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Issue 36, 2011
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Highly enantioselective recognition of a wide range of carboxylic acids based on enantioselectively aggregation-induced emission

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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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Publication details

The article was received on 18 Jun 2011, accepted on 27 Jul 2011 and first published on 10 Aug 2011


Article type: Communication
DOI: 10.1039/C1CC13622D
Citation: 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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