Search results for "ALAT"

showing 10 items of 4241 documents

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)
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Self-assembly of the tetrachlorido(oxalato)rhenate( iv ) anion with protonated organic cations: X-ray structures and magnetic properties

2016

Two novel ReIV compounds of formulae [H2bpy][ReIVCl4(ox)] (1) and [H3biim]2[ReIVCl4(ox)] (2) [H2bpy2+ = 4,4′-bipyridinium dication, H3biim+ = 2,2′-biimidazolium monocation, and ox2− = oxalate dianion] have been synthesised and magneto-structurally characterised. 1 crystallises in the monoclinic system with space group C2/c, and 2 crystallises in the triclinic system with space group P[1 with combining macron]. The ReIV ion in 1 and 2 is six-coordinate, bonded to four chloride ions and two oxalate-oxygen atoms in a distorted octahedral geometry. Short intermolecular ReIV–Cl⋯Cl–ReIV contacts, Cl⋯π type interactions and hydrogen bonds are present in the crystal lattice of both compounds, gener…

010405 organic chemistryChemistryInorganic chemistrySupramolecular chemistryGeneral ChemistryCrystal structureTriclinic crystal system010402 general chemistryCondensed Matter Physics01 natural sciencesMagnetic susceptibilityOxalate0104 chemical sciencesDicationchemistry.chemical_compoundCrystallographyOctahedral molecular geometryGeneral Materials ScienceMonoclinic crystal system
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Synthesis of copper(II) and gold(III) bis(NHC)-pincer complexes

2016

Abstract CuII and AuIII chlorido complexes bearing the bis(NHC) carbazolide pincer ligand (bimca) were synthesized by transmetallation from the respective lithium complex [Li(bimca)] (NHC=N-heterocyclic carbene). In the case of copper, two different molecular structures were obtained depending on the copper source. With Cu(II) chloride the paramagnetic mononuclear [Cu(bimca)Cl] complex is formed and has been characterized by EPR spectroscopy and X-ray structure analysis, while copper(I) chloride leads under oxidation to a dinuclear structure in which two cationic [CuII(bimca)] moieties are bridged by one chlorido ligand. The positive charge is compensated by the [CuCl2]− counter ion, as pro…

010405 organic chemistryChemistryLigandCationic polymerizationchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCopperMedicinal chemistry0104 chemical sciencesPincer movementlaw.inventionchemistry.chemical_compoundTransmetalationlawElectron paramagnetic resonancePincer ligandCarbeneZeitschrift für Naturforschung B
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A Molecular Electron Density Theory Study of the Role of the Copper Metalation of Azomethine Ylides in [3 + 2] Cycloaddition Reactions.

2018

The copper metalation of azomethine ylides (AYs) in [3 + 2] cycloaddition (32CA) reactions with electron-deficient ethylenes has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) level, in order to shed light on the electronic effect of the metalation in the course of the reaction. Analysis of the Conceptual Density Functional Theory reactivity indices indicates that the metalation of AYs markedly enhances the nucleophilicity of these species given the anionic character of the AY framework. These 32CA reactions take place through stepwise mechanisms characterized by the formation of a molecular complex. Both nonmetalated and metalated 32CA reactions …

010405 organic chemistryChemistryMetalationOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciencesNucleophileElectronic effectSingle bondDensity functional theoryReactivity (chemistry)The Journal of organic chemistry
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Supramolecular open-framework architectures based on dicarboxylate H-bond acceptors and polytopic cations with three/four N–H+donor units

2015

International audience; Supramolecular assemblages based on anionic H-acceptors and cationic H-donors have been envisioned to elaborate open frameworks maintained by ionic H-bonds. Combinations of di-anionic chloranilate (CA2-), oxalate (Ox2-), or terephthalate (BDC2-) and trisimidazolium or tetrapyridinium derivatives (three and four N-H+ donors, respectively) yielded five architectures of formulae [(H3TrIB)(CA)1.5[middle dot]2DMF[middle dot]2.5H2O] (1), [(H4Tetrapy)(CA)2[middle dot]3DMF] (2), [(H3TrIB)(HOx)(Ox)[middle dot]5H2O] (3), [(H4Tetrapy)(Ox)2[middle dot]5H2O] (4), and [(H4Tetrapy)(BDC)2(H2O)[middle dot]1DMF[middle dot]3H2O] (5) (with TrIB = 1,3,5-trisimidazolylbenzene and Tetrapy …

010405 organic chemistryChemistryStereochemistryHydrogen bondSupramolecular chemistryCationic polymerizationIonic bondingSorptionGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciencesOxalate0104 chemical sciencesSolventchemistry.chemical_compoundCrystallography[CHIM.COOR]Chemical Sciences/Coordination chemistryGeneral Materials ScienceCrystEngComm
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A hybrid magnet with coexistence of ferromagnetism and photoinduced Fe(iii) spin-crossover

2011

International audience; The insertion of a [Fe(sal2-trien)]+ complex cation into a 2D oxalate network results in a hybrid magnet with coexistence of magnetic ordering and photoinduced spin-crossover (LIESST effect) in compound [FeIII(sal2-trien)][MnIICrIII(ox)3]*(CH2Cl2) (1). A complete photomagnetic characterization together with a detailed structural analysis of the low-spin (LS) and high-spin (HS) structures of 1 is presented in order to understand such unusual behavior. This very rare and unexpected property in a FeIII spin-crossover complex, has been attributed to the strong distortion exhibited by the metastable HS state. Furthermore, 1 has shown that, in contrast to what has been pre…

010405 organic chemistryChemistryStereochemistry[CHIM.MATE]Chemical Sciences/Material chemistryGeneral Chemistry010402 general chemistry01 natural sciencesLIESSTOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographyFerromagnetismSpin crossoverMetastabilityMagnetSpin (physics)Chemical Science
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Oxotris(oxalate)niobate(V): An oxalate delivery agent in the design of building blocks

2018

This work concerns the oxalate delivery process that occurs when using (NH4)3[NbO(C2O4)3]·6H2O as a suitable oxalate source in the synthesis of two compounds, [Cu(dmphen)(C2O4)(H2O)] (1) and [{Cu(dmphen)(CH3OH)}2(μ-C2O4)](ClO4)2 (2) (dmphen = 2,9-dimethyl-1,10-phenanthroline). {[Fe{HB(pz)3}(CN)2(μ-CN)]2[{Cu(dmphen)}2(μ-C2O4)]}∙xCH3OH (3) (2.0 ≤ x ≤ 2.4) was obtained by reacting 2 and PPh4[Fe{HB(pz)3}(CN)3]∙H2O [ = tetraphenylphosphonium and = tris(pyrazolyl)borate]. Crystal structures of 1–3 have been determined by single-crystal X-ray diffraction experiments: 1 is a mononuclear trigonal bipyramidal copper(II) species, 2 is a centrosymmetric oxalato-bridged dicopper(II) complex, and 3 consi…

010405 organic chemistryChemistrychemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesCopperOxalate0104 chemical scienceschemistry.chemical_compoundCrystallographyTrigonal bipyramidal molecular geometryIntramolecular forceMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryBoronNatural bond orbital
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Versatile behavior of conjugated diynes with zirconocene reactive species

2008

Thermal decomposition of Cp2ZrPh2 in the presence of the buta-1,3-diynes RC≡CC≡CR (R = Ph, SiMe3) can lead to seven- or five-membered metallacycles. In both cases a stable benzo-fused seven-membered zirconacyclocumulene arising from a 2-fold insertion of the triple bonds of the dialkyne in the in situ generated zirconocene benzyne is formed. In the case of Me3SiC≡CC≡CSiMe3 a second minor complex is isolated: a 3-alkynyl-substituted zirconaindene arising from a β monoinsertion of one acetylenic function of the conjugated diyne in the zirconocene benzyne. No stable 2-alkynyl-substituted zirconacycle was isolated. This α monoinsertion complex is an intermediate in the exchange of the metalated…

010405 organic chemistryChemistrycycloaddition reactionOrganic ChemistryThermal decomposition[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementmetalationConjugated system010402 general chemistryTriple bond01 natural sciencesAryne0104 chemical sciencesInorganic ChemistrycyclometalationAntimonyReagentAtomPolymer chemistryMoiety[CHIM.COOR]Chemical Sciences/Coordination chemistryzirconocene- benzyn intermediatePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS
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Hydrogen-Bonded Open-Framework with Pyridyl-Decorated Channels: Straightforward Preparation and Insight into Its Affinity for Acidic Molecules in Sol…

2017

International audience; An hydrogen-bonded open framework with pores decorated by pyridyl groups has been constructed following an off-charge-stoichiometry assemblage of protonated tetrakis(4-pyridyl-oxymethyl)methane and [Al(oxalate)3]3-, respectively the H-bond donor and acceptor of the ionic H-bond interactions. This supramolecular porous architecture (SPA-2) possesses 1 nm-large pores interconnected in 3D with high solvent accessible void (53%). It demonstrated remarkable affinity for acidic organic molecules in solution, which was investigated by the means of various carboxylic acids including larger drug molecules. Noteworthy, competing sorption between acetic acid and its halogenated…

010405 organic chemistryHydrogen bondChemistryOrganic ChemistrySupramolecular chemistryIonic bondingProtonationSorptionGeneral ChemistryHydrogen-Bonding010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencessupramolecular chemistryCatalysis0104 chemical sciencesSolventPolymer chemistryhost-guest chemistry[CHIM]Chemical SciencesMoleculeOrganic chemistryoxalate complexporous materialHost–guest chemistryChemistry (Weinheim an der Bergstrasse, Germany)
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Heterobimetallic Oxalate‐Bridged M II Re IV (M = Zn, Cu, Ni, Co and Mn) Complexes Incorporating Bis(3,5‐dimethylpyrazol‐1‐yl)methane: Synthesis and M…

2016

Five oxalato-bridged heterobimetallic compounds of general formula [ReCl4(ox)M(bdmpzm)2].2MeCN [ox = oxalate, bdmpzm = bis(3,5-dimethylpyrazol-1-yl)methane and M = Zn (1),Cu (2), Ni (3), Co (4) and Mn (5)] have been successfully synthesized in self-assembly reactions of the [ReCl4(ox)]2- metalloligand with the coordinatively unsaturated [M(bdmpzm)2]2+ complex generated in situ by the reaction of the suitable metal(II) salt with the bdmpzm ligand. 1-5 are isostructural compounds whose crystal structures consist of neutral heterodinuclear [ReCl4(ox)M(bdmpzm)2] units and free acetonitrile molecules. The magnetic properties of 1-5 were investigated in the temperature range 2.0-300 K. The nature…

010405 organic chemistryLigandInorganic chemistryCrystal structure010402 general chemistry01 natural sciencesOxalate0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryTransition metalX-ray crystallographyMoleculeIsostructuralAcetonitrileEuropean Journal of Inorganic Chemistry
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