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Reduction and Rearrangement of a Boron(I) Carbonyl Complex.


ABSTRACT: The one-electron reduction of a cyclic (alkyl)(amino)carbene (CAAC)-stabilized arylborylene carbonyl complex yields a dimeric borylketyl radical anion, resulting from an intramolecular aryl migration to the CO carbon atom. Computational analyses support the existence of a [(CAAC)B(CO)Ar].- radical anion intermediate. Further reduction leads to a highly nucleophilic dianionic (boraneylidene)methanolate.

SUBMITTER: Rang M 

PROVIDER: S-EPMC7898892 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

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The one-electron reduction of a cyclic (alkyl)(amino)carbene (CAAC)-stabilized arylborylene carbonyl complex yields a dimeric borylketyl radical anion, resulting from an intramolecular aryl migration to the CO carbon atom. Computational analyses support the existence of a [(CAAC)B(CO)Ar]<sup>.-</sup> radical anion intermediate. Further reduction leads to a highly nucleophilic dianionic (boraneylidene)methanolate. ...[more]

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