514 0

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

Title
Metal-Organic Frameworks from Group 4 Metals and 2,5-Dihydroxyterephthalic Acid: Reinvestigation, New Structure, and Challenges Toward Gas Storage and Separation
Author
전형필
Keywords
X-RAY-DIFFRACTION; HETEROMETALLIC APPROACH; STABILITY; ADSORPTION; LIGAND; CRYSTALLOGRAPHY; TOPOLOGIES; CRYSTALS; MOFS
Issue Date
2017-03
Publisher
AMER CHEMICAL SOC
Citation
CRYSTAL GROWTH & DESIGN, v. 17, No. 4, Page. 2140-2146
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.
URI
https://pubs.acs.org/doi/abs/10.1021/acs.cgd.7b00092https://repository.hanyang.ac.kr/handle/20.500.11754/103177
ISSN
1528-7483; 1528-7505
DOI
10.1021/acs.cgd.7b00092
Appears in Collections:
COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E](과학기술융합대학) > CHEMICAL AND MOLECULAR ENGINEERING(화학분자공학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE