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Low-Temperature Curable Thermosetting Resins with Cycloaddition-Driven Cross-Linking Based on Sydnone and Silylacetylene  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Low-Temperature Curable Thermosetting Resins with Cycloaddition-Driven Cross-Linking Based on Sydnone and Silylacetylene

作者:Jiang, Fengguang[1];Yang, Yanping[1];Zhang, Yongcheng[1];Liu, Min[1];Qian, Jun[1];Zhou, Quan[1]

机构:[1]East China Univ Sci & Technol, Sch Mat Sci & Engn, Key Lab Specially Funct Polymer Mat & Related Tech, Minist Educ, Shanghai, Peoples R China

年份:2025

卷号:226

期号:21

外文期刊名:MACROMOLECULAR CHEMISTRY AND PHYSICS

收录:;EI(收录号:20253619094202);WOS:【SCI-EXPANDED(收录号:WOS:001560567800001)】;

基金:This work was supported by the National Natural Science Foundation of China (No. 52173074) and the Fundamental Research Funds for the Central Universities (No. JKD01251701).

语种:英文

外文关键词:1,3-dipolar cycloaddition reaction; low-temperature curable; silicon-alkyne hybrid resin; sydnone

摘要:Silicon-alkyne hybrid resins (PSA) possess considerable potential in aerospace and electronic applications. However, their practical use is limited by high curing temperatures (>350 degrees C) and complex cross-linking processes. To address these challenges, a click chemistry approach based on the 1,3-dipolar cycloaddition of sydnones is introduced to replace the conventional self-curing of alkynes. A monofunctional model compound is synthesized to elucidate the structural evolution during curing. A solution-based prepolymerization strategy is developed to produce B-stage prepolymers capable of efficient cross-linking upon mild thermal activation. This method significantly reduces the curing temperature, minimizes processing risks, and enables precise control over the polymer network. The final cross-linked structure forms stable pyrazole rings with carbon dioxide as the only by-product. The cured resin exhibits excellent thermal stability with a decomposition temperature (T d5) exceeding 450 degrees C, providing a promising strategy for the advancement of PSA resins.

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