This research explores the alteration of metal-organic frameworks (MOFs) using a method called postsynthetic metal exchange. We focus on the shift from a Zn-based MOF containing a [ZnO(COO)] secondary building unit (SBU) of octahedral site symmetry (ANT-1(Zn)) to a Fe-based one with a [FeO(COO)] SBU of trigonal prismatic site symmetry (ANT-1(Fe)). The symmetry-mismatched SBU transformation cleverly maintains the MOF's overall structure by adjusting the conformation of the flexible 1,3,5-benzenetribenzoate linker to alleviate the framework strain.
View Article and Find Full Text PDFA few metal-organic frameworks (MOFs), which typically use strong acids as proton sources, display superprotonic conductivity (≈10 S cm ); however, they are rare due to the instability of MOFs in highly acidic conditions. For the first time, we report superprotonic conductivity using a moderately acidic guest, zwitterionic sulfamic acid (HSA), which is encapsulated in MOF-808 and MIL-101. HSA acts not only as a proton source but also as a proton-conducting medium due to its extensive hydrogen bonding ability and zwitterion effect.
View Article and Find Full Text PDFFront Cell Neurosci
December 2022
Neurodegenerative diseases (NDDs) are characterized by the progressive loss of selectively vulnerable populations of neurons, which is responsible for the clinical symptoms. Although degeneration of neurons is a prominent feature that undoubtedly contributes to and defines NDD pathology, it is now clear that neuronal cell death is by no means mediated solely by cell-autonomous mechanisms. Oligodendrocytes (OLs), the myelinating cells of the central nervous system (CNS), enable rapid transmission of electrical signals and provide metabolic and trophic support to neurons.
View Article and Find Full Text PDFThe pore space partition approach via post-synthetic linker insertion was used to modulate the porosity of a fragile Ag(i)-carboxylate framework with potentially large pore space. The resulting Ag(i)-MOFs with partitioned pores showed enhanced permanent porosity compared with a nonpartitioned Ag(i)-carboxylate framework.
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