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Published on: March 24, 2018
A zwitterionic hydrocarbon-soluble borenium ion based on a β-diketiminate backbone
Joseph A B Abdalla1, Rémi C Tirfoin, Haoyu Niu
1Inorganic Chemistry Laboratory, Department of Chemistry, University of Oxford, South Parks Road, Oxford, OX1 3QR, UK. simon.aldridge@chem.ox.ac.uk.
Abstract:
A versatile synthetic route has been developed to access strongly Lewis acidic borenium cations (and heavier group 13 analogues) featuring a pendant weakly-coordinating borate function. The hydrocarbon-soluble borenium/borate zwitterion is more strongly Lewis acidic than B(C6F5)3, despite featuring a pendant (non-fluorinated) aryl group and two flanking N-donors.
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