Switchable gate-opening effect in metal-organic polyhedra assemblies through solution processing

被引:41
|
作者
Craig, Gavin A. [1 ]
Larpent, Patrick [1 ]
Kusaka, Shinpei [1 ,3 ]
Matsuda, Ryotaro [1 ,3 ]
Kitagawa, Susumu [1 ]
Furukawa, Shuhei [1 ,2 ]
机构
[1] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
[3] Nagoya Univ, Grad Sch Engn, Dept Mat Chem, Nagoya, Aichi, Japan
基金
日本学术振兴会;
关键词
SPIN-CROSSOVER; COOPERATIVE ADSORPTION; FRAMEWORKS; CO2; POLYMERIZATION; SELECTIVITY; BEHAVIOR; CRYSTAL; MIL-53; CH4;
D O I
10.1039/c8sc02263a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gate-opening gas sorption is known for metal-organic frameworks, and is associated with structural flexibility and advantageous properties for sensing and gas uptake. Here, we show that gate-opening is also possible for metal-organic polyhedra (MOPs), and depends on the molecular organisation in the lattice. Thanks to the solubility of MOPs, several interchangeable solvatomorphs of a lantern-type MOP were synthesised via treatment with different solvents. One phase obtained through use of methanol induced a gate-opening effect in the lattice in response to carbon dioxide uptake. The sorption process was thoroughly investigated with in situ powder X-ray diffraction and simultaneous adsorption experiments. Meanwhile, solution processing of this flexible phase using THF led to a permanently porous phase without a gate-opening effect. Furthermore, we find that we can change the metallic composition of the MOP, and yet retain flexibility. By showing that gate-opening can be switched on and off depending on the solvent of crystallisation, these findings have implications for the solution-based processing of MOPs.
引用
收藏
页码:6463 / 6469
页数:8
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