聚合
材料科学
化学工程
结晶学
聚合物
化学
复合材料
工程类
作者
Chongqing Yang,Jianfang Liu,Rebecca Shu Hui Khoo,Maged Abdelsamie,Miao Qi,He Li,Haiyan Mao,Sydney Hemenway,Qiang Xu,Yunfei Wang,Beihang Yu,Qingsong Zhang,Xinxin Liu,Liana M. Klivansky,Xiaodan Gu,Chenhui Zhu,Jeffrey A. Reimer,Ganglong Cui,Carolin M. Sutter‐Fella,Jian Zhang
标识
DOI:10.1038/s41467-025-58822-2
摘要
Topochemical polymerization (TCP) emerges as a leading approach for synthesizing single crystalline polymers, but is traditionally restricted to transformations in solid-medium. The complexity in achieving single-crystal-to-single-crystal (SCSC) transformations due to lattice disparities and the untapped potential of performing TCP in a liquid medium with solid-state structural fidelity present unsolved challenges. Herein, by using X-rays as the primary means to overcome crystal disintegration, we reveal the details of SCSC transformation during the TCP of chiral azaquinodimethane (AQM) monomers through in situ crystallographic analysis while spotlighting a rare metastable crystalline phase. Complementary in situ investigations of powders and thin films provide critical insights into the side-chain dependent polymerization kinetics of solid-state reactions. Furthermore, we enable TCP of AQM monomers in a liquid medium via an antisolvent-reinforced aggregated state, yielding polymer nanofibers with high crystallinity akin to that of solid-state. This study testifies high structural precision of TCP performed in different states and media, offering critical insights into the synthesis of processable nanostructured polymers with desired structural integrity.
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