Metal‐Free, Light‐Catalyzed ATRP For the Synthesis of Functional PVDF‐Based Block Copolymers and Their Characterization

Abstract: The synthesis and characterization of poly (vinylidene fluoride) (PVDF)‐based block copolymers using a metal‐free light‐catalyzed atom transfer radical polymerization (ATRP) approach are described. A PVDF macroinitiator with C─Br bonds at both ends of the chain is synthesized, and an organic photoredox catalyst (OPRC) is used to control the process. The metal‐free process expands the possibilities for the synthesis and application of PVDF‐based block copolymers, as it allows the use of monomers that is previously incompatible with classical ATRP due to their interaction with metal catalysts. The synthesized block copolymers are characterized structurally and thermally as powder materials and in thin films. Fourier‐transform infrared spectroscopy (FT‐IR) analysis revealed that the crystalline phase of PVDF changes when thin films are formed. Specifically, the disappearance of the FT‐IR peaks related to the gamma phase and the presence of characteristic peaks related to the alpha and beta phases indicate that film formation rearranged the PVDF chains, leading to changes in their crystalline phases. These PVDF‐based block copolymers have unique properties, including high thermal stability, chemical resistance, and piezoelectricity, making them potential candidates for use in various fields, such as biomedical engineering, energy storage, and electronic devices.

Object Details

• Location: Deutsche Nationalbibliothek Frankfurt am Main
• Extent: Online-Ressource
• Language: Englisch

References and Relationships

• Bibliographic citation: Metal‐Free, Light‐Catalyzed ATRP For the Synthesis of Functional PVDF‐Based Block Copolymers and Their Characterization ; day:16 ; month:10 ; year:2024 ; extent:10 ; Macromolecular chemistry and physics ; (16.10.2024) (gesamt 10)

Contributors, Places and Time

• Creator: Altomare, Aldo ; Sognane, Rouguy ; Fiorito, Alice ; Loos, Katja

Further information

• DOI: 10.1002/macp.202400251
• URN: urn:nbn:de:101:1-2410171406087.220238273749
• Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Last update: 15.08.2025, 7:31 AM CEST