共价键
共聚物
材料科学
高分子化学
聚苯乙烯
马来酰亚胺
聚合物
链式转移
动态光散射
聚合
化学工程
自由基聚合
化学
纳米技术
复合材料
有机化学
纳米颗粒
工程类
作者
Kyle D. Mehringer,Brad J. Davis,Lisa K. Kemp,Guorong Ma,Samuel B. Hunt,Robson F. Storey,Xiaodan Gu,Travis L. Thornell,Dane N. Wedgeworth,Yoan C. Simon,Sarah E. Morgan
标识
DOI:10.1002/marc.202200487
摘要
Abstract Incorporating dynamic covalent bonds into block copolymers provides useful molecular level information during mechanical testing, but it is currently unknown how the incorporation of these units affects the resultant polymer morphology. High‐molecular‐weight polyisobutylene‐ b ‐polystyrene block copolymers containing an anthracene/maleimide dynamic covalent bond are synthesized through a combination of postpolymerization modification, reversible addition–fragmentation chain‐transfer polymerization, and Diels–Alder coupling. The bulk morphologies with and without dynamic covalent bond are characterized by atomic force microscopy and small‐angle X‐ray scattering, which reveal a strong dependence on annealing time and casting solvent. Morphology is largely unaffected by the inclusion of the mechanophore. The high‐molecular‐weight polymers synthesized allow interrogation of a large range of polymer domain sizes.
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