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Last updated January 31, 2026
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Cyclic monothiocarbonate polymer networks: BASFRecent Research Landscape

Traditional isocyanate-based urethane synthesis poses significant toxicity risks and moisture sensitivity during application. These innovations utilize ethylenically unsaturated monothiocarbonate monomers to enable a safer, non-isocyanate pathway for high-performance coatings.

What technical problems is BASF addressing in Cyclic monothiocarbonate polymer networks?

Inefficient sulfur functionalization pathways

(8)evidences

Inefficient chemical pathways for integrating sulfur into stable polymer architectures. Overcoming this limitation enables the production of high-refractive index materials with controlled thermal properties.

Hazardous phosgene dependence

(3)evidences

Conventional polyurethane synthesis relies on hazardous isocyanates that react prematurely with environmental humidity. Utilizing cyclic monothiocarbonates enables high-performance thermosets without toxic precursors or moisture-induced defects.

Limited non-isocyanate monomer diversity

(2)evidences

Difficulty in accessing high-purity cyclic carbonate precursors with reactive exocyclic groups. Streamlining this synthesis reduces production costs and enables functional polymer architectures.

Limited polymer chain end-functionalization

(2)evidences

Conventional polyurethane synthesis relies on hazardous isocyanate chemistry which poses severe health and environmental risks. Utilizing cyclic monothiocarbonates provides a non-toxic pathway to high-performance networks.