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Photocontrolled RAFT Polymerization Catalyzed by Conjugated Polymers under Aerobic Aqueous Conditions.
Lu, Huan; Huang, Yiming; Zhang, Endong; Liu, Yiming; Lv, Fengting; Liu, Libing; Ma, Yuguo; Wang, Shu.
Afiliación
  • Lu H; Beijing National Laboratory for Molecular Sciences, Beijing 100190, P. R. China.
  • Huang Y; Centre for the Soft Matter Science and Engineering, The Key Lab of Polymer Chemistry & Physics of the Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P. R. China.
  • Zhang E; Beijing National Laboratory for Molecular Sciences, Beijing 100190, P. R. China.
  • Liu Y; Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
  • Lv F; Beijing National Laboratory for Molecular Sciences, Beijing 100190, P. R. China.
  • Liu L; Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
  • Ma Y; Beijing National Laboratory for Molecular Sciences, Beijing 100190, P. R. China.
  • Wang S; Centre for the Soft Matter Science and Engineering, The Key Lab of Polymer Chemistry & Physics of the Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P. R. China.
ACS Macro Lett ; 10(8): 996-1001, 2021 08 17.
Article en En | MEDLINE | ID: mdl-35549118
ABSTRACT
Photocontrolled polymerization offers a convenient way to direct the reaction progress and tailor the polymer structures. Nevertheless, conjugated polymers are yet to be utilized as the photocatalyst in associated reactions. Herein, we employed poly(boron dipyrromethene-alt-fluorene) (PBF), a conjugated polymer with better photostability than eosin Y, as the photocatalyst for photo-RAFT polymerizations of acrylic monomers, and the polymers were obtained with moderately narrow molecular weight distributions. The reaction progress was effectively controlled by switching irradiation conditions, and the block copolymers were prepared from chain extension of a macroinitiator. As electron spin resonance (ESR) and optical spectra results suggested, the reductive quenching of PBF* by ascorbate was the key step leading to the reduction of a chain transfer agent (CTA), whereas the hydroxyl radical derived from superoxide was considered as a byproduct of deoxygenation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Agua Idioma: En Revista: ACS Macro Lett Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Agua Idioma: En Revista: ACS Macro Lett Año: 2021 Tipo del documento: Article