A new triphenylamine-based acylhydrazone derivative (TPAH-B8) was synthesized. TPAH-B8 could form organogels in cyclohexane through ultrasonic treatment. A typical gelation-induced fluorescence enhancement property was observed, which was attributed to the formation of J-aggregate in the gel state. More interestingly, TPAH-B8 exhibited multistimuli responsive behaviors. First, TPAH-B8 showed a solvatochromic effect, with the emission color changing from blue to cyan with the change in solvent from nonpolar cyclohexane to polar dimethyl sulfoxide (DMSO). Second, TPAH-B8 showed a reversible mechanofluorochromism. The xerogel of TPAH-B8 emitted a blue fluorescence, while the fluorescence color changed to cyan after grinding. The cyan and blue colors could be repeated with the treatment of grinding and annealing, which was explored and ascribed to the transformation between crystalline and amorphous states. Third, TPAH-B8 revealed acidochromic property. The fluorescence color of TPAH-B8 in organogel and solid states could be switched by trifluoroacetic acid (TFA)/triethylamine (TEA). This work not only demonstrated the multistimuli-responsive fluorescent properties of TPAH-B8 but also offered an easy way to develop new kinds of multistimuli-responsive fluorescent materials.
Switchable reversible addition-fragmentation chain-transfer (RAFT) agents, so-called because they can be reversibly switched by the acid/ base stimulus to offer very good control over polymerization of both “more-activated” monomers (MAMs)...
Herein, we report the gelation behaviour and gel properties of two-component organogels consisting of 1,4-bis[(3,4-bisoctyloxyphenyl) hydrozide] phenylene (BPH-8) and a photoresponsive gelator 4-[3,5-(bisoctyloxyphenyl)]-9-anthracene formyl hydrazine (MB8).
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