Synthesis and applications of tricarbonyliron complexes of dendralenes

Henry Toombs-Ruane, Nik Osinski, Thomas Fallon, Cindy Wills, Anthony C. Willis*, Michael N. Paddon-Row, Michael S. Sherburn

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    16 Citations (Scopus)

    Abstract

    [3]Dendralene and [4]dendralene are converted smoothly into tricarbonyliron complexes. The structures of four complexes analyzed by DFT and single-crystal X-ray analysis show that, in contrast to free hydrocarbons, complexed dendralenes prefer a roughly in-plane conformation. The complexes are stable towards Fe(CO)3 group migration up to 150 °C. The synthetic value of Fe(CO)3 complexation in the dendralene series is demonstrated through a variety of selective synthetic manipulations (Diels-Alder reaction, dipolar cycloaddition, Simmons-Smith cyclopropanation, dihydroxylation, olefin cross metathesis) that are not achievable by direct transformation of the free hydrocarbons. Application to the synthesis of a previously unreported, highly reactive linear/cross-conjugated hydrocarbon is also described. Simplicity through complexation: Tricarbonyliron complexes of dendralenes are readily prepared and stable. They allow the formation of products that cannot be accessed directly from dendralenes, including unprecedented structures (see scheme).

    Original languageEnglish
    Pages (from-to)3243-3250
    Number of pages8
    JournalChemistry - An Asian Journal
    Volume6
    Issue number12
    DOIs
    Publication statusPublished - 2 Dec 2011

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