Search results for "Schiff Base"

showing 10 items of 180 documents

A Discrete μ 4 ‐Oxido Tetranuclear Iron(III) Cluster

2012

Reaction of a Schiff base ligand derived from salicyloyl hydrazide and diacetyl monooxime (H2L) with a triangular μ3-oxido-centered [Fe3(μ3-O)]7+ core yields a new tetranuclear iron(III) complex. FeIII4(μ4-O) crystallizes in the triclinic space group P. Structural studies reveal that this tetranuclear iron(III) complex is a new structure type of an uncharged (alkoxido)(oxido)iron(III) cluster in which the four iron(III) ions are located at the corners of a distorted tetrahedron. A study of the magnetic properties supports the presence of antiferromagnetic interactions through the central μ4-oxido ion as well as the μ2-methoxy groups present, giving an an S = 0 ground state. Mossbauer spectr…

Inorganic ChemistryCrystallographychemistry.chemical_compoundSchiff basechemistryLigandStereochemistryX-ray crystallographyMössbauer spectroscopyAntiferromagnetismTriclinic crystal systemGround stateHydrazideEuropean Journal of Inorganic Chemistry
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Control of Exchange Interactions in Trinuclear Complexes Based on Orthogonal Magnetic Orbitals

2009

The reaction of copper(II) acetate with the tetradentate Schiff base like ligand H4L {(E,E)-[{diethyl 2,2′-[4,5-dihydroxy-1,2-phenylenebis(iminomethylidyne)]bis(3-oxobutanoate)}] leads to the formation of the square planar N2O2 coordinated complex [H2CuL]. Reaction of two equivalents of this complex with copper(II) acetylacetonato or vanadyl(IV) acetylacetonato yields the trinuclear complexes [V(O)Cu2L2][N(nBu)4]2·2MeOH (1) and [Cu3L2][N(nBu)4]2·2DMF (2). Both complexes were characterised by using magnetic measurements and X-ray crystallography. Special attention was given to the spin-exchange coupling through the bridging phenylene ring. The principle of strict orthogonality of the magneti…

Inorganic ChemistryMagnetic measurementschemistry.chemical_compoundCrystallographySchiff basechemistryAtomic orbitalPhenyleneStereochemistrychemistry.chemical_elementVanadiumCopperEuropean Journal of Inorganic Chemistry
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Multifunctional Ni(II)-Based Metamagnetic Coordination Polymers for Electronic Device Fabrication

2020

The combination of two 8-aminoquinoline-based Schiff base ligands (L1 and L2) with SCN– and Ni(II) has led to the synthesis of two new one-dimensional thiocyanato-bridged coordination polymers: [Ni...

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundSchiff baseFabricationchemistry010405 organic chemistryPolymer chemistryPolymerPhysical and Theoretical Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistry
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(Ni2), (Ni3), and (Ni2 + Ni3): A Unique Example of Isolated and Cocrystallized Ni2 and Ni3 Complexes

2009

Structural and magnetic characterization of compound {[Ni(2)(L)(2)(OAc)(2)][Ni(3)(L)(2)(OAc)(4)]}.2CH(3)CN (3) (HL = the tridentate Schiff base ligand, 2-[(3-methylamino-propylimino)-methyl]-phenol) shows that it is a rare example of a crystal incorporating a dinuclear Ni(II) compound, [Ni(2)(L)(2)(OAc)(2)], and a trinuclear one, [Ni(3)(L)(2)(OAc)(4)]. Even more unusual is the fact that both Ni(II) complexes, [Ni(2)(L)(2)(OAc)(2)] (1) and [Ni(3)(L)(2)(OAc)(4)(H(2)O)(2)].CH(2)Cl(2).2CH(3)OH (2), have also been isolated and structurally and magnetically characterized. The structural analysis reveals that the dimeric complexes [Ni(2)(L)(2)(OAc)(2)] in cocrystal 3 and in compound 1 are almost i…

Inorganic Chemistrychemistry.chemical_compoundCrystallographySchiff baseMolecular geometryTridentate ligandchemistryOctahedral molecular geometryChelationPhysical and Theoretical ChemistryAcetate ionCocrystalInorganic Chemistry
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First Crystallographic Investigation of Complexes of cis-VO2+, cis-MoO22+, and trans-UO22+ Species with Schiff-Base Molecules Derived from 4,6-O-Ethy…

2001

The interaction of Schiff-base ligands derived from 4,6-O-ethylidene-β-D-glucopyranosylamine with cis-VO 2 + , cis-MoO 2 2+ , and trans-UO 2 2+ species have been studied by isolating and characterizing the corresponding products. The structures of one complex of each type of species have been established by single-crystal X-ray diffraction analysis. In all the complexes, the saccharide moiety adopts a chair conformation and has a β-anomeric form. A gradual increase in coordination number (5, 6, and 7) and a gradual variation in the geometry (distorted trigonal-bipyramidal, distorted octahedral, and pentagonal-bipyramidal) are observed on going from the complexes of cis-VO 2 + (mononuclear) …

Inorganic Chemistrychemistry.chemical_compoundCrystallographySchiff baseOctahedronLigandChemistryStereochemistryCoordination numberCyclohexane conformationMoietyMoleculeVanadateEuropean Journal of Inorganic Chemistry
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Trinuclear Nickel(II) and Cobalt(II) Complexes Constructed from Mannich–Schiff‐Base Ligands: Synthesis, Crystal Structures, and Magnetic Properties

2019

Inorganic Chemistrychemistry.chemical_compoundNickelSchiff basechemistryPolymer chemistrychemistry.chemical_elementCrystal structureCobaltEuropean Journal of Inorganic Chemistry
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Spectroscopic, density functional theory, nonlinear optical properties and in vitro biological studies of Co(II), Ni(II), and Cu(II) complexes of hyd…

2021

Inorganic Chemistrychemistry.chemical_compoundNonlinear opticalSchiff baseBiological studieschemistryComputational chemistryBiological activityDensity functional theoryGeneral ChemistryHydrazideX ray analysisIn vitroApplied Organometallic Chemistry
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Fluorescence emission and enhanced photochemical stability of Zn(II)-5-triethyl ammonium methyl salicylidene ortho-phenylendiiminate interacting with…

2010

Abstract The photophysical and photochemical properties of the cationic Zn II complex of 5-triethyl ammonium methyl salicylidene ortho-phenylendiimine (ZnL 2+ ) interacting with native DNA were investigated by steady state and time-resolved fluorescence spectroscopies. Experimental results indicate that, in the presence of DNA, ZnL 2+ is efficiently protected from a photochemical process, which occurs when it is in the free state dispersed in aqueous solution. The analysis of the absorption and emission spectra of ZnL 2+ , both stored in the dark and after exposure to tungsten lamp light for 24 h, corroborated by quantum chemical calculations, allowed us to point out that ZnL 2+ undergoes a…

Intercalation (chemistry)Context (language use)PhotochemistryBiochemistryFluorescence spectroscopyFluorescenceInorganic ChemistrySchiff baseIntercalationOrganometallic CompoundsMoleculeFluorescence spectroscopyPhotooxidationSettore CHIM/02 - Chimica FisicaAqueous solutionChemistrySpectrum AnalysisDNAPhotochemical ProcessesFluorescenceIntercalating AgentsSolventZincSettore CHIM/03 - Chimica Generale E InorganicaSolventsSteady state (chemistry)Oxidation-ReductionJournal of inorganic biochemistry
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Co-crystallization of Keggin type polyoxometalates [HL]3[PW12O40] and [Ln(DMF)8][PW12O40] (Ln=La, Dy, Yb) (L=N-(2-hydroxyphenyl)-3-methoxy-salicylide…

2016

Abstract Four new Keggin type polyoxometalate clusters [HL]3[PW12O40]·5MeOH (1) and [Ln(DMF)8][PW12O40] {Ln = La (2), Dy (3), Yb (4)} (L = N-(2-hydroxyphenyl)-3-methoxy-salicylideneamine) have been synthesized. Co-crystallization of complex 1 with each of the three complexes 2–4 takes place when the Schiff base ligand is treated with hydrated phosphotungstic acid, H3[PW12O40]·xH2O, hydrated lanthanide nitrate, Ln(NO3)3·6H2O in the presence of Ni(NO3)2·6H2O. The Schiff base ligand is protonated in complex 1 and thus it is neutralizing the charge of the polyoxotungstate anion, [PW12O40]3−. A dimethylformamide (DMF) coordinated trivalent lanthanide ion balances the negative charge of the polyo…

LanthanideSchiff base010405 organic chemistryLigandInorganic chemistryProtonationCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPolyoxometalateMaterials ChemistryDimethylformamidePhosphotungstic acidPhysical and Theoretical ChemistryPolyhedron
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Syntheses, characterisation, magnetism and photoluminescence of a homodinuclear Ln(III)-Schiff base family.

2009

A novel family of homodinuclear complexes of the general formula [Ln(2)L(2)(X)(2)] (where Ln = Nd(3+), Pr(3+), Sm(3+) and Tb(3+) for 1, 2, 3 and 4, respectively and X, the coordinated NO(3)(-) or Cl(-) anion) has been synthesised from the corresponding lanthanide(III) salts with the pentadentate dianionic Schiff base ligand, H(2)L [N(1),N(3)-bis(salicylideneimino)diethylenetriamine], that exhibits a N(3)O(2) donor set. Single crystal X-ray diffraction studies evidenced the isostructurality of this family of centrosymmetric neutral dinuclear entities where the Ln(III) metal centres are coupled together by two phenolato oxygen atoms belonging to two units of ligand (H(2)L). Interestingly, the…

LanthanideSchiff base010405 organic chemistryStereochemistryLigandMetal ions in aqueous solution[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryvisual_artDiethylenetriamine[CHIM.CRIS]Chemical Sciences/Cristallographyvisual_art.visual_art_medium[CHIM]Chemical SciencesSingle crystalDalton transactions (Cambridge, England : 2003)
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