Your browser doesn't support javascript.
loading
Organometallic-Mediated Radical Polymerization of Vinylidene Fluoride.
Banerjee, Sanjib; Ladmiral, Vincent; Debuigne, Antoine; Detrembleur, Christophe; Poli, Rinaldo; Améduri, Bruno.
  • Banerjee S; Ingénierie et Architectures Macromoléculaires, Institut Charles Gerhardt, UMR 5253 CNRS, UM, ENSCM, Place Eugène Bataillon, 34095, Montpellier Cedex 5, France.
  • Ladmiral V; Present address: Department of Chemistry, Indian Institute of Technology Bhilai, Raipur, 492015, Chhattisgarh, India.
  • Debuigne A; Ingénierie et Architectures Macromoléculaires, Institut Charles Gerhardt, UMR 5253 CNRS, UM, ENSCM, Place Eugène Bataillon, 34095, Montpellier Cedex 5, France.
  • Detrembleur C; Center for Education and Research on Macromolecules (CERM), CESAM Research Unit, University of Liege, Department of Chemistry, Sart-Tilman B6a, 4000, Liege, Belgium.
  • Poli R; Center for Education and Research on Macromolecules (CERM), CESAM Research Unit, University of Liege, Department of Chemistry, Sart-Tilman B6a, 4000, Liege, Belgium.
  • Améduri B; CNRS, LCC (Laboratoire de Chimie de Coordination) and Université de Toulouse, UPS, INPT, 205 route de Narbonne, BP 44099, 31077, Toulouse Cedex 4, France.
Angew Chem Int Ed Engl ; 57(11): 2934-2937, 2018 03 05.
Article en En | MEDLINE | ID: mdl-29329495
An unprecedented level of control for the radical polymerization of vinylidene fluoride (VDF), yielding well-defined PVDF (at least up to 14 500 g mol-1 ) with low dispersity (≤1.32), was achieved using organometallic-mediated radical polymerization (OMRP) with an organocobalt compound as initiator. The high chain-end fidelity was demonstrated by the synthesis of PVDF- and PVAc-containing di-and triblock copolymers. DFT calculations rationalize the efficient reactivation of both head and tail chain end dormant species.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2018 Tipo del documento: Article