a.Department of Biomedical Sciences, City University of Hong Kong, Hong Kong 999077, China
b.City University of Hong Kong, Shenzhen Research Institute, Shenzhen 518075, China
xi.yao@cityu.edu.hk
收稿:2021-04-18,
修回:2021-5-13,
录用:2021-5-15,
网络首发:2021-07-23,
纸质出版:2021-08-20
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Huang, X.; Lv, D.; Ai, L. Q.; Cheng, S. H.; Yao, X. Aggregate engineering in supramolecular polymers via extensive non-covalent networks. Chinese J. Polym. Sci. 2021, 39, 1310–1318
Xin Huang, Dong Lv, Li-Qing Ai, et al. Aggregate Engineering in Supramolecular Polymers
Huang, X.; Lv, D.; Ai, L. Q.; Cheng, S. H.; Yao, X. Aggregate engineering in supramolecular polymers via extensive non-covalent networks. Chinese J. Polym. Sci. 2021, 39, 1310–1318 DOI: 10.1007/s10118-021-2608-x.
Xin Huang, Dong Lv, Li-Qing Ai, et al. Aggregate Engineering in Supramolecular Polymers
Aggregate engineering of non-covalent networks endows supramolecular polymers with thermo-mechanical versatility
stimuli-responsive phase transitions and intrinsic damage-healing capabilities. However
most non-covalent networks are vulnerable at elevated temperatures
which suppresses the robustness of supramolecular polymers. Herein
ureidocytosine (UCy) motifs
which are capable of forming extensive non-covalent networks and thus robust molecular aggregates
via
multivalent hydrogen bonds and aromatic stackings
are proposed to enable precise programming of the thermo-mechanical versatility. Molecular simulations reveal that the enthalpic contributions from the UCy aggregates play dominant roles to compensate the entropic loss from the redistributions of polymeric spacers and stabilize the non-covalent networks over wide temperature windows. Such aggregate-level strategy offers prospects for applications which require thermo-mechanical versatility of supramolecular polymers
such as 3D printing
microfabrication and damage-healing coating.
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