Issue 10, 2021

Pairing Suzuki–Miyaura cross-coupling and catalyst transfer polymerization

Abstract

Suzuki–Miyaura catalyst transfer polymerization (SM CTP) is a versatile method to prepare conjugated polymers with control over molecular weight, sequence, and dispersity. This perspective aims to highlight some of the progress in using Suzuki–Miyaura coupling to prepare well-defined conjugated polymers via a chain-growth mechanism. We detail some of the advantages and challenges of this coupling to make aromatic polymers from monomers bearing two functional groups. The advances in arene borylation over the last twenty years are briefly highlighted, as these strategies should serve to diversify monomer scope in the future. The proposed mechanism for transmetalation in Suzuki–Miyaura polymerization is discussed, as it is different from the more typical Kumada coupling. We describe the versatility of the organoboron group used for this reaction and how it can be used tune polymerization behavior. Finally, some of the advances in catalyst design to prepare conjugated polymers using SM CTP are noted.

Graphical abstract: Pairing Suzuki–Miyaura cross-coupling and catalyst transfer polymerization

Article information

Article type
Perspective
Submitted
28 Oct 2020
Accepted
28 Dec 2020
First published
22 Jan 2021

Polym. Chem., 2021,12, 1404-1414

Author version available

Pairing Suzuki–Miyaura cross-coupling and catalyst transfer polymerization

M. V. Bautista, A. J. Varni, J. Ayuso-Carrillo, M. C. Carson and K. J. T. Noonan, Polym. Chem., 2021, 12, 1404 DOI: 10.1039/D0PY01507E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements