Search results for "Doublet state"

showing 6 items of 6 documents

Transient FTIR spectroscopy after one- and two-colour excitation on a highly luminescent chromium(III) complex.

2021

The development of photoactive transition metal complexes with Earth-abundant metals is a rapidly growing research field, where a deeper understanding of the underlying photophysical processes is of great importance. A multitude of potential applications in the fields of photosensitizing, optical sensing, photoluminescence and photoredox catalysis motivates demanding spectroscopic studies. We applied a series of high-level spectroscopic methods on the previously reported highly luminescent chromium(iii) complex [Cr(ddpd)2](BF4)3 (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine) possessing two near-IR emissive doublet states with microsecond lifetimes. Luminescence measurements…

PhotoluminescenceMaterials science010405 organic chemistryGeneral Physics and Astronomy010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesMicrosecondsymbols.namesakeExcited statesymbolsPhysical and Theoretical ChemistryLuminescenceRaman spectroscopyGround stateSpectroscopyDoublet statePhysical chemistry chemical physics : PCCP
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Computational modeling of isotropic electron paramagnetic resonance spectra of doublet state main group radicals

2007

The combined use of theoretical and mathematical methods in the analysis of electron paramagnetic resonance data has greatly increased the ability to interpret even the most complex spectra reported for doublet state inorganic main group radicals. This personal account summarizes the theoretical basis of such an approach and provides an in-depth discussion of some recent illustrative examples of the utilization of this methodology in practical applications. The emphasis is on displaying the enormous potential embodied within the approach. peerReviewed

Electron nuclear double resonanceBasis (linear algebra)ChemistryRadicalOrganic ChemistryIsotropypääryhmien alkuaineiden radikaalitBiochemistrySpectral linelaw.inventionInorganic Chemistryspectral simulationlawGroup (periodic table)Computational chemistryMaterials ChemistrysimulointiPhysical and Theoretical ChemistryAtomic physicsEPR spektroskopiaElectron paramagnetic resonancemain group radicalsEPR spectroscopyDoublet stateJournal of Organometallic Chemistry
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A mutliconfigurational study of low-lying electronic states of KO

1992

Abstract Potential energy curves and spectroscopic parameters of several electronic states of the KO molecule have been calculated using multi-configurational methods. The KO B 2Π state, first time theoretically described, presents a strong avoided crossing with the A 2Π state, and allows for the explanation of the observed fluorescence of the KO molecule. Eleven electronic states have been studied at all the internuclear distances. Effects of complete active space and basis set selections on the results are also analyzed.

ChemistryComputational chemistryAvoided crossingGeneral Physics and AstronomyComplete active spacePhysical and Theoretical ChemistryConfiguration interactionAtomic physicsPotential energyDiatomic moleculeBasis setMolecular electronic transitionDoublet stateChemical Physics
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Hund's Rules and Spin Density Waves in Quantum Dots

1997

Spin density functional theory is used to calculate the ground state electronic structures of circular parabolic quantum dots. We find that such dots either have a spin configuration determined by Hund's rule or make a spin-density-wave-like state with zero total spin. The dependence of the spin-density-wave amplitudes on the density of the two-dimensional electron gas is studied.

PhysicsSpin polarizationCondensed matter physicsQuantum spin Hall effectTerm symbolQuantum mechanicsHund's rulesGeneral Physics and AstronomyCondensed Matter::Strongly Correlated ElectronsHund's rule of maximum multiplicityQuantum spin liquidSpin quantum numberDoublet statePhysical Review Letters
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Dynamical stabilization of spin systems in time-dependent magnetic fields

2011

The quantum dynamics of a spin system subjected to a Rabi magnetic field configuration modified by a weak oscillating field along the Z-axis is investigated. We show that when the Rabi frequency is appropriately matched with the frequency of the perturbative field, the spin system exhibits a dynamical stabilization phenomenon defined as the tendency to occupy a fixed quantum superposition during a finite period of time.

PhysicsRabi cycleCondensed matter physicsField (physics)Spin polarizationQuantum dynamicsCondensed Matter PhysicsNitrogen-vacancy centerMathematical PhysicsAtomic and Molecular Physics and OpticsRabi frequencySpin-½Doublet statePhysica Scripta
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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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