Journal
CHEMSUSCHEM
Volume 7, Issue 7, Pages 1964-1969Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201400019
Keywords
biomass; coupling reaction; materials science; polymers; renewable resources
Funding
- Strategic Environmental Research and Development Program (SERDP) [WP-2214]
- Office of Naval Research In-House Laboratory Independent Research Program
Ask authors/readers for more resources
A renewable bisphenol, 4,4'-(butane-1,4-diyl)bis(2-methoxyphenol), was synthesized on a preparative scale by a solvent-free, Ru-catalyzed olefin metathesis coupling reaction of eugenol followed by hydrogenation. After purification, the bisphenol was converted to a new bis(cyanate) ester by standard techniques. The bisphenol and cyanate ester were characterized rigorously by NMR spectroscopy and single-crystal X-ray diffraction studies. After complete cure, the cyanate ester exhibited thermal stability in excess of 350 degrees C and a glass transition temperature (T-g) of 186 degrees C . As a result of the four-carbon chain between the aromatic rings, the thermoset displayed a water uptake of only 1.8% after a four day immersion in 85 degrees C water. The wet T-g of the material (167 degrees C) was only 19 degrees C lower than the dry T-g, and the material showed no significant degradation as a result of the water treatment. These results suggest that this resin is well suited for maritime environments and provide further evidence that full-performance resins can be generated from sustainable feedstocks.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available