scispace - formally typeset
Search or ask a question
Author

Joseph Bunnett

Bio: Joseph Bunnett is an academic researcher. The author has contributed to research in topics: Electron transfer & Nuclear warfare. The author has an hindex of 4, co-authored 22 publications receiving 230 citations.

Papers
More filters

Cited by
More filters
Journal ArticleDOI
TL;DR: In this article, the authors present the latest progress in two related polymerization methodologies that rely on singleelectron transfer (SET), single-electron-transfer degenerative chain transfer living radical polymerization (SET-DTLRP), and single-Electron Transfer Living Radical Poly(SET-LRP) for the synthesis of tailored polymers.
Abstract: The special of Chemical Review informs about studies conducted on single-electron transfer and single-electron transfer degenerative chain transfer living radical polymerization. Researchers have demonstrated that living radical polymerization (LRP) can be significantly effective for the synthesis of tailored polymers. The special issue aims at covering the latest progress in two related polymerization methodologies that rely on single-electron transfer (SET), single-electron transfer degenerative chain transfer living radical polymerization (SET-DTLRP), and single-electron transfer living radical polymerization (SET-LRP). It is demonstrated that SET-DTLRP proceeds through SET initiation and competition of SET activation, deactivation, and degenerative transfer (DT). SET-LRP proceeds exclusively through a SET initiation, activation, and deactivation. It is also revealed that the two techniques have arose from investigations into Cu-catalyzed LRP initiated with sulfonyl halides.

814 citations

Journal ArticleDOI
01 Aug 1981-Polymer
TL;DR: In this paper, Farnham et al. showed that copolytherketones and copolyaryletherketone-sulphones can be obtained by polycondensation of bis-4-halogenophenyl ketones with the potassium salt of 4-fluorophenyl 4-hydroxyphenyl ketone using certain diaryl sulphones as solvents for the reactions.

451 citations

Journal ArticleDOI
TL;DR: Recent published "organocatalytic C-H activation reactions" have now been interpreted as base-promoted homolytic substitutions, which could be experimental breakthroughs because they presage new transformations in radical (anion) chemistry.
Abstract: A radical outlook: Recently published "organocatalytic C-H activation reactions" have now been interpreted as base-promoted homolytic substitutions. The addition of an aryl radical to an arene followed by deprotonation (see above) and electron transfer form part of the chain reaction. Although these new results are not conceptual breakthroughs, they could be experimental breakthroughs because they presage new transformations in radical (anion) chemistry. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

407 citations