A Selenenium-Bridged 10-Boratriptycene Lewis Acid

Dedicated to Prof Alain Krief for his 80^th birthday.

Abstract

A non-planar triarylborane and a new member of the boratriptycene family bearing a selenium atom in bridgehead position of triptycene scaffold was generated and isolated as a boron-‘ate’ complex paired with a weakly coordinating anion. With similar electronegativity while possessing longer atom radius with respect to sulfur, the introduction a selenium atom, in the form of a selenenium moiety, at the bridgehead of a triptycene scaffold allows a very precise modification of the pyramidalization of the boron atom environment. Experimental and computational evaluation of the Lewis acidity of this new boratriptycene derivative gave qualitative information on how a modification of the pyramidalization of the boron environment affects alone Lewis acidity parameters of such pyramidal triarylborane.

Key words

Lewis acids - main-group chemistry - organoboron compounds - triptycene - acidity scale

Publication History

Received: 21 March 2022

Accepted after revision: 02 May 2022

Accepted Manuscript online:
02 May 2022

Article published online:
09 June 2022

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