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Synthesis and radical polymerization of novel vinyl monomers having the imidazoline and pyrimidine moiety

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dc.contributor.author Seçkin, T.
dc.contributor.author Alici, B.
dc.contributor.author Çetinkaya, E.
dc.contributor.author Özdemir, I.
dc.date.accessioned 2022-10-06T09:35:30Z
dc.date.available 2022-10-06T09:35:30Z
dc.date.issued 1996
dc.identifier.issn 01700839 (ISSN)
dc.identifier.uri http://hdl.handle.net/11616/62891
dc.description.abstract Alkylation of the methylene bridged tetrahydropyrimidine derivatives by chloromethylstyrene produces the bridged bis(4-vinylbenzyl)-1,4,5,6,-tetrahydropyrimidinium salts in high yields. Similar procedures are used to prepare 2-imidazolinium derivatives. The quaternary salts which support functional side groups of potential biomedical interest are characterized by means of spectroscopic methods. These monomers are readily polymerized free radically in solution of dimethyl formamide at moderate temperatures. The soluble and insoluble polymers containing 2-imidazolinium and 1,4,5,6-tetrahydropyrimidinium salts were found to exhibit antibacterial activites against Escberichia coli.
dc.source Polymer Bulletin
dc.title Synthesis and radical polymerization of novel vinyl monomers having the imidazoline and pyrimidine moiety


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