Search results for "Gas phase"

showing 10 items of 64 documents

Photophysics and photostability of adenine in aqueous solution: A theoretical study

2010

Abstract The sequential Monte Carlo/CASPT2 approach was employed to investigate deactivation and emission processes from the lowest-lying ππ∗ and n π∗ excited states of 9H-adenine in aqueous solution. It is found that conical intersections connecting the ππ∗ and n π∗ states with the ground state are also present in solution, whereas the barriers for the deactivation paths are significantly smaller on solvated conditions. The large destabilization of the n π∗ state found in solution possibly prevents its involvement in the deactivation photophysics and explains the change from a bi- to a mono-exponential decay for the molecule in the gas phase and solution, respectively.

Aqueous solutionChemical physicsChemistryExcited stateGeneral Physics and AstronomyMoleculePhysical and Theoretical ChemistryPhotochemistryGround stateGas phaseChemical Physics Letters
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Evidence for heterogeneous chlorine activation in the tropical UTLS

2011

Airborne in-situ observations of ClO in the tropics were made during the TROCCINOX (Aracatuba, Brazil, February 2005) and SCOUT-O<sub>3</sub> (Darwin, Australia, November/December 2005) field campaigns. While during most flights significant amounts of ClO (≈10–20 parts per trillion, ppt) were present only in aged stratospheric air, instances of enhanced ClO mixing ratios of up to 40 ppt – significantly exceeding those expected from gas phase chemistry – were observed in air masses of a more tropospheric character. Most of these observations are associated with low temperatures or with the presence of cirrus clouds (often both), suggesting that cirrus ice particles and/or liquid …

Atmospheric Scienceairborne in-situ observationChemistrychemistry.chemical_elementAtmosphärische SpurenstoffeAtmospheric sciencesNitrogenlcsh:QC1-999JGas phaseAerosollcsh:ChemistryTropospherelcsh:QD1-999ddc:550ChlorineLife ScienceCirrusStratospherelcsh:Physics
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Chemistry inside molecular containers in the gas phase.

2013

Inner-phase chemical reactions of guest molecules encapsulated in a macromolecular cavity give fundamental insight into the relative stabilization of transition states by the surrounding walls of the host, thereby modelling the situation of substrates in enzymatic binding pockets. Although in solution several examples of inner-phase reactions are known, the use of cucurbiturils as macrocyclic hosts and bicyclic azoalkanes as guests has now enabled a systematic mass spectrometric investigation of inner-phase reactions in the gas phase, where typically the supply of thermal energy results in dissociation of the supramolecular host-guest assembly. The results reveal a sensitive interplay in wh…

Bicyclic molecule010405 organic chemistryChemistryGeneral Chemical EngineeringGeneral ChemistryActivation energy010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciences3. Good healthGas phaseChemical physicsCucurbiturilta116Nature chemistry
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Discrimination of nerve gases mimics and other organophosphorous derivatives in gas phase using a colorimetric probe array.

2012

A colorimetric array for the chromogenic discrimination of organophosphorous derivatives in gas phase has been developed. The array allows us to classify the nerve agent simulants DFP, DCP and DCNP.

Chemical warfare agentsNerve gasesSensitivity and SpecificityCatalysisGas phaseQUIMICA ORGANICAOrganophosphorus CompoundsMaterials ChemistryChemical Warfare AgentsChromogenic detectionPROYECTOS DE INGENIERIAChromatographyChemistryChromogenicSensorsQUIMICA INORGANICAMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsProbe arrayRecognitionMultivariate AnalysisCeramics and CompositesColorimetryGasesDCNPChemical communications (Cambridge, England)
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Basis set and correlation effects in the calculation of accurate gas phase dimerization energies of two M+2 to give M2+4 (M = S, Se)

2000

The dimerization energies of two M2+ to give M42+ (M = S, Se) were calcd. They depend strongly on the size of the basis set and the correlation method used (ranging from 217 to 522 kJ/mol, M = S) and, therefore, a systematic study of basis set and correlation effects was performed [MP2, MP3, MP4(SDQ), CCSD, CCSD(T)]. The introduction of a second set of polarizing d-functions caused a significant redn. of the dimerization energies, but neither of the above limits is reached by the MPn (n = 2, 3, 4) theory, even with the largest basis sets [cc-pVQZ]. However, convergence was achieved by CCSD(T), compd. methods or hybrid HF/DFT calcns. employing flexible basis sets [e.g., CCSD(T)/cc-pV5Z, CBS-…

Computational MathematicsBasis (linear algebra)M.2Computational chemistryChemistryPhysical chemistryCorrelation methodGeneral ChemistryBasis setGas phaseJournal of Computational Chemistry
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A density functional theory evaluation of hydrophobic solvation: Ne, Ar and Kr in a 50-water cluster – Implications for the hydrophobic effect

2012

The physical explanation for the hydrophobic effect has been the subject of disagreement. Physical organic chemists tend to use a explanation related to pressure, while many biochemists prefer an explanation that involves decreased entropy of the aqueous solvent. We present DFT calculations at the B3LYP/6-31G(d,p) and X3LYP/6-31G(d,p) levels on the solvation of three noble gases (Ne, Ar, and Kr) in clusters of 50 waters. Vibrational analyses show no substantial decreases in the vibrational entropies of the waters in any of the three clusters. The observed positive free energies of transfer from the gas phase or from nonpolar solvents to water appear to be due to the work needed to make a su…

Conformational changeAqueous solutionChemistrySolvationCondensed Matter PhysicsBiochemistryArticleGas phaseSolventHydrophobic effectChemical physicsComputational chemistryDensity functional theoryWater clusterPhysical and Theoretical ChemistryComputational and Theoretical Chemistry
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Coupled cluster calculations of the vertical excitation energies of tetracyanoethylene

2003

The vertical spectrum of tetracyanoethylene was studied using coupled cluster theory. It was found that the lowest singlet-singlet transition, which corresponds to the excitation from the highest occupied molecular orbital (HOMO) to the lowest unoccupied molecular orbital (LUMO) excitation, occurs at 5.16 eV in the gas phase and is lowered approximately 0.1 eV due to solvent effects in acetonitrile. A parallel study on the ethene spectrum showed the quality of the basis sets and methods used, by placing the V state 7.92 eV above the ground state and giving an energy for the 0-0 transition of 5.42 eV to be compared with the experimental value of 5.50 eV.

Coupled Cluster CalculationsOrganic CompoundsUltraviolet SpectraGeneral Physics and AstronomyTetracyanoethyleneOrganic Compounds ; Coupled Cluster Calculations ; Ultraviolet Spectra ; Visible SpectraUpper and lower boundsGas phaseUNESCO::FÍSICA::Química físicaPhysics and Astronomy (all)chemistry.chemical_compoundFormalism (philosophy of mathematics)Coupled clusterchemistryVisible SpectraComputer Science::Systems and ControlMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physics:FÍSICA::Química física [UNESCO]AcetonitrileAstrophysics::Galaxy AstrophysicsExcitation
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Determination of inorganic species by thermal lens spectrometry

1997

Abstract The application of thermal lens spectrometry (TLS) to the determination of inorganic species is reviewed. The requirements of a chromogenic reaction to be advantageously adapted to TLS detection, and the necessary conditions for reaching very low limits of detection are discussed. Methods for the determination of metals and P, Si, S and N compounds in several samples are examined. Flow-injection and extraction methods, associated photoinduced reactions and surface phenomena, speciation and equilibrium studies are discussed. Gas phase NO 2 methods are also commented upon. Trends are given.

Detection limitChromogenicChemistryAnalytical chemistryMass spectrometryN compoundsAnalytical ChemistryGas phaselaw.inventionLens (optics)lawThermalExtraction methodsSpectroscopyTrAC Trends in Analytical Chemistry
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Impact of the ΔPhe configuration on the Boc-Gly-ΔPhe-NHMe conformation: experiment and theory

2019

Conformational propensities of N-t-butoxycarbonyl-glycine-(E/Z)-dehydrophenylalanine N′-methylamides (Boc-Gly-(E/Z)-ΔPhe-NHMe) in chloroform were investigated by NMR and IR techniques. The low-temperature crystal structure of the E isomer was determined by single crystal X-ray diffraction and the experimental data were elaborated by theoretical calculations using DFT (B3LYP, M06-2X) and MP2 approaches. The β-turn tendencies for both isomers were determined in the gas phase and in the presence of solvent. The obtained results reveal that the configuration of ΔPhe residue significantly affects the conformations of the studied dehydropeptides. The tendency to adopt β-turn conformations is sign…

Diffractionβ-turn tendencyCrystal structure010402 general chemistry01 natural sciencesGas phaseX-ray crystal structure analysischemistry.chemical_compoundResidue (chemistry)Peptide conformational analysisZ isomer0103 physical sciencesPhysical and Theoretical Chemistry13C NMRChloroform010304 chemical physicsDehydrophenylalanineE isomer1H NMRCondensed Matter Physics0104 chemical sciencesSolventCrystallographychemistryIR spectroscopyDFT-GIAO calculationsSingle crystalStructural Chemistry
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ION MOBILITY STUDIES ON SODIUM-BIS (2- ETHYLHEXIL)SULFOSUCCINATE (AOTNa) AGGREGATES

2012

The supramolecular charged aggregates formed during ESI ionization of AOTNa solutions under critical micelle concentration have been studied thorough ion mobility experiments. In particular, positively charged clusters with several charge states, ranging from +1 to +4, have been investigated. It has been found that, despite to previous investigations (Siuzdak et al. 1995, Nohara et al. 1998), specific ionic aggregates with a peculiar cross section are observed. Indeed a single drift time is observed for each charged aggregate. Using both calculated cross section and experimental calibration curves the experimental cross section of the observed cation has been determined. It is worth noting …

ESISettore CHIM/01 - Chimica AnaliticaSettore CHIM/06 - Chimica OrganicaSettore CHIM/08 - Chimica Farmaceuticasupramolecular aggregates Surfactant Micelles Gas phase mass spectrometrySettore CHIM/02 - Chimica Fisica
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