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Metal-Organic Frameworks from Group 4 Metals and 2,5-Dihydroxyterephthalic Acid: Reinvestigation, New Structure, and Challenges Toward Gas Storage and Separation

Authors
Chun, HyungphilMoon, Dohyun
Issue Date
Apr-2017
Publisher
American Chemical Society
Keywords
X-RAY-DIFFRACTION; HETEROMETALLIC APPROACH; STABILITY; ADSORPTION; LIGAND; CRYSTALLOGRAPHY; TOPOLOGIES; CRYSTALS; MOFS
Citation
Crystal Growth & Design, v.17, no.4, pp.2140 - 2146
Indexed
SCIE
SCOPUS
Journal Title
Crystal Growth & Design
Volume
17
Number
4
Start Page
2140
End Page
2146
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/10057
DOI
10.1021/acs.cgd.7b00092
ISSN
1528-7483
Abstract
The reactions of group 4 metals (Ti, Zr, and Hf) and 2,5-dihydroxyterephthalic acid (H(4)dobdc) under solvothermal conditions have been systematically explored, and their major crystalline phases have been investigated by single-crystal diffractions. Ti(IV) forms a layered framework [Ti-2(Hdobdc)(3)] where honeycomb-type sheets are interconnected through strong hydrogen bonding. Various gases are reversibly adsorbed within the straight one-dimensional channels decorated with polar O atoms, and H-2 and CO2 show relatively high isosteric heats of adsorption at 6.6 and 29.4 kJ/mol, respectively. Zr(IV)- and Hf(IV)-based MOFs have also been synthesized using the same ligand and are isostructural with the formula (H3O)(x)[M(dobdc)(bz)(x)] (M = Zr or Hf). They have a unique, nonoxo-trinuclear building block that forms a polyhedral network of 6-connected topology. Unlike the two-dimensional net of Ti, the Zr and Hf metal-organic frameworks are hydrothermally stable as unambiguously shown by variable-temperature X-ray diffraction.
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY (DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING)
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