4.7 Article

Iron-Organic Framework Nanoparticle-Supported Tungstosilicic Acid as a Catalyst for the Biginelli Reaction

Journal

ACS APPLIED NANO MATERIALS
Volume 5, Issue 11, Pages 16987-16995

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.2c03906

Keywords

MOF; heteropolyacid; heterogeneous catalyst; Biginelli reaction; dihydropyrimidinones

Funding

  1. Science and Technology Plan Project of Gansu Province [20YF8GA044]
  2. National Natural Science Foundation ofACS Applied Nano Materials China [21962017]
  3. Postgraduate Research Innovation Team Project of the Northwest Minzu University [Yxm2021004]
  4. Key Laboratory for Utility of Environmental Friendly Composite Materials and Biomass at the University of Gansu Province (Northwest Minzu University)

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In this study, a metal-organic framework with an octahedral morphology supported by a tungstosilicic acid (TSA) nanocatalyst was successfully synthesized. The hybrid material showed high catalytic activity due to the synergistic effect of exposed metal iron sites and the supported Bronsted acid sites. The environmentally friendly nano-catalyst could be recycled multiple times without significant loss in catalytic performance. This study also provides insights into the application of porous organic polymer functionalization in organic synthesis.
In this work, a metal-organic framework with an octahedral morphology supported by a tungstosilicic acid (TSA) nanocatalyst has been successfully synthesized through a post-synthetic modification approach and referred to as TSA/MIL-88B. The as-prepared catalyst was efficiently obtained from Biginelli reactions among benzaldehyde, urea, and 1,3-dicarbonyl compound. Depending on the synergistic effect of exposed metal iron sites and the supported Bronsted acid sites, the hybrid materials exhibited high catalytic activity. Additionally, the environmentally friendly nano-catalyst could be recycled seven times with a little reduction in the catalytic performance. This study also provides a way for the application of such porous organic polymer functionalization in organic synthesis.

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