4.7 Article

Construction of hexanuclear Ce(III) metal-porphyrin frameworks through linker induce strategy for CO2 capture and conversion

Journal

CATALYSIS TODAY
Volume 374, Issue -, Pages 38-43

Publisher

ELSEVIER
DOI: 10.1016/j.cattod.2020.12.038

Keywords

Metal-organic frameworks (MOFs); Linker induce strategy; CO2

Funding

  1. National Natural Science Foundation of China [NSFC21701187]
  2. Natural Science Basic Research Program of Shaanxi [2020JQ-142]
  3. Ningbo Natural Science Foundation [202003N4066]
  4. Fundamental Research Funds for the Central Universities [31020180QD115]

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In this study, a series of hexanuclear rare-earth MOFs based on Ce (III) and 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin are reported, with Ce-PCN-224 showing a new zln topology through linker induce strategy. Ce-PCN224 exhibits permanent porosity, high water and thermal stabilities, and the ability to adsorb dye molecules in the aqueous environment. Additionally, Ce-PCN-224(Fe) and Ce-PCN224(Co) were proved to be efficient heterogeneous catalysts for the cycloaddition of CO2 with epoxides after post-metallation with Fe, Co, and Ni, attributed to the combination of multiple Lewis acidic sites.
In this article, we report a series of hexanuclear rare-earth MOFs based on Ce (III) and 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin, namely Ce-PCN-224, with a new zln topology through linker induce strategy. Ce-PCN224 exhibits permanent porosity, high water and thermal stabilities, and the ability to adsorb dye molecules in the aqueous environment. Moreover, after post-metallation with Fe, Co, and Ni, Ce-PCN-224(Fe) and Ce-PCN224(Co) were proved to be efficient heterogeneous catalysts for the cycloaddition of CO2 with epoxides, attributed to the combination of multiple Lewis acidic sites.

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