Crystallization-driven self-assembly of semicrystalline block copolymers and end-functionalized polymers: A minireview

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Abstract

Self-assembly has been a powerful method to fabricate the polymer materials with well-defined structures and morphologies. Such assembled materials have shown wide potential applications in many fields such as nanomaterial, nanomedicine, lithography, and microelectronic. Crystallization has been a general behavior of stereoregular polymers. Besides the various noncovalent interactions, crystallization of polymer blocks or end groups can be an efficient way to manipulate the self-assembly pathway and assembled structures of polymers in both solid and solution. Crystallization-driven self-assembly has been widely implemented for the semicrystalline block copolymers (BCPs) and end-functionalized polymers. This minireview briefly presents the recent progresses in the crystallization-driven self-assembly of BCPs and end-functionalized polymers in both solid and solution states. Formation process, mechanism, and hierarchical structure of the crystallization-induced assemblies for BCPs and end-functionalized polymers are highlighted.

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Xu, W., Zheng, Y., & Pan, P. (2022, August 1). Crystallization-driven self-assembly of semicrystalline block copolymers and end-functionalized polymers: A minireview. Journal of Polymer Science. John Wiley and Sons Inc. https://doi.org/10.1002/pol.20210789

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