Multivariate sodalite zeolitic imidazolate frameworks: a direct solvent-free synthesis
Different mixed-ligand Zeolitic Imidazolate Frameworks (ZIFs) with sodalite topology, i.e. isoreticular to ZIF-8 , unachievable by conventional synthetic routes, have been prepared using a solvent-free methodology. In particular, the versatility of this method is demonstrated with three different me...
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Published in | Chemical science (Cambridge) Vol. 13; no. 3; pp. 842 - 847 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
19.01.2022
The Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
ISSN | 2041-6520 2041-6539 |
DOI | 10.1039/d1sc04779e |
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Summary: | Different mixed-ligand Zeolitic Imidazolate Frameworks (ZIFs) with sodalite topology,
i.e.
isoreticular to
ZIF-8
, unachievable by conventional synthetic routes, have been prepared using a solvent-free methodology. In particular, the versatility of this method is demonstrated with three different metal centres (Zn, Co and Fe) and binary combinations of three different ligands (2-methylimidazole, 2-ethylimidazole and 2-methylbenzimidazole). One combination of ligands, 2-ethylimidazole and 2-methylbenzimidazole, results in the formation of SOD frameworks for the three metal centres despite this topology not being obtained for the individual ligands. Theoretical calculations confirm that this topology is the lowest in energy upon ligand mixing.
Different mixed-ligand Zeolitic Imidazolate Frameworks (ZIFs) with sodalite topology,
i.e.
isoreticular to
ZIF-8
, unachievable by conventional synthetic routes, have been prepared using a solvent-free methodology. |
---|---|
Bibliography: | Electronic supplementary information (ESI) available. CCDC For ESI and crystallographic data in CIF or other electronic format see DOI 2095300 2095301 10.1039/d1sc04779e ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d1sc04779e |