Enabling Racemization of Axially Chiral Subphthalocyanine‐Tetracyanobutadiene‐Aniline Enantiomers by Triplet State Photogeneration
Volume: 59, Issue: 47, Pages: 21224 - 21229
Published: Sep 11, 2020
Abstract
In recent years, several tetracyanobuta‐1,3‐diene (TCBD) conjugates have been prepared by linking the tetracyano unit to various electroactive moieties. These push–pull conjugates, besides showing interesting physicochemical properties, are axially chiral, a feature arising from the restricted rotation around the central bond of the butadiene. Yet, only in a few cases, separation and isolation of the enantiomers have been successfully achieved,...
Paper Details
Title
Enabling Racemization of Axially Chiral Subphthalocyanine‐Tetracyanobutadiene‐Aniline Enantiomers by Triplet State Photogeneration
Published Date
Sep 11, 2020
Volume
59
Issue
47
Pages
21224 - 21229
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