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Synthesis and properties of novel organogelators functionalized with 5-iodo-1,2,3-triazole and azobenzene groups
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Two series of 5-iodo-1,2,3-triazole derivatives containing azobenzene group(s) were synthesized and their gelling properties were tested. Those containing two azobenzene groups (B series) have better gelation performance than those containing one azobenzene group (A series). The microstructure of organogels and the driving force of gelation were investigated by scanning electron microscopy and 1H NMR, respectively. It was found that π-π stacking, van der Waals interaction, and dipole-dipole interaction were the main forces of gelation. All the tested organogels are photoresponsive and those from B series are smarter than that from A series. Henry δph diagrams of compounds A1, A2, and B2 were constructed on the basis of their gelation performance and the Hansen solubility parameters of related solvents. 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Chemistry of Materials, 2012, 24(19): 3751–3757CrossRefGoogle ScholarCopyright information© Higher Education Press and Springer-Verlag Berlin Heidelberg 2016Authors and AffiliationsZiyan Li1Yaodong Huang1Email authorDongli Fan1Huimin Li1Shuxue Liu1Luyuan Wang11.Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and TechnologyTianjin UniversityTianjinChina About this article CrossMark Publisher Name Higher Education Press Print ISSN 2095-0179 Online ISSN 2095-0187 About this journal Reprints and Permissions Article actions Export citation .RIS Papers Reference Manager RefWorks Zotero .ENW EndNote .BIB BibTeX JabRef Mendeley Share article Email Facebook Twitter LinkedIn Cookies We use cookies to improve your experience with our site. More information Accept Over 10 million scientific documents at your fingertips

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