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The 9-Borataphenanthrene Anion
Authors:Tyler A Bartholome  Aishvaryadeep Kaur  Prof Dr David J D Wilson  Prof Dr Jason L Dutton  Prof Dr Caleb D Martin
Institution:1. Department of Chemistry and Biochemistry, Baylor University, One Bear Place #97348, Waco, TX, 76798-7343 USA;2. Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria, 3086 Australia
Abstract:The 9-borataphenanthrene anion is easily accessed by deprotonation of a 9,10-dihydro-9-boraphenanthrene and its diverse reactivity is investigated. Alkylation occurs at the carbon atom adjacent to boron, and room temperature hydroboration occurs across the B=C bond. The π-manifold of the central BC5 ring coordinates to chromium in an η6 fashion while only the B=C unit binds η2 to gold, indicating versatility of the 9-borataphenanthrene anion as a ligand. Supporting calculations rationalize the reactivity and aromaticity is corroborated by nucleus-independent chemical shift (NICS) indices.
Keywords:borataalkene  boratabenzene  boron  heterocycles  hydroboration
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