Solvent-mediated framework flexibility of interdigitated 2D layered metal-organic frameworks†

被引:8
|
作者
Lee, Seonghwan [1 ]
Jeong, Seok [1 ]
Seong, Junmo [1 ]
Lim, Jaewoong [1 ]
Sharma, Amitosh [1 ]
Won, Somi [1 ]
Moon, Dohyun [2 ]
Baek, Seung Bin [1 ]
Lah, Myoung Soo [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol, Dept Chem, Ulsan 44919, South Korea
[2] Pohang Acceleratory Lab, Pohang 37673, South Korea
基金
新加坡国家研究基金会;
关键词
POROUS COORDINATION POLYMERS; GAS-ADSORPTION; SORPTION; LIGANDS; STORAGE; CO2;
D O I
10.1039/d1qm00251a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new interdigitated two-dimensional (2D) layered metal-organic framework (MOF) with switchable framework flexibility is synthesized using a highly flexible multifunctional dicarboxylate ligand capable of pi-pi stacking and hydrogen bonding interactions. The framework flexibility and CO2 adsorption behavior of the 2D layered MOF can be controlled by guest N,N-dimethylacetamide (DMA) molecules encapsulated in the solvent pores. Partial removal of the DMA molecule results in partial contraction of the framework, and the interlayer interactions of this partially contracted framework allow reversible expansion and contraction of the framework under CO2 at 195 K. On the other hand, the flexibility of a fully contracted interdigitated 2D framework with no DMA molecules in the solvent pores is distinctly different from that of a partially contracted framework. The interlayer interactions in a fully contracted framework are significantly stronger than those in a partially contracted framework. Notably, this framework does not exhibit framework expansion under the same conditions.
引用
收藏
页码:3621 / 3627
页数:7
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