Ruthenium-catalyzed dimerization of vanillin for the formation of a biobased epoxy thermoset resin
Journal article, 2025

Vanillin is one of few lignin platform chemicals that are currently available on industrial scale. Seeking to find biobased alternatives to the reprotoxic compound bisphenol A (BPA), we have successfully dimerized three different monomeric vanillin derivatives in a ruthenium-catalyzed Tischenko reaction. The resulting esters were characterized by NMR, FTIR, HRMS, and single crystal X-ray diffraction. The thermal behaviour of one of these derivatives, the epoxy divanillin ester EDVE, was studied further by DSC and TGA. EDVE was subsequently applied towards the preparation of an epoxy thermoset resin via curing with Jeffamine D-400. The thermoset formulation was thermally cured, monitoring the curing with DSC and FTIR. The final thermoset was then characterized with respect to physical and mechanical properties with DSC, TGA, and DMA. This catalytic approach provides a new strategy to access vanillin-based epoxides that could potentially replace bisphenol A.

Author

Flavia Ferrara

Chemistry and Biochemistry Phd Students and Postdocs

Iuliana Ribca

Royal Institute of Technology (KTH)

Namratha Prabhu

Student at Chalmers

Josselin Mante

Maureen Gumbo

Chemistry and Biochemistry Phd Students and Postdocs

Andreas Ekebergh

Chalmers, Chemistry and Chemical Engineering, Chemistry and Biochemistry

Mats Johansson

Royal Institute of Technology (KTH)

Nina Kann

Chalmers, Chemistry and Chemical Engineering, Chemistry and Biochemistry

RSC Sustainability

27538125 (eISSN)

Vol. In Press

Subject Categories (SSIF 2025)

Polymer Chemistry

Organic Chemistry

Polymer Technologies

DOI

10.1039/d5su00165j

More information

Latest update

5/5/2025 5