SEARCH Articles Figures Tables 1.3- dipolar cycloaddition reactions HOMO-LUMO interaction 7t*LUMO AMI LUMO isosurface Acceptor LUMO Acetone, LUMO Alkenes HOMO and LUMO Alkenes LUMO values, table Alkyl halides LUMO energies Arynes LUMOs) Bridging ligand LUMO) C-Glycosyl compounds SOMO-LUMO interactions Carbanions HOMO-LUMO interactions Carbocations HOMO-LUMO interactions Carbocyclic dianions, HOMO—LUMO Carbonyl groups, 40. HOMO-LUMO interactions Chemical reactivity LUMO-HOMO interaction Coupling HOMO-LUMO Cycloaddition reactions HOMO-LUMO interactions Delocalized LUMO Density-electrostatic potential LUMO maps Diazoalkanes, cycloaddition with HOMO—LUMO interaction Diels-Alder HOMO-LUMO interactions Diels-Alder reaction HOMO-LUMO) Diels-Alder reactions HOMO-LUMO interactions Dienes LUMO energies Diketones 1.2- , LUMO Dipole LUMO control Electrochemical reduction LUMOs Electron affinity and LUMO Energy HOMO/LUMO Energy levels, HOMO/LUMO Energy small HOMO-LUMO Ethylene, HOMO/LUMO Fluorinated alkenes LUMOs Free electron from HOMO into LUMO Frontier Orbitals HOMO and LUMO Frontier orbital approximation HOMO-LUMO interactions Frontier orbital positions LUMO) HOMO LUMO transitions in ultraviolet visible HOMO LUMO transitions in ultraviolet visible spectroscopy HOMO and LUMO HOMO and LUMO coefficients HOMO and LUMO energy levels HOMO and LUMO orbitals, energy HOMO, LUMO (also HOMO-LUMO crossing HOMO-LUMO diagrams HOMO-LUMO energy gaps dianions HOMO-LUMO excitation HOMO-LUMO gap HOMO-LUMO interaction 474 INDEX HOMO-LUMO interaction faces, example HOMO-LUMO interaction in cycloadditions HOMO-LUMO interaction photochemical HOMO-LUMO interaction strength HOMO-LUMO interaction symmetry HOMO-LUMO interactions HOMO-LUMO interactions 4 + 2 cycloadditions HOMO-LUMO interactions Perturbation theory HOMO-LUMO interactions carbene HOMO-LUMO interactions carbonyl group with HOMO-LUMO interactions in cycloaddition HOMO-LUMO interactions in the 2 2 cycloaddition of an alkene and a ketene HOMO-LUMO interactions theory HOMO-LUMO properties HOMO-LUMO reaction HOMO-LUMO separation HOMO-LUMO separation structure HOMO-LUMO splitting HOMO-LUMO structures HOMO-LUMO transition polyenes HOMO-LUMO transitions HOMO-LUMO transitions spectroscopy HOMO-dipole LUMO-dipolarophile HOMO-dipole LUMO-dipolarophile interaction HOMO/LUMO HOMOs and LUMOs in Reactions HOMO—LUMO transition substituent effect HUMO-LUMO gap Heterocyclic dianions, HOMO-LUMO Highest occupied molecular orbital and LUMO Highest occupied molecular orbital/lowest LUMO) overlap LUMO LUMO LUMO (Lowest Unoccupied Molecular LUMO (lowest energy unoccupied LUMO (lowest occupied molecular LUMO (lowest unoccupied LUMO (lowest unoccupied Diels-Alder reactions LUMO (lowest unoccupied electronic effects LUMO (lowest unoccupied molecular in borane clusters LUMO (lowest unoccupied reaction LUMO (lowest unoccupied substituent effects LUMO 4+2)-cycloaddition LUMO Energies and Orbital Coefficients LUMO HOMO orbitals LUMO activation LUMO coefficients LUMO diene-controlled LUMO energies LUMO energies determination LUMO energy, correlation with half-wave LUMO energy, imine formation LUMO lowering LUMO manifold LUMO map LUMO map, for LUMO map, for cyclohexenone LUMO molecular orbitals LUMO of the carbonyl group LUMO orbital LUMO orbital energies LUMO states LUMO umpolung LUMO, definition LUMO, for LUMO, level LUMO-HOMO difference LUMO-HOMO energy gap LUMO-dipole/HOMO-dipolarophile reaction LUMO-lowering activation LUMOs orbitals Lewis acids HOMO-LUMO interactions Lewis bases HOMO-LUMO interactions Low-lying LUMO Lowest HOMO-LUMO gap Lowest Occupied Molecular Orbital LUMO) Lowest Unoccupied Molecular Orbital LUMO) Lowest Unoccupied Molecular Orbitals LUMOs) Lowest unoccupied molecular orbit LUMO) Lowest unoccupied molecular orbital HOMO-LUMO levels Lowest unoccupied molecular orbital LUMO energy levels Lowest unoccupied molecular orbital LUMO) energies Lowest unoccupied molecular orbital LUMO) level Lowest unoccupied molecular orbital LUMO), pericyclic reaction Lowest unoccupied molecular orbital LUMO-controlled dipole Lowest unoccupied molecular orbitals LUMO) Lowest unoccupied molecular orbitals LUMOs), electron promotion Methyl acetate, LUMO Molecular orbital HOMO-LUMO gap Molecular orbitals HOMO and LUMO Naphthalene HOMO—»LUMO transition Nitrones, cycloaddition with HOMO-LUMO interactions Orbitals HOMO-LUMO interactions Orbitals LUMO) Ozone HOMO-LUMO interactions Paratropic shift, HOMO-LUMO energy Perturbation of the HOMO And LUMO Poly LUMO energy level Qualitative Consideration of the HOMO—LUMO Interaction Reactivity HOMO-LUMO gaps Rearrangements HOMO-LUMO theory Reduction potentials LUMO energies Resonance, HOMO-LUMO interaction SOMO-LUMO orbital interactions SOMO—LUMO interaction SOMO—►LUMO excitation Substituent effects LUMO energy Substitution HOMO-LUMO interactions Thiophene HOMO-LUMO energies Transfer LUMO-lowering activation Transition state HOMO-LUMO energies Transition state HOMO-LUMO interactions Ultraviolet spectroscopy HOMO-LUMO transition