Search results for "Ionic polymerization"

showing 10 items of 481 documents

Transfer of Some Alkyl Substituted Ferrocenes from Water to Cationic Surfactant Micelles Studied by Kinetic Method

1994

Abstract Binding of ferrocene and its 1,1′-dimethyl and n -butyl derivatives to dodecyl and tetradecyltrimethylammonium nitrate micellar aggregates has been studied at 20.0°C and ionic strength 0.02 tool dm -3 by examining the micellar retarding effects on the rates of iron(III) oxidation of these substrates. Solubilization of the ferrocenes in the cationic micellar phase increases as the substrate hydrophobic character increases and, to a lesser extent, as the surfactant hydrocarbon chain length becomes longer. The critical micelle concentrations of the surfactants used and the incremental free energy of transfer of methylene groups of both the substrate and the surfactant from the aqueous…

chemistry.chemical_classificationAqueous solutionChemistryInorganic chemistryCationic polymerizationMicelleSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantFerroceneIonic strengthMethyleneAlkylJournal of Colloid and Interface Science
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Temperature-responsive inclusion complex of cationic PNIPAAM diblock copolymer and γ-cyclodextrin

2012

Aqueous mixtures of γ-cyclodextrin (γ-CD) and the thermosensitive cationic diblock copolymer poly(N-isopropylacrylamide)-b-poly(3-acrylamidopropyl)trimethylammonium chloride (PNIPAAM24-b-PAMPTAM(+)9) or the PNIPAAM homopolymer PNIPAAM47 have been investigated using various experimental methods. Solid γ-CD–polymer inclusion complexes (pseudopolyrotaxanes) form at ambient temperatures in fairly concentrated CD solutions. The NMR measurements showed that the stoichiometry of the inclusion complexes is close to two NIPAAM units per CD molecule. The cationic block of the copolymer is not incorporated into the CD cavity. Synchrotron radiation X-ray diffraction spectra of the solid inclusion compl…

chemistry.chemical_classificationAqueous solutionCyclodextrinChemistrysupramolecule cyclodextrin PNIPAAM rotaxanesCationic polymerizationGeneral ChemistryCondensed Matter PhysicsLower critical solution temperatureFluorescence spectroscopyDynamic light scatteringPolymer chemistryCopolymerMoleculeSettore CHIM/02 - Chimica FisicaSoft Matter
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Polymerization of Mono- and Bi-functional Diacetylene Derivatives in Monolayers at the Gas-Water Interface

1979

The spreading and polymerization behaviour of long chain acids and phospholipid analogues containing diacetylene groups is described. Especially the polymerization in monolayers is followed spectroscopically with a new device used in connection with a commercial UV spectrometer. The polymerization is topochemically controlled. Sonification of the phospholipid analogues in water results in the formation of liposomes with multilayered membranes. Polymerization of the liposomes in water forms aqueous solutions of polymer vesicles.

chemistry.chemical_classificationAqueous solutionDiacetyleneChemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesGeneral ChemistryPolymerPhotochemistryEnd-groupchemistry.chemical_compoundMembranePolymerizationMonolayerIsrael Journal of Chemistry
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Kinetic studies of the interaction between DNA and polycations based on polyasparthylhydrazide

2008

Abstract In the present paper, a systematic kinetic study on the interaction between interpolyelectrolytes such as positive-charged polymers and DNA was carried out. In particular, a qualitative–quantitative kinetic investigation on the interaction between copolymers of the α,β-poly(aspartylhydrazide) and DNA calf thymus filaments was performed. This study gives a new model starting from a well known “pseudo-phase model”, and permits to give a qualitative explanation about the trends of experimentally observed kinetic constants by varying the concentration of one of the two poly-electrolytes. Moreover, this study permits to verify the dependence of the binding constants KPAHy–CPTA and KDNA …

chemistry.chemical_classificationAqueous solutionKineticsCationic polymerizationThermodynamicsElectrolytePolymerKinetic energychemistry.chemical_compoundColloid and Surface ChemistrychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCopolymerOrganic chemistryDNA polycationsDNA
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Atomistic Simulations of Functional Au_{144}(SR)_{60} Gold Nanoparticles in Aqueous Environment

2012

Charged monolayer-protected gold nanoparticles (AuNPs) have been studied in aqueous solution by performing atomistic molecular dynamics simulations at physiological temperature (310 K). Particular attention has been paid to electrostatic properties that modulate the formation of a complex comprised of the nanoparticle together with surrounding ions and water. We focus on Au-144 nanoparticles that comprise a nearly spherical Au core (diameter similar to 2 nm), a passivating Au-S interface, and functionalized alkanethiol chains. Cationic and anionic AuNPs have been modeled with amine and carboxyl terminal groups and Cl-/Na+ counterions, respectively. The radial distribution functions show tha…

chemistry.chemical_classificationAqueous solutionta114ChemistryCationic polymerizationNanoparticleNanotechnologySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMolecular dynamicsGeneral EnergySolvation shellChemical engineeringColloidal goldSide chainPhysical and Theoretical ChemistryCounterionThe Journal of Physical Chemistry C
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Membrane Transport of l-Arginine and Cationic Amino Acid Analogs

2000

Publisher Summary This chapter reviews the current knowledge of the mechanisms and regulation of cationic amino acids (CAA) carrier proteins and discusses the potential involvement of each transporter in supplying L-arginine for nitric oxide biosynthesis. The CAA L-arginine, the substrate for nitric oxide synthases (NOSs), is considered a semi-essential amino acid in most mammals. Consequently, mammalian cells must be capable of exchanging CAA with the environment. The bilayer of the plasma membrane is impermeable to polar molecules, and thus, specialized carrier proteins with distinct substrate specificity transport hydrophilic solutes such as amino acids. L-arginine shares the same transp…

chemistry.chemical_classificationArginineChemistryCationic polymerizationnutritional and metabolic diseasesSubstrate (chemistry)TransporterMembrane transportAmino acidNitric oxidechemistry.chemical_compoundMembraneBiochemistrymental disorderscardiovascular diseases
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Weak interactions between resorcinarenes and diquaternary alkyl ammonium cations

2005

The interactions of resorcin[4]arenes 1 with alkyl ammonium cations bearing a 1,4-diazabicyclo[2.2.2]octane (DABCO) scaffold (32+, 42+ and 52+) were analyzed in the solid state by X-ray crystallography, in solution by 1H NMR spectroscopy, and in the gas phase by ESI-TOF mass spectrometry. The results are complemented with AM1 calculations and compared to previous reports on complexation studies of resorcinarenes with quaternary alkyl ammonium cations. The NMR titration results indicate that there are hardly any differences in the binding of the quaternary tetramethyl ammonium cation 2+ and the diquaternary N,N’-dimethyl DABCO dication 42+. The large N,N’-dibenzyl DABCO dication 52+ has two …

chemistry.chemical_classificationArylInorganic chemistryCationic polymerizationGeneral ChemistryDABCOMass spectrometryMedicinal chemistryCatalysisDicationchemistry.chemical_compoundchemistryMaterials ChemistryAmmoniumAlkylOctaneNew J. Chem.
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Antidiabetic Behavior of Biguanides

1983

The existence of active electron pairs on some nitrogen atoms in phenformin hydrochloride is inferred from the presence of a hydrogen catalytic polarographic wave. This finding emphasizes the ability of biguanides to form hydrogen bridges with other molecular species such as amino acids and proteins, as well as to form coordination complexes with zinc and other metallic cations by means of these electron pairs. The antidiabetic action of phenformin and other related biguanides can be explained in terms of competition between these molecules and insulin to coordinate cationic oligoelements together with their ability to form hydrogen bonds between the biguanide moiety and insulin itself.

chemistry.chemical_classificationChemical PhenomenaChemistry PhysicalHydrogen bondChemistryBiguanidemedicine.drug_classInorganic chemistryBiguanidesCationic polymerizationPharmaceutical ScienceHydrogen-Ion ConcentrationPhenforminCombinatorial chemistryAmino acidchemistry.chemical_compoundPhenforminmedicineHypoglycemic AgentsInsulinMoleculeMoietyPhenformin HydrochloridePolarographyJournal of Pharmaceutical Sciences
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Cationic and Zwitterionic Polymerizable SurfactantsQuaternary Ammonium Dialkyl Maleates. 2. Emulsion Polymerization of Styrene and Butyl Acrylate

1998

Polymerizable cationic and zwitterionic dialkyl maleates with different hydrophobic chain lengths (R = C10H21, C12H25, C16H33, C18H37) and different counterions (I, Br, HSO4) for the cationic hydrophilic part, as well as some similar surfactants, dialkyl succinates, were used in batch and seeded emulsion polymerization of styrene and butyl acrylate. All surfactants, when used in emulsion polymerization, provide good stability to the styrene/butyl acrylate latices. A styrene/butyl acrylate latex prepared with sodium dodecyl sulfate (SDS) was used as a reference. Some stability tests for latices were performed, and the glass transition temperatures, as well as the molecular weights of the pol…

chemistry.chemical_classificationChemistryButyl acrylateCationic polymerizationEmulsion polymerizationSurfaces and InterfacesPolymerCondensed Matter PhysicsStyrenechemistry.chemical_compoundSuccinatesPolymer chemistryElectrochemistryOrganic chemistryGeneral Materials ScienceSodium dodecyl sulfateGlass transitionSpectroscopyLangmuir
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Hydrophobically Modified Halloysite Nanotubes as Reverse Micelles for Water-in-Oil Emulsion.

2015

An easy strategy to obtain inorganic reverse micelles based on halloysite nanotubes (HNTs) and alkyltrimethylammonium bromides has been developed. The selective modification of the HNTs external surface with cationic surfactants endows to generate tubular nanostructures with a hydrophobic shell and a hydrophilic cavity. The influence of the surfactants alkyl chain on the HNTs functionalization degree has been investigated. The dynamic behavior of the surfactant/HNT hybrids in solvents with variable polarity has been correlated to their affinity toward hydrophobic media explored through partition experiments. The water-in-oil emulsion is able to solubilize copper sulfate, proving the incorpo…

chemistry.chemical_classificationChemistryCationic polymerizationCondensed Matter PhysicSurfaces and Interfacesengineering.materialCondensed Matter PhysicsHalloysiteMicellechemistry.chemical_compoundPulmonary surfactantChemical engineeringEmulsionElectrochemistryengineeringOrganic chemistrySurface modificationGeneral Materials ScienceOrganic synthesisMaterials Science (all)Surfaces and InterfaceSpectroscopyAlkylSettore CHIM/02 - Chimica FisicaLangmuir : the ACS journal of surfaces and colloids
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