2012
DOI: 10.1007/s10965-012-0028-x
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Activated polymers. II: Synthesis and exchange reactions of biologically active poly(8-acryloxyquinoline)

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Cited by 6 publications
(1 citation statement)
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“…By free radical polymerization, 8-acryloxyquinoline (8-AQ) monomer was prepared through the reaction of 8-hydroxyquinoline with either acryloyl chloride or acrylic acid in the presence of triethylamine or N, N-dicyclohexylcarbodiimide. The antimicrobial activity of all compounds demonstrated moderate to good activity against the tested strains providing wider possibilities for the synthesis of pharmacologically active polymers [8]. Improved polymerizations of monomers bearing electron transporting substituents based on 2,5-diphenyloxadiazole and 2,3-diphenylquinoxaline attached directly to a vinyl group were reported, these materials have been incorporated into light emitting polymer devices in which hole conduction properties are provided by 4-vinyltriphenylamine groups for usage in optimized devices [9].…”
Section: Introductionmentioning
confidence: 98%
“…By free radical polymerization, 8-acryloxyquinoline (8-AQ) monomer was prepared through the reaction of 8-hydroxyquinoline with either acryloyl chloride or acrylic acid in the presence of triethylamine or N, N-dicyclohexylcarbodiimide. The antimicrobial activity of all compounds demonstrated moderate to good activity against the tested strains providing wider possibilities for the synthesis of pharmacologically active polymers [8]. Improved polymerizations of monomers bearing electron transporting substituents based on 2,5-diphenyloxadiazole and 2,3-diphenylquinoxaline attached directly to a vinyl group were reported, these materials have been incorporated into light emitting polymer devices in which hole conduction properties are provided by 4-vinyltriphenylamine groups for usage in optimized devices [9].…”
Section: Introductionmentioning
confidence: 98%