Reversible Intramolecular Coupling of the Terminal Borylene and a Carbonyl Ligand of [Cp(CO)2Mn[DOUBLE BOND]B[BOND]tBu]

Authors


  • We are grateful to the European Research Council (Advanced Investigator Grant to H.B.) for financial support.

Abstract

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Cyclic complex 2 with bridging carbonyl ligands was synthesized from a facile and reversible intermolecular carbonyl–borylene ligand coupling reaction at room temperature. Complex 2 exhibits an unprecedented coordination mode for boron–metal complexes, which is also reflected in its remarkable 11B NMR chemical shift of −57.2 ppm. Findings from spectroscopic, X-ray, and computational studies are presented, along with a proposed mechanism.

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