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Thiatruxene-Based Conductive MOF: Harnessing Sulfur Chemistry for Enhanced Proton Transport.
Lu, Chenwei; Choi, Ji Yong; Check, Brianna; Fang, Xiaoyu; Spotts, Samuel; Nuñez, Dario; Park, Jihye.
Afiliación
  • Lu C; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Choi JY; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Check B; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Fang X; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Spotts S; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Nuñez D; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
  • Park J; Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, United States.
J Am Chem Soc ; 146(38): 26313-26319, 2024 Sep 25.
Article en En | MEDLINE | ID: mdl-39283998
ABSTRACT
Functionalizing the organic building blocks of electrically conductive MOFs (EC-MOFs) can be a powerful method for adjusting the electronic structure and introducing a specific chemistry. However, designing EC-MOF linkers with reactive functional groups for postsynthetic modification is challenging due to the requirements of d-p conjugation. This work addresses such design limitations by synthesizing an EC-MOF, Cu-thiatruxene (Cu-thiaTRX). This conductive framework incorporated a truxene-based linker with heterocyclic sulfur, allowing for efficient conjugation and an electrical conductivity of 2.2 × 10-2 S cm-1. Harnessing sulfur chemistry in Cu-thiaTRX involves a two-step postsynthetic modification oxidation and SNAr. The sulfinic groups introduced in the framework enabled tunable proton conductivity, leading to a 200-fold improvement. These results highlight the importance of a rational linker design for functionalization.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Am Chem Soc Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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