International Edition
    Volume58
    Issue number24
    DOIs
    Publication statusPublished - 11 Jun 2019

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