Ionization of gold (γ-methoxy)vinyl complexes generates reactive gold vinyl carbene complexes.

ABSTRACT: Cationic gold vinyl carbene/allylic cation complexes of the form (E)-[(L)AuC(H)C(H)CAr₂]⁺ OTf^- {L = IPr, Ar = Ph [(E)-5a], L = IPr, Ar = 4-C₆H₄OMe [(E)-5b], L = P(t-Bu)₂ o-biphenyl, Ar = 4-C₆H₄OMe [(E)-5c]} were generated in solution via Lewis acid-mediated ionization of the corresponding gold (γ-methoxy)vinyl complexes (E)-(L)AuC(H)C(H)C(OMe)Ar₂ at or below -95 °C. Complexes (E)-5b and (E)-5c were fully characterized in solution employing multinuclear NMR spectroscopy, which established the predominant contribution of the aurated allylic cation resonance structure and the significant distribution of positive charge into the γ-anisyl rings. Complex (E)-5b reacted rapidly at -95 °C with neutral two-electron, hydride, and oxygen atom donors exclusively at the C1 position of the vinyl carbene moiety and with p-methoxystyrene to form the corresponding vinylcyclopropane. In the absence of nucleophile (E)-5a decomposed predominantly via intermolecular carbene dimerization whereas formation of 1-aryl-5-methoxy indene upon ionization of (Z)-(IPr)AuC(H)C(H)C(OMe)(4-C₆H₄OMe)₂ [(Z)-6b] implicated an intramolecular Friedel-Crafts or electrocyclic Nazarov pathway for the decomposition of the unobserved vinyl carbene complex (Z)-[(IPr)AuC(H)C(H)C(4-C₆H₄OMe)₂]⁺ OTf^- [(Z)-5b].

SUBMITTER: Kim N 

PROVIDER: S-EPMC6585879 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature