Effect of linker substituent nature on performance of active sites in UiO-66: combined FT-IR and DFT study

The nature of organic linker substituents plays an important role in gas sorption and separation as well as in catalytic applications of metal-organic frameworks. Zirconium-based UiO-66 is one of the most tunable members of this class of materials. However, the prediction of its properties is still...

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Bibliographic Details
Published in:International journal of molecular sciences Vol. 24, № 19. P. 14893 (1-11)
Other Authors: Torbina, Viktoriia V., Salaev, Mikhail A., Paukshtis, Еvgeny A., Liotta, Leonarda Francesca, Vodyankina, Olga V.
Format: Article
Language:English
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Online Access:http://vital.lib.tsu.ru/vital/access/manager/Repository/koha:001139586
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245 1 0 |a Effect of linker substituent nature on performance of active sites in UiO-66: combined FT-IR and DFT study  |c V. V. Torbina, M. A. Salaev, Е. A. Paukshtis [et al.] 
336 |a Текст 
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504 |a Библиогр.: 40 назв. 
520 3 |a The nature of organic linker substituents plays an important role in gas sorption and separation as well as in catalytic applications of metal-organic frameworks. Zirconium-based UiO-66 is one of the most tunable members of this class of materials. However, the prediction of its properties is still not a fully solved problem. Here, the infrared spectroscopic measurements using highly sensitive CO probe molecules, combined with DFT calculations, are used in order to characterize the performance of different acidic sites caused by the presence of different organic linker substituents. The proposed model allowed differentiation between various active sites over the UiO-66 and clarification of their behavior. The experimental IR bands related to CO adsorption can be unambiguously assigned to one type of site or another. The previously undescribed highly red-shifted band is attributed to CO adsorbed on coordinatively unsaturated zirconium sites through an O atom. The results confirm the lower and higher Lewis's acidity of coordinatively unsaturated Zr sites on linker defects in the UiO-66 structure when electron-withdrawing and electron-donating groups are, respectively, included in a terephthalate moiety, whilst the Brønsted acidity of zirconium oxo-cluster remains almost unchanged. 
653 |a металлоорганические каркасы 
653 |a химические линкеры 
653 |a инфракрасная спектроскопия 
655 4 |a статьи в журналах  |9 962000 
700 1 |a Torbina, Viktoriia V.  |9 138773 
700 1 |a Salaev, Mikhail A.  |9 563314 
700 1 |a Paukshtis, Еvgeny A.  |9 103741 
700 1 |a Liotta, Leonarda Francesca  |9 917603 
700 1 |a Vodyankina, Olga V.  |9 36805 
773 0 |t International journal of molecular sciences  |d 2023  |g Vol. 24, № 19. P. 14893 (1-11)  |x 1661-6596 
852 4 |a RU-ToGU 
856 4 |u http://vital.lib.tsu.ru/vital/access/manager/Repository/koha:001139586 
856 |y Перейти в каталог НБ ТГУ  |u https://koha.lib.tsu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=1139586 
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039 |b 100 
999 |c 1139586  |d 1139586