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Supramolecular Assembly of pH-Sensitive Triphenylene Derived ?-Gelators and Their Application as Molecular Template for the Preparation of Silica Nanotubes.


ABSTRACT: The gelation properties and mode of self-assembly of six asymmetrical hexaether triphenylene derivatives mono-functionalized with carboxylic and primary amine groups were investigated. The presence of a carboxylic and amine group attached to the triphenylene core generated stable, thermo- and pH-sensitive supramolecular ?-organogels with a reversible response to both stimuli. In order to understand the gelation process, we studied the effect of the spacer length and found a different gelation scope for the acid and basic derivatives that accounts for a different supramolecular self-assembly. The presence of the basic group on the amino derivatives was used to guide and catalyze the templated in situ sol-gel polymerization of TEOS and allowed us, under controlled hydrolytic conditions, to prepare an entangled fibrillar network of silica nanotubes.

SUBMITTER: Munoz Resta I 

PROVIDER: S-EPMC6318639 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature

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Supramolecular Assembly of pH-Sensitive Triphenylene Derived π-Gelators and Their Application as Molecular Template for the Preparation of Silica Nanotubes.

Muñoz Resta Ignacio I   Manzano Verónica E VE   Cecchi Florencia F   Spagnuolo Carla C CC   Cukiernik Fabio D FD   Di Chenna Pablo H PH  

Gels (Basel, Switzerland) 20160201 1


The gelation properties and mode of self-assembly of six asymmetrical hexaether triphenylene derivatives mono-functionalized with carboxylic and primary amine groups were investigated. The presence of a carboxylic and amine group attached to the triphenylene core generated stable, thermo- and pH-sensitive supramolecular π-organogels with a reversible response to both stimuli. In order to understand the gelation process, we studied the effect of the spacer length and found a different gelation sc  ...[more]

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