共价键
材料科学
格子(音乐)
结晶学
控制重构
化学物理
纳米技术
融合
晶体结构
衍射
稳健性(进化)
转化(遗传学)
X射线晶体学
聚合物
化学键
化学
机械化学
晶体工程
晶格常数
金属有机骨架
作者
Lan Xia,Hongfei Ma,Zhilv Wang,Y Li,Zeyue Zhang,J W Li,Zhipeng Zhou,Yi Yang,Z D Zhang,Yuexian Hong,Rui‐Biao Lin,Jingyun Fang,Jie‐Peng Zhang,Liu W,Junliang Sun,Zhikun Zheng
摘要
ABSTRACT Covalent organic frameworks (COFs) typically rely on reversible covalent chemistry to achieve crystallinity, whereas irreversible and rigid linkages are generally required to achieve enhanced robustness and extended π‐conjugation. Single‐crystal‐to‐single‐crystal (SCSC) transformation offers a promising route to access such frameworks; however, irreversible bond reconfiguration imposes permanent mechanical strain that often disrupts lattice order. Here, we demonstrate sulfur‐assisted SCSC transformation of imine‐linked COFs into rigid benzothiazole‐linked frameworks with experimentally resolved atomic structures. Time‐resolved structural analyses uncover two distinct stress‐accommodation pathways‐cooperative lattice adaptation and stress‐driven transient domain reconstruction that enable irreversible bond fusion while preserving long‐range crystallographic order. The resulting single‐crystalline thiazole‐linked COFs exhibit enhanced chemical stability, rigidified pore architectures, and improved optoelectronic performance. This study establishes a mechanistic framework for managing lattice strain during irreversible covalent transformation and provides a general design principle for constructing structurally robust crystalline polymers.
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