Search results for "Singlet"

showing 10 items of 352 documents

First-principles characterization of the singlet excited state manifold in DNA/RNA nucleobases

2020

An extensive theoretical characterization of the singlet excited state manifold of the five canonical DNA/RNA nucleobases (thymine, cytosine, uracil, adenine and guanine) in gas-phase is carried out with time-dependent density functional theory (TD-DFT) and restricted active space second-order perturbation theory (RASPT2) approaches. Both ground state and excited state absorptions are analyzed and compared between these different theoretical approaches, assessing the performance of the hybrid B3LYP and CAM-B3LYP (long-range corrected) functionals with respect to the RASPT2 reference. By comparing the TD-DFT estimates with our reference for high-lying excited states, we are able to narrow do…

GuanineGuanineGeneral Physics and Astronomy010402 general chemistry01 natural sciencesMolecular physicsNucleobasechemistry.chemical_compoundCytosine0103 physical sciencesSinglet statePhysical and Theoretical ChemistryPerturbation theoryUracilDensity Functional TheoryPhysics010304 chemical physicsAdenineDNA0104 chemical sciencesThyminechemistryExcited stateRNADensity functional theoryGround stateThyminePhysical Chemistry Chemical Physics
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Forward $J/\psi$ and very backward jet inclusive production at the LHC

2018

In the spirit of Mueller-Navelet dijet production, we propose and study the inclusive production of a forward $J/\psi$ and a very backward jet at the LHC as an observable to reveal high-energy resummation effects \`a la BFKL. We obtain several predictions, which are based on the various mechanisms discussed in the literature to describe the production of the $J/\psi$, namely, NRQCD singlet and octet contributions, and the color evaporation model.

HADRONIC COLLISIONSdijet: productionParticle physicsHEAVY FLAVOR PRODUCTIONOctetOCTET QUARKONIA PRODUCTIONJet (particle physics)01 natural sciencesComputer Science::Digital Libraries114 Physical sciencesDECAYSHigh Energy Physics - ExperimentNuclear physicsPomeron[ PHYS.HEXP ] Physics [physics]/High Energy Physics - Experiment [hep-ex]0103 physical sciencesquantum chromodynamics[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]Resummation010306 general physicsMUELLER-NAVELET JETSBFKL equationoctetQuantum chromodynamicsPhysicsPOMERONLarge Hadron Colliderquantum chromodynamics: nonrelativisticcolor: evaporationta114010308 nuclear & particles physicsHigh Energy Physics::PhenomenologyVERTEXObservablesingletQCDHigh Energy Physics - PhenomenologyJ/psi mesonsCERN LHC Collforward productionjet: inclusive productionresummation[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]PHOTON SCATTERINGProduction (computer science)[ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]High Energy Physics::ExperimentJ/psi(3100): production
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Study of the Mode and Efficiency of DNA Binding in the Damage Induced by Photoactivated Water Soluble Porphyrins

2013

We have investigated the DNA binding interactions and in vitro photoactivated DNA damage induced by a neutral water soluble porphyrin derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrin (TTHPP) and its zinc derivative 5,10,15,20-tetrakis(2,4,6-trihydroxyphenyl)porphyrinato zinc(II) (Zn-TTHPP) upon visible light irradiation through various spectroscopic techniques and employing repair endonucleases. These porphyrin derivatives exhibited high affinity toward DNA through groove binding interactions as evidenced through the UV-vis absorption, emission, circular dichroism spectral and viscosity changes. Interestingly, the free base porphyrin derivative, TTHPP generated efficient sing…

HematoporphyrinCircular dichroismPorphyrinsSinglet oxygenDNA damageCircular DichroismSpectrum AnalysisWaterDNAGeneral MedicinePhotochemical ProcessesPhotochemistryBiochemistryPorphyrinchemistry.chemical_compoundchemistryDNA glycosylasePhotosensitizerPhysical and Theoretical ChemistryDNADNA DamagePhotochemistry and Photobiology
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Singlet‐Contrast Magnetic Resonance Imaging: Unlocking Hyperpolarization with Metabolism

2020

Abstract Hyperpolarization‐enhanced magnetic resonance imaging can be used to study biomolecular processes in the body, but typically requires nuclei such as 13C, 15N, or 129Xe due to their long spin‐polarization lifetimes and the absence of a proton‐background signal from water and fat in the images. Here we present a novel type of 1H imaging, in which hyperpolarized spin order is locked in a nonmagnetic long‐lived correlated (singlet) state, and is only liberated for imaging by a specific biochemical reaction. In this work we produce hyperpolarized fumarate via chemical reaction of a precursor molecule with para‐enriched hydrogen gas, and the proton singlet order in fumarate is released a…

Hydrogenchemistry.chemical_elementHyperpolarization; MRI; Metabolism; NMRparahydrogensinglet order010402 general chemistrySpin isomers of hydrogen01 natural sciencesChemical reactionCatalysisNuclear magnetic resonancemedicineMoleculeSinglet stateHyperpolarization (physics)Research Articlesmedicine.diagnostic_test010405 organic chemistryChemistryMagnetic resonance imagingMagnetic Resonance Imaging | Hot PaperGeneral ChemistryMetabolism540NMR0104 chemical sciencesHyperpolarizationMetabolismddc:540Research ArticleMRI
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A theoretical study of the emission spectra of indole and its analogs: indene, benzimidazole, and 7-azaindole

2000

Abstract The complete active space (CAS) SCF method and multiconfigurational second-order perturbation theory (CASPT2) have been used to study the electronic spectra of indole, indene, benzimidazole, and 7-azaindole. The paper is focused on the study of the low-lying valence triplet and singlet electronic states at the optimized geometries of the excited states. The geometries have been optimized by using analytic CASSCF derivatives. CASPT2 point calculations have been performed in order to obtain band origins and relaxed emission energies. The results are analyzed in the context of the complex emission processes, both fluorescence and phosphorescence, displayed by the title compounds, whic…

Indole testchemistry.chemical_compoundValence (chemistry)Absorption spectroscopychemistryComputational chemistryExcited stateGeneral Physics and AstronomyComplete active spaceSinglet statePhysical and Theoretical ChemistryIndenePhosphorescenceChemical Physics
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Essential on the Photophysics and Photochemistry of the Indole Chromophore by Using a Totally Unconstrained Theoretical Approach

2015

Indole is a chromophore present in many different molecules of biological interest, such as the essential amino acid tryptophan and the neurotransmitter serotonin. On the basis of CASPT2//CASSCF quantum chemical calculations, the photophysical properties of the system after UV irradiation have been studied through the exploration of the potential energy hypersurfaces of the singlet and triplet low-lying valence excited states. In contrast to previous studies, the present work has been carried out without imposing any restriction to the geometry of the molecule (C1 symmetry) and by performing minimum energy path calculations, which is the only instrument able to provide the lowest-energy evo…

Indole testeducation.field_of_study010304 chemical physicsChemistryPopulationQuantum yieldConical intersectionChromophore010402 general chemistryPhotochemistry01 natural sciencesPotential energy0104 chemical sciencesComputer Science ApplicationsExcited state0103 physical sciencesSinglet statePhysical and Theoretical ChemistryeducationJournal of Chemical Theory and Computation
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Synthesis and crystal structure of the low-spin iron(II) complex [Fe(bpym)3](ClO4)2·1/4H2O (bpym=2,2′-bipyrimidine)

1997

Abstract Single crystals of the mononuclear iron(II) complex of formula [Fe(bpym)3](ClO4)2·1/4H2O (bpym=2,2′-bipyrimidine) have been prepared and characterized crystallographically. The complex is monoclinic, P21/c, a=13.688(5), b=19.391(6), c=11.554(5) A, β=102.22(3)°, V=2997(2) A3, Z=4, R=0.063 and Rw=0.068. The structure analysis reveals a distorted octahedral geometry around the iron atom. The average Fe–N bond length and N–Fe–N bidentate angle are 1.970(5) A and 81.0(1)°, respectively. The value of the Fe–N distance and that of the room temperature magnetic moment are in agreement with its singlet 1A1 ground state.

Inorganic ChemistryBond lengthCrystallographyDenticityMagnetic momentChemistryOctahedral molecular geometryMaterials ChemistrySinglet stateCrystal structurePhysical and Theoretical ChemistryGround stateMonoclinic crystal systemInorganica Chimica Acta
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Fluoreszenz‐Untersuchungen an styrylsubstituierten Benzolen

1986

Die Fluoreszenz-Abklingzeiten der stilbenartigen Verbindungen 1 – 4 zeigen, das die mittleren Lebensdauern dieser Molekule im elektronisch angeregten Singulettzustand um rund zwei Zehnerpotenzen hoher sind als bei trans-Stilben selbst. Anhand von UV-Absorptions-und Anregungsspektren wird das auf einen neu gefundenen S1-Zustand zuruckgefuhrt, der einem verbotenen Ubergang S0 S1 auf der langwelligen Seite der intensiven Absorption entspricht. Investigations on the Fluorescence of Styryl-substituted Benzenes Fluorescence decay measurements of the stilbene-like compounds 1 – 4 demonstrate that the average lifetimes of these molecules in the electronically excited singlet state are about 102 tim…

Inorganic ChemistryChemistryExcitation spectraUv absorptionAnalytical chemistryChemical solutionAbsorption (chemistry)PhotochemistryFluorescenceExcited singletChemische Berichte
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Nature of Bonding in Group 13 Dimetallenes: a Delicate Balance between Singlet Diradical Character and Closed Shell Interactions

2010

The nature of metal-metal bonding in group 13 dimetallenes REER (E = Al, Ga, In, Tl; R = H, Me, (t)Bu, Ph) was investigated by use of quantum chemical methods that include HF, second order Møller-Plesset perturbation theory (MP2), coupled cluster (CCSD(T)), complete active space with (CASPT2) and without (CAS) second order perturbation theory, and two density functionals, namely, B3LYP and M06-2X. The results show that the metal-metal interaction in group 13 dimetallenes stems almost exclusively from static and dynamic electron correlation effects: both dialuminenes and digallenes have an important singlet diradical component in their wave function, whereas the bonding in the heavier diinde…

Inorganic ChemistryCoupled clusterElectronic correlationDiradicalChemical physicsChemistrySinglet stateComplete active spacePhysical and Theoretical ChemistryPerturbation theoryAtomic physicsWave functionOpen shellInorganic Chemistry
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Five-Coordinate Complexes [FeX(depe)2]BPh4, X = Cl, Br:  Electronic Structure and Spin-Forbidden Reaction with N2

2002

The bonding of N(2) to the five-coordinate complexes [FeX(depe)(2)](+), X = Cl (1a) and Br (1b), has been investigated with the help of X-ray crystallography, spectroscopy, and quantum-chemical calculations. Complexes 1a and 1b are found to have an XP(4) coordination that is intermediate between square-pyramidal and trigonal-bipyramidal. Mössbauer and optical absorption spectroscopy coupled with angular overlap model (AOM) calculations reveal that 1a and 1b have (3)B(1) ground states deriving from a (xz)(1)(z(2))(1) configuration. The zero-field splitting for this state is found to be 30-35 cm(-1). In contrast, the analogous dinitrogen complexes [FeX(N(2))(depe)(2)](+), X = Cl (2a) and Br (…

Inorganic ChemistryCrystallographyAbsorption spectroscopyComputational chemistryChemistryMössbauer spectroscopyDensity functional theoryElectronic structureSinglet statePhysical and Theoretical ChemistrySpectroscopySpin (physics)Inorganic Chemistry
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