Issue 73, 2017

Fluorescent chirality recognition by simple boronate ensembles with aggregation-induced emission capability

Abstract

Chiral ensembles were spontaneously formed in solution through boronate esterification of structurally defined di(boronic acid)-appended tetraphenylethylene (DB-TPE) and commercially available L- or D-tartaric acid, showing enantioselective aggregation behavior for chiral diamines as well as cinchona alkaloids enabling the fluorescent recognition of their chirality.

Graphical abstract: Fluorescent chirality recognition by simple boronate ensembles with aggregation-induced emission capability

Supplementary files

Article information

Article type
Communication
Submitted
25 jul. 2017
Accepted
22 ago. 2017
First published
22 ago. 2017

Chem. Commun., 2017,53, 10144-10147

Fluorescent chirality recognition by simple boronate ensembles with aggregation-induced emission capability

M. Kawai, A. Hoshi, R. Nishiyabu and Y. Kubo, Chem. Commun., 2017, 53, 10144 DOI: 10.1039/C7CC05784A

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