Thomas E. Karis, C. Mark Seymour, et al.
Rheologica Acta
A novel family of functionalized polystyrenes that can undergo base-catalyzed intramolecular side-chain imidization is reported. The thermal behaviors of poly(4-vinylphenyl succinamate), poly(4-vinylphenyl glutaramate), poly(4-vinylphenyl 3,3-dimethylglutaramate), and poly(4-vinylphenyl phthalamate), as well as their optical properties and chemical reactivities in the presence of an added amine have been studied. With the exception of poly(4-vinylphenyl phthalamate), the polymers are thermally stable up to 200 °C and have a relatively low optical density below 300 nm. A general trend for the ease of imidization of the polymers is summarized as follows: poly(4-vinylphenyl phthalamate) > poly(4-vinylphenyl succinamate) > poly(4-vinylphenyl 3,3-dimethylglutaramate) > poly(4-vinylphenyl glutaramate). Photoactive polymer systems were obtained by mixing either poly(4-vinylphenyl succinamate) or poly(4-vinylphenyl 3,3-dimethylglutaramate) with some bis((2,6-dinitrobenzyl)oxycarbonyl)hexane-1,6-diamine used as an amine photogenerator. Imaging of films of the polymers, as well as the effect of structure on their reactivity is discussed. © 1995, American Chemical Society. All rights reserved.
Thomas E. Karis, C. Mark Seymour, et al.
Rheologica Acta
Thomas H. Baum, Carl E. Larson, et al.
Journal of Organometallic Chemistry
Michael Ray, Yves C. Martin
Proceedings of SPIE - The International Society for Optical Engineering
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Journal of Applied Mechanics, Transactions ASME