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Coordination-bond-directed synthesis of hydrogen-bonded organic frameworks from metal–organic frameworks as templates

Controlled synthesis of hydrogen-bonded organic frameworks (HOFs) remains challenging, because the self-assembly of ligands is not only directed by weak hydrogen bonds, but also affected by other competing van der Waals forces. Herein, we demonstrate the coordination-bond-directed synthesis of HOFs...

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Detalles Bibliográficos
Autores principales: Su, Jian, Yuan, Shuai, Cheng, Yi-Xun, Yang, Zhi-Mei, Zuo, Jing-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565389/
https://www.ncbi.nlm.nih.gov/pubmed/34760211
http://dx.doi.org/10.1039/d1sc03962h
Descripción
Sumario:Controlled synthesis of hydrogen-bonded organic frameworks (HOFs) remains challenging, because the self-assembly of ligands is not only directed by weak hydrogen bonds, but also affected by other competing van der Waals forces. Herein, we demonstrate the coordination-bond-directed synthesis of HOFs using a preformed metal–organic framework (MOF) as the template. A MOF (Cu(I)-TTFTB) based on two-coordinated Cu(I) centers and tetrathiafulvalene-tetrabenzoate (TTFTB) ligands was initially synthesized. Cu(I)-TTFTB was subsequently oxidized to the intermediate (Cu(II)-TTFTB) and hydrated to the HOF product (TTFTB-HOF). Single-crystal-to-single-crystal (SC-SC) transformation was realized throughout the MOF-to-HOF transformation so that the evolution of structures was directly observed by single-crystal X-ray diffraction. The oxidation and hydration of the Cu(I) center are critical to breaking the Cu–carboxylate bonds, while the synergic corbelled S⋯S and π⋯π interactions in the framework ensured stability of materials during post-synthetic modification. This work not only provided a strategy to guide the design and discovery of new HOFs, but also linked the research of MOFs and HOFs.