Issue 36, 2011
From the journal:

Chemical Communications

Highly enantioselective recognition of a wide range of carboxylic acids based on enantioselectively aggregation-induced emission†

Dong-Mi Lia  and  Yan-Song Zheng*a  

* Corresponding authors

a Department of Chemistry, Huazhong University of Science and Technology, Wuhan 430074, P. R. China
E-mail: zyansong@hotmail.com
Fax: 0086-27-87543632
Tel: 0086-27-87543232

Abstract

A new chiral fluorescence receptor, designed to exploit aggregation-induced emission (AIE), exhibited not only an exceptionally high enantioselectivity but was also applicable to a wide range of chiral carboxylic acids. The fluorescence intensity ratio of two enantiomers ranged from 10 to 1.6 × 104 and could be used to determine the purity of the enantiomers.

Graphical abstract: Highly enantioselective recognition of a wide range of carboxylic acids based on enantioselectively aggregation-induced emission

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Article information

DOI
https://doi.org/10.1039/C1CC13622D
Article type
Communication
Submitted
18 Jun 2011
Accepted
27 Jul 2011
First published
10 Aug 2011

Chem. Commun., 2011,47, 10139-10141

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Highly enantioselective recognition of a wide range of carboxylic acids based on enantioselectively aggregation-induced emission

D. Li and Y. Zheng, Chem. Commun., 2011, 47, 10139 DOI: 10.1039/C1CC13622D

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