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In Situ Electrochemical Interfacial Polymerization for Covalent Organic Frameworks with Tunable Electrochromism.
Wang, Ying-Ao; Wu, Qiong; Wang, Xun; Jiang, Min; Zhang, Rui; Chen, Xiao-Juan; Liang, Ru-Ping; Qiu, Jian-Ding.
Afiliación
  • Wang YA; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Wu Q; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Wang X; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Jiang M; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Zhang R; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Chen XJ; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Liang RP; Nanchang University, College of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
  • Qiu JD; Nanchang University, Department of Chemistry, 999 Xue Fu Road, 330031, Nanchang, CHINA.
Angew Chem Int Ed Engl ; : e202413071, 2024 Aug 05.
Article en En | MEDLINE | ID: mdl-39103902
ABSTRACT
A rapid in situ synthesis of electrochromic covalent organic frameworks (EC-COFs) was proposed by using green electrochemical interface polymerization of N,N,N',N'-tetrakis(p-aminophenyl)p-phenylenediamine (TPDA) and 2,5-dihydroxy-p-phenylenedicarboxaldehyde (DHBD). The synthetized TPDA-DHBD films exhibit stable polymorphic colour variations under different applied potentials, which can be attributed to the redox state changes of bis(triphenylamine) and imine electroactive functional groups within the COFs skeleton. TPDA-DHBD represents markedly different electrochromisms from red to cyan due to the steric hindrance effect caused by the presence of UO22+, demonstrating the unique tunability of COFs materials. This work offers a new feasible idea for rapid EC-COFs synthesis and tunable EC-COFs realization.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2024 Tipo del documento: Article País de afiliación: China