Thickness Transition of a Rigid Supramolecular Polymer
Author(s) -
Laurent Bouteiller,
Olivier Colombani,
Frédéric Lortie,
Pierre Térech
Publication year - 2005
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja0511016
Subject(s) - chemistry , cooperativity , supramolecular chemistry , viscosity , polymer , glass transition , solvent , hydrogen bond , supramolecular polymers , chemical physics , intrinsic viscosity , polymer chemistry , transition temperature , molecule , chemical engineering , crystallography , thermodynamics , organic chemistry , condensed matter physics , biochemistry , physics , superconductivity , engineering
A low molecular weight bisurea in nonpolar solvents is shown to self-assemble by hydrogen bonding into two distinct high molecular weight structures. At low temperature and high concentration, the most stable structure is a thick cylindrical assembly, responsible for the very high viscosity of the solution. At higher temperature or lower concentration, the thick filaments disappear in favor of thinner filaments, leading to a lower viscosity. The reversible transition occurs over a temperature range of 5 degrees C only, showing that it is highly cooperative. The structural switch can also be triggered by changing the nature of the solvent or the composition in the case of a mixture of two bisureas. The high cooperativity and the tunability of this transition are useful for the design of responsive materials.
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