Carmean R Nicholas, Figg C Adrian, Scheutz Georg M, Kubo Tomohiro, Sumerlin Brent S
George and Josephine Butler Polymer Research Laboratory, Center for Macromolecular Science and Engineering, Department of Chemistry, University of Florida, Gainesville, Florida 32611, United States.
ACS Macro Lett. 2017 Feb 21;6(2):185-189. doi: 10.1021/acsmacrolett.7b00038. Epub 2017 Feb 9.
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.
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。