| Literature DB >> 28039942 |
Rongchang Luo1, Yaju Chen1, Qian He1, Xiaowei Lin1, Qihang Xu1, Xiaohui He1, Wuying Zhang1, Xiantai Zhou2, Hongbing Ji1.
Abstract
A series of new metallosalen-based ionic porous organic polymers (POPs) were synthesized for the first time using a simple unique strategy based on the free-radical copolymerization reaction. Various techniques were used to characterize the physicochemical properties of these catalysts. These well-designed materials endowed high surface area, hierarchical porous structures, and enhanced CO2 /N2 adsorptive selectivity. Moreover, these POPs having both metal centers (Lewis acid) and ionic units (nucleophile) could serve as bifunctional catalysts in the catalytic conversion of CO2 into high value-added chemicals without any additional co-catalyst under mild and solvent-free conditions, for example, CO2 /epoxides cycloaddition and Nformylation of amines from CO2 and hydrosilanes. The results demonstrated that the irregular porous structure was very favorable for the diffusion of substrates and products, and the microporous structural property resulted in the enrichment of CO2 near the catalytic centers in the CO2 -involved transformations. Additionally, the superhydrophobic property could not only enhance the chemoselectivity of products but also promote the stability and recyclability of catalysts.Entities:
Keywords: bifunctional catalyst; carbon dioxide; ionic liquids; porous organic polymers; salen
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Year: 2017 PMID: 28039942 DOI: 10.1002/cssc.201601846
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928