Franziska Debatin, Karsten Behrens, Jens Weber, Igor A. Baburin, Arne Thomas, Johannes Schmidt, Irena Senkovska, Stefan Kaskel, Alexandra Kelling, Niklas Hedin, Zoltan Bacsik, Stefano Leoni, Gotthard Seifert, Christian Jäger, Christina Günter, Uwe Schilde, Alwin Friedrich, Hans-Jürgen Holdt
- We report on a new series of isoreticular frameworks based on zinc and 2-substituted imidazolate-4-amide-5-imidate (IFP-14, IFP=imidazolate framework Potsdam) that form one-dimensional, microporous hexagonal channels. Varying R in the 2-substitued linker (R=Me (IFP-1), Cl (IFP-2), Br (IFP-3), Et (IFP-4)) allowed the channel diameter (4.01.7 angstrom), the polarisability and functionality of the channel walls to be tuned. Frameworks IFP-2, IFP-3 and IFP-4 are isostructural to previously reported IFP-1. The structures of IFP-2 and IFP-3 were solved by X-ray crystallographic analyses. The structure of IFP-4 was determined by a combination of PXRD and structure modelling and was confirmed by IR spectroscopy and 1H MAS and 13C CP-MAS NMR spectroscopy. All IFPs showed high thermal stability (345400?degrees C); IFP-1 and IFP-4 were stable in boiling water for 7 d. A detailed porosity analysis was performed on the basis of adsorption measurements by using various gases. The potential of the materials to undergo specific interactions with CO2We report on a new series of isoreticular frameworks based on zinc and 2-substituted imidazolate-4-amide-5-imidate (IFP-14, IFP=imidazolate framework Potsdam) that form one-dimensional, microporous hexagonal channels. Varying R in the 2-substitued linker (R=Me (IFP-1), Cl (IFP-2), Br (IFP-3), Et (IFP-4)) allowed the channel diameter (4.01.7 angstrom), the polarisability and functionality of the channel walls to be tuned. Frameworks IFP-2, IFP-3 and IFP-4 are isostructural to previously reported IFP-1. The structures of IFP-2 and IFP-3 were solved by X-ray crystallographic analyses. The structure of IFP-4 was determined by a combination of PXRD and structure modelling and was confirmed by IR spectroscopy and 1H MAS and 13C CP-MAS NMR spectroscopy. All IFPs showed high thermal stability (345400?degrees C); IFP-1 and IFP-4 were stable in boiling water for 7 d. A detailed porosity analysis was performed on the basis of adsorption measurements by using various gases. The potential of the materials to undergo specific interactions with CO2 was investigated by measuring the isosteric heats of adsorption. The capacity to adsorb CH4 (at 298 K), CO2 (at 298 K) and H2 (at 77 K) at high pressure were also investigated. In situ IR spectroscopy showed that CO2 is physisorbed on IFP-14 under dry conditions and that both CO2 and H2O are physisorbed on IFP-1 under moist conditions.…
MetadatenVerfasserangaben: | Franziska Debatin, Karsten BehrensGND, Jens Weber, Igor A. Baburin, Arne Thomas, Johannes Schmidt, Irena Senkovska, Stefan Kaskel, Alexandra Kelling, Niklas Hedin, Zoltan Bacsik, Stefano Leoni, Gotthard Seifert, Christian Jäger, Christina GünterGND, Uwe SchildeORCiDGND, Alwin Friedrich, Hans-Jürgen HoldtORCiD |
---|
DOI: | https://doi.org/10.1002/chem.201200889 |
---|
ISSN: | 0947-6539 |
---|
Titel des übergeordneten Werks (Englisch): | Chemistry - a European journal |
---|
Verlag: | Wiley-VCH |
---|
Verlagsort: | Weinheim |
---|
Publikationstyp: | Wissenschaftlicher Artikel |
---|
Sprache: | Englisch |
---|
Jahr der Erstveröffentlichung: | 2012 |
---|
Erscheinungsjahr: | 2012 |
---|
Datum der Freischaltung: | 26.03.2017 |
---|
Freies Schlagwort / Tag: | N; O ligands; adsorption; metal- organic frameworks; microporous materials; zinc |
---|
Band: | 18 |
---|
Ausgabe: | 37 |
---|
Seitenanzahl: | 11 |
---|
Erste Seite: | 11630 |
---|
Letzte Seite: | 11640 |
---|
Fördernde Institution: | Deutsche Forschungsgemeinschaft [SPP-1362] |
---|
Organisationseinheiten: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Geowissenschaften |
---|
Peer Review: | Referiert |
---|
Name der Einrichtung zum Zeitpunkt der Publikation: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Erd- und Umweltwissenschaften |
---|