Small molecule activation by frustrated Lewis pairs
Alastair L. Travis, Samantha C. Binding, Hasna Zaher, Thomas Arnold, Jean‐Charles Buffet, Dermot O’Hare
Abstract
Alastair L. Travis, Samantha C. Binding, Hasna Zaher, Thomas Arnold, Jean‐Charles Buffet, Dermot O’Hare
Abstract
A series of frustrated Lewis pairs (FLPs) based on the Lewis acids tris(perchloroaryl)borane (BAr(Cl)), and tris(2,2',2''-perfluorobiphenyl)borane (PBB) and trialkylphosphines were prepared; their ability to effect the heterolytic cleavage of dihydrogen, insert carbon dioxide into the borohydride, and reduce the resulting formatoborate to methanol were studied. Additionally, the insertion of CO(2) into a B-OH bond is explored with the ultimate aim of developing a homogeneous, catalytic preparation of carbonates. The compound [PBB-OH][H-P((t)Bu)(3)] was characterised by single crystal X-ray crystallography.
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A series of frustrated Lewis pairs (FLPs) based on the Lewis acids tris(perchloroaryl)borane (BAr(Cl)), and tris(2,2',2''-perfluorobiphenyl)borane (PBB) and trialkylphosphines were prepared; their ability to effect the heterolytic cleavage of dihydrogen, insert carbon dioxide into the borohydride, and reduce the resulting formatoborate to methanol were studied. Additionally, the insertion of CO(2) into a B-OH bond is explored with the ultimate aim of developing a homogeneous, catalytic preparation of carbonates. The compound [PBB-OH][H-P((t)Bu)(3)] was characterised by single crystal X-ray crystallography.
Key concepts: Heterolysis, Frustrated Lewis pair, Borane, Chemistry, Borohydride, Lewis acids and bases, Crystallography, Tris