Ambient conversion of CO2 and epoxides to cyclic carbonates using 3D amide-functionalized MOFs

Zafar A.K. Khattak, Nazir Ahmad*, Hussein A. Younus, Habib Ullah, Baoyi Yu, Khurram S. Munawar, Muhammad Ashfaq, Muhammad Yaseen, Muhammad Danish, Mohammed Al-Abri, Rashid AlHajri, Francis Verpoort*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Metal(II)-carboxylate frameworks are an important class of MOF materials finding applications in gas storage, separation, sensing, catalysis, etc. Recently, their design, synthesis, and characterization have been established at a very...Metal(II)-carboxylate frameworks are an important class of MOF materials finding applications in gas storage, separation, sensing, catalysis, etc. Recently, their design, synthesis, and characterization have been established at a very high pace. Here two novel MOFs based on 5,5'-(([1,1'-biphenyl]-4,4'-dicarbonyl)bis(azanediyl))diisophthalic acid (H4L, an amide containing ligand) and transition metals (copper and zinc) are reported. Several characterization tools e.g., FT-IR, XRD, SEM, TGA, and XPS are used to characterize these MOFs. The single-crystal X-ray diffraction and Hirshfeld surface analyses are used to characterize the 3D structural framework. The voids and cavities analyses revealed the strength of the crystal packing. Both MOFs followed multistage thermogravimetric disintegration profiles. The solvent molecules escaped around 200 ⁰C and the structural changes due to decompositions in the frameworks continued till 500 °C. The morphological analysis for ZnMOF and CuMOF showed uniform wedge-shaped rectangular blocks and spherical balls with dimensions around 100 and 50 μm, respectively. Amide functionalized Zn(II)-carboxylate framework exhibited high catalytic activity (85->99%) towards the solvent-free cycloaddition of CO2 to different epoxides e.g., epichlorohydrin, propylene oxide, allyl glycidyl ether and glycidyl isopropyl ether with 100% selectivity under ambient conditions (i.e., 1 bar at 40 ⁰C in 24 h) at very low catalyst loading. By adjusting reaction conditions (T, P, and co-catalyst), the catalytic conversion reached 100% within only 2 hours. The results showed ZnMOF as a superior and efficient catalyst compared to other reported MOFs. Additionally, the catalyst can be easily recovered and regenerated for repeated use without performance loss.
Original languageEnglish
Pages (from-to)1888-1901
Number of pages14
JournalCatalysis Science and Technology
Volume14
Issue number7
DOIs
Publication statusPublished - Feb 7 2024

ASJC Scopus subject areas

  • Catalysis

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