Search results for "polymers"

showing 10 items of 3567 documents

Tribute to Axel Müller on the occasion of his 65th birthday

2012

Polymers and PlasticsChemistryOrganic ChemistryMaterials ChemistryArt historyTributePolymer
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Chemical stiffening of constructs between polymeric microparticles based on a hyaluronic acid derivative and mesenchymal stem cells: rheological and …

2018

Polymers and PlasticsChemistryOrganic ChemistryMesenchymal stem cell02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIn vitro0104 chemical sciencesStiffeningchemistry.chemical_compoundRheologyHyaluronic acidMaterials ChemistryBiophysics0210 nano-technologyDerivative (chemistry)Polymer International
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Syndiospecific polymerization of styrene using methylaluminoxane-activated bis(phenolato)titanium complexes

1998

Styrene was polymerized using a series of methylaluminoxane-activated bis(phenolato)titanium complexes of the type ((OC 6 H 2 -4-Me-6- 1 Bu) 2 Z)TiX 2 (X = Cl, O 1 Pr, η 5 -C 5 Me 5 ) to give syndiotactic polystyrene. Catalyst activity was found to depend on the nature of the bridging group Z, where Z = CH 2 , CH 2 CH 2 , S, S=O. Activity was found to be highest for Z = S.

Polymers and PlasticsChemistryOrganic ChemistryMethylaluminoxanechemistry.chemical_elementCondensed Matter PhysicsCatalysisStyrenechemistry.chemical_compoundStereospecificityPolymerizationTacticityPolymer chemistryMaterials ChemistryPolystyrenePhysical and Theoretical ChemistryTitaniumMacromolecular Chemistry and Physics
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Amphiphilic dyes for NLO in LB-films

1991

The influence of structural variations of phenyl-hydrazones and stilbazium salts on monolayer behaviour and second-harmonic generation in LB-monolayers is discussed. In contrast to the stilbazium salts the variation of the substituents of the phenylhydrazones does not influence the absorption maximum of the dyes in resonance enhancement of the nonlinearity. This allows a direct comparison of the substitution pattern on SHG.

Polymers and PlasticsChemistryOrganic ChemistryMonolayerAmphiphileInorganic chemistryMaterials ChemistryAbsorption (chemistry)Condensed Matter PhysicsPhotochemistryResonance (chemistry)Makromolekulare Chemie. Macromolecular Symposia
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RAFT Synthesis of Reactive Multifunctional Triblock‐Copolymers for Polyplex Formation

2021

Polymers and PlasticsChemistryOrganic ChemistryPolymer chemistryMaterials ChemistryCopolymerReversible addition−fragmentation chain-transfer polymerizationRaftPhysical and Theoretical ChemistryCondensed Matter PhysicsMacromolecular Chemistry and Physics
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Trend report macromolecular chemistry 2001

2002

Polymers and PlasticsChemistryOrganic ChemistryPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryCondensed Matter PhysicsMacromolecular Chemistry and Physics
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Poly(phosphonate)s via Olefin Metathesis: Adjusting Hydrophobicity and Morphology

2014

Olefin metathesis step-growth (acyclic diene metathesis (ADMET)) and chain-growth (ring-opening metathesis) polymerization was used to prepare linear poly(phosphonate)s with variable hydrophilicity. The first phosphonate monomer, i.e., di(undec-10-en-1-yl) methylphosphonate, for ADMET polymerization was developed, and potentially degradable and biocompatible, unsaturated poly(phosphonate)s were prepared with molecular weights up to 23 000 g mol–1 with molecular weight dispersities Đ < 2. These polymers were studied with respect to their interaction with a calcium phosphate bone substitute material from an aqueous nanoparticle dispersion that was prepared by a solvent evaporation miniemulsio…

Polymers and PlasticsChemistryOrganic ChemistryROMPMetathesisPhosphonateInorganic Chemistrychemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryRing-opening metathesis polymerisationAcyclic diene metathesisMacromolecules
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Polyether Core-Shell Cylinder-Polymerization of Polyglycidol Macromonomers

2005

The synthesis and polymerization of macromonomers containing a polymerizable styrene head group and a tail of ethylene oxide derivatives of different character were investigated. The synthesis of macromonomers was based on living anionic polymerization of oxiranes. Two monomers were used: 1-ethoxyethyl glycidyl ether (glycidol acetal), which after hydrolysis forms hydrophilic glycidol blocks and glycidyl phenyl ether forming hydrophobic blocks. Polymerizable double bonds were introduced by terminating the living chain with p-(chloromethyl)styrene. The radical polymerization of the macromonomers was carried out in water with addition of a non-polar solvent (benzene) and AIBN as initiator. Co…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationCondensed Matter PhysicsMacromonomerRing-opening polymerizationLiving free-radical polymerizationAnionic addition polymerizationPolymerizationPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPhysical and Theoretical ChemistryLiving anionic polymerizationMacromolecular Chemistry and Physics
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Pyrene Containing Polymers for the Non-Covalent Functionalization of Carbon Nanotubes

2009

Pyrene containing diblock copolymers based on poly(methyl methacrylate) were synthesized and investigated regarding their adsorption on carbon nanotubes (CNT). The pyrene units were introduced using a reactive ester monomer for the build up of the second block which later on was reacted polymer-analogously with amine functionalized pyrene derivatives. As we started from the same reactive ester intermediate, full block length identity is given. We varied the length of the anchor block to find an optimal block length and used pyren-1-yl-methylamine as well as 4-pyren-1-yl-butylamine as anchor units. For both anchor units a maximal adsorption was found for 13 and 20 anchor units, respectively.…

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationCondensed Matter Physicschemistry.chemical_compoundEnd-groupMonomerAdsorptionPolymer chemistryDispersion stabilityMaterials ChemistryCopolymerPyrenePhysical and Theoretical ChemistryMethyl methacrylateMacromolecular Chemistry and Physics
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Polymeric mesoions, 4. Synthesis of polymerizable mesoionic 4,6-dioxo-1,3-diazines derived from vinylbenzylmalonic acid

2000

Vinylbenzylmalonic acid (4) was condensed with N,N'-diphenylformamidine (5a), N,N'-diphenylacetamidene (5b), S-propyl-1,3-diphenylisothiourea (6) and anilinopyridine (7) in the presence of dicyclohexylcarbodiimide (DDC). The resulting new mesoionic monomers 8a-d were polymerized with 2,2'-azoisobutyronitrile (AIBN) as an initiator and dodecanethiol as a chain transfer agent. The low molecular weight model compounds 5-benzyl-pyrido[1,2-a]pyrimidine-2,4-dione (9a) and 5-hexadecyl-4,6-dioxo-1,3-diphenyl-2-hexadecylthio-1,3-diazine (9b) were prepared for X-ray diffraction analysis and comparison of spectrospical data.

Polymers and PlasticsChemistryOrganic ChemistryRadical polymerizationMesoionicCrystal structureCondensed Matter PhysicsChemical synthesischemistry.chemical_compoundMonomerPolymerizationTransfer agentPolymer chemistryMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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