Issue 20, 2013

Hybrid organogels and aerogels from co-assembly of structurally different low molecular weight gelators

Abstract

The blending of perfluorinated bile ester derivatives with the gelator 2,3-didecyloxyanthracene (DDOA) yields a new class of hybrid organo- and aerogels displaying a combination of optical and mechanical properties that differ from those of pure gels. Indeed, the nanofibers constituting the hybrid organogels emit polarized blue light and display dichroic near-UV absorption via the achiral DDOA molecules, thanks to their association with a chiral bile ester. Moreover, the thermal stability and the mechanical yield stress of the mixed organogels in DMSO are enhanced for blends of DDOA with the deoxycholic gelator (DC11) having a C11 chain, as compared to the pure components' gels. When the chain length of the ester is increased to C13 (DC13) a novel compound for aerogel formation directly in scCO2 is obtained under the studied conditions. A mixture of this compound with DDOA is also able to gelate scCO2 leading to novel composite aerogel materials. As revealed by SAXS measurements, the hybrid and the pure DDOA and DC13 aerogels display cell parameters that are very similar. These SAXS experiments suggest that crystallographic conditions are very favorable for the growth of hybrid molecular arrangements in which DDOA and DC13 units could be interchanged. Specific molecular interactions between two components are not always a pre-requisite condition for the formation of a hybrid nanostructured material in which the components mutually induce properties.

Graphical abstract: Hybrid organogels and aerogels from co-assembly of structurally different low molecular weight gelators

Article information

Article type
Paper
Submitted
17 Jan 2013
Accepted
26 Mar 2013
First published
27 Mar 2013

J. Mater. Chem. C, 2013,1, 3305-3316

Hybrid organogels and aerogels from co-assembly of structurally different low molecular weight gelators

S. Banerjee, R. K. Das, P. Terech, A. de Geyer, C. Aymonier, A. Loppinet-Serani, G. Raffy, U. Maitra, A. Del Guerzo and J. Desvergne, J. Mater. Chem. C, 2013, 1, 3305 DOI: 10.1039/C3TC30104D

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