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Rapid Postgrafting Reaction to Prepare Quaternized Polycarbazoles.
Adhikari, Santosh; Matanovic, Ivana; Leonard, Daniel; Klein, Jeffrey M; Agarwal, Tanya; Kim, Yu Seung.
Afiliação
  • Adhikari S; C-CDE: Chemical Diagnostics and Engineering Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Matanovic I; T-1: Physics and Chemistry of Materials Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Leonard D; MPA-11: Materials Synthesis and Integrated Devices Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Klein JM; MPA-11: Materials Synthesis and Integrated Devices Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Agarwal T; MPA-11: Materials Synthesis and Integrated Devices Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
  • Kim YS; MPA-11: Materials Synthesis and Integrated Devices Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
ACS Macro Lett ; 13(1): 28-33, 2024 Jan 16.
Article em En | MEDLINE | ID: mdl-38100721
ABSTRACT
We report a rapid postgrafting reaction to prepare alkyl ammonium functionalized polycarbazoles from a commercially available monomer. This novel synthetic approach provides benefit to preparing the high molecular weight quaternized polycarbazoles within 1 h of Friedel-Crafts polycondensation, avoiding the synthesis and purification step to prepare a functionalized monomer. The postgrafting reaction produces hexyl alkyl ammonium functionalized polycarbazole with 100% grafting degree. However, the postgrafting reaction produced only 60% grafting with propyl alkyl ammonium due to the competitive elimination reaction because of the higher acidity of ß-hydrogen in the propyl alkyl group resulting from the proximity of the bromide and ammonium groups. The hexyl alkyl ammonium functionalized polycarbazole has a high hydroxide conductivity of 103 mS cm-1 at 80 °C and showed excellent alkaline stability with less than 3% loss of ion group after 1 M NaOH treatment at 80 °C for 500 h. This study highlights that the postgrafting reaction provides a pathway for the scale-up synthesis of quaternized aryl ether-free polyaromatics.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Macro Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Macro Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos