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Ultra-Slow Dynamics of Framework Linker in MIL-53 (Al) as a Sensor for Different Isomers of Xylene Conference Abstracts

Conference International Workshop on Porous Coordination Compounds
19-23 Sep 2016 , Altay
Source International Workshop on Porous Coordination Compounds (IWPCC-2016): book of abstracts
Compilation, NIIC SB RAS. Novosibirsk.2016. 81 c.
Output data Year: 2016, Pages: 76-77 Pages count : 2
Authors Khudozhitkov Alexander E. 1,2 , Jobic Hervé 3 , Freude Dieter 4 , Haase Juergen 4 , Kolokolov Daniil I. 1,2 , Stepanov Alexander G. 1,2
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia
2 Department of Physical Chemistry, Faculty of Natural Sciences, Novosibirsk State University, Novosibirsk, Russia
3 Institut de Recherches sur la Catalyse et l’Environnement de Lyon, CNRS, Université de Lyon, Villeurbanne, France
4 Fakultät für Physik und Geowissenschaften, Universität Leipzig, Leipzig, Germany

Funding (2)

1 Russian Foundation for Basic Research 14-03-91333
2 German Research Foundation HA 1893/16

Abstract: MIL-53 (Al) is an important example of the metal?organic frameworks (MOFs) with a flexible framework capable to efficiently separate ortho and para isomers of xylene at moderate temperatures. The batch adsorption and breakthrough experiments have demonstrated that the o-/p-xylenes separation factor was ~ 3.5 at saturation conditions and T = 298 K. The MIL-53 MOF contains mobile terephthalate phenylene fragments that can be used as dynamical probe to investigate the guest-host interactions and the origin of the separation selectivity. 2H NMR spin alignment echo technique was applied for the first time to identify and characterize an ultra-slow motion (0.1-1 kHz) in MOFs. Xylene isomers influence the mobility of the linkers in a different way causing drastic discrepancy in its rates of motion. It has been established that phenylenes rotation perform one order of magnitude slower in the presence of o-xylene (kortho = 70 s-1) compared to the same rotation in the presence of the other isomer, p-xylene (kpara = 800 s-1) at T ~ 373 K. This is explained by the stronger interaction of ortho isomer with the linker than para isomer. However, this difference in rotation rates is irregular and depends on the temperature.
Cite: Khudozhitkov A.E. , Jobic H. , Freude D. , Haase J. , Kolokolov D.I. , Stepanov A.G.
Ultra-Slow Dynamics of Framework Linker in MIL-53 (Al) as a Sensor for Different Isomers of Xylene
In compilation International Workshop on Porous Coordination Compounds (IWPCC-2016): book of abstracts. – NIIC SB RAS., 2016. – C.76-77.
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Citing: Пока нет цитирований