Journal
CHEMISTRY OF MATERIALS
Volume 30, Issue 5, Pages 1667-1676Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.7b05052
Keywords
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Funding
- DFG [FOR 2433]
- research cluster SusChemSys
- European Regional Development Fund (ERDF)
- state of North Rhine-Westphalia, Germany
- Alexander von Humboldt Foundation
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The pillared-layered metalorganic framework compounds M-2(BME-bdc)(2)(dabco) (M2+ = Zn2+, Co2+, Ni2+, Cu2+; BME-bdc(2-) = 2,5-bis(2-methoxyethoxy)-1,4-benzenedicarboxylate; dabco = diazabicyclo[2.2.2]octane) exhibit structural flexibility and undergo guest and temperature-induced reversible phase transitions between a narrow pore (np) and a large pore (lp) form. These transitions were analyzed in detail by powder X-ray diffraction ex and in situ, isothermal gas adsorption measurements and differential scanning calorimetry. The threshold parameters (gas pressure or temperature), the magnitude of the phase transitions (volume change) as well as their transition enthalpies are strikingly dependent on the chosen metal cation M2+. This observation is assigned to the different electronic structures and ligand field effects on the coordination bonds. Accordingly, in situ powder X-ray diffraction measurements as a function of CO2 pressure reveal different mechanisms for the np to lp phase transition during CO2 adsorption.
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