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Hydrodehalogenation of alkyl halides catalyzed by a trichloroniobium complex with a redox active α-diimine ligand†
Haruka Nishiyama,Hiromu Hosoya,John Arnold,Hayato Tsurugi,Kazushi Mashima
Chemical Communications Pub Date : 05/29/2019 00:00:00 , DOI:10.1039/C9CC03268A
Abstract

A high-valent d0 niobium(V) complex, (α-diimine)NbCl3 (1), bearing a dianionic redox-active α-diimine ligand served as a catalyst for a hydrodehalogenation reaction of alkyl halides in the presence of PhSiH3. During the catalytic reaction, the redox-active α-diimine ligand allowed the complex to reversibly release and accept one-electron through switching its coordination mode between a dianionic folded form and a monoanionic planar one.

Graphical abstract: Hydrodehalogenation of alkyl halides catalyzed by a trichloroniobium complex with a redox active α-diimine ligand
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