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Structural diversity and solvent-induced transformations of a copper-based metal-organic framework with highly aromatic ligands.

作者信息

Edwards Abigail, Elkins Landon J, Slebodnick Carla, Wang Jinglei, Zhang Qiang, Makal Tegan A

机构信息

Department of Natural Sciences, The University of Virginia's College at Wise, 1 College Avenue, Wise, VA 24293, USA.

Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24060, USA.

出版信息

Dalton Trans. 2024 Aug 27;53(34):14496-14504. doi: 10.1039/d4dt02085e.

DOI:10.1039/d4dt02085e
PMID:39157929
Abstract

A newly designed tetracarboxylic acid ligand precursor 5,5'-([9,9'-bianthracene]-10,10'-diyl)diisophthalic acid (HBADI) has been used to prepare a series of copper-based metal-organic frameworks (MOFs) with the formula [Cu(BADI)()]· (denoted as 1-, where = solvent) and exhibiting solvent-induced structural transformations. Single-crystal-to-single-crystal transformation occurs upon exchanging 1-DMF (DMF = ,-dimethylformamide) with DMSO (DMSO = dimethylsulfoxide). 1-DMF exhibits reversible structural transformation upon treatment with a variety of solvents; of particular interest is the reversible crystalline-to-amorphous phase transformations observed upon exchange with volatile, polar solvents. A thorough structural investigation of the three framework isomers characterized single-crystal X-ray diffraction experiments is reported and compared to several other tetracarboxylate-based MOFs composed of dimetal secondary building units.

摘要

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