Publication | Closed Access
Photo-induced fiber–vesicle morphological change in an organogel based on an azophenyl hydrazide derivative
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Citations
42
References
2011
Year
Macromolecular ChemistryEngineeringBiomimetic MaterialsOrganic ChemistryChemistrySol-gel SynthesisPolymersHydrogelsMacromolecular EngineeringPhotopolymer NetworkAzophenyl Hydrazide DerivativeHybrid MaterialsBiophysicsPhotochemistryBiopolymersAzobenzene GroupsBiophotonicsCis-bnb-t8 PhotoisomerizationMolecular EngineeringSupramolecular PhotochemistryPhotochromismSupramolecular PolymerBiomolecular EngineeringBiopolymer GelPolymer ScienceStable Organogels
A new low molecular mass organic gelator (LMOG) bearing hydrazide and azobenzene groups, namely N-(3,4,5-octanoxyphenyl)-N′-4-[(4-hydroxyphenyl)azophenyl] benzohydrazide (BNB-t8), was designed and synthesized. The organogelator has shown great ability to gel a variety of organic solvents to form stable organogels with a critical gelation concentration as low as 0.5 mg mL−1. Xerogels from chloroform exhibited entangled and dense fibrous aggregates with diameters of 50–60 nm. The organogel showed photoinduced gel-to-precipitate transition under the irradiation by 365 nm UV-light, which was attributed to trans-BNB-t8 to cis-BNB-t8 photoisomerization. The trans–cisisomerization in BNB-t8 gels further caused the morphological change from fibers to vesicles at the supramolecular level.
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