Pressure-Driven Solid-State Radical Polymerization toward Carbon Nanothread

Mechanochemical radical polymerization has unique advantages in the synthesis of polymers due to its reduced solvent consumption and adaptability of insoluble monomers. However, it suffers from the uncontrollable degradation of the formed polymers during reaction, and a new synthetic strategy with precise controllability needs to be developed. Here, by employing high static pressure up to 30 GPa, we found 1,3,5-trifluorobenzene undergoes radical polymerization by breaking the conjugated π-bonds and forms a carbon nanothread with high selectivity (Polymer-I polymorph). Based on the crystal structure at the threshold pressure and the calculated energy barriers for the bonding pathway, we concluded that the benzene rings react via a radical 1,2-addition pathway. Our work highlights that high pressure is a robust method to initiate solid-state radical polymerization, even for very stable aromatics, and offers fresh insights for the synthesis of polymeric carbon-based materials with high selectivity.

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Publication Details

Journal
Nano Letters
Published
2025-09-18
DOI
https://doi.org/10.1021/acs.nanolett.5c03977
Primary Topic
Advanced Polymer Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
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article

Pressure-Driven Solid-State Radical Polymerization toward Carbon Nanothread

Xiao Dong, Xin Yang, Haiyan Zheng, Jing Ju et al.
Nano Letters
Advanced Polymer Synthesis and Characterization
article

Pressure-Driven Solid-State Radical Polymerization toward Carbon Nanothread

Xiao Dong, Xin Yang, Haiyan Zheng, Jing Ju, Xingyu Tang, Aijiao Guan, Jun Abe, Guangwei Che, Takanori Hattori, Kuo Li, Jie Liu, Yajie Wang, Junfeng Xiang, Xiaoge Wang, Dexiang Gao, Yunfan Fei, Puyi Lang
article en

Abstract

Mechanochemical radical polymerization has unique advantages in the synthesis of polymers due to its reduced solvent consumption and adaptability of insoluble monomers. However, it suffers from the uncontrollable degradation of the formed polymers during reaction, and a new synthetic strategy with precise controllability needs to be developed. Here, by employing high static pressure up to 30 GPa, we found 1,3,5-trifluorobenzene undergoes radical polymerization by breaking the conjugated π-bonds and forms a carbon nanothread with high selectivity (Polymer-I polymorph). Based on the crystal structure at the threshold pressure and the calculated energy barriers for the bonding pathway, we concluded that the benzene rings react via a radical 1,2-addition pathway. Our work highlights that high pressure is a robust method to initiate solid-state radical polymerization, even for very stable aromatics, and offers fresh insights for the synthesis of polymeric carbon-based materials with high selectivity.

Nano LettersVol. 25(39)
Japan Atomic Energy Agency (JP), Peking University (CN), Nankai University (CN), Japan Proton Accelerator Research Complex (JP), Comprehensive Research Organization for Science and Society (JP), Center for High Pressure Science and Technology Advanced Research (CN), Institute of Applied Physics (RU), Institute of Chemistry (CN)
Openalex Percentile: Top 81%
Advanced Polymer Synthesis and Characterization
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