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Novel Templated Polyphenol for Ionic Conductivity

Published online by Cambridge University Press:  14 March 2011

Ferdinando F. Bruno
Affiliation:
Materials Science Team, Natick Soldier Center, U.S. Army Soldier and Biological, Chemical Command, Natick, MA 01760
Ramaswamy Nagarajan
Affiliation:
Departments of Physics and Chemistry, Center for Advanced Materials, University of Massachusetts Lowell, Lowell, MA 01854
Jayant Kumar
Affiliation:
Departments of Physics and Chemistry, Center for Advanced Materials, University of Massachusetts Lowell, Lowell, MA 01854
Lynne A. Samuelson
Affiliation:
Materials Science Team, Natick Soldier Center, U.S. Army Soldier and Biological, Chemical Command, Natick, MA 01760
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Abstract

Phenolic polymers and phenol formaldehyde resins are of great interest for a number of electronic and industrial applications. Unfortunately, the toxic nature of the starting materials (formaldehyde) and harsh reaction conditions required for the synthesis of these polymers have severely limited their use in today’s markets. We present here an alternative, biocatalytic approach where the enzyme horseradish peroxidase is used to polymerize phenol in the presence of a template such as polyethylene oxide. Here the template serves as a surfactant that can both emulsify the phenol and polyphenol chains during polymerization and maintain water/solvent solubility of the final polyphenol/template complex. The reactants and the reaction conditions of this approach are mild and result in high molecular weight, electrically and optically active, water-soluble complexes of polyphenol and the template used. High molecular weight water-soluble polyphenol/polyethylene oxide complexes were formed. The ionic conductivity and potential use of these polymers as polyelectrolytes for battery and solution cell applications will be discussed.

Type
Research Article
Copyright
Copyright © Materials Research Society 2002

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References

REFERENCES

1. Brode, G. L.V, in Kirk-Othmer Encyclopedia of Chemical Technology, (John Wiley & Sons, New York, NY, 1982), 17, 384.Google Scholar
2. White, D. M., Cooper, G. D., in Kirk-Othmer Encyclopedia of Chemical Technology, (John Wiley & Sons, New York, NY, 1982), 18, 594.Google Scholar
3. Clary, J. J., Gibson, J. E., Waritz, R. S., in Formaldehyde: Toxicology, Epidemiology, Mechanisms, (Decker New York, NY, 1983).Google Scholar
4. Akkara, J. A., Senecal, K. J., Kaplan, D. L., J. Polym. Sci. Part A: Polym. Chem., 29, 1561 (1991).Google Scholar
5. Dordick, J. S., Marletta, M. A., Klibanov, A. M., Biotechnol. Bioeng., 30, 31 (1987).Google Scholar
6. Kobayashi, S., Ikeda, R., Sugihara, J., Macromolecules, 29, 8702 and ref. in the paper (1996).Google Scholar
7. Rao, M., John, V. T., Gonzalez, R. D., Akkara, J. A., Kaplan, D. L., Biotechnol. Bioeng., 41, 531 (1993).Google Scholar
8. Bruno, F. F., Akkara, J. A., Samuelson, L. A., Kaplan, D. L., Mandal, B. K., Marx, K. A., Kumar, J., Tripathy, S., Langmuir, 11, 889 (1995).Google Scholar
9. Bruno, F. F., Nagarajan, R., Sidhartha, J. S., Yang, K., Kumar, J., Tripathy, S., Samuelson, L., Mater. Res. Soc. Symp. Proc., 600, 255 (2000).Google Scholar
10. Liu, W., Kumar, J., Tripathy, S., Senecal, K., Samuelson, L., J. Am. Chem. Soc. 121, 71 (1999).Google Scholar
11.W Liu, Choli, A. L., Nagarajan, R., Bruno, F. F., Kumar, J., Tripathy, S. K., Samuelson, L., J. Am. Chem. Soc., 121, 11345 (1999).Google Scholar
12. Higashimura, H., Fujisawa, K., Y. Moro-oka, Kubota, M., Shiga, A., Terahara, A., Uyama, H., Kobayashi, S., J. Am. Chem. Soc. 120, 8529 (1998).Google Scholar
13. Sperling, L. H. Physical Polymer Science, (John Wiley & Sons; New York, NY, 1996) pp.394.Google Scholar