Search results for "Addition polymer"

showing 10 items of 114 documents

1976

A number of acryl and methacryl derivatives of different sulfanilamides (1a—I) were prepared and polymerized. The fixation of the sulfonamide to the polymerizable group was carried out directly, using the acryl- and methacrylamides, and by means of spacer groups, to favour the enzymatic or hydrolytic release of the drug moiety. Selected sulfonamide types of different pKA values were used, and the pH-dependant solubility of the corresponding polymers was studied. The monomeric acryloyl and methacryloyl sulfonamides were homopolymerized radically by AIBN. For distribution studies polysulfadiazineacrylamide, 14C-labelled in the main chain (2e'), was synthesized. Copolymerization with 2-methyls…

chemistry.chemical_classificationSulfanilamideMethacrylateBiodegradable polymerSulfonamidechemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymer chemistrymedicineCopolymerMoietymedicine.drugDie Makromolekulare Chemie
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Ylide als polymerisationsinitiatoren. I. Salzhaltige und salzfreie phosphoniumylide

1972

Phosphorylide, R3PCHX und R3PCH2·LiBr, konnen eine anionische Polymerisation von Vinylmonomeren starten. Dabei werden im Falle des Methacrylnitrils und des Methylmethacrylats die Ylide als Endgruppen in die Polymeren eingebaut. Bei den salzfreien Yliden hangt die Startwirksamkeit von der Basizitat des Ylidcarbanions ab, die Struktur dieser Ylide hat aber keinen mesbaren Einflus auf das Molekulargewicht und die Taktizitat der entstehenden Polymeren. Im Gegensatz dazu wird bei der Initiierung mit den salzhaltigen Yliden auch die Taktizitat der Polymeren von den Substituenten der Phosphorylide beeinflust. Phosphorous ylids, R3PCHX and R3PCH2·LiBr, are able to start an anionic polymerization of…

chemistry.chemical_classificationchemistry.chemical_compoundAnionic addition polymerizationMonomerPolymerizationChemistryYlideTacticityPolymer chemistryPolymerDie Makromolekulare Chemie
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1981

chemistry.chemical_classificationchemistry.chemical_compoundAnionic addition polymerizationchemistrySodiumKineticsPolymer chemistrychemistry.chemical_elementOrganic chemistryCounterionMethyl methacrylateTetrahydrofuranLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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1991

Telechelic α,ω-macrozwitterions — narrowly distributed polystyrene chains oppositely charged at each end — were synthesized via anionic polymerization using direct functionalization with the initiator and the termination agent. The resulting products were purified (zwitterion content ≥ 0,95) and characterized with gel permeation chromatography, viscometry, static and dynamic light scattering and small-angle neutron scattering. In unpolar solvents as toluene, the polymeric zwitterions form clusters with molecular weights depending on concentration. In the dilute case, the clusters are relatively small and consist of approximately 8 zwitterions. The structure of these clusters is discussed by…

chemistry.chemical_classificationchemistry.chemical_compoundEnd-groupTelechelic polymerAnionic addition polymerizationchemistryDynamic light scatteringZwitterionPolymer chemistryPolymerPolystyreneSmall-angle neutron scatteringDie Makromolekulare Chemie
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Electrochemical production of initiators for polymerization processes

2007

The most important technological interest in initiator production lies, in the electrosynthesis of complex catalytic systems, i. e. coordination compounds and Ziegler-Natta catalysts, although the choice of olefins to be polymerized with these electrosynthesized complexes is still limited to ethylene and to very few other monomers.

chemistry.chemical_classificationchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationCationic polymerizationReversible addition−fragmentation chain-transfer polymerizationIonic polymerizationElectrosynthesisCombinatorial chemistryCoordination complex
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Synthesis and thermoresponsive properties of four arm, amphiphilic poly(tert-butyl-glycidylether)-block-polyglycidol stars

2011

Abstract A series of four arm stars with copolymer arms composed of poly(tert-butyl-glycidylether)-b-polyglycidol were prepared using a multi-step process based on anionic ring-opening polymerization. Control of the length of the arms and the number of functional (hydroxyl) reactive groups was achieved by anionic polymerization. Stars with molar masses up to 12200 g/mol were prepared. The amphiphilic character of the star structure was varied using different polyglycidol block lengths. The star structure and molar mass of the obtained stars were characterized by SEC–MALLS and NMR spectroscopy. The temperature behavior of an aqueous solution of the obtained polymers was also investigated. Th…

chemistry.chemical_classificationendocrine systemMaterials scienceMolar massAqueous solutionPolymers and PlasticsOrganic ChemistryNuclear magnetic resonance spectroscopyPolymerAnionic addition polymerizationchemistryPolymerizationAmphiphilePolymer chemistryMaterials ChemistryCopolymerPolymer
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1980

chemistry.chemical_compoundAnionic addition polymerizationChemistryKineticsPolymer chemistryMethyl methacrylateIonic polymerizationPhotochemistryDimethoxyethaneLiving anionic polymerizationDie Makromolekulare Chemie, Rapid Communications
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1974

chemistry.chemical_compoundAnionic addition polymerizationMonomerReaction rate constantChemistryPolymer chemistryMethyl methacrylateDie Makromolekulare Chemie
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1978

A newly designed automatically controlled stirred reactor suitable for kinetic measurements of reactions with half lives ≥2s has been applied to follow the anionic polymerization of methyl methacrylate in THF with Na+ as a counter ion in the presence of an excess of NaB(C6H5)4. As initiators were used: benzylsodium reacted with α-methylstyrene (I), fluorenylsodium (II), and 9-methylfluorenylsodium (III). With I the initiation is fast as compared with the polymerization reaction which is first order in monomer concentration. Within the range of −50°C to −100°C an almost unperturbed “living” polymerization is observed. The Arrhenius plot of the rate constants results in a straight line with a…

chemistry.chemical_compoundAnionic addition polymerizationMonomerReaction rate constantPolymerizationChemistryTacticityPolymer chemistryActivation energyMethyl methacrylateArrhenius plotDie Makromolekulare Chemie
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1984

The decomposition reactions of the lithiated dimer, trimer, and tetramer of methyl methacrylate (MMA) in THF at 25°C were investigated. The decomposition of the lithiated dimer proceeds via depolymerization to lithiated monomer and MMA, addition of MMA to residual lithiated dimer, resulting the trimer (“disproportionation” of the dimer), and subsequent autocondensation of the products. The lithiated trimer almost exclusively undergoes cyclo-autocondensation, whereas for the lithiated tetramer both reactions proceed simultaneously to a remarkable degree. It is shown that the relative rate of autocondensation, which is highly dependent on the degree of polymerization of the oligomer, controls…

chemistry.chemical_compoundAnionic addition polymerizationMonomerTetramerChemistryDepolymerizationDimerPolymer chemistryfood and beveragesDisproportionationTrimerDegree of polymerizationDie Makromolekulare Chemie
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