活化/失活过程对表面引发的原子转移自由基聚合的影响:一项硅学研究

IF 5.4 1区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY GIANT Pub Date : 2024-11-06 DOI:10.1016/j.giant.2024.100345
Zhongyan Zhang , Hui Li , Yuqi Guo , Yao-Hong Xue , Hong Liu
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引用次数: 0

摘要

我们提出了一种探索表面引发原子转移自由基聚合(SI-ATPR)的模拟方法,其中可以明确考虑激活/失活过程对聚合物链增长的影响。我们的研究结果表明,这些激活和失活机制为所有聚合物链提供了平等的生长机会。这一过程显著增加了接枝密度,同时降低了接枝链的分散性。理论证明,活化链和休眠链的比例最终会在活化/失活过程中达到平衡。较短的激活/失活周期会使所有链的生长机会均等,并加快 "停止-继续 "的速度。我们的研究有助于从微观角度更好地理解活化/去活化过程在 SI-ATRP 中的作用。
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Influence of activation/deactivation process on surface-initiated atom transfer radical polymerization: An in silico investigation
We propose a simulation approach to explore surface-initiated atom transfer radical polymerization (SI-ATRP), in which how the chain growth is affected by activation/deactivation process could be considered explicitly. Our findings indicate that these activation and deactivation mechanisms provide all polymer chains with equal growth opportunities. This process leads to a significant increase of grafting density while concurrently reducing the dispersity of the grafted chains. The ratio of activated and dormant chains is theoretically proved to eventually reach equilibrated within the activation/deactivation process. The shorter lifetime of activation/deactivation cycle leads to an even equal opportunity and a faster “stop-continue” pace for the growth of all chains. Our study is helpful for better understanding the role of activation/deactivation process in SI-ATRP from a microscopic perspective.
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来源期刊
GIANT
GIANT Multiple-
CiteScore
8.50
自引率
8.60%
发文量
46
审稿时长
42 days
期刊介绍: Giant is an interdisciplinary title focusing on fundamental and applied macromolecular science spanning all chemistry, physics, biology, and materials aspects of the field in the broadest sense. Key areas covered include macromolecular chemistry, supramolecular assembly, multiscale and multifunctional materials, organic-inorganic hybrid materials, biophysics, biomimetics and surface science. Core topics range from developments in synthesis, characterisation and assembly towards creating uniformly sized precision macromolecules with tailored properties, to the design and assembly of nanostructured materials in multiple dimensions, and further to the study of smart or living designer materials with tuneable multiscale properties.
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