Issue 44, 2020

Tacticity, molecular weight, and temporal control by lanthanide triflate-catalyzed stereoselective radical polymerization of acrylamides with an organotellurium chain transfer agent

Abstract

Dual control over molecular weight and tacticity in the polymerization of N,N-dimethylacyrlamide, N,N-diethylacrylamide, N-isopropylacrylamide, and acrylamide was achieved by organotellurium-mediated radical polymerization (TERP) in the presence of Y(OTf)3 or Yb(OTf)3 as a Lewis acid catalyst. While previous dual-control reactions have been limited to the synthesis of low-molecular-weight polyacrylamides, the current conditions significantly expanded this limitation. The high compatibility of the TERP chain transfer agent and dormant species to the Lewis acid was demonstrated by nearly complete end-group fidelity. Stereoblock copolymers consisting of atactic and isotactic PDEAA blocks were also successfully synthesized. Temporal control while maintaining dual control was also achieved by using photoactivation of organotellurium species. The effect of tacticity on the polymer structure in the gas phase was estimated for the first time by ion mobility spectrometry, revealing that the collision cross section increased as the meso diad selectivity of the polyacrylamide increased.

Graphical abstract: Tacticity, molecular weight, and temporal control by lanthanide triflate-catalyzed stereoselective radical polymerization of acrylamides with an organotellurium chain transfer agent

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
19 محرم 1442
Accepted
15 ربيع الأول 1442
First published
17 ربيع الأول 1442

Polym. Chem., 2020,11, 7042-7049

Tacticity, molecular weight, and temporal control by lanthanide triflate-catalyzed stereoselective radical polymerization of acrylamides with an organotellurium chain transfer agent

Y. Imamura, T. Fujita, Y. Kobayashi and S. Yamago, Polym. Chem., 2020, 11, 7042 DOI: 10.1039/D0PY01280G

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