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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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Published in: | Chemistry : a European journal 2019-09, Vol.25 (52), p.12098-12104 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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). |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201901422 |