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showing 10 items of 4813 documents

Deposition of binder-free oxygen-vacancies NiCo2O4 based films with hollow microspheres via solution precursor thermal spray for supercapacitors

2019

Abstract Hollow micro-/nanostructures and oxygen vacancies are highly desirable for supercapacitors due to high active surface area and outstanding electrochemical properties. In order to benefiting from the both effect, binder-free oxygen-vacancies NiCo2O4 based films with hollow microspheres were pioneering directly deposited via one kind thermal spray technology, named solution precursor thermal spray (SPTS) process. To our best knowledge, the rapid one-step SPTS route was firstly employed to synthesize and deposit NiCo2O4 films for supercapacitor applications. The CV data clearly demonstrated that the specific capacitances of more oxygen-deficient NiCo2O4 electrodes with hollow microsph…

010302 applied physicsSupercapacitorHorizontal scan rateNanostructureMaterials scienceProcess Chemistry and Technology02 engineering and technology021001 nanoscience & nanotechnologyElectrochemistry01 natural sciences7. Clean energyCapacitanceSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineering0103 physical sciencesElectrodeMaterials ChemistryCeramics and Composites[CHIM]Chemical Sciences0210 nano-technologyThermal sprayingCurrent densityCeramics International
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Force probe simulations of a reversibly rebinding system: Impact of pulling device stiffness.

2017

We present a detailed study of the parameter dependence of force probe molecular dynamics (FPMD) simulations. Using a well studied calix[4]arene catenane dimer as a model system, we systematically vary the pulling velocity and the stiffness of the applied external potential. This allows us to investigate how the results of pulling simulations operating in the constant velocity mode (force-ramp mode) depend on the details of the simulation setup. The system studied has the further advantage of showing reversible rebinding meaning that we can monitor the opening and the rebinding transition. Many models designed to extract kinetic information from rupture force distributions work in the limit…

010304 chemical physicsChemistryWork (physics)General Physics and AstronomyEnergy landscapeStiffnessMechanics010402 general chemistryKinetic energy01 natural sciences0104 chemical sciencesMolecular dynamicsSpring (device)Computational chemistry0103 physical sciencesJumpmedicinePhysical and Theoretical Chemistrymedicine.symptomConstant (mathematics)The Journal of chemical physics
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Novel Stannatrane N(CH2CMe2O)2(CMe2CH2O)SnO-t-Bu and Related Oligonuclear Tin(IV) Oxoclusters. Two Isomers in One Crystal

2016

The syntheses of the alkanolamine N(CH2CMe2OH)2(CMe2CH2OH) (1), of the stannatrane N(CH2CMe2O)2(CMe2CH2O)SnO-t-Bu (2), and of the trinuclear tin oxocluster 3 consisting of the two isomers [(μ3-O)(O-t-Bu){Sn(OCH2CMe2)(OCMe2CH2)2N}3] (3a) and [(μ3-O)(μ3-O-t-Bu){Sn(OCH2CMe2)(OCMe2CH2)2N}3] (3b) as well as the isolation of a few crystals of the hexanuclear tin oxocluster [LSnOSn(OH)3LSnOH]2 [L = N(CH2CMe2O)2(CMe2CH2O)] (4) are reported. The compounds were characterized by 1H, 13C, 15N, and 119Sn (1–3) nuclear magnetic resonance and infrared spectroscopy, electrospray ionization mass spectrometry, and single-crystal X-ray diffraction analysis (1–4). A graph set analysis was performed for compoun…

010405 organic chemistryChemistryElectrospray ionizationAnalytical chemistryInfrared spectroscopychemistry.chemical_element010402 general chemistry01 natural sciencesGraph0104 chemical sciencesInorganic ChemistryCrystalCrystallographychemistry.chemical_compoundDensity functional theoryAlkanolaminePhysical and Theoretical ChemistryTinInorganic Chemistry
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Exploring the Chemoselectivity towards Cysteine Arylation by Cyclometallated Au III Compounds: New Mechanistic Insights

2020

To gain more insight into the factors controlling the efficient cysteine arylation by cyclometalated Au(III) complexes, the reaction between selected gold compounds and different peptides was investigated by high‐resolution liquid chromatography electrospray ionization mass spectrometry (HR‐LC‐ESI‐MS). The deducted mechanisms of C–S cross‐coupling, also supported by density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations, evidenced the key role of secondary peptidic gold binding sites in favouring the process of reductive elimination.

010405 organic chemistryChemistryElectrospray ionizationOrganic Chemistrycyclometallated gold complexes010402 general chemistryMass spectrometry01 natural sciencesBiochemistryCombinatorial chemistryMolecular mechanicsReductive elimination0104 chemical sciencesddc:cysteine arylationGold CompoundschemoselectivitySettore CHIM/03 - Chimica Generale E InorganicapeptidesMolecular MedicineDensity functional theoryChemoselectivityMolecular BiologyCysteinemass spectrometry
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Photochemistry and Redox Chemistry of an Unsymmetrical Bimetallic Copper(I) Complex

2016

The bimetallic copper(I) complex Cu2L2 (cis-1) is formed with high diasteroselectivity from [Cu(NCCH3)4][BF4] and HL (4-tert-butyl phenyl(pyrrolato-2-yl-methylene)amine) in a kinetically controlled reaction. cis-1 features a rather short Cu···Cu distance of 2.4756(6) A and is weakly emissive at room temperature in solution. Oxidatively triggered disproportionation of cis-1 yields elemental copper and the mononuclear copper(II) complex CuL2 (trans-2). One-electron reduction of trans-2 gives cuprate [2]– with a bent bis(pyrrolato) coordinated copper(I) entity. The imine donor atoms of [2]– can insert an additional copper(I) ion giving exclusively the bimetallic complex cis-1 closing the oxida…

010405 organic chemistryChemistryIminechemistry.chemical_elementDisproportionation010402 general chemistryPhotochemistry01 natural sciencesRedoxCopper0104 chemical sciencesIonInorganic Chemistrychemistry.chemical_compoundAmine gas treatingCupratePhysical and Theoretical ChemistryBimetallic stripInorganic Chemistry
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Exploring the Slow Relaxation of the Magnetization in CoIII -Decorated {DyIII 2 } Units

2016

We have prepared and structurally characterized a new member of the butterfly-like {CoIII 2DyIII 2} single-molecule magnets (SMMs) through further CoIIIdecoration, with the formula [CoIII 4DyIII 2(OH)2(teaH)2(tea)2(Piv)6] (teaH3=triethanolamine; Piv=trimethylacetate or pivalate). Direct current (DC) susceptibility and magnetization measurements were performed allowing the extraction of possible crystal-field parameters. A simple electrostatic modeling shows reasonable agreement with experimental data. Alternating current (AC) susceptibility measurements under a zero DC field and under small applied fields were performed at different frequencies (i.e., 10–1500 Hz) and at low temperatures (i.…

010405 organic chemistryChemistryOtras Ciencias QuímicasOrganic ChemistryCiencias QuímicasAnalytical chemistryGeneral ChemistryCOORDINATION COMPLEXLANTHANIDESMAGNETIC PROPERTIES010402 general chemistry01 natural sciencesSINGLE-MOLECULE MAGNETSCatalysisDYSPROSIUM0104 chemical sciencesMagnetizationRelaxation (physics)Physical chemistryCIENCIAS NATURALES Y EXACTASChemistry - A European Journal
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Switching of Slow Magnetic Relaxation Dynamics in Mononuclear Dysprosium(III) Compounds with Charge Density

2016

The symmetry around a Dy ion is recognized to be a crucial parameter dictating magnetization relaxation dynamics. We prepared two similar square-antiprismatic complexes, [Dy(LOMe)2(H2O)2](PF6) (1) and Dy(LOMe)2(NO3) (2), where LOMe = [CpCo{P(O)(O(CH3))2}3], including either two neutral water molecules (1) or an anionic nitrate ligand (2). We demonstrated that in this case relaxation dynamics is dramatically affected by the introduction of a charged ligand, stabilizing the easy axis of magnetization along the nitrate direction. We also showed that the application of either a direct-current field or chemical dilution effectively stops quantum tunneling in the ground state of 2, thereby increa…

010405 organic chemistryChemistryUNESCO::QUÍMICARelaxation (NMR)Charge densitychemistry.chemical_element010402 general chemistry:QUÍMICA [UNESCO]01 natural sciences0104 chemical sciencesIonInorganic ChemistryCrystallographyMagnetic anisotropyMagnetizationNuclear magnetic resonanceDysprosiumMoleculePhysical and Theoretical ChemistryGround state
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Stepwise Construction of Heterobimetallic Cages by an Extended Molecular Library Approach.

2017

Two novel heterobimetallic complexes, a trigonal-bipyramidal and a cubic one, have been synthesized and characterized using the same C3-symmetric metalloligand, prepared by a simple subcomponent self-assembly strategy. Adopting the molecular library approach, we chose a mononuclear, preorganized iron(II) complex as the metalloligand capable of self-assembly into a trigonal-bipyramidal or a cubic aggregate upon coordination to cis-protected C2-symmetric palladium(II) or unprotected tetravalent palladium(II) ions, respectively. The trigonal-bipyramidal complex was characterized by NMR and UV–vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and single-crystal X-ray diffrac…

010405 organic chemistryChemistrytrigonal-bipyramidal and cubic heterobimetallic cagesElectrospray ionizationchemistry.chemical_element010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesIonInorganic ChemistryCrystallographyPhysical and Theoretical ChemistrySpectroscopyta116extended molecular library approachPalladiumInorganic chemistry
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Studies on the Reduction of [(C 5 Me 5 ) 2 Mo 2 O 5 ] in Methanol/Water/Acetate Solutions by On‐Line Electrochemical Flowcell and Electrospray Mass S…

2003

The complex [Cp*2Mo2O5] (Cp* = η5-C5Me5) and its electrochemical reduction products in acetic acid/acetate-buffered (pH = 4.0) water/methanol solutions were investigated by combined electrochemical (EC) flowcell and on-line electrospray ionization mass spectrometry (ESI-MS). Mono-, di-, tri-, and tetranuclear organometallic molybdenum oxides were identified in the starting solution. The effect of the relevant ESI-MS parameters (ionic mode, heated capillary voltage, and heated capillary temperature) and of the concentration on the observed distribution of ions in the mass spectrometer was studied in order to minimize side reactions in the ESI chamber. It was verified that reduction in the ES…

010405 organic chemistryElectrospray ionizationInorganic chemistrychemistry.chemical_element010402 general chemistryMass spectrometryElectrochemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundAcetic acidchemistryOxidation stateMolybdenumMethanolIon trapEuropean Journal of Inorganic Chemistry
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Palladium Catalyzed [3+2] Cycloaddition of Vinyl Aziridine and Indane-1,3-diones: Diastereo- and Enantioselective Access to Spiro-Pyrrolidines

2020

A mild and efficient palladium-catalyzed [3+2] cycloaddition of vinylaziridine and indane-1,3-diones has been realized. The resulting spiro-pyrrolidines were provided in excellent yields and, with the introduction of the leucine-derived phosphine ligand, moderate to good enantio­- and diastereoselectivities.

010405 organic chemistryLigandOrganic Chemistryasymmetric synthesisIndaneEnantioselective synthesischemistry.chemical_elementspriopyrrolidines010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisCycloaddition0104 chemical sciencesCatalysis3-dioneschemistry.chemical_compoundchemistryaziridinesinsane-1palladium catalysis; asymmetric synthesis; spriopyrrolidines; aziridines; insane-13-dionespalladium catalysisPhosphinePalladium
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