Traditionally, α-olefins have been regarded as non-homopolymerizable substrates in textbook examples. However, they have the ability to copolymerize with sulfur dioxide, leading to the creation of alternating copolymers. These commodity poly(olefin sulfone)s exhibite a wide array of applications. Nevertheless, the synthesis process involving sulfur dioxide pose considerable hazards and practical difficulties. In this study, we report on the "SO2-free" radical homopolymerization of sulfonyl α-olefin monomers, resulting in the production of ABC sequence-controlled poly(vinylbenzothiazole-olefin-sulfone)s. This unique radical polymerization process is enhanced by 1,4/1,5-aryl migration, facilitated by the sulfonyl radicals involved in propagation. This demonstrated aryl group migration radical polymerization opens up new possibilities for synthesizing polysulfones with unprecedented main chain sequences and structures, which hold great promise as candidates for innovative polymeric materials.
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http://dx.doi.org/10.1002/anie.202421906 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
ShanghaiTech University, School of Physicl Science and Technology, 393 Middle Huaxia Road, Pudong, Shanghai, 201210, Shanghai, CHINA.
Traditionally, α-olefins have been regarded as non-homopolymerizable substrates in textbook examples. However, they have the ability to copolymerize with sulfur dioxide, leading to the creation of alternating copolymers. These commodity poly(olefin sulfone)s exhibite a wide array of applications.
View Article and Find Full Text PDFPolymers (Basel)
November 2024
School of Physical and Chemical Sciences, University of Canterbury, Private Bag 4800, Christchurch 8140, New Zealand.
The chain-length-dependent nature of the termination reaction in radical polymerization (RP) renders the overall termination rate coefficient, <>, a complex parameter in the usual situation where the radical chain-length distribution is non-uniform. This applies also for the activation energy of termination, (<>), which we subject to detailed mechanistic investigation for the first time. The experimental side of this work measures (<>) for the dilute-solution, low-conversion, chemically initiated homopolymerization of styrene (ST), methyl methacrylate (MMA), butyl methacrylate, and dodecyl methacrylate.
View Article and Find Full Text PDFSci Adv
September 2024
Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study, and Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Radical polymerization is a powerful technique for producing a variety of polymeric materials. However, the chain transfer reaction impedes the formation of polymers from many common α-olefins such as propene and 1-butene using this method. Consequently, poly(α-olefins) are predominantly produced via coordination polymerization.
View Article and Find Full Text PDFMacromol Rapid Commun
November 2024
Department of Chemical Engineering - Product Technology, University of Groningen, Nijenborgh 4, Groningen, 9747 AG, The Netherlands.
The development of cleaner, more environmentally friendly processes in polymerization technology is crucial due to the prevalent use of volatile organic solvents (VOCs), which are harmful and toxic. Future regulations are likely to limit or ban VOCs. This review explores the use of supercritical solvents, specifically supercritical CO (scCO), in polymerization processes.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2024
Materials Science and Engineering Program, University of Colorado Boulder, Boulder, Colorado 80309, United States.
High refractive index, low birefringence photopolymers were created via the radical-mediated, ring opening homopolymerization of 1,2-dithiolane functionalized monomers and were subsequently evaluated as holographic recording media. This investigation systematically characterized the reaction kinetics, thermodynamics, and volume shrinkage of the 1,2-dithiolane homopolymerization as well as the optical transparency, refractive index, birefringence, and holographic performance of multifunctional 1,2-dithiolane functionalized monomers and their resultant polymers. Real-time kinetic and thermodynamic analyses of a monofunctional 1,2-dithiolane monomer, lipoic acid methyl ester (LipOMe), indicated rapid monomer conversion, exceeding 90% in 60 s, with an overall enthalpy of reaction of 18 ± 1 kJ/mol.
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