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The Enzymatic Mediated Polymerization of Phenol and Aniline Derivatives on a Langmuir Trough

Published online by Cambridge University Press:  15 February 2011

Ferdinando F. Bruno
Affiliation:
Center for Advanced Materials, Department of Chemistry, University of Massachusetts-Lowell, Lowell, Massachusetts 01854.
Joseph A. Akkara
Affiliation:
Biotechnology Division, U.S. Army Natick Research, Development & Engineering Center, Natick, Massachusetts, 01760–5020
Lynne A. Samuelson
Affiliation:
Biotechnology Division, U.S. Army Natick Research, Development & Engineering Center, Natick, Massachusetts, 01760–5020
David L. Kaplan
Affiliation:
Biotechnology Division, U.S. Army Natick Research, Development & Engineering Center, Natick, Massachusetts, 01760–5020
Kenneth A. Marx
Affiliation:
Center for Advanced Materials, Department of Chemistry, University of Massachusetts-Lowell, Lowell, Massachusetts 01854.
Sukant K. Tripathy
Affiliation:
Center for Advanced Materials, Department of Chemistry, University of Massachusetts-Lowell, Lowell, Massachusetts 01854.
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Abstract

Enzymatic polymerization of a number of monomers in an ordered lattice on a Langmuir trough (L-T) was investigated. The assembly and polymerization of two mixed monomeric systems consisting of 4-tetradecyloxyphenol (C14PP) with phenol, and 4-hexadecylaniline (C16PA) with aniline, in various ratios were carried out. Polymerization was obtained with C14PP and phenol (in the ratio 1:10), and C16PA and aniline (in the ratio 1:2) on buffered MilliQ water (pH 7.5) using the enzyme horseradish peroxidase (HRP) at 20°C. Polymerized monolayers were then transferred to appropriate substrates for UV-Vis, third order non linear optical (NLO) properties, and thickness measurements. Thermogravimetric analysis (TGA) was performed on the final polymers. Results suggest that the lattice controlled polymerization results in highly ordered conjugated polymers with improved functional, electronic, NLO and processability properties, which form a basis for intelligent materials design and applications.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

1) Dordick, J., Marietta, M. A. and Klibanov, A. M., Biotechnol. Bioeng. 30, 31 (1987).Google Scholar
2) Akkara, J.A., Senecal, K.J. and Kaplan, D. L., J. Polym. Sci. Part A: Polym. Chem. 29, 1561 (1991).Google Scholar
3) Akkara, J. A., Bruno, F. F., Samuelson, L. A., Mandal, B., Kaplan, D. L., Marx, K. A. and Tripathy, S., U. S. Patent 5143828, (1992).Google Scholar
4) Gaines, G. L., in Insoluble Monolayers at Liquid-Gas Interfaces, Interscience Publishers edited by Prigogine, I., New York (1966).Google Scholar
5) Bruno, F. F., Akkara, J. A., Samuelson, L. A., Mandal, B., Kaplan, D. L., Marx, K. A. and Tripathy, S., Polymer Preprints - ACS Div. Poly. Chem. 32 (1), 232 (1991).Google Scholar
6) Allara, D. L., Nuzzo, R. G., Langmuir 1, 45 (1985).Google Scholar
7) Bruno, F. F., Akkara, J. A., Samuelson, L. A., Kaplan, D. L., Marx, K. A. and Tripathy, S., Proceedings of The First Intern. Confer. on Intel. Materials, Technomic Press, edited by Takagi, T., 78 (1992).Google Scholar
8) Ryu, K., Stafford, D. R. and Dordick, J. S., ACS Symposium Series 389, 141 (1989).Google Scholar