Search results for " energy."

showing 10 items of 27368 documents

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
researchProduct

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
researchProduct

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
researchProduct

Variable Cooperative Interactions in the Pressure and Thermally Induced Multistep Spin Transition in a Two-Dimensional Iron(II) Coordination Polymer

2020

Two types of experiments conducted to investigate the effect of pressure on the spin crossover (SCO) properties of the 2D Fe(II) coordination polymer formulated {Fe[bipy(ttr)2]}n are reported, namely, (1) magnetic measurements performed at variable temperature and at fixed pressure and (2) visible spectroscopy at variable pressure and fixed temperature. The magnetic experiments carried out under a hydrostatic pressure constraint of 0.04, 0.08, and 0.8 GPa reveal a two-step spin transition behavior. The characteristic critical temperatures of the spin transition are shifted upward in temperature as pressure increases. The slope of the straight-line of the Tc vs P plot, dTc/dP, is 775 K/GPa a…

010405 organic chemistryCoordination polymerHydrostatic pressureSpin transitionElastic energyThermodynamicsFlory–Huggins solution theory010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundUltraviolet visible spectroscopychemistrySpin crossoverLattice (order)Physical and Theoretical ChemistryInorganic Chemistry
researchProduct

2-Methyltetrahydrofuran: A Green Solvent for Iron-Catalyzed Cross-Coupling Reactions

2018

Iron‐catalyzed cross‐coupling reactions allow sustainable formation of C−C bonds using cost‐effective, earth‐abundant base‐metal catalysis for complex syntheses of pharmaceuticals, natural products, and fine chemicals. The major challenge to maintain full sustainability of the process is the identification of green and renewable solvents that can be harnessed to replace the conventional solvents for this highly attractive reaction. Herein, iron‐catalyzed cross‐coupling of aryl chlorides and tosylates with challenging organometallic reagents possessing β‐hydrogens is found to proceed in good to excellent yields with the green, sustainable, and eco‐friendly 2‐methyltetrahydrofuran (2‐MeTHF) a…

010405 organic chemistryGeneral Chemical EngineeringAryl2-MethyltetrahydrofuranHomogeneous catalysis010402 general chemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesCatalysisSolventchemistry.chemical_compoundGeneral EnergychemistryReagentFunctional groupEnvironmental ChemistryGeneral Materials ScienceChemSusChem
researchProduct

Energetic study of bifurcated hydrogen bonds in secondary structures of salts composed with dicarboxylic acids and ethylamine

2020

Abstract The nature of bifurcated hydrogen bonds prompted us to analyze the energy of supramolecular motifs on the example of new structures of carboxylic acids salts with amines, which guarantee a multitude of such interactions. Experimental and theoretical studies of four dicarboxylic salts with primary amine: ethylammonium succinate hydrate (1), tartrate hydrate (2) phthalate hydrate (3) and terephthalate (4) has been investigated along with study of the strength of interactions between the anions and cations. The complete topological analysis of the charge density for all new structures allowed designation of the estimated Cumulative Dissociation Energy (eCDE).

010405 organic chemistryHydrogen bondOrganic ChemistrySupramolecular chemistryCharge densityTartrate010402 general chemistry01 natural sciencesBond-dissociation energy0104 chemical sciencesAnalytical ChemistryHydrogen bondsInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryAmine gas treatingEthylamineSupramolecular synthonsCharge densityHydrateTopological analysisSpectroscopyJournal of Molecular Structure
researchProduct

PdII-mediated integration of isocyanides and azide ions might proceed via formal 1,3-dipolar cycloaddition between RNC ligands and uncomplexed azide

2016

Reaction between equimolar amounts of trans-[PdCl(PPh3)2(CNR)][BF4] (R = t-Bu 1, Xyl 2) and diisopropylammonium azide 3 gives the tetrazolate trans-[PdCl(PPh3)2(N4t-Bu)] (67%, 4) or trans-[PdCl(PPh3)2(N4Xyl)] (72%, 5) complexes. 4 and 5 were characterized by elemental analyses (C, H, N), HRESI+-MS, 1H and 13C{1H} NMR spectroscopies. In addition, the structure of 4 was elucidated by a single-crystal X-ray diffraction. DFT calculations showed that the mechanism for the formal cycloaddition (CA) of N3− to trans-[PdCl(PH3)2(CNMe)]+ is stepwise. The process is both kinetically and thermodynamically favorable and occurs via the formation of an acyclic NNNCN-intermediate. The second step of the fo…

010405 organic chemistryLigandStereochemistryIsocyanidechemistry.chemical_elementGeneral Chemistrypalladium complexes010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisCycloadditionazides0104 chemical sciencesIonchemistry.chemical_compoundisocyanideschemistry13-Dipolar cycloadditionPotential energy surfaceMaterials ChemistryAzideta116PalladiumNew Journal of Chemistry
researchProduct

Kinetic and Electrochemical Studies of the Oxidative Addition of Demanding Organic Halides to Pd(0): the Efficiency of Polyphosphane Ligands in Low P…

2013

International audience; Oxidative addition (OA) of organic halides to palladium(0) species is a fundamental reaction step which initiates the C–C bond formation catalytic processes typical of Pd(0)/Pd(II) chemistry. The use of structurally congested polyphosphane ligands in palladium-catalyzed C–C bond formation has generated very high turnover numbers (TONs) in topical reactions such as Heck, Suzuki, Sonogashira couplings, and direct sp2C–H functionalization. Herein, the OA of aryl bromides to Pd(0) complexes stabilized by ferrocenylpolyphosphane ligands L1 (tetraphosphane), L2 (triphosphane), and L3 (diphosphane) is considered. The investigation of kinetic constants for the addition of Ph…

010405 organic chemistryReaction stepInorganic chemistrychemistry.chemical_elementHalide[CHIM.CATA]Chemical Sciences/CatalysisBond formation010402 general chemistryPhotochemistryKinetic energyElectrochemistry01 natural sciencesOxidative addition0104 chemical sciencesCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/CatalysischemistryPhysical and Theoretical ChemistryPalladium
researchProduct

A thermally/chemically robust and easily regenerable anilato-based ultramicroporous 3D MOF for CO 2 uptake and separation

2021

The combination of the properly designed novel organic linker, 3,6-N-ditriazoyil-2,5-dihydroxy-1,4-benzoquinone (trz2An), with CoII ions results in a 3D ultramicroporous MOF with high CO2 uptake capacity and separation efficiency, with particular attention to CO2/N2 and CO2/CH4 gas mixtures. This material consists of 1D chains of octahedrally coordinated CoII ions linked through the anilato ligands in the equatorial positions and to the triazole substituents from two neighbouring chains in the two axial positions. This leads to a 3D microporous structure with voids with an affinity for CO2 molecules and channels that enable the selective entrance of CO2 but not of molecules with larger kine…

010405 organic chemistryRenewable Energy Sustainability and the EnvironmentUNESCO::QUÍMICAHigh selectivityTriazoleGeneral ChemistryMicroporous materialQuímica010402 general chemistry01 natural sciences:QUÍMICA [UNESCO]0104 chemical sciencesIonchemistry.chemical_compoundAdsorptionchemistryChemical engineeringCarbon dioxideMoleculeGeneral Materials ScienceLinkerMaterialsKinetic diameterJournal of Materials Chemistry A
researchProduct

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
researchProduct