Synthesis of optically clear molecular organogels using phenol and a sulfosuccinic surfactant in various solvents with cyclic geometries
Synthesis of optically clear molecular organogels using phenol and a sulfosuccinic surfactant in various solvents with cyclic geometries
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DOI:
10.1016/j.molliq.2018.07.091
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发表时间:
2018-10
影响因子:
6
通讯作者:
K. Nishiyama;Masaru Kinoshita;Takashi Harada;Yukiteru Katsumoto
中科院分区:
文献类型:
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作者:
K. Nishiyama;Masaru Kinoshita;Takashi Harada;Yukiteru Katsumoto
Equal concentration mixtures ofp-chlorophenol and a sulfosuccinic surfactant bis(2-ethylhexyl)sulfosuccinate (AOT) are known to form optically clear gels in cyclic organic solvents like cyclohexane, whereas turbid gels are obtained in acyclic alkanes and aromatic solvents with the same gelators. Clear organogels are necessary when emitting devices are dispersed inside the gel. As such, in this study, we employed 16 cyclic solvents including cyclic alkanes, cyclic alkenes, cycloalkanones, and chlorocyclohexane. Eventually we were to obtain clear gels in 12 cyclic alkane and cyclic alkene solvents at immediately after the gelation, while 2 of those gels turned out to be turbid in a few days. A cyclic solvent geometry was shown to be unnecessary to obtain clear gels. Transmittance spectra, drop-point temperature, and nuclear magnetic resonance were employed to characterize the organogels. The rigid structure in the π-stack caused byp-chlorophenol self-assembly brought about a higher drop point.