Search results for "Lithium Hydrides"

showing 2 items of 2 documents

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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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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