Search results for " CLE"

showing 10 items of 3398 documents

Supercontinuum generation in titanium dioxide waveguides

2019

International audience; Optical supercontinua are a fundamental topic that has stimulated a tremendous practical interest since the early works of Alfano et al. in the 70’s in bulk components. Photonic crystal fibers have then brought some remarkable potentialities in tailoring the dispersive properties of a waveguide while maintaining a high level of confinement over significant propagation distances. The next breakthrough is to further reduce the footprint of the nonlinear component and to achieve the generation of optical supercontinuum on a photonic chip. To reach this aim, several platforms have been successfully investigated such as silicon, silicon germanium, silicon nitride, chalcog…

010309 optics[PHYS.PHYS.PHYS-OPTICS] Physics [physics]/Physics [physics]/Optics [physics.optics][PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]0103 physical sciencesPhysics::Optics02 engineering and technology021001 nanoscience & nanotechnology0210 nano-technology7. Clean energy01 natural sciencesComputingMilieux_MISCELLANEOUS
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Tetrasubstituted Thieno[3,2- b]thiophenes as Hole-Transporting Materials for Perovskite Solar Cells

2019

Three hole-transporting materials (HTMs) were prepared following a straightforward synthetic route by cross-linking arylamine-based ligands with a simple thieno[3,2-b]thiophene (TbT) core. The novel HTMs were fully characterized with standard techniques to gain insight into their optical and electrochemical properties and were incorporated in solution-processed mesoporous (FAPbI3)0.85(MAPbBr3)0.15 perovskite-based solar cells. The similar molecular structure of the synthesized HTMs was leveraged to investigate the role that the bridging units between the conjugated TbT core and the peripheral arylamine units plays on their properties and thereby on the photovoltaic response. A remarkable po…

010405 organic chemistryChemistryOrganic ChemistryPhotovoltaic systemEnergy conversion efficiencyConjugated system010402 general chemistryElectrochemistry7. Clean energy01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundThiopheneMoleculeMesoporous material
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Light-Induced Alkylation of (Hetero)aromatic Nitriles in a Transition-Metal-Free C–C-Bond Metathesis

2017

A light-induced C–C-σ-bond metathesis was achieved through transition-metal-free activation of an unstrained C(sp3)–C(sp3)-σ-bond in 1-benzyl-1,2,3,4-tetrahydroisoquinolines. A photoredox-mediated single-electron oxidation of these precursor amines yield radical cations which undergo a homolytic cleavage of a C(sp3)–C(sp3)-σ-bond rather than the well-known α-C–H-scission. The resulting carbon-centered radicals are used in the ipso-substitution of (hetero)aromatic nitriles proceeding through another single-electron transfer-mediated C–C-bond cleavage and formation.

010405 organic chemistryChemistryRadicalOrganic ChemistryAlkylation010402 general chemistryPhotochemistryCleavage (embryo)Metathesis01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesTransition metalYield (chemistry)Light inducedPhysical and Theoretical ChemistryBond cleavageOrganic Letters
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Green synthesis of cavity-containing manganese oxides with superior catalytic performance in toluene oxidation

2019

10 Figuras.- 2 Tablas.- Datos suplementarios disponibles en línea en la página web del editor.-- © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

010405 organic chemistryChemistryStructural waterProcess Chemistry and TechnologyInorganic chemistryCationic polymerizationVOCs oxidationchemistry.chemical_elementNanoparticleManganeseCavities010402 general chemistry01 natural sciences7. Clean energyOxygenTolueneCatalysisHydrothermal circulationToluene oxidation0104 chemical sciencesCatalysischemistry.chemical_compoundManganese oxideToluene
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Reversible O–H bond activation by an intramolecular frustrated Lewis pair

2019

The interactions of the O-H bonds in alcohols, water and phenol with dimethylxanthene-derived frustrated Lewis pairs (FLPs) have been probed. Within the constraints of this backbone framework, the preference for adduct formation or O-H bond cleavage to give the corresponding zwitterion is largely determined by pKa considerations. In the case of the PPh2/B(C6F5)2 system and p-tBuC6H4OH, an equilibrium is established between the two isomeric forms which allows the thermodynamic parameters associated with zwitterion formation via O-H bond cleavage to be probed.

010405 organic chemistryHydrogen bondintramolecular frustrated Lewis pair010402 general chemistry01 natural sciencesFrustrated Lewis pair0104 chemical sciencesAdductInorganic Chemistrykemialliset sidoksetCrystallographychemistry.chemical_compoundchemistryreversible O-H bond activationZwitterionIntramolecular forceta116Bond cleavageDalton Transactions
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Carbon monoxide activation by a molecular aluminium imide: C-O bond cleavage and C-C bond formation

2020

Anionic molecular imide complexes of aluminium are accessible via a rational synthetic approach involving the reactions of organo azides with a potassium aluminyl reagent. In the case of K2 [(NON)Al(NDipp)]2 (NON=4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethyl-xanthene; Dipp=2,6-diisopropylphenyl) structural characterization by X-ray crystallography reveals a short Al-N distance, which is thought primarily to be due to the low coordinate nature of the nitrogen centre. The Al-N unit is highly polar, and capable of the activation of relatively inert chemical bonds, such as those found in dihydrogen and carbon monoxide. In the case of CO, uptake of two molecules of the substrate…

010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesIsocyanateCatalysis3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryChemical bondReagentPolymer chemistryMoleculeImideBond cleavageCarbon monoxide
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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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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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The high-resolution far-infrared spectrum of methane at the SOLEIL synchrotron

2010

International audience; As a tetrahedral molecule, methane has no permanent dipole moment. Its spectrum, however, displays faint absorption lines in the THz region, due to centrifugal distorsion effects. This is important for planetary applications since this region is used to measure methane concentration in some planetary atmospheres, in particular on Titan. Up to now, all measurements relied either on some old low resolution infrared absorption spectra, or on high resolution Stark measurements for low J values only. Even if these results have been reexamined recently [E. H. Wishnow, G. S. Orton, I. Ozier and H. P. Gush, J. Quant. Spectrosc. Radiat. Transfer 103, 102-117 (2007)], it seeme…

010504 meteorology & atmospheric sciencesAbsorption spectroscopyAnalytical chemistrySynchrotron radiationFar infrared7. Clean energy01 natural sciencesSpectral linelaw.inventionOpticsFar infraredlaw0103 physical sciencesAbsorption (logic)010303 astronomy & astrophysicsSpectroscopy0105 earth and related environmental sciencesPhysicsRadiationSynchrotron radiationbusiness.industryResolution (electron density)BremsstrahlungAtomic and Molecular Physics and OpticsSynchrotron[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry13. Climate action[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrybusinessTitanMethaneLine intensities
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Modeling the Effects of Climate Change on the Supply of Phosphate-Phosphorus

2009

The transfer of phosphorus from terrestrial to aquatic ecosystems is a key route through which climate can influence aquatic ecosystems. A number of climatic factors interact in complex ways to regulate the transfer of phosphorus and modulate its ecological effects on downstream lakes and reservoirs. Processes influencing both the amount and timing of phosphorus export from terrestrial watersheds must be quantified before we can assess the direct and indirect effects of the weather on the supply and recycling of phosphorus. Simulation of the export of phosphorus from the terrestrial environment is complicated by the fact that it is difficult to describe seasonal and inter-annual variations …

010504 meteorology & atmospheric sciencesAquatic ecosystemPhosphorus0207 environmental engineeringchemistry.chemical_elementSoil science02 engineering and technology15. Life on landAtmospheric sciences01 natural sciences6. Clean waterExtreme weatherchemistry13. Climate actionEffects of global warmingEvapotranspirationEnvironmental scienceTerrestrial ecosystemPrecipitation020701 environmental engineeringSurface runoff0105 earth and related environmental sciences
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