Abstract

While polysulfones constitute a class of well‐established, highly valuable applied materials, knowledge about polymers based on the related sulfoximine group is very limited. We have employed functionalized diaryl sulfoximines and a p‐phenylene bisborane as building blocks for unprecedented BN‐ and BO‐doped alternating inorganic–organic hybrid copolymers. While the former were accessed by a facile silicon/boron exchange protocol, the synthesis of polymers with main‐chain B–O linkages was achieved by salt elimination.

Highlights

  • While polysulfones constitute a class of well-established, highly valuable applied materials, knowledge about polymers based on the related sulfoximine group is very limited

  • Following an analogous reaction sequence, sulfoximine 2 was prepared by imida

  • Copolymers with main-chain BÀO linkages[17] were targeted. Hypothesizing that such products could be accessed by analogous Si/B exchange reactions as applied before in the synthesis of 11, organic starting materials with silylated phenolic hydroxyl groups became of interest

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Summary

Introduction

While polysulfones constitute a class of well-established, highly valuable applied materials, knowledge about polymers based on the related sulfoximine group is very limited. Bolm Institute of Organic Chemistry, RWTH Aachen University Landoltweg 1, 52074 Helten Institute of Inorganic Chemistry, RWTH Aachen University Landoltweg 1, 52074 Following an analogous reaction sequence, sulfoximine 2 was prepared by imida-

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