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作 者:Munir Ullah Khan Safir Ullah Khan Jiraya Kiriratnikom Shah Zareen Xinghong Zhang
机构地区:[1]MOE Key Laboratory of Macromolecular Synthesis and Functionalization,Department of Polymer Science and Engineering,Zhejiang University,Hangzhou 310027,China [2]Hefei National Laboratory for Physical Science at the Microscale,School of Life Sciences,University of Science and Technology of China,Hefei 230027,China [3]National Synchrotron Radiation Laboratory,Department of Chemical Physics and Key Laboratory of Surface and Interface Chemistry and Energy Catalysis of Anhui Higher Education Institutes,University of Science and Technology of China,Hefei 230029,China
出 处:《Chinese Chemical Letters》2022年第2期1081-1086,共6页中国化学快报(英文版)
基 金:financial support of the National Natural Science Foundation of China (Nos.21774108 and 51973190)。
摘 要:The development of effective and low-energy-consumption catalysts for CO_(2)conversion into high-value-added products by constructing versatile active sites on the surface of heterogeneous compounds is an ur-gent and challenging task.In this study,a stable and well-defined heterogeneous cobalt hexacyanocobal-tate(Co_(3)[Co(CN)_(6)]_(2)),typical cobalt Prussian blue analogue(CoCo-PBA)modified with tetrabutylammo-nium bromide(TBAB),is proven to be the superior catalyst for CO_(2)and epoxide coupling to produce cyclic carbonates with>99%yield under mild reaction conditions(1.0 MPa,65℃).Based on a series of characterizations,it is revealed that the CoCo-PBA structure can maintain relatively high thermal and chemical stability.Recycling experiments exhibited that the CoCo-PBA system could retain 98%of the original activity after six reaction rounds.The CoCo-PBA/TBAB catalytic system was also highly active for coupling CO_(2)with other industrial-grade epoxides.These results show the Co Co-PBA catalytic system potential flexibility and the generality of the catalyst preparation strategy.
关 键 词:CO_(2)conversion Cyclic carbonates Prussian blue analogue Heterogeneous catalysis Co_(3)[Co(CN)_(6)]_(2)
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