0000000000465262

AUTHOR

Laura Preiss

showing 3 related works from this author

Macromol. Rapid Commun. 17/2016

2016

Materials sciencePolymers and PlasticslawChemical physicsOrganic ChemistryMaterials ChemistryCrystallizationChirality (chemistry)law.inventionMacromolecular Rapid Communications
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Amino-Acid-Based Polymerizable Surfactants for the Synthesis of Chiral Nanoparticles

2016

Amino-acid-based chiral surfactants with polymerizable moieties are synthesized, and a versatile approach to prepare particles thereof with a chiral surface functionality is presented. As an example of an application, the synthesized particles are tested for their ability as nucleating agents in the enantioselective crystallization of amino acid conglomerate systems, taking rac-asparagine as a model system. Particles resulting from chiral surfactants with different tail groups are compared and the results demonstrate that only the chiral nanoparticles made of the polymerizable surfactant are able to act efficiently as nucleation agent in enantioselective crystallization.

inorganic chemicalsMaterials sciencePolymers and PlasticsPolymersNucleationNanoparticleModel system02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationlaw.inventionSurface-Active AgentsPulmonary surfactantlawMaterials ChemistryOrganic chemistryAmino AcidsCrystallizationchemistry.chemical_classificationMolecular Structureorganic chemicalsOrganic Chemistrytechnology industry and agricultureEnantioselective synthesisStereoisomerism021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesAmino acidchemistryNanoparticles0210 nano-technologyChirality (chemistry)Macromolecular Rapid Communications
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ALTMET Polymerization of Amino Acid-Based Monomers Targeting Controlled Drug Release

2016

Giving the imminent necessity of a new generation of biodegradable and biocompatible polymers prepared from feedstock, the synthesis of a potentially biodegradable amino acid-based copolymer by the alternating diene metathesis (ALTMET) strategy is herein presented. The reaction was tailored to minimize isomerization and deactivation of ruthenium catalysts by intramolecular coordination with the amide carbonyl group of the amino-acid-based monomer. Alternated l-lysine–phosphoester copolymers with molar masses higher than 18 000 g/mol were obtained using Hoveyda–Grubbs second-generation and Umicore M2 catalysts. The copolymer was further used to prepare nanoparticles loaded with rifampicin (u…

Molar massPolymers and PlasticsDieneOrganic Chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesRutheniumInorganic ChemistryMiniemulsionchemistry.chemical_compoundMonomerchemistryPolymerizationAmidePolymer chemistryMaterials ChemistryCopolymer0210 nano-technologyMacromolecules
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