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The Special “Morse Code” between Solvent Polarity and Morphology Flexibility in a POSS–Dendrimer Supramolecular System

An amazing phenomenon of the relative magnitude of modulus of two liquid‐crystal (LC) gels is found inverted under/above their phase transition temperature TLC‐iso, which is further proved to be caused by their diverse morphology flexibility. By testing the polarity of two LCs, gelator POSS‐G1‐Boc (...

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Bibliographic Details
Published in:Chemistry : a European journal 2019-09, Vol.25 (52), p.12098-12104
Main Authors: Shan, Tianyu, Gao, Liang, Tong, Xiaoqian, Du, Qinqing, An, Zhihang, He, Huiwen, Lin, Jiaping, Chen, Si, Wang, Xu
Format: Article
Language:English
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Summary:An amazing phenomenon of the relative magnitude of modulus of two liquid‐crystal (LC) gels is found inverted under/above their phase transition temperature TLC‐iso, which is further proved to be caused by their diverse morphology flexibility. By testing the polarity of two LCs, gelator POSS‐G1‐Boc (POSS=polyhedral oligomeric silsesquioxane) was discovered to self‐assemble into more flexible structures in a relatively low polar LC, whereas more rigid ones are formed in higher polar LC. Hence, a fitting function to connect morphology flexibility with solvent polarity was established, which can even be generalized to a number of common solvents. Experimental observations and coarse‐grained molecular dynamics simulations revealed that solvent polarity mirrors a “Morse code”, with each “code” corresponding to a specific morphology flexibility. Decoding morphology: With the help of the “Decoding software 2019”, the special “Morse code” of solvent polarity can be translated into morphology flexibility of liquid‐crystal (LC) gels (see figure).
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201901422