Search results for "Reaction"

showing 10 items of 6134 documents

Toward an Understanding of Ultrafast Electron Transfer in Photosynthesis

2008

The mechanism of electron transfer (ET) from reduced pheophytin (Pheo−) to the primary stable photosynthetic acceptor, a quinone (Q) molecule, is addressed by using high-level ab initio computations and realistic molecular models. The results reveal that the ET process involving the (Pheo−+Q) and (Pheo+Q−) oxidation states can be seen essentially as an ultrafast radiationless transition between the two hypersurfaces taking place via conical intersections (CIs) and is favoured when the topology of the interacting moieties makes possible some overlap between the lowest occupied molecular orbitals (LUMO) of the two systems. Thus, it is anticipated that large scale motions, which are difficult …

PheophytinPhotosynthetic reaction centrechemistry.chemical_compoundElectron transferchemistryChemical physicsMoleculeMolecular orbitalConical intersectionHOMO/LUMOAcceptor
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Electrochemical and Spectroelectrochemical Studies of Diphosphorylated Metalloporphyrins. Generation of a Phlorin Anion Product

2015

Two series of diphosphoryl-substituted porphyrins were synthesized and characterized by electrochemistry and spectroelectrochemistry in nonaqueous media containing 0.1 M tetra-n-butylammonium perchlorate (TBAP). The investigated compounds are 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrins (Ph)2(P(O)(OEt)2)2PorM and 5,15-bis(diethoxyphosphoryl)-10,20-di(para-carbomethoxyphenyl)porphyrins (PhCOOMe)2(P(O)(OEt)2)2PorM where M = 2H, Co(II), Ni(II), Cu(II), Zn(II), Cd(II), or Pd(II). The free-base and five metalated porphyrins with nonredox active centers undergo two ring-centered oxidations and two ring-centered reductions, the latter of which is followed by a chemical reaction of the por…

PhotochemistryElectrochemistryMedicinal chemistryPorphyrinChemical reactionIonInorganic ChemistryPerchloratechemistry.chemical_compoundchemistryChemical conversion[CHIM]Chemical SciencesPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Photochemistry of 1,2,4-oxadiazoles. A DFT study on photoinduced competitive rearrangements of 3-amino- and 3-N-methylamino-5-perfluoroalkyl-1,2,4-ox…

2006

The photoinduced competitive rearrangements of 5-perfluoroalkyl-3-amino(N-alkylamino)-1,2,4-oxadia- zoles have been investigated by DFT calculations and UV-vis spectroscopy. The observed product selectivity depends on the number of hydrogen atoms present in the amino moiety and involves two or three possible routes: (i) ring contraction-ring expansion (RCRE), (ii) internal-cyclization isomerization (ICI), or (iii) C(3)-N(2) migration-nucleophilic attack-cyclization (MNAC). UV absorption and fluorescence spectra of the reactants, and vertical excitation energy values, calculated by time dependent DFT, support the involvement of a neutral singlet excited state in the photoexcitation process. …

PhotochemistryUltraviolet RaysFluorescence spectrometryReaction intermediatePhotochemistryDENSITY-FUNCTIONAL THEORYSinglet stateHUMAN 5-HT1B RECEPTORBASIS-SETSOxadiazolesRING-PHOTOISOMERIZATIONMolecular StructureChemistryOrganic ChemistryEXPEDIENT ROUTETautomerTransition statePhotoexcitationMOLECULAR-ORBITAL METHODSModels ChemicalLUORINATED HETEROCYCLIC-COMPOUNDSAROMATICITY INDEXExcited state5-MEMBERED HETEROCYCLESEXCITATION-ENERGIESIsomerization
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Photochromic System among Boron Hydrides: The Hawthorne Rearrangement

2019

Photoswitchable molecules have attracted wide interest for many applications in chemistry, physics, and materials science. In this work, we revisit the reversible photochemical and thermal rearrangements of the two B20H182– isomers reported by Hawthorne and Pilling in 1966, whose mechanism had not been understood so far. We investigate the rearrangements by means of a joint experimental and computational study with the outcome that B20H182– represents the first boron-based photochromic system ever reported. Both photochemical and thermal isomerizations occur through the same intermediate and involve a diamond–square–diamond (DSD) mechanism. Given the absence within boron chemistry of named …

Photochromismchemistrychemistry.chemical_elementMoleculeGeneral Materials ScienceBoron HydridesPhysical and Theoretical ChemistryPhotochemistryBoronChemical reactionIsomerization
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Photoelectrocatalytic oxidation of 3-pyridinemethanol to 3-pyridinemethanal and vitamin B3 by TiO2 nanotubes

2020

In this paper, the first photoelectrocatalytic (PEC) 3-pyridinemethanol oxidation to 3-pyridinemethanal and vitamin B-3 was investigated. To meet this aim, efficient nanotube structured TiO2 on a Ti plate as a photoanode was prepared by an anodic oxidation method in ethylene glycol and characterized by XRD, SEM, and photocurrent techniques. The effect of nanotube morphology, applied potential, Na2SO4 concentration, stirring speed of solution, and pH on the reaction activity and product selectivities were investigated. The TiO2 phase of all of the anodes was mainly the anatase one. The PEC activity, the intensity of the XRD peak and the photocurrent increased by increasing the nanotube lengt…

PhotocurrentAnatasechemistry.chemical_compoundNanotubeSelective oxidation TiO2 nanotubes PEC reactionschemistryPhase (matter)Inorganic chemistryPhotocatalysisSelectivityEthylene glycolCatalysisCatalysis
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Electro- and photo-electrooxidation of 2,4,5-trichlorophenoxiacetic acid (2,4,5-T) in aqueous media with PbO2, Sb-doped SnO2, BDD and TiO2-NTs anodes…

2020

Abstract In this work, the 2,4,5-T degradation in aqueous media was studied by electro- (EC) and photoelectrochemical (PEC) oxidation methods, which are two of the most important advanced oxidation processes (AOPs) for wastewater treatment. Both EC and PEC experiments were carried out in a single compartment cell under galvanostatic conditions (30 mA cm−2) at 298 K by using 0.05 M Na2SO4 + 200 ppm 2,4,5-T at pH 3 and pH 9, as model solutions. EC oxidation was performed using Sb-doped SnO2, PbO2 and boron doped diamond (BDD) as anodic materials. Besides these anodes, TiO2 in a nanotubular structure (TiO2 NTs) with or without PbO2 dispersed nanoparticles (TiO2::PbO2) were also used for PEC ox…

Photocurrentchemistry.chemical_classificationElectrolysisAqueous solutionmedicine.diagnostic_testChemistryGeneral Chemical EngineeringCarboxylic acidInorganic chemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionReaction rate constantlawSpectrophotometryElectrodeElectrochemistrymedicine0210 nano-technologyVoltammetryJournal of Electroanalytical Chemistry
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Charge-Separation and Charge-Recombination Rate Constants in a Donor–Acceptor Buckybowl-Based Supramolecular Complex: Multistate and Solvent Effects

2021

The kinetics of the nonradiative photoinduced processes (charge-separation and charge-recombination) experimented in solution by a supramolecular complex formed by an electron-donating bowl-shaped truxene-tetrathiafulvalene (truxTTF) derivative and an electron-accepting fullerene fragment (hemifullerene, C30H12) has been theoretically investigated. The truxTTF·C30H12 heterodimer shows a complex decay mechanism after photoexcitation with the participation of several low-lying excited states of different nature (local and charge-transfer excitations) all close in energy. In this scenario, the absolute rate constants for all of the plausible charge-separation (CS) and charge-recombination (CR)…

PhotoexcitationReaction rate constantFullereneChemistryExcited stateSupramolecular chemistryCharge (physics)Electronic structurePhysical and Theoretical ChemistrySolvent effectsMolecular physicsArticleThe Journal of Physical Chemistry. a
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Anharmonic Vibrational Spectrum and Experimental Matrix Isolation Study of Thioformic Acid Conformers -- Potential Candidates for Molecular Cloud and…

2021

Thioformic acid (TFA) is the sulfur analog of formic acid, the simplest organic acid. It has three analogues HCOSH, HCSOH, and HCSSH, each of them having two rotational isomeric (rotameric) forms: trans and cis where the trans form is energetically more stable. In this article, we study computational energetics and anharmonic vibrational spectrum of TFA including overtone and combination vibrations. We also studied experimental photoisomerization and photodecomposition channels of HCOSH molecules with different wavelengths. We suggest that TFA is a potential sulfur containing candidate molecule for interstellar and planetary observations and discuss these in a light of different radiation e…

PhotoisomerizationFormic acidInfraredAb initioFOS: Physical sciences02 engineering and technology01 natural sciences7. Clean energyChemical reactionchemistry.chemical_compoundComputational chemistryPhysics - Chemical Physics0103 physical sciencesMolecule010303 astronomy & astrophysicsConformational isomerismPhysicsChemical Physics (physics.chem-ph)Matrix isolationAstronomy and Astrophysics021001 nanoscience & nanotechnologyAstrophysics - Astrophysics of Galaxieschemistry13. Climate actionSpace and Planetary ScienceAstrophysics of Galaxies (astro-ph.GA)0210 nano-technology
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Carborane-stilbene dyads: influence of substituents and cluster isomers on the photoluminescence properties

2017

Two novel styrene-containing meta-carborane derivatives substituted at the second carbon cluster atom (Cc) with either a methyl (Me), or a phenyl (Ph) group, are introduced herein alongside with a new set of stilbene-containing ortho- (o-) and meta- (m-) carborane dyads. The latter set of compounds has been prepared from styrenecontaining carborane derivatives via Heck coupling reaction. High regioselectivity has been achieved for these compounds by using a combination of palladium complexes [Pd2(dba)3]/[Pd(t-Bu3P)2] as a catalytic system, yielding exclusively E isomers. All compounds have been fully characterized and the crystal structures of seven of them analyzed by X-ray diffraction. Th…

PhotoluminescenceAbsorption spectroscopy010405 organic chemistryStereochemistryChemistrySubstituentRegioselectivityQuantum yield010402 general chemistry01 natural sciencesFluorescence spectroscopy0104 chemical sciencesInorganic Chemistrycluster isomersCrystallographychemistry.chemical_compoundsubstituentsHeck reactionphotoluminescence propertiesCarboranecarborane-stilbene dyadsta116
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Isolated photon production in proton-nucleus collisions at forward rapidity

2018

We calculate isolated photon production at forward rapidities in proton-nucleus collisions in the Color Glass Condensate framework. Our calculation uses dipole cross sections solved from the running coupling Balitsky-Kovchegov equation with an initial condition fit to deep inelastic scattering data. For comparison, we also update the results for the nuclear modification factor for pion production in the same kinematics. We present predictions for future forward RHIC and LHC measurements at $\sqrt{s_{NN}}=200$ GeV and $\sqrt{s_{NN}}=8$ TeV.

PhotonNuclear TheoryProton7. Clean energy01 natural sciencesColor-glass condensateHigh Energy Physics - Phenomenology (hep-ph)coupling constant: energy dependenceDEPENDENCEPIONNuclear Experiment[ PHYS.NUCL ] Physics [physics]/Nuclear Theory [nucl-th]Brookhaven RHIC CollPhysicsphoton lepton and quark productionLarge Hadron ColliderD+AU COLLISIONSphotonBalitsky-Kovchegov equationP-PB COLLISIONSHigh Energy Physics - PhenomenologyCERN LHC Colllepton and quark productionLHCphoton: forward production[PHYS.NUCL]Physics [physics]/Nuclear Theory [nucl-th]FOS: Physical sciencespi: hadroproduction114 Physical sciencesNuclear Theory (nucl-th)Nuclear physicsPiondeep inelastic scatteringquantum chromodynamics0103 physical sciencesRapidity010306 general physicsp nucleus: scatteringta114010308 nuclear & particles physicsCOLOR GLASS CONDENSATEDeep inelastic scatteringHADRON-PRODUCTIONboundary conditionDipolerapidityQCD in nuclear reactions[PHYS.HPHE]Physics [physics]/High Energy Physics - Phenomenology [hep-ph]TEV[ PHYS.HPHE ] Physics [physics]/High Energy Physics - Phenomenology [hep-ph]cross section: dipole
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