Synthesis, Characterization, and Functionalization of 1-Boraphenalenes

Rachel J. Kahan, Daniel L. Crossley, Jessica Cid, James E. Radcliffe, Michael J. Ingleson

    Research output: Contribution to journalArticlepeer-review

    Abstract

    1‐Boraphenalenes have been synthesized by reaction of BBr3 with 1‐(aryl‐ethynyl)naphthalenes, 1‐ethynylnaphthalene, and 1‐(pent‐1‐yn‐1‐yl)naphthalene and they can be selectively functionalized at boron or carbon to form bench‐stable products. All of these 1‐boraphenalenes have LUMOs localized on the planar C12B core that are closely comparable in character to isoelectronic phenalenyl cations. In contrast to the comparable LUMOs, the aromatic stabilization of the C5B ring in 1‐boraphenalenes is dramatically lower than the C6 rings in phenalenyl cations. This is due to the occupied orbitals of π symmetry being less delocalised in the 1‐boraphenalenes.
    Original languageEnglish
    Pages (from-to)8084-8088
    JournalAngewandte Chemie - International Edition
    Volume57
    Issue number27
    Early online date11 May 2018
    DOIs
    Publication statusPublished - 26 Jun 2018

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