Hong Seung-Mo, Kim Oh Young, Hwang Seok-Ho
Department of Polymer Science & Engineering, Dankook University, Yongin 16890, Republic of Korea.
Advanced Materials Division, Shin-A T&C Co., Ltd., Seoul 08501, Republic of Korea.
Materials (Basel). 2024 Mar 14;17(6):1343. doi: 10.3390/ma17061343.
Thiols can react with readily available organic substrates under benign conditions, making them suitable for use in chemical, biological, physical, and materials and engineering research areas. In particular, the highly efficient thiol-based click reaction includes the reaction of radicals with electron-rich enes, Michael addition with electron-poor enes, carbonyl addition with isocyanate S2 ring opening with epoxies, and S2 nucleophilic substitution with halogens. This mini review provides insights into emerging venues for their industrial applications, especially for the applications of thiol-ene, thiol-isocyanate, and thiol-epoxy reactions, highlighting a brief chemistry of thiols as well as various approaches to polythiol synthesis.
硫醇可以在温和条件下与易得的有机底物发生反应,这使得它们适用于化学、生物、物理、材料和工程研究领域。特别地,高效的基于硫醇的点击反应包括自由基与富电子烯的反应、与缺电子烯的迈克尔加成、与异氰酸酯的羰基加成、与环氧化合物的S2开环反应以及与卤素的S2亲核取代反应。本综述对其工业应用的新兴领域进行了深入探讨,尤其是硫醇-烯、硫醇-异氰酸酯和硫醇-环氧化合物反应的应用,同时简要介绍了硫醇的化学性质以及多硫醇合成的各种方法。