期刊
CRYSTAL GROWTH & DESIGN
卷 8, 期 7, 页码 2478-2483出版社
AMER CHEMICAL SOC
DOI: 10.1021/cg8001114
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Three 3D multifunctional microporous metal-organic frameworks (MOFs), Cu-2(ABTC)(H2O)(2)center dot(DMF)(2)(H2O) (JUC-62), Cd)(2)(ABTC)(DMF)(3)center dot(DMF)(2) (JUC-63), and Mn(H(2)ABTC)(DMF)(2) (JUC-64)(H(4)ABTC = 3,3',5,5'-azobenzenetetracarboxylic acid, DMF = NN'-dimeihylformamide, and JUC = Jilin University China) have been synthesized by self-assembly of a rigid tetra-carboxylate ligand H4ABTC and corresponding transition metal salts under mild conditions. X-ray crystallography reveals that their topologies are based on NbO (JUC-62) and PtS (JUC-63 and JUC-64) nets, constructed of 4-connected rectangular ABTC(4-) units with 4-connected square paddle-wheel CU2(CO2)(4)(H2O)(2) secondary building units (SBUs), tetrahedral bimetallic Cd-2(CO2)(4)(DMF)(3) -)(4)(DMF)(3) SBUs, and tetrahedral monometallic Mn(CO2)(4)(DMF)(3) SBUs, respectively. High-pressure hydrogen sorption of the activated JUC-SBUs, 62 reveals a type I profile at 77 K, which is saturated at 40 bar with a hydrogen uptake of about 4.71 wt%. Photoluminescence investigations reveal that JUC-62 and JUC-63 display strong main emission spectra peaks at 392 and 402 urn, respectively.
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