0000000000053319

AUTHOR

Ralf Mruk

showing 8 related works from this author

CdSe/ZnS Nanocrystals with Dye-Functionalized Polymer Ligands Containing Many Anchor Groups

2005

chemistry.chemical_compoundFunctionalized polymerMaterials scienceCadmium selenidechemistryNanocrystalEnergy transferInorganic chemistryPolymer chemistryGeneral ChemistryCatalysisAngewandte Chemie International Edition
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Poly(N-isopropylacrylamide)-Modified Styrene-Butadiene Rubber as Thermoresponsive Material

2013

Styrene-butadienePolymers and PlasticsThiol-ene reactionOrganic ChemistryCondensed Matter Physicschemistry.chemical_compoundchemistryNatural rubbervisual_artPolymer chemistryMaterials ChemistryPoly(N-isopropylacrylamide)visual_art.visual_art_mediumOrganic chemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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CdSe/ZnS-Nanokristalle mit farbstoffmarkierten Polymerliganden mit mehrfachen Ankergruppen

2005

Materials scienceGeneral MedicineAngewandte Chemie
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Chiral Polyisocyanates from an Azomonomer with a Very High Chiral Induction

2001

The synthesis of new chiral polyisocyanates is described. For this purpose a new chiral azobenzene containing monomer with the chiral center in α-position to the isocyanate group was synthesized. The anionic copolymerization was carried out in THF as solvent with potassium cyanide that was complexed by 18-crown-6 as initiator. This allowed a better control of the reaction and thereby the synthesis of polyisocyanates with a fairly low polydispersity. The copolymers show an extremely high transfer of chirality from the chiral side groups to the helical backbone in dilute solution. Copolymers with only 1.6 mol % of chiral side groups show nearly the full optical rotation and exist predominantl…

Azo compoundPolymers and PlasticsPhotoisomerizationOrganic ChemistryPhotochemistryCis trans isomerizationInorganic Chemistrychemistry.chemical_compoundAzobenzenechemistryLyotropicPolymer chemistryMaterials ChemistrySide chainOptical rotationChirality (chemistry)Macromolecules
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Thin Films by Multilayer Build-Up of Electron Transport Materials

2003

We present the synthesis and the electrochemical characterization of polymeric electron transport materials, synthesized by polycondensation of substituted triazines and α,ω-dihaloalkanes. They can be reversibly reduced with the least negative potential at −0.39 V, which is below the reduction potential of oxygen. In addition, the formation of polyelectrolyte multilayers is possible by the electrostatic self-assembly method. This multilayer formation takes place in a very defined way up to thirty double layers. An example of one of the polymeric triazine electron transport materials synthesized and a schematic diagram of a self-assembled multilayer film.

Conductive polymerMaterials sciencePolymers and PlasticsOrganic ChemistryElectrochemistryElectron transport chainPolyelectrolyteCharacterization (materials science)chemistry.chemical_compoundchemistryChemical engineeringPolymer chemistryMaterials ChemistrySelf-assemblyThin filmTriazineMacromolecular Rapid Communications
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Semiconductor Nanocrystals with Multifunctional Polymer Ligands

2002

In this letter, we describe the preparation of a versatile polymer ligand, which can be attached to CdSe/ZnS semiconductor nanocrystals via a phase transfer reaction. The ligand is based on a chain of reactive esters, which can, in principle, be substituted by any compound containing amino-functionalities. The polymer/nanocrystal complexes are characterized in terms of structure and photostability.

chemistry.chemical_classificationLigandfungiInorganic chemistryfood and beveragesQuantum yieldGeneral ChemistryPolymerBiochemistryCombinatorial chemistryCatalysisFluorescence spectroscopyColloid and Surface ChemistryNanocrystalchemistryPhase (matter)Surface modificationSemiconductor nanocrystalsJournal of the American Chemical Society
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Synthesis of pentafluorophenyl(meth)acrylate polymers: New precursor polymers for the synthesis of multifunctional materials

2005

Pentafluorophenyl acrylate and -methacrylate were polymerized using AIBN as a thermal initiator. The obtained polymers were soluble polymeric active esters that could be used for the preparation of multifunctional polymers. The reactivity of poly(pentafluorophenylacrylate) and poly(pentafluorophenylmethacrylate) towards primary and secondary amines, as well as alcohols was investigated in a quantitative way. Both poly(active esters) reacted satisfactorily with aliphatic primary and secondary amines but only low conversion was found in the case of aromatic amines. Conversions of only 30% were reached when poly(pentafluorophenylacrylate) was treated with one equivalent of alcohol under base c…

chemistry.chemical_classificationAcrylatePolymers and PlasticsChemistryOrganic ChemistryGeneral Physics and AstronomyAlcoholPolymerMethacrylateCatalysischemistry.chemical_compoundReaction rate constantPolymerizationPolymer chemistryMaterials ChemistryOrganic chemistryReactivity (chemistry)European Polymer Journal
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Amphotropic Ionomers by Attachment of Secondary Amines to a Reactive Ester Polymer

2004

We report on the synthesis of polyacrylamides that were prepared by the reaction of a reactive ester polymer with a mesogen-containing secondary amine and N-methyl-piperazine. As the polymers do not form hydrogen bonds near the amide groups, their mobility is significantly higher than that of poly(N-monoalkylacrylamides). The initially nonionic polymer shows no liquid-crystalline behavior in bulk and in mixture with ethylene glycol. This is due to the low polarity difference between the different side chains. The polarity difference can be increased by protonation or quarter-nization of the tertiary amino groups, and liquid-crystalline behavior is observed. The self-assembly multilayer buil…

Acrylate polymerchemistry.chemical_classificationPolymers and PlasticsHydrogen bondOrganic ChemistryPolymerCondensed Matter PhysicsPolyelectrolytechemistry.chemical_compoundchemistryAmidePolymer chemistryMaterials ChemistrySide chainPhysical and Theoretical ChemistryEthylene glycolIonomerMacromolecular Chemistry and Physics
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