Search results for " hydrides"

showing 7 items of 7 documents

Ag11(SG)7 : A New Cluster Identified by Mass Spectrometry and Optical Spectroscopy

2014

We report a one-step and high yield synthesis of a red-luminescent silver cluster with the molecular formula, Ag11(SG)7 (SG: glutathionate) via reduction of silver ions by sodium borohydride in the presence of the tripeptide, glutathione (GSH). The as-prepared cluster shows prominent absorption features at 485 and 625 nm in its UV-vis absorption spectrum. Aging of the as-prepared cluster solution led to the disappearance of the 625 nm peak, followed by broadening of the 485 nm peak to give three maxima at ?487, 437, and 393 nm in its absorption spectrum. These peaks remain unchanged even after polyacrylamide gel electrophoresis (PAGE), where a single band was observed confirming high purity…

Absorption spectroscopyta114Electrospray ionizationAnalytical chemistryMass spectrometryAbsorption spectra; Density functional theory; Electrodeposition; Electromagnetic wave absorption; Electrophoresis; Electrospray ionization; Isotopes; Light absorption; Mass spectrometry; Metal ions; Potable water; Spectrometry; Ultraviolet spectroscopy; Absorption features; Electrospray ionization mass spectrometry; High yield synthesis; Molecular formula; Optical spectroscopy; Polyacrylamide gel electrophoresis; Sodium boro hydrides; UV-VIS absorption spectra; Absorption spectroscopySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonSodium borohydridechemistry.chemical_compoundGeneral EnergyUltraviolet visible spectroscopychemistryPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)Spectroscopyta116Journal of Physical Chemistry C
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Electronic aspects of the hydride transfer mechanism. Ab initio analytical gradient studies of the cyclopropenyl‐cation/lithium hydride model reactan…

1985

The electronic mechanisms of a model hydride transfer reaction are theoretically studied with ab inito RHF and UHF SCF MO procedures at the 4‐31G basis set level and analytical gradient methods. The model system describes the reduction of cyclopropenyl cation to cyclopropene by the oxidation of lithium hydride to lithium cation. The molecular fragments corresponding to the asymptotic reactive channels characterizing the stepwise mechanisms currently discussed in the literature have been characterized. The binding energy between the fragments is estimated within a simple electrostatic approximate scheme. The results show that a hydride‐ion mechanism is a likely pathway for this particular sy…

Biological MaterialsAb initioGeneral Physics and Astronomychemistry.chemical_elementchemistry.chemical_compoundElectron transferAb initio quantum chemistry methodsComputational chemistry:FÍSICA [UNESCO]CationsRedox ProcessPhysical and Theoretical ChemistryTriplet stateCycloalkenes:FÍSICA::Química física [UNESCO]HydrideUNESCO::FÍSICAChemical ReactionsUNESCO::FÍSICA::Química físicachemistryLithium hydrideChemical physicsLithium HydridesAb Initio Calculations ; Chemical Reactions ; Cycloalkenes ; Cations ; Lithium Hydrides ; Redox Process ; Biological MaterialsLithiumLithium CationAb Initio Calculations
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The chemical bonds in CuH, Cu2, NiH, and Ni2 studied with multiconfigurational second order perturbation theory

1994

The performance of multiconfigurational second order perturbation theory has been analyzed for the description of the bonding in CuH, Cu2, NiH, and Ni2. Large basis sets based on atomic natural orbitals (ANOS) were employed. The effects of enlarging the active space and including the core‐valence correlation contributions have also been analyzed. Spectroscopic constants have been computed for the corresponding ground state. The Ni2 molecule has been found to have a 0+g ground state with a computed dissociation energy of 2.10 eV, exp. 2.09 eV, and a bond distance of 2.23 Å. The dipole moments of NiH and CuH are computed to be 2.34 (exp. 2.4±0.1) and 2.66 D, respectively. pou@uv.es ; merchan@…

Chemical BondsGeneral Physics and AstronomyDissociation EnergyDipole MomentsPerturbation Theory ; Chemical Bonds ; Configuration Interaction ; Copper Hydrides ; Nickel Hydrides ; Copper ; Nickel ; Electron Correlation ; Core Levels ; Dissociation Energy ; Dipole Moments ; Bond Lengths ; Diatomic MoleculesCore LevelsBond LengthsNickelPhysical and Theoretical ChemistryPerturbation theory:FÍSICA::Química física [UNESCO]Nickel HydridesDiatomic MoleculesElectronic correlationChemistryConfiguration interactionBond-dissociation energyDiatomic moleculeUNESCO::FÍSICA::Química físicaBond lengthConfiguration InteractionChemical bondCopper HydridesPerturbation TheoryElectron CorrelationAtomic physicsGround stateCopper
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Calculation of size‐intensive transition moments from the coupled cluster singles and doubles linear response function

1994

Coupled cluster singles and doubles linear response (CCLR) calculations have been carried out for excitation energies and dipole transition strengths for the lowest excitations in LiH, CH+, and C4and the results compared with the results from a CI-like approach to equation of motion coupled cluster (EOMCC). The transition strengths are similar in the two approaches for single molecule calculations on small systems. However, the CCLR approach gives size-intensive dipole transition strengths, while title EOMCC formalism does not. Thus, EOMCC calculations can give unphysically dipole transition strengths, e.g., in EOMCC calculations on a sequence of noninteracting LiH systems we obtained a neg…

DipolesGeneral Physics and AstronomySmall systemsExcitation ; Dipoles ; Lithium Hydrides ; Carbynes ; Cations ; Molecular Ions ; Carbon Molecules ; Equations Of Motion ; Correlations ; Response FunctionsPhysics and Astronomy (all)CationsMoleculePhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]ExcitationCorrelationsChemistryEquations of motionCarbon MoleculesLinear response functionUNESCO::FÍSICA::Química físicaFormalism (philosophy of mathematics)DipoleCoupled clusterLithium HydridesCarbynesResponse FunctionsAtomic physicsEquations Of MotionMolecular IonsExcitationThe Journal of Chemical Physics
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Photochromic System among Boron Hydrides: The Hawthorne Rearrangement

2019

Photoswitchable molecules have attracted wide interest for many applications in chemistry, physics, and materials science. In this work, we revisit the reversible photochemical and thermal rearrangements of the two B20H182– isomers reported by Hawthorne and Pilling in 1966, whose mechanism had not been understood so far. We investigate the rearrangements by means of a joint experimental and computational study with the outcome that B20H182– represents the first boron-based photochromic system ever reported. Both photochemical and thermal isomerizations occur through the same intermediate and involve a diamond–square–diamond (DSD) mechanism. Given the absence within boron chemistry of named …

Photochromismchemistrychemistry.chemical_elementMoleculeGeneral Materials ScienceBoron HydridesPhysical and Theoretical ChemistryPhotochemistryBoronChemical reactionIsomerization
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Effect of nano-structuring on hydrogen sorption properties of LaNi5 systems

2010

hydrogen storage LaNi5 nanostructuring hydrides ball milling
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Nanostructured Materials and Systems for Hydrogen Technology

2011

hydrogen storage nanostructuring hydrides ball milling borohydrides hydrogen tank nanoconfinement
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