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A Dicationic Bismuth(III) Lewis Acid: Catalytic Hydrosilylation of Olefins

Balasubramaniam, S and Kumar, S and Andrews, AP and Varghese, B and Jemmis, ED and Venugopal, A (2019) A Dicationic Bismuth(III) Lewis Acid: Catalytic Hydrosilylation of Olefins. In: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY (28).

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Official URL: https://dx.doi.org/ 10.1002/ejic.201900459

Abstract

Lewis acid promoted activation of inert chemical bonds is central to catalysis. The presence of a highly electrophilic central atom having minimum interactions with anions and solvent molecules is a requisite for a reactive Lewis acid. This requirement for a strong Lewis acid is met with by designing a reactive cation of a heavy element, bismuth, bearing the tridentate trispyrazolylborate ligand. The coordination sphere of the electrophilic bismuth dication is stabilized by very weak interactions with the halogen atoms of the weakly nucleophilic tetrakis(pentafluorophenyl)borate anion, chlorobenzene, and ortho-dichlorobenzene in the solid state. The high electrophilicity at bismuth is demonstrated by the ability of the dication to efficiently catalyze the addition of Si–H to olefins.

Item Type: Journal Article
Publication: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Publisher: Wiley-VCH Verlag
Additional Information: The copyright for this article belongs to the Author(s).
Keywords: Bismuth; Lewis acids; Reactive cations; Weakly coordinating anions; Bond activation; Hydrosilylation
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 04 Sep 2019 10:45
Last Modified: 21 Oct 2022 11:52
URI: https://eprints.iisc.ac.in/id/eprint/63457

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