Literature DB >> 31283869

An Alkenyl Boronate as a Monomer for Radical Polymerizations: Boron as a Guide for Chain Growth and as a Replaceable Side Chain for Post-Polymerization Transformation.

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  1 in total

1.  Synthesis of 1,3-Bis-(boryl)alkanes through Boronic Ester Induced Consecutive Double 1,2-Migration.

Authors:  Cai You; Armido Studer
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-07       Impact factor: 15.336

  1 in total

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