Search results for "Positive Ions"

showing 8 items of 8 documents

Assessment for the mean value total dressing method: Comparison with coupled cluster including triples methods for BF, NO+, CN+, C2, BeO, NH3, CH2, H…

1997

Limited previous experience with the mean value total dressing (MVTD) method had shown that MVTD energies for closed shell systems are generally better than CCSD(T) ones compared to FCI. The method, previously published as total dressing 2′(td-2′), is based on the single reference intermediate Hamiltonian theory. It is not a CC method but deals in a great part with the same physical effects that CC methods that incorporate amplitudes of triples such as CCSDT or its CCSDT-1n approaches. A number of test calculations comparing to diverse CC methods, as well as FCI and experiment when available, have been performed. The tests concern equilibrium energies in NH3 and CH2, equilibrium energies an…

Carbon compoundsGeneral Physics and AstronomyBoron compounds ; Nitrogen compounds ; Water ; Ammonia ; Ozone ; Organic compounds ; Carbon compounds ; Beryllium compounds ; Hydrogen compounds ; Silicon compounds ; Lithium ; Lithium compounds ; Carbon ; Neon compounds ; Coupled cluster calculations ; Dissociation ; Dissociation energies ; Positive ionsLithiumDissociation (chemistry)Nitrogen compoundsIonDissociation energiesOzoneCoupled cluster calculationsAmmoniaBeryllium compoundsOrganic compoundsMoleculeSilicon compoundsPhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]Open shellChemistryNeon compoundsMean valueWaterLithium compoundsHydrogen compoundsDiatomic moleculeCarbonUNESCO::FÍSICA::Química físicaCoupled clusterAmplitudeBoron compoundsPositive ionsAtomic physicsDissociation
researchProduct

Kinetic modeling of ion conduction in KcsA potassium channel.

2005

KcsA constitutes a potassium channel of known structure that shows both high conduction rates and selectivity among monovalent cations. A kinetic model for ion conduction through this channel that assumes rapid ion transport within the filter has recently been presented by Nelson. In a recent, brief communication, we used the model to provide preliminary explanations to the experimental current-voltage J-V and conductance-concentration g-S curves obtained for a series of monovalent ions (K(+),Tl(+), and Rb(+)). We did not assume rapid ion transport in the calculations, since ion transport within the selectivity filter could be rate limiting for ions other than native K(+). This previous wor…

ChemistrySodiumPositive IonsIonic ConductivityAnalytical chemistryKcsA potassium channelUNESCO::FÍSICAGeneral Physics and AstronomyConductanceIon-associationRubidiumIonReaction rate constant:FÍSICA [UNESCO]Biomembrane TransportPotassium ; Thallium ; Rubidium ; Sodium ; Positive Ions ; Ionic Conductivity ; Biomembrane TransportPotassiumIonic conductivityPhysical and Theoretical ChemistryThalliumIon transporterIon channelThe Journal of chemical physics
researchProduct

Carbon nanotubes embedded in a polyimide foil for proton acceleration with a sub-ns laser

2021

A series of thin films made of aligned carbon nanotubes (CNTs) embedded in a polyimide substrate was designed, fabricated and used for the first time to accelerate protons and C ions by interaction with a sub-nanosecond, high power laser beam (600 J energy and 300 ps pulse width) with peak intensity of about 3 × 1016 W/cm2 on target. Each target was 5 μm thick, and the composite material contained CNTs aligned in different directions in the substrate. The results obtained from the analysis of a Thomson Parabola spectrometer, and of the spots imprinted by ions on a series of PM355 nuclear track detectors, indicate high energies (up to 3 MeV for protons and 9 MeV for C ions) and a marked infl…

Ion sources (positive ionsMaterials scienceProtonbusiness.industrySettore ING-IND/20 - Misure E Strumentazione NucleariCarbon nanotubeLaserNegative ionsSettore FIS/03 - Fisica Della Materialaw.inventionElectron beam (EBIS))AccelerationManufacturinglawOptoelectronicsPolyimide foilbusinessElectron cyclotron resonance (ECR)InstrumentationMathematical Physics
researchProduct

Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
researchProduct

Smart High-κ Nanodielectrics Using Solid Supported Polyoxometalate-Rich Nanostructures

2011

Utilizing Langmuir-Blodgett deposition and scanning probe microscopy, we have investigated the extent to which cations alter the self-assembly processes of hybrid polyoxometalates (POMs) on surfaces. The well-defined 2D hexagonal nanostructures obtained were extensively characterized and their properties were studied, and this has revealed fascinating dielectric behavior and reversible capacitive properties. The nanostructures are extremely stable under ambient conditions, and yet exhibit fascinating self-patterning upon heating. These findings present POMs as effective smart nanodielectrics and open up a new field for future POM applications. (c) 2011 American Chemical Society.

Materials scienceNanostructureMacromolecular SubstancesSurface PropertiesMolecular ConformationGeneral Physics and AstronomyNanotechnologyDielectricsurfacesSmart materialScanning probe microscopyMaterials TestingElectric ImpedanceIntelligent materialsGeneral Materials ScienceParticle SizeCation exchangesDielectric behaviorPolyoxometalateHexagonal crystal systemPolyoxometalatesGeneral EngineeringOxidesself-assemblyTungsten CompoundsSelf assemblyNanodielectricsNanostructuresHigh-κ NanodielectricSelf assembly processScanning probe microscopyLangmuir-Blodgett depositionPositive ionsPolyoxometalateSelf-assembly2D-hexagonalAmbient conditions
researchProduct

Electrical Pumping of Potassium Ions Against an External Concentration Gradient in a Biological Ion Channel

2013

We show experimentally and theoretically that significant currents can be obtained with a biological ion channel, the OmpF porin of Escherichia coli, using zero-average potentials as driving forces. The channel rectifying properties can be used to pump potassium ions against an external concentration gradient under asymmetric pH conditions. The results are discussed in terms of the ionic selectivity and rectification ratio of the channel. The physical concepts involved may be applied to separation processes with synthetic nanopores and to bioelectrical phenomena. (C) 2013 AIP Publishing LLC.

MicroorganismosPhysics and Astronomy (miscellaneous)PotassiumSeparaciónRatchetAnalytical chemistryBiophysicschemistry.chemical_elementRATCHETPotassium ionsFenómenos bioeléctricosIonSeparationBioelelectric phenomenaRectificationPORINVOLTAGEPotasiomicroorganismsIon channelChemistrypHNANOFLUIDIC DIODEBiomembrane transportIones positivosRECTIFICATIONOMPFTransporte de biomembranasCanales iónicosNanoporeSELECTIVITYPositive ionsFISICA APLICADAIon channelsPotassiumSelectivityConcentration gradientCommunication channelNANOPORES
researchProduct

Picomolar inhibition of cholera toxin by a pentavalent ganglioside GM1os-calix[5]arene

2013

Cholera toxin (CT), the causative agent of cholera, displays a pentavalent binding domain that targets the oligosaccharide of ganglioside GM1 (GM1os) on the periphery of human abdominal epithelial cells. Here, we report the first GM1os-based CT inhibitor that matches the valency of the CT binding domain (CTB). This pentavalent inhibitor contains five GM1os moieties linked to a calix[5]arene scaffold. When evaluated by an inhibition assay, it achieved a picomolar inhibition potency (IC50 = 450 pM) for CTB. This represents a significant multivalency effect, with a relative inhibitory potency of 100000 compared to a monovalent GM1os derivative, making GM1os-calix[5]arene one of the most potent…

Models MolecularCholera ToxinbindingStereochemistrydesignCalix[5]areneEpithelial cellsG(M1) GangliosideHeat-labile enterotoxinmedicine.disease_causeligandBiochemistrycrystalMultivalency effectsCholeraCausative agentsmedicinePotencyHumansoligosaccharidePhysical and Theoretical ChemistryIC50Vibrio choleraeheat-labile enterotoxinVLAGchemistry.chemical_classificationgm1 mimicsGangliosideInhibition assaysChemistryCholera toxinOrganic ChemistryOligosaccharideBinding domainLigand (biochemistry)ValenciesOrganische ChemiehexamethylenetetramineChemistryPositive ionsaffinityAntitoxinsCalixarenesrecognitionBinding domain
researchProduct

Studies in organic mass spectrometry. Part 23. Role of the aroyl group on the competitive fragmentation reactions of the molecular ion of aroylanilid…

1999

The 70 eV and mass-analysed ion kinetic energy (MIKE) spectra of some thiophenecarboxanilides and benzoylanilides (1–10) have been compared in order to investigate the role of the aroyl (or heteroaroyl) moiety on the abundance of the competitive fragmentation reactions occurring in their molecular ions (amide–bond cleavage and phenol radical ion formation). It has been shown that the electron ionisation induced decompositions with high (70 eV) and low (MIKE) internal energy excess are qualitatively similar, but remarkable quantitative differences have been observed that can be accounted for in terms of the different effectiveness in the transmission of electronic effects of substituents in …

substituent effectsChemistryrearrangement processesPolyatomic ionAnalytical chemistryaroylanilidesMass spectrometryPhotochemistryelectron ionisation; positive ions; ion chemistry; aroylanilides; substituent effects; rearrangement processesIonchemistry.chemical_compoundRadical ionFragmentation (mass spectrometry)positive ionsThiopheneElectronic effectMoietyion chemistryelectron ionisationSpectroscopy
researchProduct