Journal
DALTON TRANSACTIONS
Volume 41, Issue 41, Pages 12759-12765Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2dt31427d
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Funding
- National Research Foundation of Korea
- Korean Government [R01-2009-0074066, 2011K000675, KRF-2008-331-C00149]
- Basic Science Research Program through the National Research Foundation of Korea (NRF)
- Ministry of Education, Science and Technology [2012-0004193]
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We report bifunctional three-dimensional (3D) Cu-MOFs with high selectivity of CO2 over N-2 and H-2 as well as high catalytic activity for transesterification of esters. The Cu-MOFs containing Cu-2 dinuclear units connected by glutarates and bipyridyl ligands are formulated as [{Cu-2(Glu)(2)(mu-bpa)}center dot(CH3CN)](n) (1) and [{Cu-2(Glu)(2)(mu-bpp)}center dot(C3H6O)](n) (2) (Glu = glutarate, bpa = 1,2-bis(4-pyridyl)ethane, bpp = 1,3-bis-(4-pyridyl)propane). These two new bifunctional 3D Cu-MOFs possess very similar pore shape with different pore dimensions. Their gas sorption behaviors were investigated by using CO2, N-2 and H-2 at suitable temperatures. Both MOFs exhibited good CO2 selectivity over N-2 and H-2. MOF 1 having a smaller pore dimension exhibited much higher CO2 adsorption enthalpy than MOF 2 having a larger pore dimension. However, MOF 2 exhibited more enhanced CO2 uptake ability than MOF 1. A subtle variation of pore dimension indeed influenced the CO2 uptake ability somewhat significantly especially at higher temperatures such as 273 K and 298 K. Heterogeneous catalytic activities of the MOFs were also investigated in detail. Only MOF 1 appeared to be an efficient, mild, and easily recyclable heterogeneous catalyst for the transesterification of esters and constitutes a promising class of heterogeneous catalysts that allowed reuse without a significant loss of activity through twenty runs with ester.
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