Search results for "Singlet"

showing 10 items of 352 documents

Toward the understanding of DNA fluorescence: The singlet excimer of cytosine

2006

By using the multiconfigurational second-order perturbation method CASPT2, including corrections for the basis set superposition error, the lowest-singlet excited state of the face-to-face π-stacked cytosine homodimer is revealed to be bound by about half an eV, being the source of an emissive feature consistent with the observed redshifted fluorescence. Gloria.Olaso@uv.es Daniel.Roca@uv.es Luis.Serrano@uv.es Manuela.Merchan@uv.es

Models MolecularDNA ; Molecular biophysics ; Fluorescence ; Excimers ; Perturbation theory ; Excited states ; Red shift ; BiochemistryTime FactorsLightUltraviolet RaysOligonucleotidesGeneral Physics and AstronomyPerturbation theoryExcimerBiochemistryFluorescenceCytosinechemistry.chemical_compoundSinglet statePhysical and Theoretical ChemistryPerturbation theory:FÍSICA::Química física [UNESCO]ExcimersChemistry PhysicalExcited statesDNAMolecular biophysicsFluorescenceRed shiftUNESCO::FÍSICA::Química físicaMicroscopy FluorescenceModels ChemicalchemistryExcited stateAtomic physicsLuminescenceDimerizationCytosineDNAThe Journal of Chemical Physics
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Experimental and Theoretical Studies on Magnetic Exchange in Silole-Bridged Diradicals.

2006

International audience; Five bis(tert-butylnitroxide) diradicals connected by a silole [2,5-R2-3,4-diphenylsilole; R = Me3CN(®O.bul.)Z; Z = p-C6H4 (7a), p-C6H4C6H4-p (7b), 1,4-naphthalenediyl (7c), m-C6H4 (7d)] or a thiophene [2,5-R2-thiophene; R = p-Me3CN(®O.bul.)C6H4 (12)] ring as a coupler were studied. Compd. 12 crystallizes in the orthorhombic space group Pna21 with a 20.752(5), b 5.826(5), and c 34.309(5) .ANG.. X-ray crystal structure detn., electronic spectroscopy, variable-temp. EPR spectroscopy, SQUID measurements and DFT computations (UB3LYP/6-31+G*) were used to study the mol. conformations and electronic spin coupling in this series of mols. Whereas compds. 7b, 7c, and 7d are q…

Models MolecularFree RadicalsSiloleCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesDFTCatalysislaw.inventionchemistry.chemical_compoundNitroxide diradicalMagnetic interactionslawComputational chemistryThiopheneAntiferromagnetismOrganosilicon CompoundsSinglet stateTriplet stateElectron paramagnetic resonance010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryElectron Spin Resonance SpectroscopyGeneral Chemistry0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyModels ChemicalButanesDiamagnetismEPR spectroscopy
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Copper-mediated DNA photocleavage by a tetrapyridoacridine (tpac) ligand.

2008

Abstract We have focused our interest on the tetrapyridoacridine ligand tetrapyrido[3,2- a :2′,3′- c :3′′,2″- h : 2‴,3‴- j ]acridine (tpac), as a model system for the preparation of novel copper-based artificial nucleases. The complex of copper(II)–tpac cleaves supercoiled pUC18 plasmid DNA in an oxidative manner by photoactivation with visible light, exhibiting maximum cleaving efficiency at 1:2 metal–ligand stoichiometric ratio. We propose an interaction of the copper–tpac complex with DNA through both major and minor grooves and a photocleavage mechanism via the formation of hydroxyl radicals and singlet oxygen or singlet oxygen-like species.

Models MolecularLightStereochemistryPhotochemistryRadicalClinical BiochemistryPharmaceutical Sciencechemistry.chemical_elementPhotochemistryLigandsBiochemistrychemistry.chemical_compoundPolycyclic compoundDrug DiscoveryPhotosensitizerSinglet stateMolecular Biologychemistry.chemical_classificationDeoxyribonucleasesMolecular StructureSinglet OxygenChemistrySinglet oxygenOrganic ChemistryDNACopperAcridineMolecular MedicineAcridinesDNACopperPhenanthrolinesBioorganicmedicinal chemistry letters
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Hyperpolarized 1H long lived states originating from parahydrogen accessed by rf irradiation

2013

Hyperpolarization has found many applications in Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging (MRI). However, its usage is still limited to the observation of relatively fast processes because of its short lifetimes. This issue can be circumvented by storing the hyperpolarization in a slowly relaxing singlet state. Symmetrical molecules hyperpolarized by Parahydrogen Induced Hyperpolarization (PHIP) provide a straightforward access to hyperpolarized singlet states because the initial parahydrogen singlet state is preserved at almost any magnetic field strength. In these systems, which show a remarkably long 1H singlet state lifetime of several minutes, the conversion of t…

Models MolecularMagnetic Resonance SpectroscopyCiencias FísicasPhysics::Medical PhysicsGeneral Physics and AstronomySpin isomers of hydrogenOtras Ciencias FísicasLong Lived StatesMagnetizationsymbols.namesakeSinglet stateHyperpolarization (physics)Physical and Theoretical ChemistryTriplet statePHIPChemistryObservableMagnetic fieldParaHydrogenMagnetic FieldsHyperpolarizationAlkynessymbolsCondensed Matter::Strongly Correlated ElectronsHydrogenationAtomic physicsHamiltonian (quantum mechanics)CIENCIAS NATURALES Y EXACTAS
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Electronic structure of the ground and excited states of beta-carboline.

2008

Coupled-cluster calculations are used to compute the energy of conversion between the neutral and the zwitterionic forms of beta-carboline. The stability of the different species is discussed in terms of charge separation and aromatic character, which is related to magnetic criteria. By means of a linear response formalism the vertical excitation energies and oscillator strengths of the lowest singlet states of both structures as well as of the cationic species are determined. General agreement of the relative position and intensity of the different peaks with experimental data is achieved, but the overall spectra are slightly displaced because of solvent effects.

Models MolecularMolecular StructureChemistryβ-carbolineSpectrum Analysisground and excited statesAromaticityElectronsElectronic structureelectronic structureMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineMagneticsComputational chemistryAb initio quantum chemistry methodsExcited stateSinglet statePhysical and Theoretical ChemistrySolvent effectsβ-carboline; electronic structure; ground and excited statesExcitationCarbolinesChemphyschem : a European journal of chemical physics and physical chemistry
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Photoreactivity of Furocoumarins and DNA in PUVA Therapy: Formation of Psoralen−Thymine Adducts

2008

The mechanism of the [2 + 2] cycloaddition photoreaction of psoralen and a DNA nucleobase, thymine, cornerstone of the furocoumarin-based PUVA (psoralen + UVA radiation) phototherapy, has been studied by the quantum-chemical multiconfigurational CASPT2 method. Triplet- and singlet-mediated mono- and diadduct formations have been determined to take place via singlet-triplet crossings and conical intersections, correlated with the initially promoted triplet or singlet states in different possible reactive orientations. Pyroneside monoadducts are suggested to be formed in the triplet manifold of the system, and to be less prone to yield diadducts because of the properties of the monoadduct low…

Models MolecularMolecular StructurePhotochemistryFurocoumarinFicusinDNAConical intersectionPhotochemistrySurfaces Coatings and FilmsThymineNucleobasechemistry.chemical_compoundFurocoumarinschemistryFurocoumarinsMaterials ChemistrySinglet statePhysical and Theoretical ChemistryTriplet statePUVA TherapyThyminePsoralenThe Journal of Physical Chemistry B
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The Role of Adenine Excimers in the Photophysics of Oligonucleotides

2009

Energies and structures of different arrangements of the stacked adenine homodimer have been computed at the ab initio CASPT2 level of theory in isolation and in an aqueous environment. Adenine dimers are shown to form excimer singlet states with different degrees of stacking and interaction. A model for a 2-fold decay dynamics of adenine oligomers can be supported in which, after initial excitation in the middle UV range, unstacked or slightly stacked pairs of nucleobases will relax by an ultrafast internal conversion to the ground state, localizing the excitation in the monomer and through the corresponding conical intersection with the ground state. On the other hand, long-lifetime intra…

Models MolecularPhotochemistryUltraviolet RaysMolecular ConformationOligonucleotidesAb initioPhotochemistryExcimerBiochemistryCatalysisNucleobaseColloid and Surface ChemistryUltrafast laser spectroscopySinglet stateQuantitative Biology::BiomoleculesChemistryAdenineDNAGeneral ChemistryConical intersectionInternal conversion (chemistry)Chemical physicsNucleic Acid ConformationSpectrophotometry UltravioletGround stateDimerizationHydrogenJournal of the American Chemical Society
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Singlet Excited-State Interactions in Naphthalene-Thymine Dyads

2004

Two thymidine-derived nucleosides 1 and 2 were prepared by attaching a chiral naphthalene to the positions 5′ and 3′ of the sugar. The resulting dyads, which contain key substructures present in drugs and nucleic acids, exhibit different spatial arrangements (transoid or cisoid) of the fluorophore relative to the thymine unit. Emission measurements on these compounds in the presence of ROH molecules revealed a remarkable intramolecular fluorescence quenching for dyad 1. The obtained results are consistent with quenching of the singlet excited state of 1 by hydrogen-bond donor solvents. Thus, a physical deactivation process (vibronically induced internal conversion) would be the pathway resp…

Models MolecularPhotolysisQuenching (fluorescence)ChemistryLasersMolecular ConformationNaphthalenesCrystallography X-RayInternal conversion (chemistry)PhotochemistryFluorescenceAtomic and Molecular Physics and OpticsThyminechemistry.chemical_compoundSpectrometry FluorescenceIntersystem crossingIntramolecular forceExcited stateSpectrophotometry UltravioletSinglet statePhysical and Theoretical ChemistryThymineChemPhysChem
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Photodynamics in stable complexes composed of a zinc porphyrin tripod and pyridyl porphyrins assembled by multiple coordination bonds

2010

A tripod zinc porphyrin (TPZn(3)) forms a stable 1:1 complex with gold(III) tetra(4-pyridyl)porphyrin (AuTPyP(+)) and free-base tris(4-pyridyl)porphyrin (2H-Py(3)P) in nonpolar solvents. The strong binding of TPZn(3) with AuTPyP(+) or 2H-Py(3)P results from the encapsulation of AuTPyP(+) or 2H-Py(3)P inside the cavity of TPZn(3) through multiple coordination bonds, as indicated by UV-vis-NIR, ESI-MS, (1)H NMR, electrochemistry and computational studies. The binding constants of monomer zinc porphyrin (MPZn) with AuTPyP(+) and 2H-Py(3)P drastically decrease as compared with TPZn(3). Detailed photophysical studies have been carried out on these composites using laser flash photolysis as well …

Models MolecularPorphyrinsMetalloporphyrinsPhotochemistryPyridinesTripod (photography)General Physics and Astronomychemistry.chemical_elementZincElectrochemistryPhotochemistryPorphyrinElectron TransportElectron transferchemistry.chemical_compoundMonomerchemistryFlash photolysisSinglet statePhysical and Theoretical ChemistryPhysical Chemistry Chemical Physics
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Structure, Spectroscopy, and Spectral Tuning of the Gas-Phase Retinal Chromophore: The β-Ionone "Handle" and Alkyl Group Effect

2005

The low-lying singlet states (i.e. S0, S1, and S2) of the chromophore of rhodopsin, the protonated Schiff base of 11-cis-retinal (PSB11), and of its all-trans photoproduct have been studied in isolated conditions by using ab initio multiconfigurational second-order perturbation theory. The computed spectroscopic features include the vertical excitation, the band origin, and the fluorescence maximum of both isomers. On the basis of the S0-->S1 vertical excitation, the gas-phase absorption maximum of PSB11 is predicted to be 545 nm (2.28 eV). Thus, the predicted absorption maximum appears to be closer to that of the rhodopsin pigment (2.48 eV) and considerably red-shifted with respect to that…

Models Molecularchemistry.chemical_classificationAlkylationDouble bondChemistrySpectrum AnalysisMolecular ConformationAb initioHydrogen BondingStereoisomerismChromophoreHydroxylationRing (chemistry)PhotochemistryVibrationRetinaGasesSinglet statePhysical and Theoretical ChemistryNorisoprenoidsSpectroscopyAbsorption (electromagnetic radiation)Alkyl
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