Search results for "Electron configuration"

showing 10 items of 44 documents

Reversible switching of the electronic ground state in a pentacoordinated Cu(ii) complex.

2013

International audience; An easy reversible switching of the electronic ground state in a pentacoordinated copper(ii) complex is reported for the first time. The simple protonation of a carboxylic group in a Cu(ii) complex with a {dx(2)-y(2)}(1) electronic configuration leads to a flip of the ground electronic configuration from {dx(2)-y(2)}(1) to {dz(2)}(1) in the metal ion.

Carboxylic groupMolecular Conformationchemistry.chemical_elementInorganic compoundsElectronsProtonationCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMetalCoordination ComplexesComputational chemistryElectronic ground stateMaterials Chemistry010405 organic chemistryChemistryMetals and AlloysGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistryCopper3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsReversible switchingvisual_artCeramics and Compositesvisual_art.visual_art_mediumQuantum TheoryPhysical chemistryElectron configurationGround stateCopper
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Magnetic exchange interaction in clusters of orbitally degenerate ions. I. Effective Hamiltonian

2001

Abstract A new effective Hamiltonian is reported for the kinetic exchange between two arbitrary terms 2S A +1 Λ A and 2S B +1 Λ B that can be ground or excited in octahedrally coordinated transition metal ions. This Hamiltonian is applicable to both homo- and heterometallic clusters. For the homonuclear cluster the resonance part of the effective Hamiltonian is also presented for the case when one of the ions is excited. The operator part of the exchange Hamiltonian contains symmetry adapted products of the cubic irreducible tensors acting in orbital spaces ΛA and ΛB and scalar product of site spin operators. The parameters of the Hamiltonian are defined by the relevant intercenter transfer…

ChemistryDegenerate energy levelsGeneral Physics and AstronomyHomonuclear moleculesymbols.namesakeOperator (computer programming)Excited statesymbolsCluster (physics)Electron configurationPhysical and Theoretical ChemistryAtomic physicsHamiltonian (quantum mechanics)Ground stateChemical Physics
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Role of the central gold atom in ligand-protected biicosahedral Au 24 and Au25 clusters

2013

The crystal structures of the ligand-protected clusters [Au24(PPh3)10(SC2H4Ph)5Cl2]+ and [Au25(PPh3)10(SC2H4Ph)5Cl2]2+ have been elucidated recently, and they comprise the same biicosahedral structural motif for the Au core. The only difference is the central Au atom joining two icosahedra which is absent in the Au24 cluster. On the basis of density functional simulations, we have evaluated the structural, electronic, optical, and vibrational properties of the clusters in question with a full presentation for the thiolate and phosphine side groups. Our spherical harmonics analysis of the electronic structure shows that the chemical stability of both clusters can be understood based on an 8 …

ChemistryIcosahedral symmetrySuperatomta221Crystal structureElectronic structureSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyGeneral EnergyAtomCluster (physics)Chemical stabilityElectron configurationPhysical and Theoretical ChemistryJournal of Physical Chemistry C
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Extension of Walsh's rules to more general systems

1972

It is demonstrated that location of hydrogen atoms within bonding distance of a simple triatomic molecule can alter the order of energy levels relative to that of the parent system without significantly changing the behavior of the orbital energies under geometrical variation. As a result the ground state electronic configurations of H n AB2 systems often differ from those of triatomics with the same number of electrons and this fact is shown to be directly responsible for the existence of such distinctive geometrical structures as those possessed by cyclopropane, cyclopropyl and allyl cations and cyclopropene. Thus the familiar prescription of Walsh's rules which states that isoelectronic …

ChemistryTriatomic moleculeWalsh diagramCyclopropenechemistry.chemical_compoundSimple (abstract algebra)Excited stateQuantum mechanicsMoleculeChiropracticsElectron configurationPhysical and Theoretical ChemistryAtomic physicsGround stateTheoretica Chimica Acta
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Multistate active spaces from local CAS-SCF molecular orbitals: the photodissociation of HFCO as an example.

2005

A recently developed algorithm to generate localized molecular orbitals (LMO) is applied to the study of excited states along a photodissociation process. The LMOs allow for the selection of a consistent complete active space (CAS) for the simultaneous description of all the electronic states involved in a multistate process on the basis of simple chemical criteria. The local nature of the orbitals is used to label them in a unique way that does not depend on the molecular geometry. The selection of the electronic configurations of interest for the set of target states on only the basis of the dominant excitations required by the simplest configuration interaction (CI) descriptions for both…

Computational MathematicsBasis (linear algebra)ChemistryQuantum mechanicsExcited stateMolecular orbitalGeneral ChemistryComplete active spaceLocalized molecular orbitalsElectron configurationConfiguration interactionAtomic physicsPotential energyJournal of computational chemistry
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Spin Transitions in Iron(II) Complexes

1996

Iron(II) has the 3d6 outer electronic configuration and hence its octahedral complexes may be either high-spin or low-spin. The high-spin configuration, t 2g 4 e g 2 , is adopted when relatively weak-field ligands are coordinated while the low-spin, t 2g 6 e g 0 , is obtained when strong-field ligands are involved. In Oh symmetry the ground states are 5T2g and lA1g, for the high-spin and low-spin configurations, respectively. While in most iron(II) six-coordinate complexes the symmetry is lower than Oh, these designations are generally adopted in the following sections for convenience. [Fe(H2O)6]2+ and [Fe(en)3]2+ (en = ethylenediamine) are typical examples of high-spin complexes, while [Fe…

CrystallographySpin statesUnpaired electronAtomic orbitalSpin crossoverChemistryAtomSpin transitionOrganic chemistryElectron configurationAntibonding molecular orbital
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Phonon Driven Floquet Matter.

2018

The effect of electron–phonon coupling in materials can be interpreted as a dressing of the electronic structure by the lattice vibration, leading to vibrational replicas and hybridization of electronic states. In solids, a resonantly excited coherent phonon leads to a periodic oscillation of the atomic lattice in a crystal structure bringing the material into a nonequilibrium electronic configuration. Periodically oscillating quantum systems can be understood in terms of Floquet theory, which has a long tradition in the study of semiclassical light-matter interaction. Here, we show that the concepts of Floquet analysis can be applied to coherent lattice vibrations. This coupling leads to p…

Floquet theoryFloquet theoryPhononphotoelectron spectroscopynonequilibrium bandstructureFOS: Physical sciencesSemiclassical physicsBioengineeringAngle-resolved photoemission spectroscopy02 engineering and technologyElectronic structureelectron?phonon coupling01 natural sciencesSettore FIS/03 - Fisica Della MateriaFirst-principles calculations0103 physical sciencesGeneral Materials Science010306 general physicsElectronic band structurePhysicsCondensed Matter - Materials Sciencepumpprobe spectroscopyCondensed matter physicsMechanical EngineeringMaterials Science (cond-mat.mtrl-sci)General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsExcited stateElectron configuration0210 nano-technologyNano letters
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The Role of C–H···H–B Interactions in Establishing Rotamer Configurations in Metallabis(dicarbollide) Systems

2010

The aim of this work is to explore the self-interaction capability of the anion [3,3′-Co(1,2-C2B9H11)2]– through Ccluster–H···H–B (Cc–H···H–B) dihydrogen bonds. A set of theoretical and empirical data aiming to establish the main rules that account for the binding mode between the negatively charged borane framework made by [3,3′-Co(1,2-C2B9H11)2]– and the [NMe4]+ ions have been compiled. The interaction between cation and anion is mainly electrostatic but the covalent contribution is also proven and quantified. The existing intermolecular H···H short contacts have been studied and are compared with available data from the Cambridge Structural Database. The results show that the electronic …

Inorganic Chemistrychemistry.chemical_compoundchemistryCovalent bondComputational chemistryHydrogen bondIntermolecular forceAtomElectron configurationBoraneConformational isomerismIonEuropean Journal of Inorganic Chemistry
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Mobility of the Singly-Charged Lanthanide and Actinide Cations: Trends and Perspectives

2020

The current status of gaseous transport studies of the singly-charged lanthanide and actinide ions is reviewed in light of potential applications to superheavy ions. The measurements and calculations for the mobility of lanthanide ions in He and Ar agree well, and they are remarkably sensitive to the electronic configuration of the ion, namely, whether the outer electronic shells are 6s, 5d6s or 6s$^2$. The previous theoretical work is extended here to ions of the actinide family with zero electron orbital momentum: Ac$^+$ (7s$^2$, $^1$S), Am$^+$ (5f$^7$7s $^9$S$^\circ$), Cm$^+$ (5f$^7$7s$^2$ $^8$S$^\circ$), No$^+$ (5f$^{14}$7s $^2$S) and Lr$^+$ (5f$^{14}$7s$^2$ $^1$S). The calculations rev…

LanthanideAtomic Physics (physics.atom-ph)Ab initioFOS: Physical sciences02 engineering and technologyElectroninteraction potential010402 general chemistry7. Clean energy01 natural sciencesPhysics - Atomic PhysicsIonlcsh:Chemistryion mobilityAtomlanthanideselectronic configurationOriginal ResearchPhysicsIonic radiussuperheavy ionsactinidesGeneral ChemistryActinide021001 nanoscience & nanotechnology3. Good health0104 chemical sciencesChemistrylcsh:QD1-999ddc:540Electron configurationAtomic physics0210 nano-technology
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Thermal and optical switching of bistable iron compounds and possible applications

1993

Abstract Iron(II) coordination compounds with ligand field strengths close to the mean spin pairing energy may undergo thermal spin transition in the solid as well as in the liquid state. The thermodynamically stable state is high spin (HS) 5T2 (under Oh symmetry) with (t2)4 e2 electron configuration above the critical transition temperature Tc, and low spin (LS) 1A1 with (t2)6 electron configuration below Tc. The spin transition curve γHS(T) (molar fraction of HS molecules as function of temperature) can be abrupt or gradual, with or without hysteresis, or even with a plateau near Tc. Tc itself can vary over the whole temperature scale between the liquid helium region up to above room temp…

Ligand field theoryNuclear and High Energy PhysicsSpin statesBistabilityChemical physicsChemistryExcited stateSpin transitionAnalytical chemistryElectron configurationSpin (physics)InstrumentationLIESSTNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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