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CO2 cycloaddition reaction at ambient temperature and pressure over metal organic framework catalysts

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Abstract

Valorisation of CO2 via cycloaddition reactions to value added cyclic carbonates is a desirable, however, challenging technique owing to the chemical and thermodynamic stability of CO2. Here, we report synthesis of Cr-based MIL-101 MOF and postsynthetic incorporation of Brønsted acid groups as active site for catalytic production of cyclic carbonate from CO2 and epoxide. For CO2 cycloaddition reaction with propylene oxide to yield cyclic carbonate, MIL-101(Cr)-N(CH2PO3H2)2 outperformed the pristine MIL-101(Cr)–NH2, while MIL-101(Cr)-NH(CH2)3-SO3H deteriorated the catalytic activity. The catalytic efficacy was found to be depending on active sites, surface areas and pore sizes of the synthesized MOFs.

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Data availability

The data that support the findings of this study are available on request from the authors.

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Acknowledgments

SR thanks SERB (Grant No. CRG/2022/000517) for the financial help.

Funding

Birla Institute of Technology and Science, Pilani.

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Authors and Affiliations

  1. Department of Chemistry, Birla Institute of Technology and Science (BITS) Pilani, Hyderabad Campus, Hyderabad, 500078, India

    Soumitra Payra & Sounak Roy

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  1. Soumitra Payra
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  2. Sounak Roy
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Contributions

SP: investigation, data curation, validation, Writing-original draft. SR: conceptualization, writing-review & editing.

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Correspondence to Sounak Roy.

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Payra, S., Roy, S. CO2 cycloaddition reaction at ambient temperature and pressure over metal organic framework catalysts. MRS Communications 13, 1309–1314 (2023). https://doi.org/10.1557/s43579-023-00456-w

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