Search results for "ELECTRON"

showing 10 items of 24810 documents

Photo-Chromium: Sensitizer for Visible-Light-Induced Oxidative C−H Bond Functionalization-Electron or Energy Transfer?

2017

The chromium(III) sensitizer [Cr(ddpd)2]3+ - based on an earth-abundant metal center - possesses a unique excited state potential energy landscape (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine). The very large energy gap between the redox active and substitutionally labile 4T2 state and the long-lived low-energy 2E spin-flip state enables a selective, efficient sensitization of triplet dioxygen to give singlet dioxygen. Ultrafast intersystem crossing after the Franck Condon point from the 4T2 to the 2E excited state within 3.5 ps precludes intermolecular electron transfer pathways from the ultrashort-lived excited 4T2 state. This specific excited state reactivity enables a …

010405 organic chemistrySinglet oxygenOrganic ChemistryIntermolecular forcechemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundChromiumElectron transferIntersystem crossingchemistryExcited stateSinglet fissionReactivity (chemistry)Physical and Theoretical ChemistryChemPhotoChem
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Helical supramolecular polymerization of C3-symmetric amides and retroamides: on the origin of cooperativity and handedness.

2016

The cooperative supramolecular polymerization of 1 and 2 yields P- or M-type helical aggregates depending on the absolute configuration (S or R) of the stereogenic centres attached to the side chains. The connectivity of the amide group does not affect the handedness of the helical aggregates, but determines a larger cooperativity for retroamides 1.

010405 organic chemistryStereochemistryMetals and AlloysSupramolecular chemistryAbsolute configurationCooperativityGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundCrystallographychemistryPolymerizationAmideMaterials ChemistryCeramics and CompositesSide chainChemical communications (Cambridge, England)
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Substituent effect on the σ- and π-electron structure of the nitro group and the ring in meta- and para-substituted nitrobenzenes

2017

An application of quantum chemical modeling allowed us to investigate a substituent effect on a σ and π electron structure of a ring and the nitro group in a series of meta- and para-X-substituted nitrobenzene derivatives (X = NMe2, NHMe, NH2, OH, OMe, Me, H, F, Cl, CF3, CN, CHO, COMe, CONH2, COOH, NO2, and NO). The obtained pEDA and sEDA parameters (the π- and σ-electron structure characteristics of a given planar fragment of the system obtained by the summation of π- and σ-orbital occupancies, respectively) of the NO2 group and the benzene ring allowed us to reveal the impact of the substituents on their mutual relations as well as to analyze them from the viewpoint of substituent charact…

010405 organic chemistryStereochemistrySubstituent010402 general chemistryRing (chemistry)Resonance (chemistry)01 natural sciences0104 chemical sciencesNitrobenzeneElectronegativitychemistry.chemical_compoundCrystallographychemistryGroup (periodic table)NitroPhysical and Theoretical ChemistryBenzeneJournal of Physical Chemistry A
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Extending the halogen-bonded supramolecular synthon concept to 1,3,4-oxadiazole derivatives

2016

A series of five crystal structures of 1:1 halogen-bonded complexes were obtained from 4-[5-(4-alkoxyphenyl)-1,3,4-oxadiazole-2-yl]pyridine and 1,3,5-trifluorotriiodobenzene. Electronic structure calculations show that the N(oxadiazole)⋯I interaction in the new synthon is as strong as the classic N(pyridine)⋯I interaction. Oxygen to sulfur atom subsitution on the oxadiazole ring results in a different supramolecular packing where the N(pyridine)⋯I interaction is favored, which could be rationalized by the changes in the molecular electrostatic potential predicted from the theoretical calculations.

010405 organic chemistryStereochemistrySynthonSupramolecular chemistryOxadiazoleGeneral ChemistryCrystal structureElectronic structure010402 general chemistryCondensed Matter PhysicsRing (chemistry)01 natural sciences0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryHalogenPyridineGeneral Materials ScienceCrystEngComm
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Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation

2018

Copper(II) complexes with the potentially tridentate Schiff bases N-[(3-ethoxy-2-hydroxyphenyl)methylidene]-N′-tosylbenzene-1,2-diamine (H2L1) and N-[(2-hydroxynaphthanyl)methylidene]-N′-tosylbenzene-1,2-diamine (H2L2) have been synthesized by electrochemical oxidation of the metal in an electrochemical cell containing a solution of the corresponding ligand in acetonitrile. Adducts of these compounds with 2,2′-bipyridine (2,2′-bpy), 4,4′-bipyridine (4,4′-bpy) or 1,10-phenanthroline (phen) were also obtained. The complexes have been characterized by microanalysis, mass spectrometry, EPR, IR and UV-Vis spectroscopies, as well as DFT calculations. The ligand H2L1 and the compounds [CuL1(H2O)]·…

010405 organic chemistrySupramolecular chemistrychemistry.chemical_elementNANOPARTÍCULASGeneral Chemistry010402 general chemistry01 natural sciencesCopperCatalysisSquare pyramidal molecular geometry0104 chemical scienceslaw.inventionAdductMetalCrystallographychemistry.chemical_compoundchemistrylawvisual_artMaterials Chemistryvisual_art.visual_art_mediumElectron paramagnetic resonanceAcetonitrileTernary complex
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Catalytic activity of biscobalt porphyrin-corrole dyads toward the reduction of dioxygen

2009

A series of biscobalt cofacial porphyrin-corrole dyads bearing mesityl substituents at the meso positions of the corrole ring were investigated as to their electrochemistry, spectroelectrochemistry, and CO binding properties in nonaqueous media and then applied to the surface of a graphite electrode and tested as electrocatalysts for the reduction of dioxygen to water or hydrogen peroxide in air-saturated aqueous solutions containing 1 M HClO(4). The catalytic reduction of O(2) with the same dyads was also investigated in the homogeneous phase using 1,1'-dimethylferrocene as a reductant in PhCN containing HClO(4). The examined compounds are represented as (PMes(2)CY)Co(2), where P = a porph…

010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry010402 general chemistryElectrocatalystPhotochemistry01 natural sciencesPorphyrin0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundElectron transferchemistrycorrolePolymer chemistryelectrocatalyst[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryCyclic voltammetryCorroleRotating disk electrodeVoltammetryporphyrinComputingMilieux_MISCELLANEOUSreduction of dioxygen
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DFT Study on the Interaction of Tris(benzene-1,2-dithiolato)molybdenum Complex with Water. A Hydrolysis Mechanism Involving a Feasible Seven-Coordina…

2016

In the present work, the reactivity of the tris(benzene-1,2-dithiolato)molybdenum complex ([Mo(bdt)3]) toward water is studied by means of the density functional theory (DFT). DFT calculations were performed using the M06, B3P86, and B3PW91 hybrid functionals for comparison purposes. The M06 method was employed to elucidate the reaction pathway, relative stability of the intermediate products, nature of the Mo–S bond cleavage, and electronic structure of the involved molybdenum species. This functional was also used to study the transference of electrons from the molybdenum center toward the ligands. The reaction pathway confirms that [Mo(bdt)3] undergoes hydrolysis, yielding dihydroxo-bis(…

010405 organic chemistrychemistry.chemical_elementElectronic structure010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesHybrid functionalchemistry.chemical_compoundCrystallographychemistryMolybdenumDensity functional theoryReactivity (chemistry)Physical and Theoretical ChemistryBenzeneLone pairBond cleavageThe Journal of Physical Chemistry A
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A reinvestigation of compound CpMo(PMe3)2(CH3)2: Alkylation by single electron transfer and radical addition?

2001

International audience; The synthesis of the half-sandwich molybdenum(III) diphosphine dimethyl complex CpMo(PMe3)2(CH3)2 has been reinvestigated. The compound was obtained from the corresponding dichloro complex CpMo(PMe3)2Cl2 and methyllithium at low temperatures and isolated as a crystalline product by conducting all operations at temperatures lower than −10 °C. The complex is thermally unstable at room temperature but has been fully characterised by EPR spectroscopy, cyclic voltammetry and X-ray diffraction. The formation reaction is retarded by excess phosphine. On the basis of this and other related observations, a mechanism involving phosphine pre-dissociation followed by single elec…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryAlkylation010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionSingle electronchemistry.chemical_compoundchemistrylawMolybdenumPolymer chemistryMethyllithium[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclic voltammetryElectron paramagnetic resonancePhosphine
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Theoretical investigation of the spin crossover transition states of the addition of methane to a series of Group 6 metallocenes using minimum energy…

2016

International audience; Density functional calculations are reported on the addition of methane to Group 6 metallocenes, M(η-C5H5)2 (M), M(CH2(η-C5H4)2) (a-M) and M(η-C5Me5)2 (M*) where M = Mo and W. Full geometry optimisations were carried out on the singlet and triplet 16 electron complexes, 1[M] and 3[M], the η2-methane complexes, 1[M(η2-CH4)], and the hydridomethyl adducts, 1[M(CH3)(H)]. The triplet state for [M] was found to be more stable for all six metallocenes, the difference being least in the case of the ansa-bridged system. Formation of the hydridomethyl complexes was exoenergetic for all tungsten systems and for a-Mo, the other two Mo systems being endoenergetic. Minumum energy…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryElectronTungsten010402 general chemistry7. Clean energy01 natural sciencesTransition stateMethane0104 chemical sciencesAdduct[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry13. Climate actionSpin crossoverComputational chemistryPhysical chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet stateTriplet stateJOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
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A comprehensive in situ and remote sensing data set from the Arctic CLoud Observations Using airborne measurements during polar Day (ACLOUD) campaign

2019

The Arctic CLoud Observations Using airborne measurements during polar Day (ACLOUD) campaign was carried out north-west of Svalbard (Norway) between 23 May and 6 June 2017. The objective of ACLOUD was to study Arctic boundary layer and mid-level clouds and their role in Arctic amplification. Two research aircraft (Polar 5 and 6) jointly performed 22 research flights over the transition zone between open ocean and closed sea ice. Both aircraft were equipped with identical instrumentation for measurements of basic meteorological parameters, as well as for turbulent and radiative energy fluxes. In addition, on Polar 5 active and passive remote sensing instruments were installed, while Polar 6 …

010504 meteorology & atmospheric sciences02 engineering and technology01 natural sciencesRadiative fluxddc:5500202 electrical engineering electronic engineering information engineeringSea icelcsh:Environmental sciences0105 earth and related environmental sciencesRemote sensinglcsh:GE1-350[SDU.OCEAN]Sciences of the Universe [physics]/Ocean AtmosphereData processinggeographygeography.geographical_feature_categorybusiness.industrylcsh:QE1-996.5020206 networking & telecommunicationsTrace gaslcsh:GeologyEarth sciencesArctic13. Climate actionRemote sensing (archaeology)Polar amplificationGeneral Earth and Planetary SciencesEnvironmental scienceData centerbusiness
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