期刊
RSC ADVANCES
卷 10, 期 12, 页码 6794-6800出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ra09919k
关键词
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资金
- National Science Foundation of China [21622406, 21871273]
- National Key Research and Development Program of China [2019YFA0210400]
An efficient polymer dimerization method is developed on a self-accelerating double strain-promoted azide-alkyne cycloaddition (DSPAAC) click reaction. In this approach, varied polymer dimers can be efficiently prepared by coupling azide terminated polymer building blocks by sym-dibenzo-1,5-cyclooctadiene-3,7-diyne (DIBOD) small linkers. The distinct advantages of this method can be summarized as follows. First, the azide terminated polymer building blocks can be easily prepared with varied molecular topologies such as linear, star, and dendritic shapes. Second, the self-accelerating property of DSPAAC coupling reaction allows the method to efficiently prepare pure polymer dimers in the presence of excess molar amounts of DIBOD small linkers to azide-terminated polymer building blocks. Third, the click property of DSPAAC coupling reaction facilitates the dimerization reaction with a very mild ambient reaction condition. As a result, this method provides a powerful tool to fabricate topological polymers with a symmetrical molecular structure such as block, star, and dendritic polymers.
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