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无催化剂光诱导硫代羰基硫官能团端基去除

Catalyst-Free Photoinduced End-Group Removal of Thiocarbonylthio Functionality.

作者信息

Carmean R Nicholas, Figg C Adrian, Scheutz Georg M, Kubo Tomohiro, Sumerlin Brent S

机构信息

George and Josephine Butler Polymer Research Laboratory, Center for Macromolecular Science and Engineering, Department of Chemistry, University of Florida, Gainesville, Florida 32611, United States.

出版信息

ACS Macro Lett. 2017 Feb 21;6(2):185-189. doi: 10.1021/acsmacrolett.7b00038. Epub 2017 Feb 9.

Abstract

An initiator- and catalyst-free method for polymer end-group modification has been designed. Under long-wave ultraviolet irradiation, polymers with thiocarbonylthio end groups undergo photolytic cleavage to reveal an active macroradical capable of irreversible termination with a suitable hydrogen source. This straightforward method was successfully demonstrated by the removal of a range of end groups that commonly result from reversible addition-fragmentation chain transfer or photoiniferter polymerizations, including trithiocarbonate, dithiobenzoate, xanthate, and dithiocarbamate mediating agents. This strategy proved efficient for polymers derived from acrylamido, acrylic, methacrylic, styrenic, and vinylpyrrolidone monomers.

摘要

设计了一种无引发剂和催化剂的聚合物端基改性方法。在长波紫外线照射下,具有硫代羰基硫端基的聚合物发生光解裂解,产生一个活性大分子自由基,该自由基能够与合适的氢源发生不可逆终止反应。通过去除一系列通常由可逆加成-断裂链转移或光引发转移终止剂聚合产生的端基,成功证明了这种直接的方法,这些端基包括三硫代碳酸酯、二硫代苯甲酸酯、黄原酸酯和二硫代氨基甲酸盐介导剂。该策略对由丙烯酰胺、丙烯酸、甲基丙烯酸、苯乙烯和乙烯基吡咯烷酮单体衍生的聚合物有效。

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