Search results for "Singlet"

showing 10 items of 352 documents

Mixed-valence polyoxometalate clusters. I. Delocalization of electronic pairs in dodecanuclear heteropoly blues with keggin structure

1995

Abstract The problem of delocalization of a pair of electrons over dodecanuclear polyoxometalate clusters with the Keggin structure is considered with the aim of explaining the spin pairing in these multi-nuclear mixed-valence systems. A general approach that considers the Coulomb interactions between the two delocalized electrons, as well as the single and double electron transfer processes which can be operative in delocalization of the electronic pairs is developed. The new approach is based on the site-symmetry concept which makes possible a group theoretical classification for the delocalized states of electronic pairs. This procedure proves to be very efficient in the calculation of t…

Valence (chemistry)Spin statesGeneral Physics and AstronomyMolecular physicsDelocalized electronKeggin structurechemistry.chemical_compoundchemistryPairingPolyoxometalateCluster (physics)Singlet statePhysical and Theoretical ChemistryAtomic physicsChemical Physics
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Xanthone-photosensitized detoxification of the veterinary anthelmintic fenbendazole

2013

Fenbendazole (1) is a common veterinary anthelmintic, toxic to water living microorganisms. Fluorescence quantum yields of 1 were found to be 0.11 in acetonitrile, 0.068 in methanol, 0.034 in cyclohexane, and 0.013 in water. The singlet excited state energy was ca. 96 kcal mol(-1) in all solvents. The phosphorescence spectrum of 1 in ethanol at 77 K displayed a maximum at 450 nm, leading to a triplet energy of 75 kcal mol(-1). Experimental excited state energies agree well with the results of OFT calculations at the time-dependent B3LYP/6-311+G(d,p)//B3LYP/6-31G(d) level. Laser flash photolysis (LFP) of 1 at 266 nm led to transients absorbing in the 300-700 nm range, ascribed to radical cat…

Veterinary medicineToxicityChemistryGeneral Chemical EngineeringDaphnia magnaEnvironmental remediationPhotodissociationGeneral Physics and AstronomyMICROBIOLOGIAFenbendazoleGeneral ChemistryPhotochemistrychemistry.chemical_compoundQUIMICA ORGANICARadical ionExcited statePhotodegradationXanthoneBIOQUIMICA Y BIOLOGIA MOLECULARFlash photolysisSinglet statePhotodegradationPhosphorescenceJournal of Photochemistry and Photobiology A: Chemistry
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Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyri…

2016

We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(…

XantphosLigand02 engineering and technologyGeneral ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences22'-Bipyridine0104 chemical scienceschemistry.chemical_compoundCrystallographyElectron transferchemistryExcited stateMaterials ChemistrySinglet state0210 nano-technology
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Polarization transfer via field sweeping in parahydrogen-enhanced nuclear magnetic resonance.

2019

<div><br></div><div><table><tr><td>We show that in a spin system of two magnetically inequivalent protons coupled to a heteronucleus such as 13C, an adiabatic magnetic field sweep, passing through zero field, transfers proton singlet order into magnetization of the coupled heteronucleus. This effect is potentially useful in parahydrogen-enhanced nuclear magnetic resonance, and is demonstrated on singlet-hyperpolarized [1-13C]maleic acid, which is prepared via the reaction between [1-13C]acetylene dicarboxylic acid and para-enriched hydrogen gas. The magnetic field sweeps are of microtesla amplitudes, and have durations on the order of seconds. We sh…

Zero field NMRMaterials science010304 chemical physicsMaleic acidHydrogenField (physics)ProtonGeneral Physics and Astronomychemistry.chemical_element010402 general chemistryPolarization (waves)Spin isomers of hydrogen01 natural sciences0104 chemical sciencesMagnetic fieldchemistry.chemical_compoundMagnetizationNuclear magnetic resonancechemistry0103 physical sciencesSinglet statePhysical and Theoretical ChemistryThe Journal of chemical physics
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Internally Contracted Multireference Coupled Cluster Calculations with a Spin-Free Dirac-Coulomb Hamiltonian: Application to the Monoxides of Titaniu…

2017

We combine internally contracted multireference coupled cluster theory with a four-component treatment of scalar-relativistic effects based on the spin-free Dirac–Coulomb Hamiltonian. This strategy allows for a rigorous treatment of static and dynamic correlation as well as scalar-relativistic effects, which makes it viable to describe molecules containing heavy transition elements. The use of a spin-free formalism limits the impact of the four-component treatment on the computational cost to the non-rate-determining steps of the calculations. We apply the newly developed method to the lowest singlet and triplet states of the monoxides of titanium, zirconium, and hafnium and show how the in…

Zirconium010304 chemical physicsElectronic correlationComputer Science Applications1707 Computer Vision and Pattern Recognition; Physical and Theoretical Chemistrychemistry.chemical_elementComputer Science Applications1707 Computer Vision and Pattern RecognitionElectronic structure010402 general chemistry01 natural sciences0104 chemical sciencesComputer Science ApplicationsHafniumsymbols.namesakeCoupled clusterchemistry0103 physical sciencessymbolsSinglet statePhysics::Chemical PhysicsAtomic physicsPhysical and Theoretical ChemistryRelativistic quantum chemistryHamiltonian (quantum mechanics)
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Coumarin-Phosphine-Based Smart Probes for Tracking Biologically Relevant Metal Complexes: From Theoretical to Biological Investigations

2016

International audience; Ten metal-based complexes and associated ligands have been synthesized and characterized. One of the metal ligands is a coumarin-phosphine derivative, which displays tunable fluorescence properties. The fluorescence is quenched in the case of the free ligand and ruthenium and osmium complexes, whereas it is strong for the gold complexes and phosphonium derivatives. These trends were rationalized by theoretical calculations, which revealed non-radiative channels involving a dark state for the free ligands that is lower in energy than the emissive state and is responsible for the quenching of fluorescence. For the Ru-II and Os-II complexes, other non-radiative channels…

ab-initiotheranosticschemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesQuantitative Biology::Cell BehaviorBioinorganic chemistryInorganic Chemistrychemistry.chemical_compound[CHIM]Chemical SciencesOsmiumSinglet statePhosphoniumtherapyAntitumor agents010405 organic chemistryChemistryLigandFluorescence0104 chemical sciencesRutheniumP ligandsagentsTheranostic agentsExcited stateFluorescent probesporphyrinPhosphine
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Theoretical and experimental studies of some main group compounds : from closed shell interactions to singlet diradicals and stable radicals

2012

Acquiring knowledge of different interactions within and between molecules is a fascinating undertaking as it not only deepens our understanding of chemical bonding but also offers insight into electronic structures, molecular properties and the connections between these two. This dissertation combines together three main group chemistry related topics within the aforementioned theme. Research presented in the first third of this dissertation describes wave function and density functional theory studies of weak inter- and intramolecular interactions in pnictogen-based dimers X3Pn···PnX3 (Pn = N-Bi; X = F-I), dithallenes RTlTlR (R = H, Me, tBu, Ph) and octachalcogen dications Ch82+ (Ch = S, …

atomitkemialliset sidoksetstable radicalssynthesisintermolecular interactionskemiatheoretical and computational chemistrysinglet diradical characterintramolecular interactionsmolekyylitsynteesimain group chemistryclosed shell interactions
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Singlet and triplet energy transfers in tetra-(meso-truxene)zinc(II)- and tetra-(meso-tritruxene)zinc(II) porphyrin and porphyrin-free base dendrimer…

2011

The synthesis, optical properties, and energy transfer features of four dendrimers composed of meso-tetrasubstituted zinc(II) porphyrin (ZnP) or a free base (P) central core, where the substituents are four truxene (Tru) or four tritruxene dendrons (TriTru), TruP, TriTruP, TruZnP, and TriTruZnP, are reported. Selective excitation of the truxene donors results in a photoinduced singlet energy transfer from the truxenes to the porphyrin acceptor. The rates for singlet energy transfer (k(ET)), evaluated from the change in the fluorescence lifetime of the donors (Tru and TriTru) in the presence and absence of the acceptor (P or ZnP) for TruP, TruZnP, TriTruP, and TriTruZnP, are 5.9, 1.2, 0.87, …

biologyChemistryFree basechemistry.chemical_elementZincbiology.organism_classificationPhotochemistryFluorescencePorphyrinAcceptorInorganic Chemistrychemistry.chemical_compoundDendrimerTetraSinglet statePhysical and Theoretical ChemistryInorganic chemistry
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[33] Use of repair endonucleases to assess DNA damage by peroxynitrite

1999

Publisher Summary This chapter discusses the use of repair endonucleases to assess DNA damage by peroxynitrite. Repair endonucleases allow a convenient quantification of various types of oxidative modifications induced by peroxynitrite, both in cultured cells and in cell-free DNA. The high sensitivity of the assays allows highly ectotoxic exposure conditions to be avoided—as well as the generation of secondary DNA modifications—that often become a problem at high levels of damage because primary DNA oxidation products can be orders of magnitude more reactive than the original bases, as demonstrated for the reaction of 8-hydroxyguanine with singlet oxygen. The ratio of the various types of m…

biologyDNA damageDNA repairSinglet oxygenDNA oxidationmedicine.disease_causechemistry.chemical_compoundchemistryBiochemistrybiology.proteinmedicineEndodeoxyribonucleasesPeroxynitriteOxidative stressDNA
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Squaraine Dyes for Photodynamic Therapy: Mechanism of Cytotoxicity and DNA Damage Induced by Halogenated Squaraine Dyes Plus Light (>600 nm)¶

2004

Halogenated squaraine dyes 1 and 2 possess favorable photophysical and in vitro photobiological properties that make these new class of molecules interesting for photodynamic therapeutic applications. For a better understanding of the mechanism of their photobiological activity, we have analyzed the DNA damage and the cytotoxicity induced by these photosensitizers in mammalian cells and cell-free systems in the presence and absence of various additives and scavengers. Both photoactivated squaraines were found to be similar efficient in inducing single-strand breaks (SSB) in cell-free DNA when compared with the cellular DNA. Superoxide dismutase and catalase did not show any influence. Howev…

biologySinglet oxygenDNA damagemedicine.medical_treatmentPhotodynamic therapyGeneral MedicineGlutathionePhotochemistryBiochemistryIn vitroSuperoxide dismutasechemistry.chemical_compoundchemistrybiology.proteinmedicinePhysical and Theoretical ChemistryCytotoxicityDNAPhotochemistry and Photobiology
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