Photocontrolled Stereoselective Cationic Polymerization

01 December 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

By virtue of noninvasive regulations by light, photocontrolled polymerizations have attracted considerable attention for the precision synthesis of macromolecules. However, a cationic polymerization with simultaneous photo-control and tacticity-regulation remains elusive and challenging to achieve. Herein, we introduce an asymmetric ion-pairing photoredox catalysis strategy, which allows for the development of a stereoselective cationic polymerization with light control for the first time. By employing a chiral ion pair photoredox catalyst (PC+/*A–) con-sisting of a photoredox active cationic part (PC+) and a sterically confined chiral anion (*A–) to deliver the stereochemical control, the stereoselective cationic polymerization of vinyl ethers with the assistance of photo control can be achieved with high isotactic selectivity (up to 91% m) at a remarkable low level of catalyst loading (50 ppm).

Keywords

cationic polymerization
photocontrolled polymerization
tacticity
ion pairing catalysis
organocatalysis

Supplementary materials

Title
Description
Actions
Title
Supporting Information
Description
Synthesis of monomer, experimental procedures, characterization data, copies of NMR spectra.
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.