Search results for "Electron pair"

showing 10 items of 22 documents

Electronic fluxes during diels-alder reactions involving 1,2-benzoquinones: mechanistic insights from the analysis of electron localization function …

2012

By means of the joint use of electron localization function (ELF) and Thom's catastrophe theory, a theoretical analysis of the energy profile for the hetero-Diels-Alder reaction of 4-methoxy-1,2-benzoquinone 1 and methoxyethylene 2 has been carried out. The 12 different structural stability domains obtained by the bonding evolution theory have been identified as well as the bifurcation catastrophes (fold and cusp) responsible for the changes in the topology of the system. This analysis permits finding a relationship between the ELF topology and the evolution of the bond breaking/forming processes and electron pair rearrangements through the reaction progress in terms of the different ways o…

Diels-Alder reactionsElectron pairElectron localization functionMolecular StructureChemistryCatastrophe theoryRegioselectivityElectronsGeneral ChemistryElectron localization function12-benzoquinonesComputational MathematicsRegioselectivityEnergy profileNucleophileChemical physicsComputational chemistryElectrophileBenzoquinonesQuantum TheoryDensity functional theoryCatastrophe theoryJournal of Computational Chemistry
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Pressure-Driven Symmetry-Preserving Phase Transitions in Co(IO3)2

2021

[EN] High-pressure synchrotron X-ray diffraction studies of cobalt iodate, Co(IO3)(2), reveal a counterintuitive pressure-induced expansion along certain crystallographic directions. High-pressure Raman and infrared spectroscopy, combined with density-functional theory calculations, reveal that with increasing pressure, it becomes energetically favorable for certain I-O bonds to increase in length over the full range of pressure studied up to 28 GPa. This phenomenon is driven by the high-pressure behavior of iodate ion lone electron pairs. Two pressure-induced isosymmetric monoclinic-monoclinic phase transitions are observed at around 3.0 and 9.0 GPa, which are characterized by increasing o…

DiffractionPhase transitionElectron pairMaterials sciencechemistry.chemical_elementInfrared spectroscopySynchrotronSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionsymbols.namesakechemistry.chemical_compoundGeneral EnergychemistrylawChemical physicsFISICA APLICADAsymbolsPhysical and Theoretical ChemistryRaman spectroscopyCobaltIodateThe Journal of Physical Chemistry C
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First-principles simulations on the aggregation of F centers in BaF2: R centers

2011

Abstract F center (an electron trapped in the fluorine vacancy) and R center (a defect composed of three F centers) in BaF 2 crystal, have been studied by using density functional theory (DFT) with hybrid exchange potentials, namely DFT-B3PW. Our calculations show that the F -center transfer barrier is equal to 1.83 eV. During the F -center transfer, the trapped electron is more delocalized than that in the static F -center case, and the gap between defect leveland CB in the α-spin state decreases obviously. The association energy calculations on R centers indicate stable aggregations of isolated F centers. During F -center aggregation, a considerable covalency between two neighbor fluorine…

Electron pairDelocalized electronValence (chemistry)Atomic electron transitionChemistryVacancy defectGeneral Materials ScienceDensity functional theoryGeneral ChemistryElectronAtomic physicsCondensed Matter PhysicsElectronic band structureSolid State Ionics
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Towards an intrinsic nucleofugality scale: the leaving group (lg) ability in ch(3)lg model system

2006

Abstract For an important class of organic reactions in which a fragment of the reactants, the leaving group (LG) or nucleofuge (Z), is detached of the substrate bearing the bonding electron pair, the global electrophilicity index of the CH3LG system is proposed as a reliable descriptor of the intrinsic nucleofugality of the LG. The model is illustrated by ranking within a unique relative scale, the LG ability of 28 functional groups commonly involved in substitution and elimination reactions in organic chemistry.

Electron pairElimination reactionOrganic reactionScale (ratio)StereochemistryChemistryElectrophileLeaving groupGeneral Physics and AstronomySubstrate (chemistry)NucleofugePhysical and Theoretical Chemistry
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Theoretical Study of the 15- and 17-Electron Structures of Cyclopentadienylchromium(III) and Cyclopentadienylmolybdenum(III) Complexes. Dichloride an…

1997

International audience; The structure and the energetics of the model systems CpMX2(PH3) + PH3 ⇄ CpMX2(PH3)2 (Cp = cyclopentadienyl; M = Cr, Mo; X = Cl, CH3) are studied by performing Møller−Plesset second order (MP2) and density functional theory (DFT) calculations. Extended basis sets are employed in the geometry optimizations. The results indicate that the structural preference can be traced back to the competition between electron pairing stabilization and M−P bond dissociation energy along the spin doublet surface. At all levels of calculation, the energy splitting, a measure of the cost of pairing the electron during the promotion process from the quartet ground state to the excited d…

Electron pairEnergy010405 organic chemistryChemistryElectrical energy010402 general chemistryLigands01 natural sciencesBond-dissociation energyQuantum mechanics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyCyclopentadienyl complexComputational chemistryMetalsExcited statePairingDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryGround stateDoublet state
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A semiempirical method based on geminal functions

1968

An attempt has been made to develop a semiempirical method which considers only the n- and π-electrons, with the eigenfunctions expressed as an antisymmetrized product of two-electron functions or geminals. These geminals are expressed as a linear combination of products of Huckel-type MO's and the matrix elements are evaluated assuming the strong orthogonality condition to hold among the geminals, with an average effective Hamiltonian where the interaction between paired electrons is explicitly included.

Electron pairGeminalChemistryElectron interactionEigenfunctionsymbols.namesakeComputational chemistrysymbolsMatrix elementChiropracticsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryLinear combinationHamiltonian (quantum mechanics)Mathematical physicsTheoretica Chimica Acta
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Energetics of hydride and electron pair attachment to EX30/+ (E=B, C, Al, Si and X=F, Cl, Br, I) and the study of bonding trends among EX30/+, EX32−/…

2004

Abstract A theoretical gas-phase “ligand-free” or “electron pair affinity” (EPA) approach, based on CCSD(T)/(SDB-)cc-pVTZ//MP2/(SDB-)cc-pVTZ electronic structure calculations, is introduced as a possible means for determining Lewis acidity trends among planar EX30/+ (E = B, C, Al, Si; X = F, Cl, Br, I) species. In this treatment, the free electron pair is considered to be an extreme Lewis base. The calculated EPA values are compared with experimental Lewis acidities, previously calculated fluoride ion affinity (FIA) and hydride ion affinity (HA) trends, and are found to exhibit reasonable correlations in all cases. The bonding in the planar and trigonal pyramidal conformations of EX30/+ and…

Electron pairHydrideChemistryOrganic ChemistryTrigonal pyramidal molecular geometryCrystal structureBiochemistryElectron localization functionInorganic ChemistryCrystallographyComputational chemistryEnvironmental ChemistryC/ALLewis acids and basesPhysical and Theoretical ChemistrycomputerNatural bond orbitalcomputer.programming_languageJournal of Fluorine Chemistry
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Size-consistent single-reference methods for electronic correlation: a unified formulation through intermediate hamiltonian theory

1996

Using the intermediate hamiltonian theory as a unique conceptual frame and the technique of CI matrix dressing, a wide series of single-reference methods for the treatment of the ground state correlation are reviewed, compared, and sometimes improved. These methods range from independent excitation approximation (the very next step beyond MP2) to coupled cluster, going through the so-called electron pair approximations and the (SC)2CI formalism. A hierarchy of these methods can be established according to two criteria: These formulations in terms of diagonalizations of dressed CI matrices avoid convergence problems, but their main advantage is their flexibility, since they apply to multi-re…

Electron pairMatrix (mathematics)Formalism (philosophy of mathematics)Coupled clusterClassical mechanicsElectronic correlationApplied mathematicsConceptual frameChiropracticsPhysical and Theoretical ChemistryGround stateExcitationMathematicsTheoretica Chimica Acta
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Quantum Chemical Calculations Show that the Uranium Molecule U2 Has a Quintuple Bond.

2005

Covalent bonding is commonly described by Lewis's theory1, with an electron pair shared between two atoms constituting one full bond. Beginning with the valence bond description2 for the hydrogen molecule, quantum chemists have further explored the fundamental nature of the chemical bond for atoms throughout the periodic table, confirming that most molecules are indeed held together by one electron pair for each bond. But more complex binding may occur when large numbers of atomic orbitals can participate in bond formation. Such behaviour is common with transition metals. When involving heavy actinide elements, metal–metal bonds might prove particularly complicated. To date, evidence for ac…

Electron pairMultidisciplinaryChemistryThree-center two-electron bondGeneral MedicineBond orderchemistry.chemical_compoundAtomic orbitalChemical bondComputational chemistryChemical physicsCovalent bondSextuple bondddc:540AtomSingle bondMoleculeValence bond theoryBond energyQuintuple bondChemInform
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2,3-Dihydro-3-methyl-2-nitrimino-1,3-thiazole

2000

The title compound ¿alternatively, 3-methyl-2-[oxido(oxo)hydrazono]-2,3-dihydro-1,3-thiazole¿, C(4)H(5)N(3)O(2)S, was obtained by methylation of N-(2-thiazolyl)nitramine. The molecule lies on a mirror plane and the thiazole ring is planar, regular in shape and aromatic. The S atom participates in the aromatic sextet via an electron pair on the 3p(z) orbital. In the crystal, the molecules are arranged in parallel layers, bound to each other by weak C-H.O and C-H.N hydrogen bonds and by S.O dipolar interactions, with an interlayer separation of 3.23 A.

Electron pairStereochemistryHydrogen bondGeneral MedicineCrystal structureRing (chemistry)General Biochemistry Genetics and Molecular BiologyCrystalCrystallographychemistry.chemical_compoundchemistryMoleculeAmine gas treatingThiazoleActa Crystallographica Section C Crystal Structure Communications
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