Original polymorphism in a naphthalene bisimide π-conjugated organogelator: a complex interplay between hydrogen bonding and heterocycle π-stacking - Archive ouverte HAL
Article Dans Une Revue Journal of Materials Chemistry C Année : 2019

Original polymorphism in a naphthalene bisimide π-conjugated organogelator: a complex interplay between hydrogen bonding and heterocycle π-stacking

Laure Biniek
Lydia Karmazin
Christophe Contal
  • Fonction : Auteur
Suhrit Ghosh
  • Fonction : Auteur
Philippe Mesini
Martin Brinkmann

Résumé

This study focuses on the structure of different supramolecular assemblies formed in the gel phase and in the solid state by a naphthalene-bisimide organogelator: N,N'-di(1-(3,4,5tri(octyloxy)benzamido))eth-1yl naphthalene-1,4,5,8 tetracarboxylic acid bisimide (NDI2). This molecule is formed by a naphthalene bisimide core with symmetric dendrons composed of a flexible alkyl linker, an amide group and a trialkoxyphenyl group. The structure, especially

Domaines

Chimie Matériaux
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Dates et versions

hal-02338686 , version 1 (23-11-2020)

Identifiants

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Morgane Diebold, Elliot Christ, Laure Biniek, Lydia Karmazin, Benoît Heinrich, et al.. Original polymorphism in a naphthalene bisimide π-conjugated organogelator: a complex interplay between hydrogen bonding and heterocycle π-stacking. Journal of Materials Chemistry C, 2019, ⟨10.1039/C9TC04402G⟩. ⟨hal-02338686⟩
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