A Breathing Zirconium Metal-Organic Framework with Reversible Loss of Crystallinity by Correlated Nanodomain Formation

被引:43
作者
Bueken, Bart [1 ]
Vermoortele, Frederik [1 ]
Cliffe, Matthew J. [2 ,7 ]
Wharmby, Michael T. [3 ,4 ]
Foucher, Damien [5 ]
Wieme, Jelle [6 ]
Vanduyfhuys, Louis [6 ]
Martineau, Charlotte [5 ]
Stock, Norbert [3 ]
Taulelle, Francis [5 ]
Van Speybroeck, Veronique [6 ]
Goodwin, Andrew L. [2 ]
De Vos, Dirk [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, Celestijnenlaan 200F,POB 2461, B-3001 Leuven, Belgium
[2] Univ Oxford, Inorgan Chem Lab, S Parks Rd, Oxford OX1 3QR, England
[3] CAU Kiel, Inst Anorgan Chem, Max Eyth Str 2, D-24118 Kiel, Germany
[4] Diamond Light Source, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England
[5] Univ Versailles, Inst Lavoisier, UMR CNRS 8180, Ave Etats Unis 45, F-78035 Versailles, France
[6] Univ Ghent, Ctr Mol Modeling, Technol Pk 903, B-9052 Zwijnaarde, Belgium
[7] Univ Cambridge, Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
dynamic porosity; metal-organic frameworks; phase transitions; structure elucidation; zirconium; STABILITY; CLUSTERS; MOFS;
D O I
10.1002/chem.201600330
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The isoreticular analogue of the metal-organic framework UiO-66(Zr), synthesized with the flexible trans-1,4-cyclohexanedicarboxylic acid as linker, shows a peculiar breathing behavior by reversibly losing long-range crystalline order upon evacuation. The underlying flexibility is attributed to a concerted conformational contraction of up to two thirds of the linkers, which breaks the local lattice symmetry. X-ray scattering data are described well by a nanodomain model in which differently oriented tetragonal-type distortions propagate over about 7-10 unit cells.
引用
收藏
页码:3264 / 3267
页数:4
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