Search results for "ionic"

showing 10 items of 2016 documents

Post-Processing via Cation Exchange Cartridges: Versatile Options

2012

New 68Ge/68Ga radionuclide generators provide the positron emitter 68Ga (T½ = 67.7 min) as an easily available and relatively inexpensive source of a PET nuclide for labeling of interesting targeting vectors. However, currently available “ionic” 68Ge/68Ga radionuclide generators are not necessarily optimized for the routine synthesis of 68Ga-labeled radiopharmaceuticals in a clinical environment. Post-processing of 68Ge/68Ga generators using cation exchange resins provides chemically and radiochemically pure 68Ga with 97±2% within less than 4 min, with 68Ge almost completely removed, and ready for online labeling. This simple, fast, and efficient technology can be extended for new applicati…

chemistry.chemical_compoundCartridgechemistryRadiochemistrySynthonAcetonePositron emittersIonic bondingRadionuclide GeneratorIon-exchange resin
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Kinetik und Molekulargewichtsverteilung eines anionischen Polymerisationsprozesses mit momentanem Start bei simultanem Monomerabbruch

1973

Die Kinetik und die Molekulargewichtsverteilung wird fur einen anionischen Polymerisationsprozes mit einem momentanen Startschritt und mit simultanem Monomerabbruch berechnet. Ein derartiger Polymerisationsablauf ist bei der anionischen Polymerisation von Methylmethacrylat in polaren Losungsmitteln zu erwarten. — Die Molekulargewichtsverteilung geht mit steigendem Monomerabbruch in eine SCHULZ-FLORY-Verteilung uber. The kinetics and the molecular weight distribution are calculated for an anionic polymerization with rapid initiation and simultaneous deactivation by the monomer. Such a process is to be expected for the anionic polymerization of methylmethacrylate in polar solvents. — The mole…

chemistry.chemical_compoundColloid and Surface ChemistryMonomerAnionic addition polymerizationPolymers and PlasticsPolymerizationchemistryKineticsPolymer chemistryMaterials ChemistryMolar mass distributionPhysical and Theoretical ChemistryColloid and Polymer Science
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1992

Phosphonomethyl-substituted phenols are readily obtained from o-hydroxymethylated phenols and trialkyl phosphites. The free acids, incorporated into phenol-formaldehyde resins, act as cation exchangers with remarkable selectivity for different metal ions.

chemistry.chemical_compoundCondensation polymerchemistryMetal ions in aqueous solutionPolymer chemistryCation-exchange capacityOrganic chemistryPhenolsSelectivityIonic selectivityDie Makromolekulare Chemie
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Physicochemical Properties of New Dicationic Ether-Functionalized Low Melting Point Ammonium Salts

2010

Eleven new and one previously known but insufficiently characterized dicationic quaternary ammonium (QA) salts were synthesized and characterized. They contain an ethoxy ethyl group either in a side chain and/or as spacer of the diammonium cation and have bromide, hexafluorophosphate (PF6–), bis(trifluoromethanesulfonyl)imide (TFSI), or trifluoromethanesulfonate (TFMS) as an anion. 1H and 13C techniques, mass spectrometry, and elemental analysis together with X-ray diffraction and thermoanalytical methods were used for their characterization both in the liquid and solid state. In addition, residual water content and viscosity measurements were made for the two room temperature ionic liquid…

chemistry.chemical_compoundCrystallinitychemistryBromideHexafluorophosphateInorganic chemistryIonic liquidSide chainPhysical chemistryGeneral ChemistryCrystal structureTrifluoromethanesulfonatePowder diffractionAustralian Journal of Chemistry
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Crystal Structures and Thermal Behavior of Bis(dibenzyldimethylammonium) Tetrabromometallates(II) [M = Mn(II), Co(II) and Zn(II)] and Their Solvates

2007

Six new A2MBr4 structures [A = dibenzyldimethylammonium cation,M = Mn(II), Co(II) or Zn(II)] were crystallized with or without solvent molecules from acetonitrile, methanol and/or aqueous solutions. The isomorphous compounds [(Bz2Me2N)2][MnBr4]·CH3CN·H2O (1) and [(Bz2Me2N)2]-[ZnBr4]·CH3CN·H2O (4) crystallize in the triclinic space group P1̄ from acetonitrile solutions. The solvent molecules participate in the hydrogen bonding network inside the crystal structure. [(Bz2Me2N)2][CoBr4]·0.5CH3CN (2) crystallizes from an acetonitrile solution in the monoclinic space group P21/c. The solvent molecules fill the voids of the crystal structure. Compound 2 is isostructural with the previously reporte…

chemistry.chemical_compoundCrystallographyAqueous solutionHydrogen bondChemistryIonic bondingGeneral ChemistryCrystal structureIsostructuralTriclinic crystal systemAcetonitrileMonoclinic crystal systemZeitschrift für Naturforschung B
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1993

The synthesis and the thermotropic phase behavior of the dipolar amphiphiles C 5 H 5 N + (CH 2 ) m OCOPhPHCOO(CH 2 ) m N + C 5 H 5 and the polymeric amphiphile [(CH 2 ) 6 OPhPhO(CH 2 ) 6 OCOCH([CH 2 ] 6 N + C 5 H 5 )COO] n are described

chemistry.chemical_compoundCrystallographyCondensation polymerMonomerChemistryLiquid crystalStereochemistryAmphiphileIonic bondingPyridiniumThermotropic crystalPolyelectrolyteDie Makromolekulare Chemie, Rapid Communications
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A quantum chemical topological analysis of the c-c bond formation in organic reactions involving cationic species

2014

ELF topological analysis of the ionic Diels-Alder (I-DA) reaction between the N,N-dimethyliminium cation and cyclopentadiene (Cp) has been performed in order to characterise the C-C single bond formation. The C-C bond formation begins in the short range of 2.00-1.96 Åvia a C-to-C pseudoradical coupling between the most electrophilic center of the iminium cation and one of the two most nucleophilic centers of Cp. The electron density of the pseudoradical center generated at the most electrophilic carbon of the iminium cation comes mainly from the global charge transfer which takes place along the reaction. Analysis of the global reactivity indices indicates that the very high electrophilic c…

chemistry.chemical_compoundCyclopentadieneNucleophileOrganic reactionChemistryElectrophileGeneral Physics and AstronomyIminiumIonic bondingSingle bondReactivity (chemistry)Physical and Theoretical ChemistryTopology
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1989

By endcapping of living polystyrene with ethylene oxide and subsequent reaction with bromoacetyl bromide a polymer with a bromoacetoxy endgroup was obtained. This was used as a macroinitiator for the living cationic polymerization of 1-azabicyclo[4.2.0]octane. The structure and composition of the so formed two-block copolymer was elucidated by different methods. The ratio of the two block and their lengths were varied within broad limits.

chemistry.chemical_compoundEnd-groupAnionic addition polymerizationchemistryEndcappingPolymer chemistryCopolymerCationic polymerizationOrganic chemistryPolystyreneLiving cationic polymerizationOctaneDie Makromolekulare Chemie
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Synthesis of Macromolecular Substances by Condensation Polymerization and Stepwise Addition Polymerization

2001

Condensation polymerizations (polycondensations) are stepwise reactions between bifunctional or polyfunctional components, with elimination of simple molecules such as water or alcohol and the formation of macromolecular substances. For the preparation of linear condensation polymers from bifunctional compounds (the same considerations apply to polyfunctional compounds which then lead to branched or crosslinked condensation polymers) there are basically two possibilities. One either starts from a monomer which has two unlike groups suitable for polycondensation (AB type), or one starts from two different monomers, each possessing a pair of identical reactive groups that can react with each …

chemistry.chemical_compoundEnd-groupCondensation polymerChain-growth polymerizationAnionic addition polymerizationPolymerizationchemistryPolymer chemistryCationic polymerizationAddition polymerOrganic chemistryBifunctional
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Fluorimetric determination of binding constants between micelles and chemical systems

1991

Abstract A fluorimetric method is adapted to determine the binding constants (K) between different systems and micelles. The method is based on the variation of the fluorescence of the system in the presence of increasing amounts of a surfactant agent. This method permits the determination of binding constants in strong acid or alkaline media. The binding constants of 1-naphthol and 2-(4-alkylamino-2 hydroxyphenyl)benzo-X azoles (X being an O or an S atom, PAS-O and PAS-S) with cationic, anionic, and nonionic surfactants have been determined by the proposed method. Values from 49,100 M−1 for the interaction between PAS-S and CTAB in basic medium to 10 M−1 for the interaction of 1-naphthol w…

chemistry.chemical_compoundEthylene oxidechemistryPulmonary surfactantInorganic chemistryFluorescence spectrometryCationic polymerizationMicelleOligomerFluorescenceSpectroscopyAnalytical ChemistryNonylphenolMicrochemical Journal
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