Search results for "ionic"

showing 10 items of 2016 documents

Hydrophobicity of ionisable compounds studied by countercurrent chromatography

2011

Countercurrent chromatography (CCC) is a liquid chromatography technique in which the stationary phase is also a liquid. The main chemical process involved in solute separation is partitioning between the two immiscible liquid phases: the mobile phase and the support-free liquid stationary phase. The octanol-water partition coefficients (P(o/w)) is the accepted parameter measuring the hydrophobicity of molecules. It is considered to estimate active principle partitioning over a biomembrane. It was related to the substance biological activity. CCC is able to work with an octanol stationary phase and an aqueous mobile phase. In this configuration, CCC is a useful and easy alternative to measu…

OctanolAdrenergic beta-AntagonistsHydrophobicityAnalytical chemistryIonic bonding01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundCountercurrent chromatographyPhase (matter)MoleculeDiureticsCountercurrent DistributionAqueous solutionChromatography010405 organic chemistryHydrophilic interaction chromatography010401 analytical chemistryOrganic ChemistryOctanol–water partition coefficientsGeneral Medicine0104 chemical sciencesPartition coefficientPharmaceutical PreparationschemistryCountercurrent chromatographyIonisable compoundsHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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Pulse radiolysis and theoretical investigation on the initial mechanism of the e-beam polymerization of epoxy resins. The results obtained on (phenox…

2007

Abstract The radical cation of (phenoxymethyl)oxirane ( PGE ⋅ + ) is generated by pulse radiolysis in dichloromethane solution and by direct action of radiation on the title compound. In the pure system its UV–vis spectrum is characterized by two bands at 340 and 430 nm, such that the electronic structure corresponds to a dipole bearing the positive charge on the phenoxy side. At the same time, the phenoxy-oxirane bridge is weakened. Then, the radical cation fragments into a phenoxonium ion and an oxyranylmethyl radical ( k PGE - fragm = 1.16 × 10 7 s - 1 ) . The latter immediately rearranges to an allyloxyl radical by ring opening. It is then conceived that the action of onium salts, as ra…

Onium saltsRadiationPulse radiolysisChemistryCationic polymerizationCationic polymerizationOniumEpoxy ring openingPhotochemistryIonchemistry.chemical_compoundRadical ionPolymerizationRadiolysisPolymer chemistryElectron beam curingCuring (chemistry)Pulse radiolysiDichloromethane
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Effect of Lithium Perchlorate on the Kinetics of the Anionic Polymerization of Methyl Methacrylate in Tetrahydrofuran

1999

The kinetics of the anionic polymerization of methyl methacrylate in the presence of lithium perchlorate (LiClO 4 ) are investigated in THF using 1,1-diphenylhexyllithium as initiator in a flow-tube reactor between -30 and 0 °C. The rate constants of propagation determined in the presence of LiClO 4 are lower than those obtained in the absence of the salt, similar to the effect observed for LiCl. For propagation, the reaction order with respect to active center concentration is found to be 0.5 in both cases, which indicates that LiClO 4 does not effectively perturb the aggregation of the enolate ion pair. The formation of various mixed aggregates is proposed. The polydispersity index of the…

Order of reactionPolymers and PlasticsOrganic ChemistryInorganic chemistryKineticsSolution polymerizationLithium perchlorateInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryMaterials ChemistryMethyl methacrylateTetrahydrofuranMacromolecules
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N,N-Di-n-octyl-N,N-dimethyl and N,N-di-n-nonyl-N,N-dimethyl ammonium cholates: 13C and 15N CPMAS NMR, powder X-ray diffraction and thermoanalytical c…

2009

Abstract N,N-Di-n-octyl-N,N-dimethyl cholate (1) and N,N-di-n-nonyl-N,N-dimethyl ammonium cholate (2) have been prepared by crystallization from equimolar mixtures of sodium cholate and quaternary N,N-di-n-alkyl-N,N-dimethyl (n-octyl or n-nonyl) ammonium bromides. The formed crystalline materials have been structurally characterized by 13C and 15N cross polarization magic angle spinning (CPMAS) NMR, powder X-ray diffraction (PXRD) and thermoanalytical (TGA/DTA and DSC) methods and compared with each other. Powder X-ray diffraction patterns of 1 and 2 reveal clear similarities. Combined with the thermoanalytical data of these structures an existence of two hydrated polymorphs (most probably …

Organic ChemistryInorganic chemistryIonic bondingAnalytical Chemistrylaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPolymorphism (materials science)lawX-ray crystallographyMagic angle spinningAmmoniumCrystallizationSodium CholateSpectroscopyPowder diffractionJournal of Molecular Structure
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A study of the influence of ionic liquids properties on the Kemp elimination reaction

2009

The morpholino-induced elimination of 5-nitrobenzisoxazole into the relevant 2-cyano-4-nitrophenolate has been used as a sample reaction in order to investigate molecular properties of some room temperature ionic liquids. The kinetic study was carried out at 298 K by means of spectrophotometric measurements. Ionic liquids, which differ in both their cation and anion properties, were used as solvent systems. In particular, aliphatic (pyrrolidinium, piperidinium, and ammonium) and aromatic (imidazolium and pyridinium) ionic liquids were used. For aromatic cations, imidazolium ions having different hydrogen-bond donor ability or a different alkyl-chain length were taken into account. The anion…

Organic ChemistryInorganic chemistryIonic bondingionic liquids Kemp elimination base catalysisGeneral ChemistrySettore CHIM/06 - Chimica OrganicaResonance (chemistry)CatalysisIonSolventchemistry.chemical_compoundElimination reactionchemistryIonic liquidPyridiniumImide
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Metal Telluride Clusters Composed of Niobocene Carbonyl, Telluride, and Cobalt Carbonyl Units: Syntheses, Structures, and Reactivity

2000

Abstract: The reaction of [Cp#2NbTe2H] (1#; Cp# = Cp* (C5Me5) or Cp(x) (C5Me4Et)) with two equivalents of [Co2(CO)8] gives a series of cobalt carbonyl telluride clusters that contain different types of niobocene carbonyl fragments. At 0 degrees C, [Cp#2NbTe2CO3(CO)7] (2#) and [Co4Te2(CO)10] (3) are formed which disappear at higher temperatures: in boiling toluene a mixture of [cat2][Co9Te6(CO)8] (5#) (cat= [Cp#2Nb(CO)2]+) and [cat2][Co11Te7(CO)10] (6#) is formed along with [cat][Co(CO)4] (4#). Complexes 6# transform into [cat][Co11Te7(CO)10] (7#) upon interaction with HPF6 or wet SiO2. The molecular structures of 2(Cp(x)), 4(Cp(x)), 5(Cp*), 6(Cp*) and 7(Cp*) have been determined by X-ray cr…

Organic ChemistryInorganic chemistrychemistry.chemical_elementIonic bondingGeneral ChemistryCatalysisMetalCrystallographyElectron transferchemistry.chemical_compoundBipyramidchemistryvisual_artTelluridevisual_art.visual_art_mediumReactivity (chemistry)TelluriumCobaltChemistry - A European Journal
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A DFT study of the ionic [2+2] cycloaddition reactions of keteniminium cations with terminal acetylenes

2015

Abstract The molecular mechanism of the ionic [2+2] cycloaddition (I-22CA) reactions of a keteniminium cation (KC) with acetylene and propyne has been investigated using DFT methods at the MPWB1K/6-311G(d,p) level. These I-22CA reactions take place via a two-step mechanism. The first step is the nucleophilic attack of these alkynes on the central carbon of KC, yielding cyclopropene intermediates, while the second step corresponds to the conversion of these intermediates into more stable cyclobuteniminium cations (CCs). The first step is the rate-determining step, while the second step is responsible for the formation of the two regioisomeric CCs experimentally observed in the reaction with …

Organic ChemistryIonic bondingCyclopropenePropynePhotochemistryBiochemistryCycloadditionchemistry.chemical_compoundNucleophilechemistryAcetyleneComputational chemistryDrug DiscoveryElectrophileReactivity (chemistry)Tetrahedron
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Crystal structure of a novel bismuth phthalocyanine-bismuth iodide complex

1999

Abstract A new phthalocyaninato complex of bismuth with formula [(BiPc) 4 (Bi 4 I 16 )] was obtained in the reaction of bismuth with 1,2-dicyanobenzene in iodine vapour. The crystal and molecular structure of the complex was determined by single crystal X-ray diffraction. The unit cell consists of four discrete (BiPc) + cations and (Bi 4 I 16 ) 4− anions. The (Bi 4 I 16 ) 4− complex anion is formed by four edge-sharing BiI 6 octahedra. The arrangement of molecules in the crystalline structure of the complex is mainly determined by ionic attraction between the (BiPc) + and (Bi 4 I 16 ) 4− moieties, i.e. each (Bi 4 I 16 ) 4− complex anion is encapsulated between four (BiPc) + cations. The str…

Organic ChemistryIonic bondingchemistry.chemical_elementCrystal structureAnalytical ChemistryBismuthInorganic ChemistryCrystalchemistry.chemical_compoundCrystallographychemistryOctahedronPhthalocyanineMoleculeSingle crystalSpectroscopyJournal of Molecular Structure
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Dialkylimidazolium dimethyl phosphates as solvents and catalysts for the Knoevenagel condensation reaction

2014

Abstract The reaction between benzaldehyde and ethyl cyanoacetate is investigated in 1,3-dialkylimidazolium salts as solvents. The impact of both ions in these ionic liquids on the yield of the condensation reaction product is examined. Potentiometric titrations are employed for quantitative analyses of the best ionic liquids, revealing these to be 1,3-dialkylimidazolium dimethyl phosphates.

Organic ChemistryPotentiometric titrationCondensation reactionBiochemistryCatalysisIonBenzaldehydechemistry.chemical_compoundchemistryYield (chemistry)Drug DiscoveryIonic liquidOrganic chemistryKnoevenagel condensationTetrahedron Letters
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Host–guest blue light-emitting electrochemical cells

2014

Carbazole, a commonly used hole-transporter for organic electronics, has been modified with an imidazolium cation and a hexafluorophosphate counter-anion to give an ionic hole-transporter. It has been applied as one of the hosts in a host–guest blue light-emitting electrochemical cell (LEC) with the neutral blue emitter FIrPic. We have obtained efficient and bright blue LECs with an electroluminescence maximum at 474 nm and efficacy of 5 cd A−1 at a luminance of 420 cd m−2, thereby demonstrating the potential of the ionic organic charge-transporters and of the host–guest architecture for LECs.

Organic electronicsMaterials scienceCarbazoleInorganic chemistryIonic bondingGeneral ChemistryElectroluminescenceElectrochemical cellchemistry.chemical_compoundchemistryHexafluorophosphateMaterials ChemistryCommon emitterBlue lightJ. Mater. Chem. C
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