4.7 Article

Radical Cations of Phenoxazine and Dihydrophenazine Photoredox Catalysts and Their Role as Deactivators in Organocatalyzed Atom Transfer Radical Polymerization

Journal

MACROMOLECULES
Volume 54, Issue 10, Pages 4726-4738

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.1c00640

Keywords

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Funding

  1. National Institute of General Medical Sciences of the National Institutes of Health [R35GM119702]
  2. Colorado State University and the Research Corporation for Science Advancement (Cottrell Scholar Award)
  3. NSF GRFP

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This study focused on synthesizing radical cations of photoredox catalysts for organocatalyzed ATRP to investigate deactivation mechanisms. The results showed that increasing radical cation concentrations improved polymerization control in O-ATRP.
Radical cations of photoredox catalysts used in organocatalyzed atom transfer radical polymerization (O-ATRP) have been synthesized and investigated to gain insight into deactivation in O-ATRP. The stability and reactivity of these compounds were studied in two solvents, N,N-dimethylacetamide and ethyl acetate, to identify possible side reactions in O-ATRP and to investigate the ability of these radical cations to deactivate alkyl radicals. A number of other factors that could influence deactivation in O-ATRP were also probed, such as ion pairing with the radical cations, radical cation oxidation potential, and halide oxidation potential. Ultimately, these studies enabled radical cations to be employed as reagents during O-ATRP to demonstrate improvements in polymerization control with increasing radical cation concentrations. In the polymerization of acrylates, this approach enabled superior molecular weight control, a decrease in polymer dispersity from 1.90 to 1.44, and an increase in initiator efficiency from 78 to 102%. This work highlights the importance of understanding the mechanism and side reactions of O-ATRP, as well as the importance of catalyst radical cations for successful O-ATRP.

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