Search results for "dron"

showing 10 items of 4363 documents

Unveiling the Occurrence of Co(III) in NiCo Layered Electroactive Hydroxides: The Role of Distorted Environments

2020

Co- and Ni-based layered hydroxides constitute a unique class of two-dimensional inorganic materials with exceptional chemical diversity, physicochemical properties and outstanding performance as supercapacitors and overall water splitting catalysts. Recently, the occurrence of Co(III) in these phases has been proposed as a key factor that enhance their electrochemical performance. However, the origin of this centers and control over its contents remains as an open question. We employed the Epoxide Route to synthesize a whole set of α-NiCo layered hydroxides. The PXRD and XAS characterization alert about the occurrence of Co(III) as a consequence of the increment in the Ni content. DFT+U si…

010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysisCatalysis//purl.org/becyt/ford/1 [https]symbols.namesake//purl.org/becyt/ford/1.4 [https]LAYERED HYDROXIDESX-ray absorption spectroscopy2D MATERIALS010405 organic chemistryChemistryOrganic ChemistryFermi levelGeneral Chemistry0104 chemical sciencesCharacterization (materials science)Chemical engineeringOctahedronWATER SPLITTINGsymbolsWater splittingENERGY STORAGESUPERCAPACITANCEChemistry – A European Journal
researchProduct

Hybrid Molecular Materials Based upon Magnetic Polyoxometalates and Organic π-Electron Donors:  Syntheses, Structures, and Properties of Bis(ethylene…

1998

International audience; The syntheses, crystal structures, and physical properties of the series of radical salts made with bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF or ET) and monosubstituted α-Keggin polyoxoanions of formula [XZ(H2O)M11O39]5- (XZM11 = Si(IV)Fe(III)Mo11, Si(IV)Cr(III)W11, P(V)Con(II)W11, P(V)Ni(II)W11, P(V)Cu(II)W11 P(V)Zn(II)W11, P(V)Mn(II)W11, and P(V)Mn(II)Mo11) containing a magnetic metal ion Z on a peripheral octahedral site of the Keggin union are reported. They all crystallize in two related series called α2 and α3. The general structure consists of alternating layers of the organic donor and the Keggin polyoxometalates. While the stoichiometry and α-packing a…

010405 organic chemistryChemistryInorganic chemistryGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesIonMetalCrystallographychemistry.chemical_compoundColloid and Surface ChemistryOctahedronPolymerizationvisual_artPhase (matter)visual_art.visual_art_medium[CHIM]Chemical SciencesStoichiometryTetrathiafulvaleneJournal of the American Chemical Society
researchProduct

A decacobalt(ii) cluster with triple-sandwich structure obtained by partial reductive hydrolysis of a pentacobalt(ii/iii) Weakley-type polyoxometalat…

2016

Partial reductive hydrolysis of a penta-CoII/III cluster [CoII4(H2O)2(CoIIIW9O34)(PW9O34)]12− (1) leads to the formation of [Co2{Co3(H2O)(Co(OH)2W7O26)(PW9O34)}2]22− (2). This polyoxometalate is made up of two capping [PW9O34]9− units and two bridging [W7O26]10− units that assemble to encapsulate a novel deca-CoII cluster core comprising octahedral and tetrahedral CoII ions.

010405 organic chemistryChemistryInorganic chemistryMetals and AlloysGeneral ChemistryType (model theory)010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHydrolysisCrystallographyOctahedronPolyoxometalateMaterials ChemistryCeramics and CompositesCluster (physics)Chemical communications (Cambridge, England)
researchProduct

Self-assembly of M4L4tetrahedral cages incorporating pendant PS and PSe functionalised ligands

2019

Herein, the synthesis of metal–organic tetrahedral cages featuring flexible thio- and selenophosphate-based ligands is described. The cages were prepared by sub-component self-assembly of AP(OC6H4NH2-4)3 (A = S, Se) or SP(SC6H4NH2-4)3, 2-pyridinecarboxaldehyde, and either Fe[BF4]2 or Co[BF4]2. Preliminary host–guest studies into the ability of the pendant PS and PSe groups to interact with suitable substrates will be discussed.

010405 organic chemistryChemistryMetals and AlloysThio-General Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymer chemistryMaterials ChemistryCeramics and CompositesTetrahedronSelf-assemblyChemical Communications
researchProduct

Chiral and Racemic Spin Crossover Polymorphs in a Family of Mononuclear Iron(II) Compounds

2017

[EN] Understanding the origin of cooperativity and the equilibrium temperature of transition (T1/2) displayed by the spin-crossover (SCO) compounds as well as controlling these parameters are of paramount importance for future applications. For this task, the occurrence of polymorphism, presented by a number of SCO complexes, may provide deep insight into the influence of the supramolecular organization on the SCO behavior. In this context, herein we present a novel family of mononuclear octahedral FeII complexes with formula cis- [Fe(bqen)(NCX)2], where bqen is the chelating tetradentate ligand N,N¿-bis(8-quinolyl)ethane-1,2-diamine and X = S, Se. Depending on the preparation method, these…

010405 organic chemistryChemistryStereochemistrySupramolecular chemistryCooperativity010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyOctahedronPolymorphism (materials science)Spin crossoverFISICA APLICADARacemic mixtureOrthorhombic crystal systemPhysical and Theoretical ChemistryEnantiomerInorganic Chemistry
researchProduct

Mixed phenoxo and azido bridged dinuclear nickel(II) and copper(II) compounds with N,N,O-donor schiff bases: Synthesis, structure, DNA binding, DFT a…

2019

Abstract Two dinuclear complexes, µ-phenoxo, µ1,1-azido bridged [Ni2(L)2(µ1,1-N3)(N3)(CH3OH)] (1) and µ-phenoxo, µ1,1-azido bridged [Cu2(L)2(µ1,1-N3)(N3)] (2) bearing HL as a blocking co-ligand produced by the 1:1 condensation of N-methyl 1,3 propanediamine with o-vanillin have been synthesized and successfully characterized by elemental analyses, IR and electronic spectroscopy, single-crystal X-ray diffraction for 1 and DFT optimization for 2. X-ray crystal structure discloses that the asymmetric unit of 1 consists of two nickel(II) ions exhibiting a six-coordinate octahedral coordination with µ-phenoxo, µ1,1-azido bridging dimeric structure. The DFT optimization of 2 reveals the five-coor…

010405 organic chemistryChemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesFluorescenceCopperElectron spectroscopySquare pyramidal molecular geometry0104 chemical sciencesInorganic ChemistryNickelCrystallographyOctahedronDocking (molecular)Materials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
researchProduct

Linking PO43− and HAsO42− anions with a dinuclear [ZnII2] complex: Formation and stabilization of novel decanuclear metallomacrocyclic [ZnII10] and t…

2017

The linkage of PO43- and HAsO42--anions with a newly synthesized five-coordinate dinuclear zinc complex, Zn-2(cpdp)(H2O)(2)]Cl (1) H(3)cpdp =N,N'-bis2-carboxybenzomethyl]-N,N'-bis2-pyridylmethyl]-1,3diamino propan-2-ol], has been explored. In methanol-water, the reaction of 1 with Na2HPO4 center dot 2H(2)O and Na2HAsO4 center dot 7H(2)O/NaBr separately, at ambient temperature, yielded the novel phosphate-bridged decanuclear zinc cluster, (H3O)(4)Zn-10(cPdP)(4)(mu(5)-PO4)(2)(H2O)(6)](6 center dot Cl)center dot 53H(2)O (2) and hydrogen arsenate bridged tetranuclear zinc cluster, Na-2Zn-4(cpdp)(2)(mu(4)-HAsO4)]ClBr center dot 13H(2)O (3), respectively. Analysis of the single crystal X-ray stru…

010405 organic chemistryInorganic chemistrychemistry.chemical_elementCrystal structureZinc010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryMetalTrigonal bipyramidal molecular geometryCrystallographychemistryOctahedronvisual_artMaterials Chemistryvisual_art.visual_art_mediumZinc ClusterTitrationPhysical and Theoretical ChemistrySingle crystalPolyhedron
researchProduct

Self‐Assembly and Characterisation of Grid‐Type Iron( II ), Cobalt( II ) and Zinc( II ) Complexes

2003

The reaction of the ligands 5 and 6, containing two tridentate binding units, with iron(II), cobalt(II) and zinc(II) leads to the self-assembly of supramolecular architectures of [2 × 2] grid type containing four ions in octahedral coordination sites. The grid-type structures have been assigned on the basis of the spectroscopic data in solution, and confirmed in the solid state in the case of complexes 6b and 6c by X-ray crystallography. The latter study revealed that each metal ion is situated in a distorted octahedral coordination environment comprising two N,N,O ligand donor sets. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

010405 organic chemistryLigandSupramolecular chemistrychemistry.chemical_elementZinc010402 general chemistry01 natural sciences0104 chemical sciencesIonInorganic ChemistryMetalCrystallographychemistryOctahedronvisual_artvisual_art.visual_art_mediumSelf-assemblyCobaltEuropean Journal of Inorganic Chemistry
researchProduct

Oxygen Transfer from Trimethylamine N ‐Oxide to Cu I Complexes Supported by Pentanitrogen Ligands

2020

[N,N-bis(1-methyl-2-benzimidazolyl)methyl-N-(bis-2-pyridylmethyl)amine] (L1) and [N,N-bis(2-quinolylmethyl)-N-bis(2-pyridyl)methylamine] (L2) were employed to prepare CuII and CuI complexes for spectroscopic and structural characterization. [L1CuII(H2O)](NO3)2 and [L2CuII(NO3)]NO3 have Jahn–Teller distorted octahedral geometries and give rise to isotropic EPR spectra in frozen solution. [L1CuI(CH3CN)]OTf and [L2CuI(CH3CN)]OTf have distorted trigonal bipyramidal and tetrahedral solid-state structures, respectively. The N-donors display labile behavior in solution, based on variable-temperature 1H NMR studies. Addition of trimethylamine N-oxide (Me3NO) to solutions of [L1CuI(CH3CN)]OTf and [L…

010405 organic chemistryMethylamineTrimethylamine010402 general chemistry01 natural sciences0104 chemical sciencesAdductlaw.inventionInorganic ChemistryCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistryOctahedronlawProton NMRElectron paramagnetic resonanceAcetonitrileEuropean Journal of Inorganic Chemistry
researchProduct

Cytosine Nucleobase Ligand: A Suitable Choice for Modulating Magnetic Anisotropy in Tetrahedrally Coordinated Mononuclear CoII Compounds

2017

A family of tetrahedral mononuclear CoII complexes with the cytosine nucleobase ligand is used as the playground for an in-depth study of the effects that the nature of the ligand, as well as their noninnocent distortions on the Co(II) environment, may have on the slow magnetic relaxation effects. Hence, those compounds with greater distortion from the ideal tetrahedral geometry showed a larger-magnitude axial magnetic anisotropy (D) together with a high rhombicity factor (E/D), and thus, slow magnetic relaxation effects also appear. In turn, the more symmetric compound possesses a much smaller value of the D parameter and, consequently, lacks single-ion magnet behavior.

010405 organic chemistryStereochemistryChemistryLigandTetrahedral molecular geometry010402 general chemistry01 natural sciences0104 chemical sciencesNucleobaseInorganic ChemistryTurn (biochemistry)Magnetic anisotropychemistry.chemical_compoundMagnetTetrahedronPhysical and Theoretical ChemistryCytosineInorganic Chemistry
researchProduct