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Published on: November 9, 2019
A Triple-Catalytic, Fully Biogenic Synthesis of Cyclic Carbonates
Robin Stuhr1, Leon Liu1, Axel Jacobi von Wangelin1
1Department of Chemistry, University of Hamburg, Hamburg, Germany.
This study introduces a sustainable method for creating cyclic carbonates from natural resources using a triple-catalytic process. These biogenic carbonates offer a green route to non-isocyanate polyurethanes.
Area of Science:
- Green chemistry and sustainable synthesis of organic carbonates.
- Catalysis and materials science.
Background:
- Organic carbonates are key platform molecules in chemical manufacturing.
- Current methods for cyclic carbonate synthesis often rely on unsustainable epoxide precursors.
- Green chemistry principles emphasize atom-economical and mild reaction conditions.
Purpose of the Study:
- To develop a highly sustainable triple-catalytic approach for synthesizing biogenic cyclic carbonates.
- To utilize all-natural building blocks for carbonate production.
- To demonstrate the application of these carbonates in creating environmentally benign polyurethanes.
Main Methods:
- A triple-catalytic system combining fatty acid derivatives, oxygen (O2), and carbon dioxide (CO2).
- Utilized catalysts include porphyrin, VO(acac)2, and pyridine.
- Key step involves photo-oxygenation for full O2 incorporation into hydrocarbons.
Main Results:
- Achieved 100% atom-economy in the formation of biogenic cyclic carbonates from natural resources.
- Successfully demonstrated a sustainable pathway bypassing traditional epoxide synthesis.
- Synthesized environmentally benign non-isocyanate polyurethanes using the novel cyclic carbonates.
Conclusions:
- The developed triple-catalytic method offers a sustainable and atom-economical route to biogenic cyclic carbonates.
- This approach aligns with green chemistry principles by using readily available, natural feedstocks.
- The synthesized cyclic carbonates are valuable precursors for sustainable polymer production, specifically non-isocyanate polyurethanes.
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