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The Synthesis Properties and Reactivity of Lewis Acidic Aminoboranes

preprint
submitted on 15.03.2021, 16:45 and posted on 16.03.2021, 12:50 by Jordan N. Bentley, Selvyn A. Simoes, Ekadashi Pradhan, Tao Zeng, Chris Caputo

The evolution of frustrated Lewis pair chemistry has led to significant research into the development of new Lewis acidic boranes. Much of this has focused on modifying aryl substituents rather than introducing heteroatoms bound to boron. We recently reported unique Lewis acidic behaviour from bis(pentafluorophenyl)phenothiazylborane (1) for the heterolytic dehydrocoupling of stannanes. In this work, we synthesize and characterize a family of Lewis acidic aminoboranes and explored their reactivity with various Lewis bases as well as their efficacy as catalysts for stannane dehydrocoupling and hydrosilylation. Quantum chemical caluclations were undertaken to understand the origins of the Lewis acidity and the most Lewis acidic aminoborane (5) was found to be an effective catalyst even in coordinating solvents such as water or acetonitrile, suggesting the amino substituent provides a level of protection against competing donors.


History

Email Address of Submitting Author

caputo@yorku.ca

Institution

York University

Country

Canada

ORCID For Submitting Author

0000-0002-7523-0324

Declaration of Conflict of Interest

No Conflict of Interest

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