Search results for "Polymers"

showing 10 items of 3567 documents

Versatile ω-end group functionalization of RAFT polymers using functional methane thiosulfonates

2009

Five different polymers, poly[methyl methacrylate] (PMMA), poly[lauryl methacrylate] (PLMA), poly[diethylene glycol methacrylate] (PDEGMA), poly[N-iso-propylacrylamide] (PNIPA), and poly[styrene] (PS) prepared by the RAFT process and thus terminated with dithioesters were aminolyzed in the presence of S-3-butynyl methane thiosulfonate (MTS), which was synthesized in two steps. Analysis of the polymers by 2D NMR, UV–vis absorbance, and gel permeation chromatogra-phy revealed them to quantitatively carry acetylene end groups connected with disul-fide bridges, indicating that functional MTS reagents can be employed for end group functionalization of RAFT polymers. This versatile method is of ad…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryRaftPolymerMethacrylateContact anglechemistry.chemical_compoundEnd-groupchemistryPolymer chemistryMaterials ChemistrySurface modificationAzideMethyl methacrylateJournal of Polymer Science Part A: Polymer Chemistry
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Hyperbranched methacrylates by self-condensing group transfer polymerization

1997

The synthesis of hyperbranched methacrylates was achieved by self-condensing group transfer polymerization of 2-(2-methyl-1-triethylsiloxy-1-propenyloxy)ethyl methacrylate (1). “Back-biting” is shown to be the predominant side reaction. In spite of this, the compact nature of the hyperbranched molecules was demonstrated through SEC-viscosity measurements and comparison with a linear analogue. The degree of branching can be controlled by copolymerization with conventional monomers, e.g. MMA, and the living polymers can be used as macroinitiators for star-shaped polymers.

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySide reactionPolymerSelf-condensationBranching (polymer chemistry)Methacrylatechemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMacromolecular Rapid Communications
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Systematic investigation of functional core variation within hyperbranched polyglycerols

2008

A novel series of hyperbranched polyether polyols with various n-alkyl amine cores (mono- and bifunctional) and photoactive cores (benzylamine and 1-naphthylmethylamine) have been prepared. Polymerization of glycidol was carried out in two ways, starting directly from primary amine initiators and from bisglycidolized amine initiators. NMR spectroscopy and size exclusion chromatography (SEC) showed good control over the molecular weights only, when bisglycidolized amines were used. Molecular weights and polydispersity of the hyperbranched polyglycerols prepared with these initiator-cores were in the range of 1600 to 8400 g/mol and of 1.5 to 2.5, respectively. MALDI-ToF mass spectrometry conf…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySize-exclusion chromatographyDispersityGlycidolPolymerRing-opening polymerizationchemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryBifunctionalJournal of Polymer Science Part A: Polymer Chemistry
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Anionic polymerization of methyl methacrylate using tetrakis[tris(dimethylamino)phosphoranylidenamino] phosphonium (P5+) as counterion in tetrahydrof…

2000

A novel metal-free initiator, i.e. the salt of the tetrakis[tris(dimethylamino)phosphoranylidenamino]phosphonium (P5+) cation with the 1,1-diphenylhexyl (DPH–) anion was prepared by cation metathesis. It initiates a very fast and controlled anionic polymerization of methyl methacrylate in THF. Kinetic investigations between –20 and +20°C using a flow tube reactor provide nearly linear first-order time-conversion plots with half-lives below 0.1 s, a linear dependence of the number-average degree of polymerization, and rather narrow molecular weight distributions (Mw/Mn ≈ 1.2). 13C NMR measurements on a model of the active chain end (the P5+ salt of ethyl isobutyrate) in THF-d8 show 15 and 25…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySolution polymerizationDegree of polymerizationchemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryPhosphoniumCounterionMethyl methacrylateTetrahydrofuranCarbanionMacromolecular Rapid Communications
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Polymerizations of Cyclic Esters Catalyzed by Titanium Complexes Having Chalcogen-Bridged Chelating Diaryloxo Ligands

2002

A series of titanium complexes having tellurium-bridged chelating bis(aryloxo) ligands, [TiX2{2,2‘-Te(4-Me-6-tBu-C6H2O)2}]2 (5:  X = Cl; 6:  X = OiPr), catalyzed the ring-opening polymerization of cyclic esters such as e-caprolactone, δ-valerolactone, and l-lactide. The strong dependence of polymerizations on the solvent was observed in this catalytic system. When the polymerizations of e-caprolactone and l-lactide were carried out in toluene at 100 °C, tellurium-bridged bis(aryloxo)titanium complex 5 was found to give polymers with rather broad molecular weight distribution due to back-biting. When the polymerizations of e-caprolactone and l-lactide was carried out in anisole or in dioxane…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySolution polymerizationPolymerAnisoleRing-opening polymerizationCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerMolar mass distributionMacromolecules
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Anionic Polymerization of Alkyl (Meth)acrylates Using Metal-Free Initiators:  Effect of Ion Pairing on Initiation Equilibria

1999

Metal-free anionic polymerizations of alkyl (meth)acrylates using tetrabutylammonium salts of diethylphenylmalonate, fluorene, and 9-ethylfluorene as initiators were performed in THF at 30 °C. A poor control of molecular weights, inconsistent initiator efficiencies, and broad or bimodal molecular weight distributions were obtained. The effect of counterion nature was studied from the polymerization of methyl methacrylate using the 1,1-diphenylhexyl anion with tetrabutylammonium, tetramethyldiethylguanidinium, and lithium as counterions under otherwise identical conditions. Metal-free initiators resulted in incomplete initiation which is attributed to the fact that the initiation is an equil…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySolution polymerizationPolymerInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymer chemistryMaterials ChemistryHofmann eliminationCounterionMethyl methacrylateAlkylMacromolecules
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Automated Large-Scale Synthesis of Supramolecular Oligo(p-benzamide) Block Copolymers

2007

A fully automated large-scale synthesis procedure has been developed that allows the preparation of supramolecular rod−coil copolymers on a 100 g scale. The new reaction cycle allows the stepwise growth of oligo(p-benzamide)s onto the chain end of amine-terminated polymers. Amine-terminated poly(ethylene glycol) (PEG, Mn = 5000 g mol-1) and poly(styrene) (PS, Mn = 2950 g mol-1) were prepared, and an octa(p-benzamide) oligomer block was grown from the chain end in an automated computer-controlled reaction cycle. Plotting the apparent molecular weight of the PEG copolymer against the number of reaction cycles revealed a linear relationship, which emphasized the high level of control this meth…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistrySupramolecular chemistryPolymerOligomerMicelleStyreneInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryPEG ratioMaterials ChemistryCopolymerEthylene glycolMacromolecules
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An Alternate Interpretation of Polymer/Solvent Jump Size Units for Free-Volume Diffusion Models

1996

Polystyrene/toluene mutual-diffusion coefficients have been measured as a function of temperature in the limit of infinite solvent dilution. The solvent to polymer jump size unit ratio (ξ) was determined from the Vrentas−Duda free-volume diffusion model for polymer self-diffusion and is in excellent agreement with values evaluated from solvent self- and binary mutual-diffusion coefficient data. Comparison of the free-volume model to a version of the Kirkwood−Riseman theory, modified for diffusion at infinite dilution under non-ϑ conditions, suggests that ξ follows the temperature dependence of the root-mean-squared end-to-end distance of the polystyrene and can be estimated without the use …

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryThermodynamicsPolymerDilutionCondensed Matter::Soft Condensed MatterInorganic ChemistrySolventchemistry.chemical_compoundchemistryVolume (thermodynamics)Materials ChemistryBrownian dynamicsJumpPolystyrenePhysics::Chemical PhysicsDiffusion (business)Macromolecules
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Thiol-functionalized ROMP polymers via Sacrificial Synthesis

2009

The synthesis of well-defined and highly functionalized thiol-functionalized polymers has been accomplished via the ring-opening metathesis polymerization (ROMP). A sacrificial synthesis-based approach was chosen for this interesting functional group since it has proven to give precise control over molecular weight and selective placement of end-groups on a different functionality before. Thiol-functionalized ROMP-polymers were successfully synthesized employing thioacetal monomers, which can be cleaved by hydrogenation leaving the desired thiol group behind. The placement of this highly reactive functional group at one chain end of a poly(norborneneimide) is demonstrated by analytical meth…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryThioacetalPolymerROMPMetathesisInorganic Chemistrychemistry.chemical_compoundEnd-groupMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryImideMacromolecules
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N,N-Diallylglycidylamine: A Key Monomer for Amino-Functional Poly(ethylene glycol) Architectures

2012

The first application of N,N-diallylglycidylamine (DAGA) as a monomer for anionic ring-opening polymerization is presented. The monomer is obtained in a one-step procedure using epichlorohydrin and N,N-diallylamine. Both random and block copolymers consisting of poly(ethylene glycol) and poly(N,N-diallylglycidylamine) with adjusted DAGA ratios from 2.5 to 24% have been prepared, yielding well-defined materials with low polydispersities (Mw/Mn) in the range 1.04–1.19. Molecular weights ranged between 2600 and 10 300 g mol–1. Isomerization of allylamine to enamine structures during polymerization depending on time, temperature, and counterion has been realized. The kinetics of the formation o…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryTriad (anatomy)Inorganic Chemistrychemistry.chemical_compoundMonomermedicine.anatomical_structurechemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymermedicineProton NMREpichlorohydrinCounterionEthylene glycolMacromolecules
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