CO2-induced dissolution of ZnO into ionic liquids and its catalytic application for the hydration of propargylic alcohols; Applied Catalysis B: Environmental; Vol. 310

Dades bibliogràfiques
Parent link:Applied Catalysis B: Environmental
Vol. 310.— 2022.— [121270, 14 p.]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Altres autors: Yongxing Zhang, Jia Hu, Xu Yong, Yan Xiangyu, Zhang Siqi, Duan Kang, Chen Cheng, Yuan Ye, Verpoort F. V. K. Frensis Valter Kornelius
Sumari:Title screen
An unexpected CO2-induced dissolution of ZnO into ionic liquids was discovered. This process exhibited high dissolution speed and the dissociated mixture was applied as an efficient Zn-based catalytic system for the CO2-promoted hydration of propargylic alcohols under atmospheric pressure with broad substrate scope. Moreover, this system could be recycled and reused for at least 16 times with excellent yields continuously obtained, which is an unprecedented record for this reaction. Significantly, this system could employ waste pigments as the ZnO source and work even under flue gas atmosphere. In the mechanistic investigations, the interaction between ZnO, CO2 and ionic liquids to give N-heterocyclic carbene/CO2 adducts proved to be the key factor for this specific dissolution. These adducts were further identified to exhibit better reactivity than the normal CO2 by experimental data and density functional theory (DFT) calculations, which might be responsible for the excellent performance of the abovementioned catalytic system.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2022
Matèries:
Accés en línia:https://doi.org/10.1016/j.apcatb.2022.121270
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=668886

MARC

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200 1 |a CO2-induced dissolution of ZnO into ionic liquids and its catalytic application for the hydration of propargylic alcohols  |f Yongxing Zhang, Jia Hu, Xu Yong [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 62 tit.] 
330 |a An unexpected CO2-induced dissolution of ZnO into ionic liquids was discovered. This process exhibited high dissolution speed and the dissociated mixture was applied as an efficient Zn-based catalytic system for the CO2-promoted hydration of propargylic alcohols under atmospheric pressure with broad substrate scope. Moreover, this system could be recycled and reused for at least 16 times with excellent yields continuously obtained, which is an unprecedented record for this reaction. Significantly, this system could employ waste pigments as the ZnO source and work even under flue gas atmosphere. In the mechanistic investigations, the interaction between ZnO, CO2 and ionic liquids to give N-heterocyclic carbene/CO2 adducts proved to be the key factor for this specific dissolution. These adducts were further identified to exhibit better reactivity than the normal CO2 by experimental data and density functional theory (DFT) calculations, which might be responsible for the excellent performance of the abovementioned catalytic system. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Applied Catalysis B: Environmental  
463 |t Vol. 310  |v [121270, 14 p.]  |d 2022 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a CO2 utilization 
610 1 |a Zn catalysis 
610 1 |a ionic liquids 
610 1 |a N-heterocyclic carbene/CO2 adducts 
610 1 |a a-Hydroxy ketones 
610 1 |a утилизация 
610 1 |a диоксид углерода 
610 1 |a катализ 
610 1 |a ионные жидкости 
610 1 |a аддукты 
610 1 |a N-гетероциклические карбены 
701 0 |a Yongxing Zhang 
701 0 |a Jia Hu 
701 0 |a Xu Yong 
701 0 |a Yan Xiangyu 
701 0 |a Zhang Siqi 
701 0 |a Duan Kang 
701 0 |a Chen Cheng 
701 0 |a Yuan Ye 
701 1 |a Verpoort  |b F. V. K.  |c Chemical Engineer  |c Professor of Tomsk Polytechnic University, doctor of chemical Sciences  |f 1963-  |g Frensis Valter Kornelius  |3 (RuTPU)RU\TPU\pers\35059  |9 18334 
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