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Chemical science (Cambridge), 2024-03, Vol.15 (11), p.416-4113
2024
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Autor(en) / Beteiligte
Titel
Polar alcohol guest molecules regulate the stacking modes of 2-D MOF nanosheets
Ist Teil von
  • Chemical science (Cambridge), 2024-03, Vol.15 (11), p.416-4113
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2024
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • The modulation of two-dimensional metal-organic framework (2-D MOF) nanosheet stacking is an effective means to improve the properties and promote the application of nanosheets in various fields. Here, we employed a series of alcohol guest molecules (MeOH, EtOH and PrOH) to modulate Zr-BTB (BTB = benzene-1,3,5-tribenzoate) nanosheets and to generate untwisted stacking. The distribution of stacking angles was statistically analyzed from high-angle annular dark-field (HAADF) and fast Fourier transform (FFT) images. The ratios of untwisted stacking were calculated, such as 77.01% untwisted stacking for MeOH, 83.45% for EtOH, and 85.61% for PrOH. The obtained untwisted Zr-BTB showed good separation abilities for different substituted benzene isomers, superior para selectivity and excellent column stability and reusability. Control experiments of 2-D Zr-TCA (TCA = 4,4′,4′′-tricarboxytriphenylamine) and Zr-TATB (TATB = 4,4′,4′′-(1,3,5-triazine-2,4,6-triyl)tribenzoic acid) nanosheets with similar pore sizes and stronger polarity regulated by the alcohol guests exhibited moderate separation performance. The electron microscopy images revealed that polar alcohol regulation dominantly generated the twisted stacking of Zr-TCA and Zr-TATB with various Moiré patterns. Polar guest molecules, such as alcohols, provide strong host-guest interactions during the regulation of MOF nanosheet stacking, providing an opportunity to design new porous Moiré materials with application prospects. Polar alcohol guest molecules strategy was proposed to modulate the stacking modes of 2-D MOF nanosheets.
Sprache
Englisch
Identifikatoren
ISSN: 2041-6520
eISSN: 2041-6539
DOI: 10.1039/d3sc06844g
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10935662

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