Search results for " functional"

showing 10 items of 1811 documents

A Combined Experimental and Theoretical Study of the Ammonium Bifluoride Catalyzed Regioselective Synthesis of Quinoxalines and Pyrido[2,3-b]pyrazines

2015

International audience; Ammonium bifluoride was efficiently used (at a 0.5 mol % loading) to catalyze the cyclocondensation between 1,2-arylenediamines and 1,2-dicarbonyl compounds at room temperature in methanol-water, affording quinoxalines and pyrido[2,3-b]pyrazines in excellent yields. Importantly, 2,8-disubstituted quinoxalines and 3-substituted pyrido[2,3-b]pyrazines were regioselectively formed by reacting aryl glyoxals with 3-methyl-1,2-phenylenediamine and 2,3-diaminopyridine, respectively. Analysis of the DFT reactivity indices allowed to explain the catalytic role of ammonium bifluoride.

010405 organic chemistryChemistryOrganic ChemistryRegioselectivityAmmonium bifluoride010402 general chemistrypyrido[201 natural sciencesCatalysisammonium bifluoride0104 chemical sciencesCatalysischemistry.chemical_compoundregioselectivity3-b]pyrazinesDFT reactivity indices[CHIM]Chemical SciencesOrganic chemistryquinoxalinesDensity functional theoryReactivity (chemistry)Synthesis
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Theoretical Investigation of the Low-Energy States of CpMoCl(PMe 3 ) 2 and Their Role in the Spin-Forbidden Addition of N 2 and CO

2003

International audience; A recent computational investigation of Jahn−Teller effects in unsaturated 16-electron d4d6 [CpMLn] complexes (Abu-Hasanayn, F.; Cheong, P.; Oliff, M. Angew. Chem.2002, 41, 2120) highlighted the typical presence of two spin-triplet and two singlet states of competing stability in these complexes and pointed out the necessity to account for more than one electronic state in studies thereof. Consequently, we have reinvestigated the addition of N2 to all the four low-energy states of CpMoCl(PH3)2, a reaction for which previously only one singlet and one triplet state have been considered (Keogh, D. W.; Poli, R. J. Am. Chem. Soc.1997, 119, 2516). The present study was pe…

010405 organic chemistryChemistryState (functional analysis)010402 general chemistry01 natural sciencesQuantum mechanics0104 chemical sciencesElectronic statesAddition reactionsChemical calculations[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryLow energyChemical structureMathematical methodsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet statePhysics::Chemical PhysicsSpin (physics)Ground state
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Copper(I)-catalysed regioselective synthesis of pyrazolo[5,1-c]-1,2,4-triazoles: A DFT mechanistic study

2017

Abstract Formation of pyrazolo[5,1-c]-1,2,4-triazoles by means of Cu(I)-catalysed [3+2] cycloaddition (32CA) reactions of C,N-cyclic azomethine imines with phenylacetylene, experimentally reported by Katritzky et al. (JOC 2012, 77, 5813), was studied using the density functional theory (DFT) method. Comparison with the uncatalysed 32CA reaction indicates that the Cu(I) catalyst provides new reaction pathways with lower electronic energy barriers in dichloromethane as solvent. The mechanism proposed by Katritzky for the Cu(I) catalysed reaction is compared with that proposed by Sharpless et al. (JACS 127, 2005, 210). The major difference between these two mechanisms lies in the coordination …

010405 organic chemistryChemistryStereochemistryAcetylideOrganic ChemistryImineRegioselectivity010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistryCycloaddition0104 chemical sciencesCatalysischemistry.chemical_compoundPhenylacetyleneDrug DiscoveryMoietyDensity functional theoryTetrahedron
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Halide-Mediated Modification of Magnetism and Electronic Structure of α-Co(II) Hydroxides: Synthesis, Characterization, and DFT+U Simulations.

2019

The present study introduces a comprehensive exploration in terms of physicochemical characterization and calculations based on density functional theory with Hubbard's correction (DFT+U) of the whole family of α-Co(II) hydroxyhalide (F, Cl, Br, I). These samples were synthesized at room temperature by employing a one-pot approach based on the epoxide route. A thorough characterization (powder X-ray diffraction, X-ray photoelectron spectroscopy, thermogravimetric analysis/mass spectroscopy, and magnetic and conductivity measurements) corroborated by simulation is presented that analyzes the structural, magnetic, and electronic aspects. Beyond the inherent tendency of intercalated anions to …

010405 organic chemistryMagnetismepoxide routechemistry.chemical_elementHalideElectronic structure010402 general chemistrycobalt01 natural sciences0104 chemical sciencesCharacterization (materials science)//purl.org/becyt/ford/1 [https]Inorganic Chemistrychemistrymagnetism//purl.org/becyt/ford/1.4 [https]Physical chemistryDensity functional theoryPhysical and Theoretical Chemistrylayered hydroxidesCobaltFisicoquímicaInorganic chemistry
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N-Cobaltocenium Amide as Reactive Nucleophilic Reagent for Donor–Acceptor Bimetallocenes

2017

Deprotonation of the aminocobaltocenium ion [Cc-NH2]+ ([H-1]+) generates the nucleophilic imine CcNH (1). Reaction of 1 with acid chlorides R–COCl (R = Ph, Fc, and Cc+) yields the reference amide [Ph-CO-NH-Cc]+ (2+) and the amide-linked hetero- and homobimetallocenes [Fc-CO-NH-Cc]+ (3+) and [Cc-CO-NH-Cc]2+ (42+), respectively. Cation–anion interactions of charged amides 2+–42+ in the solid state and in solution are probed by single crystal X-ray diffraction and NMR and IR spectroscopy. Intramolecular metal–metal interactions in donor–acceptor heterobimetallocene 3+ and in mixed-valent homobimetallocene 4+ (prepared electrochemically) are discussed within the Marcus–Hush framework aided by s…

010405 organic chemistryOrganic ChemistryImineInfrared spectroscopy010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistryNucleophileIntramolecular forceReagentAmideDensity functional theoryPhysical and Theoretical ChemistryOrganometallics
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Unexpected Scholl Reaction of 6,7,13,14-Tetraarylbenzo[k]tetraphene: Selective Formation of Five-Membered Rings in Polycyclic Aromatic Hydrocarbons

2016

Cyclodehydrogenation is a versatile reaction that has enabled the syntheses of numerous polycyclic aromatic hydrocarbons (PAHs). We now describe a unique Scholl reaction of 6,7,13,14-tetraarylbenzo[k]tetraphene, which "unexpectedly" forms five-membered rings accompanying highly selective 1,2-shift of aryl groups. The geometric and optoelectronic nature of the resulting bistetracene analogue with five-membered rings is comprehensively investigated by single-crystal X-ray, NMR, UV-vis absorption, and cyclic voltammetry analyses. Furthermore, a possible mechanism is proposed to account for the selective five-membered-ring formation with the rearrangement of the aryl groups, which can be ration…

010405 organic chemistryStereochemistryArylGeneral Chemistry010402 general chemistryHighly selective01 natural sciencesBiochemistryCatalysis0104 chemical sciencesScholl reactionchemistry.chemical_compoundColloid and Surface ChemistrychemistryComputational chemistryDensity functional theoryAbsorption (chemistry)Cyclic voltammetryTetrapheneJournal of the American Chemical Society
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Controlling the Host-Guest Interaction Mode through a Redox Stimulus

2017

International audience; A proof-of-concept related to the redox-control of the binding/releasing process in a host-guest system is achieved by designing a neutral and robust Pt-based redox-active metallacage involving two extended-tetrathiafulvalene (exTTF) ligands. When neutral, the cage is able to bind a planar polyaromatic guest (coronene). Remarkably, the chemical or electrochemical oxidation of the host-guest complex leads to the reversible expulsion of the guest outside the cavity, which is assigned to a drastic change of the host-guest interaction mode, illustrating the key role of counteranions along the exchange process. The reversible process is supported by various experimental d…

010405 organic chemistryStereochemistrySupramolecular chemistryGeneral MedicineGeneral ChemistryReversible processself-assembly010402 general chemistryElectrochemistry01 natural sciencesRedoxsupramolecular cageCatalysisCoronene0104 chemical scienceschemistry.chemical_compoundchemistryChemical physicsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySelf-assemblyTetrathiafulvaleneexTTF
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Bowl-shape electron donors with absorptions in the visible range of the solar spectrum and their supramolecular assemblies with C 60

2012

We describe the synthesis, electronic, optical and photophysical properties of a family of three electron-donor bowl-shaped organic molecules that absorb light in the whole range of the visible spectrum (up to 800 nm in one case), and associate C60 in solution with binding constants in the range of 104–102 M−1 as measured from both UV-vis and fluorescence titrations in several solvents. These molecules are π-extended derivatives of tetrathiafulvalene, based on a truxene core to which two or three units of dithiole are covalently attached. The inclusion of the bulky dithiole groups is responsible for their bowl-shape geometry, which allows them to associate with C60, and their electron-donor…

010405 organic chemistrySupramolecular chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesPhotoexcitationchemistry.chemical_compoundchemistryIntramolecular forceUltrafast laser spectroscopyDensity functional theoryAbsorption (chemistry)TetrathiafulvaleneVisible spectrum
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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 study on the decomposition mechanism of bisphenol A polycarbonate induced by the combined effect of humidity and UV irradiation.

2020

Polycarbonate (PC) is a good material for covering and protecting cultural heritage sites because of its durability, mechanical properties, and transparency. When bisphenol A polycarbonate is subjected to weathering conditions this polymer shows several degradation processes depending on the irradiation wavelength, humidity and temperature. In particular, the combined effects of humidity and UV irradiation speed up the PC molecular weight reduction. In this work, the decomposition mechanisms associated to the hydrolysis process are scrutinized and the effects of UV irradiation on the hydrolysis process are evaluated throughout the Density Functional Theory (DFT) approach. It was found that …

010407 polymersMaterials sciencePolymersUltraviolet Rays02 engineering and technologyPhotochemistry01 natural sciencesHydrolysisDFT modeling; hydrolysis process; polycarbonate; weathering degradationMaterials ChemistryIrradiationPhysical and Theoretical ChemistryPolycarbonateBenzhydryl CompoundsSpectroscopychemistry.chemical_classificationHumidityHumidityPolymerModels Theoretical021001 nanoscience & nanotechnologyComputer Graphics and Computer-Aided DesignDecomposition0104 chemical sciencespolycarbonatechemistryhydrolysis processvisual_artvisual_art.visual_art_mediumDegradation (geology)Density functional theoryDFT modeling0210 nano-technologyweathering degradationJournal of molecular graphicsmodelling
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