Core-shell metal-organic frameworks and metal functionalization to access highest efficiency in catalytic carboxylation; Journal of Catalysis; Vol. 371

Dades bibliogràfiques
Parent link:Journal of Catalysis
Vol. 371.— 2019.— [P. 106-115]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Altres autors: Gong Yanyan, Yuan Ye, Chen Cheng, Zhang Pan, Wang Jichao, Zhuiykov S. Serge, Chaemchuen S. Somboon, Verpoort F. V. K. Frensis Valter Kornelius
Sumari:Title screen
A core-shell metal-organic frameworks (MOF@MOF) based on the Zr-MOFs assembly from core-structure UiO-66 combined with shell-structure UiO-67-BPY were explored. The synthesized materials were characterized via XRD, FTIR, SEM, TEM, and surface area analysis, etc. indicating the presence of a core-shell structure of UiO-66@UiO-67-BPY. Furthermore, incorporation of the bipyridinic (BPY) group in the linker used to construct the shell layer (UiO-67-BPY) could coordinate with active metal species and thus create an advantage for site-selective metal incorporation in the core-shell structure. Silver (Ag) was selected for the selective metal incorporation and an excellent Ag-dispersion via coordination with the bipyridinic groups in the UiO-67-BPY layer of the core-shell material was obtained. The synthesized material (UiO-66@UiO-67-BPY-Ag) was successfully applied as a heterogeneous catalyst for the CO2 fixation via carboxylation of terminal alkynes. The catalytic material showed excellent yields using at a low Ag-loading under mild reaction condition (50?°C, 1?bar). Moreover, the catalyst can be recycled for at least 5 times maintaining a stable catalytic performance. Interestingly, the high catalytic activity of the synthesized material demonstrated clearly the beneficial advantage of the metalated core-shell structure over the reported routes to synthesize silver catalysts such as encapsulated Ag nanoparticles (AgNP@MOF) or Ag-bidentately coordinated on traditional MOFs applying the same reaction model.
Режим доступа: по договору с организацией-держателем ресурса
Idioma:anglès
Publicat: 2019
Matèries:
Accés en línia:https://doi.org/10.1016/j.jcat.2019.01.036
Format: MixedMaterials Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=660257

MARC

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200 1 |a Core-shell metal-organic frameworks and metal functionalization to access highest efficiency in catalytic carboxylation  |f Gong Yanyan [et al.] 
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300 |a Title screen 
320 |a [References: 74 tit.] 
330 |a A core-shell metal-organic frameworks (MOF@MOF) based on the Zr-MOFs assembly from core-structure UiO-66 combined with shell-structure UiO-67-BPY were explored. The synthesized materials were characterized via XRD, FTIR, SEM, TEM, and surface area analysis, etc. indicating the presence of a core-shell structure of UiO-66@UiO-67-BPY. Furthermore, incorporation of the bipyridinic (BPY) group in the linker used to construct the shell layer (UiO-67-BPY) could coordinate with active metal species and thus create an advantage for site-selective metal incorporation in the core-shell structure. Silver (Ag) was selected for the selective metal incorporation and an excellent Ag-dispersion via coordination with the bipyridinic groups in the UiO-67-BPY layer of the core-shell material was obtained. The synthesized material (UiO-66@UiO-67-BPY-Ag) was successfully applied as a heterogeneous catalyst for the CO2 fixation via carboxylation of terminal alkynes. The catalytic material showed excellent yields using at a low Ag-loading under mild reaction condition (50?°C, 1?bar). Moreover, the catalyst can be recycled for at least 5 times maintaining a stable catalytic performance. Interestingly, the high catalytic activity of the synthesized material demonstrated clearly the beneficial advantage of the metalated core-shell structure over the reported routes to synthesize silver catalysts such as encapsulated Ag nanoparticles (AgNP@MOF) or Ag-bidentately coordinated on traditional MOFs applying the same reaction model. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Catalysis 
463 |t Vol. 371  |v [P. 106-115]  |d 2019 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a MOF@MOF 
610 1 |a core-shell structure 
610 1 |a heterogeneous catalysis 
610 1 |a carboxylation 
610 1 |a CO2 fixation 
610 1 |a propiolic acids 
610 1 |a гетерогенный катализ 
610 1 |a карбоксилирование 
701 0 |a Gong Yanyan 
701 0 |a Yuan Ye 
701 0 |a Chen Cheng 
701 0 |a Zhang Pan 
701 0 |a Wang Jichao 
701 1 |a Zhuiykov  |b S.  |g Serge 
701 0 |a Chaemchuen  |b S.  |c chemist-technologist  |c researcher at Tomsk Polytechnic University  |f 1984-  |g Somboon  |3 (RuTPU)RU\TPU\pers\42620 
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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