Search results for "Ion pairs"

showing 10 items of 19 documents

Ion-Pairing Effects in the Self-Assembly of a Fluorescent Pseudorotaxane

2006

Herein we report on the self-assembly, in a low polarity solvent, of a pseudorotaxane species comprising binaphthyl-26-crown-8 (BN26C8) as the macrocyclic host and anthracenyl-benzylammonium as the threadlike positively charged guest (ABH+). Absorption and luminescence data reveal a very efficient energy transfer process occurring from the binaphthyl to the anthracene singlet excited states. The self-assembly is highly dependent on the nature of the counteranion confirming the crucial role played by it in the competition between the self-assembly process and the formation of ion pairs (ABH+X-). This behavior can be readily evidenced in dilute solutions from the analysis of the luminescence …

AnthraceneIon pairsRotaxanesPhotochemistryStereochemistryOrganic ChemistrySupramolecular chemistrySelf-assemblychemistry.chemical_compoundCrystallographyTRISPHATMolecular recognitionchemistryHexafluorophosphateddc:540Proton NMRSinglet stateMolecular recognitionPhysical and Theoretical ChemistryLuminescenceEuropean Journal of Organic Chemistry
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Protonation of Carbonate in Aqueous Tetraalkylammonium Salts at 25°C.

2006

Protonation constants of carbonate were determined in tetramethylammonium chloride (Me4NClaq 0.1≤I/mol kg−1 ≤4) and tetraethylammonium iodide (Et4NIaq 0.1≤I/mol kg−1 ≤1) by potentiometric ([H+]-glass electrode) measurements. Dependence of protonation constants on ionic strength was taken into account by modified specific ion interaction theory (SIT) and by Pitzer models. Literature data on the protonation of carbonate in NaClaq (0.1≤I/mol kg−1 ≤6) were also critically analysed. Both protonation constants of carbonate follow the trend Et4NI>Me4NCl > NaCl. An ion pair formation model designed to take into account the different protonation behaviours of carbonate in different supporting electr…

Aqueous solutionProtonation of carbonateSpecific ion interaction theory (SIT)Ion pair formation modelChemistryInorganic chemistryTetraalkylammonium saltProtonationDependence on ionic strengthElectrolyteIon pairsAnalytical Chemistrychemistry.chemical_compoundIonic strengthTetramethylammonium chlorideAqueous solutionPitzer equationsCarbonateSettore CHIM/01 - Chimica AnaliticaProtonation of carbonate; Dependence on ionic strength; Aqueous solution; Tetraalkylammonium salts; Ion pair formation model; Specific ion interaction theory (SIT); Pitzer equationPitzer equation
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Amine basicity: measurements of ion pair stability in ionic liquid media

2007

Abstract The stability constants relevant to the formation of amine/p-nitrophenol ion pairs have been determined in [bmim][BF4] solution, in the presence of butylamine, piperidine, and triethylamine, by using spectrophotometric measurements. In order to evaluate how the ion pair stability is affected by ionic liquid structure, piperidine has been chosen as model amine for studies in [bmim][PF6], [bmim][NTf2], [bm2im][NTf2] and in several [bmim][BF4]/1,4-dioxane binary mixtures. Data obtained in ionic liquid solutions have been compared with those previously reported in conventional organic solvents.

ButylamineOrganic ChemistryInorganic chemistrySettore CHIM/06 - Chimica OrganicaIon pairsBiochemistrychemistry.chemical_compoundchemistryIonic liquids amine basicity ion pairDrug DiscoveryIonic liquidAmine gas treatingPiperidineTriethylamineTetrahedron
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Über den einfluß der monomerkonzentration auf die geschwindigkeitskonstante kw der monomeraddition an das ionenpaar eines „lebenden” polymeren

1966

Fur den Zahlenwert der Geschwindigkeit skonstante kw(±) fanden die Arbeitsgruppen in Mainz und Syracuse voneinander abweichende Werte. Es wurde angenommen, das die Ursache dieser Diskrepanz die um Grosenordnungen verschiedenen Konzentrationsbereiche sind, in denen die Messungen ausgefuhrt wurden. Nachfolgend wird ein Reaktionsschema vorgeschlagen und kinetisch durchgerechnet, welches eine schneller polymerisierende Komplexverbindung zwischen dem Ionenpaar und dem Monomeren voraussetzt. The rate constant kw(±) for the addition of monomer to the ion pair of a „living” polymer was measured by workers in Mainz and in Syracuse. Their results lack agreement. It was assumed that this disparity is …

ChemistryPolymer chemistryIon pairsDie Makromolekulare Chemie
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Extractive Spectrophotometric Determination of Ondansetron by Ion-Pair Formation with Bromocresol Green

1996

Abstract An empirical spectrophotometric procedure for the determination of the antiemetic ondansetron is carried out. The method is based on the formation of a 1:1 ion pair with bromocresol green in the pH range over 3.2 – 4.4, extraction into chloroform layer and spectrophotometric measurement at 420.8 nm. The calibration graph is linear over the range 0.1 – 20 μg ml−1 ondansetron, with a relative standard deviation of 2.7%; the influence of foreign substances is also studied. The method is applied to ondansetron determination in human urine.

ChromatographyChloroformBromocresol greenmedicine.diagnostic_testCalibration curveBiochemistry (medical)Clinical BiochemistryExtraction (chemistry)Ion pairsBiochemistryAnalytical ChemistryOndansetronchemistry.chemical_compoundchemistrySpectrophotometryElectrochemistrymedicineQuantitative analysis (chemistry)Spectroscopymedicine.drugAnalytical Letters
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Kinetic control in the chiral recognition of three-bladed propellers

2010

The ion pair of the stereolabile C(3)-symmetric, i(+)o proton complex [1H](+) of diaza-macropentacycle 1 and the configurationally stable Delta-TRISPHAT ([Delta-3](-)) anion exists in the form of two diastereomers, namely, [Delta-(1.H)][Delta-3] and [Lambda-(1.H)][Delta-3], the ratio of which, in terms of diastereomeric excess (de) decreases in the order [D(8)]THF (28%)CD(2)Cl(2) (22%)CDCl(3) (20%)[D(8)]toluene (16%)C(6)D(6) (7%)[D(6)]acetone (0%) at thermodynamic equilibrium. Except in the case of [D(6)]acetone, the latter is reached after a period of time that increases from 1 h ([D(8)]THF) to 24 h (CDCl(3)). Moreover, the initial value of the de of [1.H][Delta-3] in CDCl(3), before the t…

CryptandsIon pairsProtonStereochemistryOrganic ChemistryKineticsDiastereomerProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyTolueneCatalysischemistry.chemical_compoundCrystallographyKineticsDeprotonationchemistryddc:540Solvent effectsSolvent effectsHelical structures
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Low-Q peak in X-ray patterns of choline-phenylalanine and homophenylalanine: a combined effect of chain and stacking

2016

Abstract In this contribution we report for the first time the X-ray patterns of choline-phenylalanine and choline-homophenylalanine ionic liquids. The presence of a low Q peak in both systems is another evidence that a long alkyl chain is not always needed to establish a nanodomain segregation in the liquid sufficient to be revealed by the diffraction experiment. These new data are compared with the diffraction patterns and the theoretical calculations of other choline-aminoacid ionic liquids recently reported. A significant role might be played by the stacking interactions between aromatic rings.

DiffractionChemical substancePhenylalanineStackingGeneral Physics and AstronomyPhenylalanine02 engineering and technologyIonic liquid010402 general chemistry01 natural sciencesCholinePhysics and Astronomy (all)chemistry.chemical_compoundAminoacidSettore CHIM/02Organic chemistryPhysical and Theoretical ChemistryAlkylcholine-amino acid ionic liquids EDXD; ion pairs; pre-peak; renewable materialschemistry.chemical_classificationSmall-angle X-ray scatteringSAXS; Choline; Phenylalanine; Aminoacids; Ionic liquidsAromaticitySAXS021001 nanoscience & nanotechnologyIonic liquids0104 chemical sciencesCrystallographychemistryIonic liquid0210 nano-technologyAminoacids
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Leitfahigkeitsmessungen an Polystyrylnatrium in Dimethoxiäthan (DME) und Tetrahydrofuran (THF)

1971

An Polystyrylnatrium werden in zwei polaren organischen Losungsmitteln Leitfahigkeitsmessungen uber einen groseren Temperaturbereich ausgefuhrt. Aus der Temperaturabhangigkeit der Dissoziationskonstante ergibt sich, das die undissoziierte Verbindung in zwei Formen, dem Kontaktionenpaar (I) und dem solvatgetrennten Ionenpaar (II), vorkommt. Enthalpie- und Entropiedifferenz beim ubergang von I nach II, sowie die entsprechenden thermodynamischen Parameter der Dissoziation von II werden ermittelt. Der effektive Ladungsabstand im solvatgetrennten Ionenpaar betragt etwa 7 A. Conductivity measurements were carried out with polystyryl sodium in two polar solvents within a large temperature range. T…

Dissociation constantSolventchemistry.chemical_compoundchemistryGeneral Chemical EngineeringEnthalpyPolymer chemistryPhysical chemistryAtmospheric temperature rangeIon pairsConductivityTetrahydrofuranEffective nuclear chargeBerichte der Bunsengesellschaft für physikalische Chemie
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Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications

2001

An efficient system for the analysis of indole alkaloids by HPLC on a reversed-phase column using an ion pair technique is described. The optimised chromatographic conditions allowed the successful separation of 22 standard monoterpenoid indole alkaloids (including some isomers) and tryptamine. The described HPLC system was applied to the analysis of alkaloids in intergeneric somatic hybrid cell cultures of Rauvolfia serpentina x Rhazya stricta.

Indole testTryptamineMonoterpenoid Indole AlkaloidsChromatographybiologyApocynaceaeChemistryPlant ScienceGeneral MedicineIon pairsRhazya strictabiology.organism_classificationBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineRauvolfia serpentinaDrug DiscoveryMolecular MedicineFood SciencePhytochemical Analysis
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N-Heterocyclic Phosphenium, Arsenium, and Stibenium Ions as Ligands in Transition Metal Complexes: A Comparative Experimental and Computational Study

2005

Reaction of 2-chloro-1,3,2-diazaarsolenes and -diazaphospholenes with Tl[Co(CO)4] gives instable complexes of type [Co(ER2)(CO)4] which decarbonylated to yield [Co(ER2)(CO)3]. Spectroscopic and X-ray diffraction studies revealed that the tetracarbonyl complexes can be formulated as ion pair for E = P and as covalent metalla-arsine for E = As, and the tricarbonyl complexes as carbene-like species with a formal E=Co double bond. A similar reactivity towards Tl[Co(CO)4] was also inferred for 1,3,2-diazastibolenes although the products were not isolable and their constitution remained uncertain. Evaluation of structural and computational data suggests that the weak and polarized Co–As bond in […

Inorganic Chemistrychemistry.chemical_classificationCrystallographyTransition metalDouble bondStereochemistryChemistryCovalent bondYield (chemistry)Reactivity (chemistry)Ion pairsIonZeitschrift für anorganische und allgemeine Chemie
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