Pressure-Dependent Structural and Chemical Changes in a Metal–Organic Framework with One-Dimensional Pore Structure
Source abstract
Abstract
Pressure-dependent structural and chemical changes of the metal–organic framework (MOF) compound MIL-47(V) have been investigated up to 3 GPa using different pore-penetrating liquids as pressure transmitting media (PTM). We find that at 0.3(1) GPa the terephthalic acid (TPA) template molecules located in the narrow channels of the as-synthesized MIL-47(V) are selectively replaced by methanol molecules from a methanol–ethanol–water mixture and form a methanol inclusion complex. Further pressure increase leads to a gradual narrowing of the channels up to 1.9(1) GPa, where a second irreversible insertion of methanol molecules leads to more methanol molecules being inserted into the pores. After pressure release methanol molecules remain within the pores and can be removed only after heating to 400 °C. In contrast, when MIL-47(V) is compressed in water, a reversible replacement of the TPA by H 2 O molecules takes place near 1 GPa. The observed structural and chemical changes observed in MIL-47(V) demonstrate unique high pressure chemistry depending on the size and type of molecules present in the liquid PTM. This allows postsynthetic nonthermal pressure-induced removal and insertion of organic molecules in MOFs forming novel and stable phases at ambient conditions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Crystallography and molecular interactions · X-ray Diffraction in Crystallography
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Earth System Sciences, Yonsei University, Seoul 03722, Republic of Korea
Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States
Department of Chemistry, Kyungpook National University, Daegu 41566, Republic of Korea
NanoCenter, Department of Chemistry & Biochemistry, University of South Carolina, Columbia, South Carolina 29208, United States
Funding
National Research Foundation of Korea
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