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The thermally induced decarboxylation mechanism of a mixed-oxidation state carboxylate-based iron metal–organic framework

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Abstract

Investigations into a thermally generated decarboxylation mechanism for metal site activation and the generation of mesopores in a carboxylate iron-based MOF, PCN-250, have been conducted. PCN-250 exhibits an interesting oxidation state change during thermal treatment under inert atmospheres or vacuum conditions, transitioning from an Fe(III)3 cluster to a Fe(II)Fe(III)2 cluster. To probe this redox event and discern a mechanism of activation, a combination of thermogravimetric analysis, gas sorption, scanning electron microscopy, 57Fe Mössbauer spectroscopy, gas chromatography-mass spectrometry, and X-ray diffraction studies were conducted. The results suggest that the iron-site activation occurs due to ligand decarboxylation above 200 °C. This is also consistent with the generation of a missing cluster mesoporous defect in the framework. The resulting mesoporous PCN-250 maintains high thermal stability, preserving crystallinity after multiple consecutive high-temperature regeneration cycles. Additionally, the thermally reduced PCN-250 shows improvements in the total uptake capacity of methane and CO2.

Graphical abstract: The thermally induced decarboxylation mechanism of a mixed-oxidation state carboxylate-based iron metal–organic framework

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Publication details

The article was received on 19 Jul 2019, accepted on 23 Sep 2019 and first published on 24 Sep 2019


Article type: Communication
DOI: 10.1039/C9CC04555D
Chem. Commun., 2019, Advance Article

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    The thermally induced decarboxylation mechanism of a mixed-oxidation state carboxylate-based iron metal–organic framework

    H. F. Drake, G. S. Day, S. W. Vali, Z. Xiao, S. Banerjee, J. Li, E. A. Joseph, J. E. Kuszynski, Z. T. Perry, A. Kirchon, O. K. Ozdemir, P. A. Lindahl and H. Zhou, Chem. Commun., 2019, Advance Article , DOI: 10.1039/C9CC04555D

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