Search results for "Inorganic chemistry"

showing 10 items of 7339 documents

Effect of Guest Molecules on Spin Transition Temperature in Loaded Hofmann‐Like Clathrates with Improved Porosity

2020

The synthesis, crystal structure, magnetic and calorimetric studies of a new clathrate compound of the Hofmann-type spin crossover (SCO) metal-organic framework (MOF) {Fe(bpb)[MII(CN)4]}·xGuest (bpb = bis(4-pyridyl)butadiyne, and MII = Ni, Pt) with characteristic fsc topology is reported. The framework {Fe(bpb)[MII(CN)4]} can host up to 1.5 guest molecules of (trifluoromethyl)benzene and display complete one-step cooperative SCO behavior. Our systematic study on {Fe(bpb)[Pt(CN)4]}·xGuest shows a general reciprocal correlation between the SCO temperature with the volume of the guest molecules.

010405 organic chemistryChemistrySpin transition010402 general chemistry01 natural sciences0104 chemical sciences3. Good healthInorganic ChemistryCrystallographySpin crossoverMoleculeMetal-organic frameworkHost–guest chemistryPorosityEuropean Journal of Inorganic Chemistry
researchProduct

Proline-Modified Porphyrin Catalysts for Enantioselective Epoxidations: Design, Synthesis, and Reactivity

2004

International audience; The syntheses of various strapped and −picket-fence× chiral porphyrins are described, and their reactivities towards the enantioselective epoxidation of alkenes are reported. Four L-proline residues provide the chiralityfor the various meso-substituted catalysts, which differ by either the spatial arrangement of the stereogenic centers or the nature and length of the straps. The resulting bridged structures possess four amide linkages ineach strap, leading to highly rigid molecules with well-defined geometries whereas the strapped Fe catalysts gave rise to only moderate enantioselectivities, the C2-symmetrical ones being superior to the D2-symmetrical compounds. The …

010405 organic chemistryChemistryStereochemistryOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciencesBiochemistryPorphyrin[ CHIM ] Chemical SciencesCatalysis0104 chemical sciencesStereocenterCatalysisInorganic Chemistrychemistry.chemical_compoundAmideDrug DiscoveryMolecule[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryChirality (chemistry)
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

Electron-Sponge Behavior, Reactivity and Electronic Structures of Cobalt-Centered Cubic Co9Te6(CO)8 Clusters

2008

Extended investigations of the reaction sequence [Cp′2Nb(Te2)H]/CH3Li/[Co2(CO)8] (Cp′ = tBuC5H4) led to the identification of Lin[3] {3 = [Co9Te6(CO)8]; n = 1, 2} salts through their transformation with [PPN]Cl into [PPN]n[3] (PPN = Ph3PNPPh3). These compounds form in the solid state columnar ([PPN][3]) or undulated 2D ([PPN]2[3]) supramolecular networks. Electrochemical studies of [Cp*2Nb(CO)2][3] (Cp* = C5Me5) or [Na(THF)6][3] revealed the presence of the redox couples [3]–/[3]2–/[3]3–/[3]4–/[3]5– regardless of the nature of the cation, whereas in the anodic part oxidative degradation of the cluster takes place. This behavior is in agreement with the observation that [3]– containing salts…

010405 organic chemistryChemistryStereochemistrySupramolecular chemistrychemistry.chemical_element[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryElectronic structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistryelectronic structure01 natural sciencesRedoxcobalt3. Good health0104 chemical sciencesInorganic ChemistryCrystallographyelectrochemistrytelluriumCluster (physics)Reactivity (chemistry)Ground stateclusterCobalt
researchProduct

Aza and cyanobridged tripodal dinuclear copper(II) complexes: Electrochemical studies and structural evidence for an original azacyanocarbanion

2014

International audience; The reactivity of the mononuclear [Cu(TMPA)(L)] n+ complex (TMPA: tris(2-methylpyridine) amine, L: CH3CN, H2O) towards two different bridging species (tetracyanoethylene, 4,40-bipyridine) was investigated. The dinuclear complex [(mu-4,40-bipy)Cu-II(TMPA)(2)](CF3SO3)(4) (1) was synthesised and analysed by Xray diffraction (XRD). Magnetic studies revealed that this derivative displays very weak antiferromagnetic interactions between the two metal centres (2J = -0.69 cm(-1)). Solution studies (EPR spectroscopy and voltammetry) evidenced the lability of the bridged neutral bipyridine ligand in acetonitrile. The reaction of TCNE (TCNE: tetracyanoethylene) with the copper(…

010405 organic chemistryChemistryStereochemistrychemistry.chemical_elementCrystal structureTetracyanoethylene010402 general chemistryElectrochemistry01 natural sciencesCopper0104 chemical scienceslaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographyBipyridinelaw[CHIM.ANAL]Chemical Sciences/Analytical chemistryMaterials ChemistryAmine gas treating[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceAcetonitrile
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

Self-assembled Pt2L2 boxes strongly bind G-quadruplex DNA and influence gene expression in cancer cells

2017

Supramolecular Pt(ii) quadrangular boxes bind native and G-quadruplex DNA motifs in a size-dependent fashion. Three Pt molecular squares of distinct size show biological activity against cancer cells and heavily influence the expression of genes known to form G-quadruplexes in their promoter regions. The smallest Pt-box displays less activity but more selectivity for a quadruplex formed in the c-Kit gene.

010405 organic chemistryChemistrySupramolecular chemistryBiological activity010402 general chemistryG-quadruplex01 natural sciencesMolecular biology0104 chemical sciencesSelf assembledCell biologyInorganic Chemistrychemistry.chemical_compoundG-quadruplex PlatinumSettore CHIM/03 - Chimica Generale E InorganicaGene expressionCancer cellheterocyclic compoundsGeneDNADalton Transactions
researchProduct

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
researchProduct

High-Pressure Behavior of Nickel Sulfate Monohydrate: Isothermal Compressibility, Structural Polymorphism, and Transition Pathway

2020

Single crystals of synthetic nickel sulfate monohydrate, α-NiSO4·H2O (space-group symmetry C2/c at ambient conditions), were subject to high-pressure behavior investigations in a diamond-anvil cell up to 10.8 GPa. By means of subtle spectral changes in Raman spectra recorded at 298 K on isothermal compression, two discontinuities were identified at 2.47(1) and 6.5(5) GPa. Both transitions turn out to be apparently second order in character, as deduced from the continuous evolution of unit-cell volumes determined from single-crystal X-ray diffraction. The first structural transition from α- to β-NiSO4·H2O is an obvious ferroelastic C2/c–P1̅ transition. It is purely displacive from a structur…

010405 organic chemistryChemistrychemistry.chemical_element010402 general chemistry01 natural sciencesArticle0104 chemical sciencesInorganic ChemistryNickelchemistry.chemical_compoundPolymorphism (materials science)High pressureCompressibilityPhysical chemistryPhysical and Theoretical ChemistrySulfateInorganic Chemistry
researchProduct

Sequential Nucleophilic−Electrophilic Reactions Selectively Produce Isomerically Pure Nona‐ B ‐Substituted o ‐Carborane Derivatives

2003

Nine equal substituents on the intensively studied o-carborane have been obtained for the first time by a combined nucleophilic-electrophilic reaction sequence. Iodine and methyl groups have been introduced to prove the generality of the method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

010405 organic chemistryChemistrychemistry.chemical_element010402 general chemistryIodine01 natural sciences0104 chemical sciences3. Good healthInorganic ChemistryReaction sequenceNucleophileElectrophileCarboraneOrganic chemistryBoronEuropean Journal of Inorganic Chemistry
researchProduct