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Issue 34, 2015
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Revisiting the assembly of amino ester-based benzene-1,3,5-tricarboxamides: chiral rods in solution

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Abstract

Some benzene-1,3,5-tricarboxamide (BTA) monomers derived from (L) α-amino esters self-assemble into long rods at millimolar concentrations, and display a strong chiral amplification effect. These rods are in competition with dimeric species.

Graphical abstract: Revisiting the assembly of amino ester-based benzene-1,3,5-tricarboxamides: chiral rods in solution

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Publication details

The article was received on 18 Feb 2015, accepted on 24 Mar 2015 and first published on 25 Mar 2015


Article type: Communication
DOI: 10.1039/C5CC01513H
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Citation: Chem. Commun., 2015,51, 7397-7400
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    Revisiting the assembly of amino ester-based benzene-1,3,5-tricarboxamides: chiral rods in solution

    A. Desmarchelier, M. Raynal, P. Brocorens, N. Vanthuyne and L. Bouteiller, Chem. Commun., 2015, 51, 7397
    DOI: 10.1039/C5CC01513H

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