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Ligation of Boratabenzene and 9-Borataphenanthrene to Coinage Metals.

作者信息

Wisofsky Greta K, Rojales Katherine, Su Xiaojun, Bartholome Tyler A, Molino Andrew, Kaur Aishvaryadeep, Wilson David J D, Dutton Jason L, Martin Caleb D

机构信息

Department of Chemistry and Biochemistry, Baylor University, One Bear Place #97348, Waco, Texas 76798, United States.

Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria, Australia 3086.

出版信息

Inorg Chem. 2021 Dec 20;60(24):18981-18989. doi: 10.1021/acs.inorgchem.1c02800. Epub 2021 Dec 8.

Abstract

The reactions of boratabenzene and borataphenanthrene anions with group 11 PhPMCl reagents furnished η coordination complexes, with the exception of the copper boratabenzene species that adopted an η mode. The binding of arene ligands to copper in an η manner is rare, and altering the ancillary ligand on copper to an N-heterocyclic carbene switched the binding of the boratabenzene to η, indicating that such ligands are capable of vacating coordination sites. The η coordination complexes bind side-on, akin to olefins, via a borataalkene unit, although with the carbon atom much more proximal to the metal center than boron.

摘要

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