| Literature DB >> 31283869 |
Tsuyoshi Nishikawa1, Makoto Ouchi1.
Abstract
The ability of isopropenyl boronate pinacol ester to serve as a monomer in radical polymerizations was established and exploited for the synthesis of polymers that are difficult to access using other polymerization techniques. Although the monomer exhibits an α-methyl-substituted unconjugated structure, which is usually unfavorable for radical propagation, both free and controlled radical polymerizations smoothly afford the corresponding polymers. A density-functional-theory-based investigation revealed that the boron atom moderately stabilizes the radical species, which leads to the suppression of the degradative chain transfer to the α-methyl groups, and thus guides the reaction towards the radical polymerization. The boronyl pendants, which are directly attached to the polymer backbone, can be replaced with -OH or -NH2 to yield poly(α-methyl vinyl amine) or poly(α-methyl vinyl alcohol), which has been inaccessible by conventional synthetic methods.Entities:
Keywords: block copolymers; boron; polymerization; radical reactions; self-assembly
Year: 2019 PMID: 31283869 DOI: 10.1002/anie.201905135
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336