BIOLOGICALLY DERIVED PHOTOACTIVE MACROMOLECULAR AZODYES
Azophenols with various substituents at the para position of the phenyl ring were enzymatically polymerized in the presence of H 2 O 2 . Structural characterization of the synthesized polymers by FTIR, FT-Raman, and NMR ( 1 H and 13 C) spectroscopy confirms our previous observation that this enzymat...
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Published in: | Journal of macromolecular science. Part A, Pure and applied chemistry Vol. 38; no. 12; pp. 1355 - 1370 |
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Main Authors: | , , , , , , , |
Format: | Journal Article Conference Proceeding |
Language: | English |
Published: |
Colchester
Taylor & Francis Group
01-01-2001
Taylor & Francis |
Subjects: | |
Online Access: | Get full text |
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Summary: | Azophenols with various substituents at the para position of the phenyl ring were enzymatically polymerized in the presence of H
2
O
2
. Structural characterization of the synthesized polymers by FTIR, FT-Raman, and NMR (
1
H and
13
C) spectroscopy confirms our previous observation that this enzymatically catalyzed coupling reaction occurs primarily at the ortho positions, with some substitution at the meta position of the phenol ring. The strong constraint and poor packing of the azobenzene chromophores in the polymer leads to a significant blue shift of the π-π
*
transition absorption and slow photoisomerization and thermal relaxation in comparison to the monomers. Surface relief gratings (SRG) with large surface modulation have been fabricated on these enzymatically synthesized polymer films.
†
Deceased. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 1060-1325 1520-5738 |
DOI: | 10.1081/MA-100108390 |