Share Email Print
cover

Proceedings Paper

Triplet-sensitized reactions of some main chain liquid-crystalline polyaryl cinnamates
Author(s): P. Subramanian; David Creed; Charles E. Hoyle; Krishnan Venkataram
Format Member Price Non-Member Price
PDF $14.40 $18.00

Paper Abstract

Thin films of a liquid crystalline polyaryl cinnamate have been irradiated at (lambda) > 400 nm in the presence of ketocoumarin triplet sensitizers. The aryl cinnamate chromophore disappears upon irradiation with concomitant loss of solubility attributed to cross-linking by interchain cyclobutane photoproduct formation. Competing loss of sensitizer absorption also occurs during irradiation. Up to ca. 80% of the aryl cinnamate chromophores in amorphous films can be destroyed using high weight percentages (>= 5%) of sensitizer. At low concentrations of sensitizer (0.5 wt.%), approximately 80 cinnamate chromophores are photolyzed for each sensitizer molecule initially present, despite the competing photolysis of sensitizer during the course of irradiation. The ketocoumarins are insoluble in the glassy (frozen) nematic films of the polymer and thus are ineffective in sensitizing photolysis in this more organized phase.

Paper Details

Date Published: 1 December 1991
PDF: 9 pages
Proc. SPIE 1559, Photopolymer Device Physics, Chemistry, and Applications II, (1 December 1991); doi: 10.1117/12.50695
Show Author Affiliations
P. Subramanian, Univ. of Southern Mississippi (United States)
David Creed, Univ. of Southern Mississippi (United States)
Charles E. Hoyle, Univ. of Southern Mississippi (United States)
Krishnan Venkataram, Univ. of Southern Mississippi (United States)


Published in SPIE Proceedings Vol. 1559:
Photopolymer Device Physics, Chemistry, and Applications II
Roger A. Lessard, Editor(s)

© SPIE. Terms of Use
Back to Top