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dc.contributor.authorPatrickios, Costas S.en
dc.contributor.authorSimmons, M. R.en
dc.creatorPatrickios, Costas S.en
dc.creatorSimmons, M. R.en
dc.date.accessioned2019-11-21T06:22:10Z
dc.date.available2019-11-21T06:22:10Z
dc.date.issued2000
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55997
dc.description.abstractImidazole-containing polymers were prepared and characterized in terms of their hydrolytic activity. Unlike similar materials synthesized in the 1960s, the polymers are of precise molecular weight and controlled structure (random or block) afforded by the group transfer polymerization (GTP) chemistry used in the synthetic procedure. The size and composition of the copolymers were determined by gel permeation chromatography (GPC) and proton nuclear magnetic resonance spectroscopy, respectively. Aqueous solutions of the polymers were evaluated in terms of their ability to hydrolyze 4-nitrophenyl acetate. The effects of pH, polymer concentration, substrate concentration, polymer size, and structure were investigated and discussed with reference to the nucleophilicity of imidazole and the self-assembly of the block copolymers into micelles. A series of model networks based on imidazole homopolymers were also prepared and characterized in terms of their aqueous degree of swelling. Copyright (C) 2000 Elsevier Science B.V. Imidazole-containing polymers were prepared and characterized in terms of their hydrolytic activity. Unlike similar materials synthesized in the 1960s, the polymers are of precise molecular weight and controlled structure (random or block) afforded by the group transfer polymerization (GTP) chemistry used in the synthetic procedure. The size and composition of the copolymers were determined by gel permeation chromatography (GPC) and proton nuclear magnetic resonance spectroscopy, respectively. Aqueous solutions of the polymers were evaluated in terms of their ability to hydrolyze 4-nitrophenyl acetate. The effects of pH, polymer concentration, substrate concentration, polymer size, and structure were investigated and discussed with reference to the nucleophilicity of imidazole and the self-assembly of the block copolymers into micelles. A series of model networks based on imidazole homopolymers were also prepared and characterized in terms of their aqueous degree of swelling.en
dc.sourceColloids and Surfaces A: Physicochemical and Engineering Aspectsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0033954029&doi=10.1016%2fS0927-7757%2899%2900483-5&partnerID=40&md5=6269fc87a02cb995acb3b47037444610
dc.subjectmodelen
dc.subjectarticleen
dc.subjectpriority journalen
dc.subjectmolecular weighten
dc.subjectSolubilityen
dc.subjectMicellesen
dc.subjectsynthesisen
dc.subjectNetworksen
dc.subjectBlock copolymersen
dc.subjectHomopolymerizationen
dc.subjectSwellingen
dc.subjectpolyelectrolyteen
dc.subjectPolymethyl methacrylatesen
dc.subjectaqueous solutionen
dc.subjectpolymeren
dc.subjectpHen
dc.subjectHomopolymersen
dc.subject2-(Dimethylamino)ethyl methacrylateen
dc.subjectcopolymeren
dc.subjectGroup transfer polymerizationen
dc.subjectmethacrylic acid derivativeen
dc.subjectproton nuclear magnetic resonanceen
dc.subjectpolymerizationen
dc.subjectConcentration (process)en
dc.subjectmicelleen
dc.subjectCatalysisen
dc.subjectMicellizationen
dc.subjectPolyelectrolytesen
dc.subjectHydrolysisen
dc.subjectGel permeation chromatographyen
dc.subjectpH effectsen
dc.subjectMolecular structureen
dc.subjectWater-soluble polymersen
dc.subjectWeak polyelectrolytesen
dc.subject2-(1-Imidazolyl)ethyl methacrylateen
dc.subject4-Nitrophenyl acetateen
dc.subjectDimethylaminoethyl methacrylateen
dc.subjectEnzyme mimicsen
dc.subjectimidazoleen
dc.subjectImidazolylethyl methacrylateen
dc.subjectNitrophenyl acetateen
dc.titleSynthesis and aqueous solution characterization of catalytically active homopolymers, block copolymers and networks containing imidazoleen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/S0927-7757(99)00483-5
dc.description.volume167
dc.description.issue1-2
dc.description.startingpage61
dc.description.endingpage72
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Manufacturers: Aldrich, United Kingdomen
dc.description.notesCited By :30</p>en
dc.source.abbreviationColloids Surf.A Physicochem.Eng.Asp.en
dc.contributor.orcidPatrickios, Costas S. [0000-0001-8855-0370]
dc.gnosis.orcid0000-0001-8855-0370


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