0000000000323438

AUTHOR

Julia Jeromin

showing 3 related works from this author

Cyclodextrins in polymer synthesis: free radical polymerisation of cyclodextrin complexes of cyclohexyl and phenyl methacrylate in aqueous medium

1998

The polymerisation mechanism of 2,6-dimethyl-β-cyclodextrin (Me2-β-CD) complexes of phenyl methacrylate (1) and cyclohexyl methacrylate (2) is described. The polymerisation of the complexes 1 a and 2a was carried out in water with potassium peroxodisulfate/potassium hydrogensulfite as initiator. The unthreading of the Me2-β-CD during the polymerisation led to water-insoluble poly(phenyl methacrylate) (1b) and poly(cyclohexyl methacrylate) (2b). By comparison, analogously prepared polymers from uncomplexed monomers 1 and 2 in homogeneous organic solvent (THF) with AIBN as radical initiator showed significantly lower viscosities and were obtained in lower yields in both cases.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinChemistryPotassiumOrganic Chemistrychemistry.chemical_elementSolution polymerizationPolymerMethacrylatechemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryRadical initiatorMacromolecular Rapid Communications
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Cyclodextrins in polymer synthesis: Free radical polymerization of cyclodextrin complexes withN-methacryloyl-11-aminoundecanoic acid orN-methacryloyl…

1998

The hydrophobic monomers N-methacryloyl-11 -aminoundecanoic acid (1) or N-methacryloyl-1-aminononane (2) were incorporated as guests into the cavity of heptakis(2,6-di-O-methyl)-β-cyclodextrin (Me 2 -β-CD) as a host, yielding the water compatible monomers N-methacryloyl-l 11-aminoundecanoic acid/ Me 2 -β-CD-complex (1a) and N-methacryloyl-1 -aminononane/Me 2 -β-Cl complex (2a). These complexes were polymerized radically in aqueous medium. The resulting polymers 1b and 2b which were obtained from the complexes 1a and 2a, are insoluble in water because of the unthreading of the cyclodextrin during the polymerization. The polymerization rate of 1a and 2a is high in comparison to the rate of th…

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinChemistryOrganic ChemistryRadical polymerizationSolution polymerizationPolymerCondensed Matter PhysicsRing-opening polymerizationPolyelectrolytechemistry.chemical_compoundMonomerPolymerizationPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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Cyclodextrins in Polymer Synthesis:  Free Radical Polymerization of a N-Methacryloyl-11-aminoundecanoic Acid/β-Cyclodextrin Pseudorotaxane in an Aque…

1999

The relatively hydrophobic monomer N-methacryloyl-11-aminoundecanoic acid (1) was incorporated as a guest into the cavity of β-cyclodextrin (β-CD) as a host, yielding the water-soluble monomer N-me...

chemistry.chemical_classificationRotaxanePolymers and PlasticsAqueous mediumCyclodextrinOrganic ChemistryRadical polymerizationSolution polymerizationmacromolecular substancesPolymerPolyelectrolyteInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryOrganic chemistryMacromolecules
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