Issue 12, 2017

Synthesis and self-assembly of unconventional C3-symmetrical trisubstituted triphenylenes

Abstract

Triphenylene-based self-assembly modules, bearing three amide groups at the 1-, 5-, and 9-positions, were designed and synthesized. Supramolecular gels could be constructed by combining hydrogen bonding, π–π stacking and van der Waals interactions. In addition, the assembly exhibited liquid crystalline mesophases by tuning of the length of the alkyl chains. This work provides an essential representative of functional assembly based on C3-symmetric triphenylenes.

Graphical abstract: Synthesis and self-assembly of unconventional C3-symmetrical trisubstituted triphenylenes

Supplementary files

Article information

Article type
Research Article
Submitted
08 8月 2017
Accepted
14 9月 2017
First published
19 9月 2017

Mater. Chem. Front., 2017,1, 2599-2605

Synthesis and self-assembly of unconventional C3-symmetrical trisubstituted triphenylenes

Y. Li, Y. Wang, X. Ren and L. Chen, Mater. Chem. Front., 2017, 1, 2599 DOI: 10.1039/C7QM00361G

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