Search results for "LUMO"

showing 10 items of 164 documents

A Comparative Analysis of the Electrophilicity of Organic Molecules between the Computed IPs and EAs and the HOMO and LUMO energies

2007

[EN] The electrophilicity index, omega, of a series of substituted ethylenes used in some relevant organic reactions has been evaluated from the ionization potential JP) and the electron affinity (EA) computed by vertical ionization at the B3LYP/aug-cc-PVTZ level. The corresponding electrophilicity values are well correlated with those obtained from the HOMO and LUMO energies of the neutral molecules. The good linear correlation found between omega(I,A) and omega(H,L)(LBS), and between omega(H,L)(LBS) and omega(H,L)(SBS) allows to confirm the use of the easily available B3LYP/6-31G(*) HOMO and LUMO energies to obtain reasonable values of the global electrophilicity index of organic molecule…

ChemistryBasis-SetsReactivityGeneral Physics and AstronomyScalesOrganic reactionDensity-Functional TheoryComputational chemistryHardnessIonizationElectron affinityElectrophileComputationMoleculeElectron-AffinitiesDensity functional theoryQuantitative characterizationPhysical and Theoretical ChemistryIonization energyHOMO/LUMO
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Orbital-controlled reactions catalysed by zeolites: Electrophilic alkylation of aromatics

1994

The role of orbital control in product selectivity during electrophilic aromatic alkylation catalysed by zeolites was studied both theoretically and experimentally. In order to discuss this, the alkylation of toluene and m-xylene by methanol was carried out on a series of large-pore zeolites (HY). The changes in the para to ortho ratio observed on changing the framework Si/Al ratio of the zeolites were related to ab initio molecular orbital calculations of the LUMO energy of structurally alike model clusters but containing different tetrahedral cations around the active site. The observed correlation is discussed in terms of the HSAB principle by taking into account the influence of the cat…

ChemistryComputational chemistryOrganic ChemistryElectrophileHSAB theoryAb initioMolecular orbitalReactivity (chemistry)Physical and Theoretical ChemistryAlkylationPhotochemistryHOMO/LUMOCatalysisJournal of Physical Organic Chemistry
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Synthesis and molecular and electronic structures of a series of Mo3CoSe4 cluster complexes with three different metal electron populations.

2008

The synthesis, crystal structure, and magnetic properties of [Mo 3(CoCO)Se 4(dmpe) 3Cl 3] ( 1), [Mo 3(CoCl)Se 4(dmpe) 3Cl 3] ( 2), and [Mo 3(CoCl)Se 4(dmpe) 3Cl 3](TCNQ) ([ 2](TCNQ)) (dmpe = 1,2-bis(dimethylphosphanyl)ethane; TCNQ = 7,7,8,8-tetracyanoquinomethane) cubane-type complexes with 16, 15, and 14 metal electrons, respectively, are reported. These compounds complete the series of cobalt-containing Mo 3CoQ 4 (Q = S, Se) cubane-type complexes, which allows a complete analysis of the consequences of replacing the inner chalcogen and the metal electron count on the structural, magnetic, and electrochemical properties. The experimental evidence is theoretically supported and rationalized…

ChemistryHeteroatomElectronCrystal structureElectrochemistrylaw.inventionInorganic ChemistryMetalChalcogenCrystallographylawComputational chemistryvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryElectron paramagnetic resonanceHOMO/LUMOInorganic chemistry
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ChemInform Abstract: Getting Discriminant Functions of Antibacterial Activity from Physicochemical and Topological Parameters.

2010

Linear discriminant analysis has been demonstrated to be a very useful tool in the selection and design of new drugs. Up to now we have used it through the search of a topological pattern of activity. In this work our goal is to calculate a complete set of physicochemical parameters using semiempirical (quantum chemical) calculations as well as topological indices (TIs) and try to find out any discriminant function for antibacterial activity through the combined use of both types of descriptors. The physicochemical parameters, such as heat of formation, HOMO, LUMO, dipole moment, polarizability, hyperpolarizability, PM3 generated IR vibrational frequencies, etc., were calculated using PM3 H…

ChemistryHyperpolarizabilityGeneral MedicineLinear discriminant analysisTopologyMaxima and minimasymbols.namesakeDiscriminantPolarizabilityPhysics::Atomic and Molecular ClusterssymbolsHamiltonian (quantum mechanics)HOMO/LUMOTopological quantum numberChemInform
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Electronic nature of the emitting triplet in SF 5 -substituted cationic Ir(III) complexes

2018

Abstract A theoretical density functional theory study has been performed on a family of cationic iridium(III) complexes of the form [Ir(C^N)2(dtBubpy)]+ (dtBubpy = 4,4′-di-tert-butyl-2,2′-bipyridine), that incorporate 2-phenylpyridine (1, 2) and 1-phenylpyrazole (3, 4) cyclometallating C^N ligands functionalized with SF5 groups. The goal is to investigate the effect that the inclusion of SF5 groups in meta (1, 3) and para position (2, 4) with respect to the Ir–C bond has on the electronic nature of the emitting triplet state and the emission wavelength. The attachment of the electron-withdrawing groups induces the stabilization of the molecular orbitals localized on the C^N ligands and, in…

ChemistryLigand02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesInorganic ChemistryExcited stateMaterials ChemistryDensity functional theoryMolecular orbitalPhysical and Theoretical ChemistryTriplet state0210 nano-technologyPhosphorescenceHOMO/LUMODiiminePolyhedron
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Photophysical Properties of Oligo(phenylene ethynylene) Iridium(III) Complexes Functionalized with Metal-Anchoring Groups

2016

[EN] The electrochemical and photophysical properties of a family of conjugated ligands and their iridium(III) cyclometallated complexes are described. They consist of a series of monocationic Ir-III bis-2-phenylpyridine complexes with p-phenylethynyl-1,10-phenanthroline ligands of different length. The structure of these ligands includes terminal acetylthiol or pyridine groups, which can provide good electrical contacts between metal electrodes. Cyclic voltammetry, absorption and emission spectroscopy, laser flash photolysis and density functional theory calculations reveal that the high conjugation of the diimine ligand affords small energy gaps between the frontier orbitals. Nevertheless…

ChemistryLigandLaser flash photolysischemistry.chemical_element02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescence0104 chemical sciencesMLCTLLCTInorganic ChemistryIr complexesQUIMICA ORGANICAExcited stateFlash photolysisDensity functional theoryIridium0210 nano-technologyHOMO/LUMODiimine
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Ultrafast Twisting of the Indoline Donor Unit Utilized in Solar Cell Dyes: Experimental and Theoretical Studies

2015

Previous time-resolved measurements on D149, the most-studied dye of the indoline family, had shown a fast time-component of 20–40 ps that had tentatively been attributed to structural relaxation. Using femtosecond transient absorption, we have investigated the isolated indoline donor unit (i.e., without acceptor group) and found an ultrafast decay characterized by two lifetimes of 3.5 and 23 ps. Density functional theory calculations show π-bonding and π*-antibonding character of the central ethylene group for the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO), respectively. The LUMO is localized on the flexible vinyl-diphenyl region of the donor unit and a twist…

ChemistryRelaxation (NMR)PhotochemistryAcceptorSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyExcited stateUltrafast laser spectroscopyIndolineDensity functional theoryMolecular orbitalPhysical and Theoretical ChemistryHOMO/LUMOThe Journal of Physical Chemistry C
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Unravelling the mechanism of the ketene-imine Staudinger reaction. An ELF quantum topological analysis

2015

The mechanism of the ketene-imine Staudinger (KI-S) reaction between t-butyl-cyano ketene and N-phenyl phenylimine has been studied using DFT methods at the MPWB1K/6-311G(d) computational level. The reaction takes place through a two-step mechanism: (i) the first step is the nucleophilic attack of the imine nitrogen lone pair on the central carbon of the ketene yielding a zwitterionic (ZW) intermediate; (ii) the second step, which is the rate- and stereoselectivity-determining step, is a ring-closure process achieved by a nucleophilic attack of the terminal carbon atom of the ketene on the imine carbon atom. Due to the unfeasibility of a cis/trans and an E/Z stereoisomerisation at the ZW in…

ChemistryStereochemistryGeneral Chemical EngineeringImineKeteneGeneral ChemistryTopologychemistry.chemical_compoundNucleophileSingle bondStaudinger reactionConrotatory and disrotatoryHOMO/LUMOLone pairRSC Advances
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Adsorption and activation of O2 at Au chains on MgO/Mo thin films

2010

We have investigated the adsorption of O(2) on Au(n) clusters (n = 1-6) supported by an ultra thin (3ML)MgO(001) film on Mo metal via density functional theory calculations. On thin films, these small clusters have chain like structures and their electronic states resemble 1D quantum well states. The Au(1-3) are charged by one electron whereas the larger Au(4-6) get two electrons from the substrate. This is confirmed both by the symmetries of the HOMO and LUMO states of the clusters and the Bader charge analysis. In contrast to the O(2) adsorption on gas-phase clusters, the adsorption energy of O(2) molecule does not show pronounced oscillations as a function of cluster size. The O(2) is ac…

ChemistryStereochemistryGeneral Physics and AstronomySubstrate (electronics)MetalCrystallographyAdsorptionvisual_artvisual_art.visual_art_mediumCluster (physics)MoleculeDensity functional theoryPhysical and Theoretical ChemistryThin filmHOMO/LUMOPhysical Chemistry Chemical Physics
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Labdane Diterpenes from Stachys plumosa

2000

Three new labdane diterpenoids were isolated from the aerial parts of Stachys plumosa. The first two (1, 2) were the dextrorotatory enantiomers of the known 6-deoxyandalusol and 13-epijabugodiol. Structures were determined using NMR and MS techniques. The absolute stereochemistry of the third compound (3) was not experimentally proved.

Chromatography GasMagnetic Resonance SpectroscopyOptical RotationStereochemistryPharmaceutical ScienceGas Chromatography-Mass SpectrometryAnalytical ChemistryDextrorotatoryLabdanechemistry.chemical_compoundBalkan peninsulaDrug DiscoveryOrganic chemistryPharmacologyLamiaceaePlant StemsChemistryOrganic ChemistryAbsolute configurationStachys plumosaTerpenoidPlant LeavesItalyComplementary and alternative medicineChromatography GelMolecular MedicineSpectrophotometry UltravioletEpimerDiterpenesDiterpeneJournal of Natural Products
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