期刊
CRYSTAL GROWTH & DESIGN
卷 12, 期 8, 页码 4083-4089出版社
AMER CHEMICAL SOC
DOI: 10.1021/cg300566x
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资金
- National Nature Science Foundation of China [201171062, 20801021]
- Program for New Century Excellent Talents in University of China [NCET-10-040]
- Program for Distinguished Young Scientist of Hubei Province [2010CDA087]
- self-determined research funds of CCNU from the colleges' basic research and operation of MOE [CCNU10A01008, CCNU09A02002, CCNU11C01002]
- Program for Innovation Group of Hubei Province of China [2009CDA048]
- Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT) [IRT0953]
Two microporous cadmium(H) metal organic frameworks, [Cd(cptpy)(Ac)(H2O)center dot(DMA)(H2O)] (1) and [Cd(cptpy)(2)center dot(DMF)(2)] (2) (Hcptpy = 4-(4-carboxyphenyl)-2,2':4',4 ''-terpyridine, DMA = N,N-dimethylacetamide, DMF = dimethylformamide) have been solvothermally synthesized under different reaction conditions. Complex 1 is a double-interpenetrating 3D network, while 2 is a noninterpenetrating (3,5)-connected 2D framework. The dehydrated forms of compounds 1 and 2 exhibit selective adsorption of CO2 over N-2 and H2O over CH3OH. In addition, the adsorption value of CO2 for 2 is higher than that of 1. The contents of uncoordinated pyridine nitrogen (Lewis basic sites) per formula unit of 1 and 2 are 2.16 and 4.36%, respectively. Obviously, the grafting of more uncoordinated pyridine nitrogen into compound 2 could enhance adsorption of the acidic CO2 molecule. Notably, both 1 and 2 display strong photoluminescence. The nature of electronic transitions for complex 1 in the photoluminescent process was investigated by means of time-dependent density functional theory (TDDFT) calculations and molecular orbital analyses, which collaborates that the luminescent property is ligand-based.
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