Search results for "Azide"

showing 10 items of 334 documents

A unique example of structural and magnetic diversity in four interconvertible copper(II)-azide complexes with the same schiff base ligand: a monomer…

2010

Four new Cu(II)-azido complexes of formula [CuL(N(3))] (1), [CuL(N(3))](2) (2), [Cu(7)L(2)(N(3))(12)](n) (3), and [Cu(2)L(dmen)(N(3))(3)](n) (4) (dmen = N,N-dimethylethylenediamine) have been synthesized using the same tridentate Schiff base ligand HL (2-[1-(2-dimethylaminoethylimino)ethyl]phenol, the condensation product of dmen and 2-hydroxyacetophenone). The four compounds have been characterized by X-ray structural analyses and variable-temperature magnetic susceptibility measurements. Complex 1 is mononuclear, whereas 2 is a single mu-1,1 azido-bridged dinuclear compound. The polymeric compound 3 possesses a 2D structure in which the Cu(II) ions are linked by phenoxo oxygen atoms and t…

Schiff baseCopper(II) azideStereochemistryLigandDimerMagnetic susceptibilityInorganic ChemistryCrystallographychemistry.chemical_compoundMonomerchemistryHelixAzidePhysical and Theoretical ChemistryInorganic chemistry
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Coordination versatility of 1,5-bis(salicylidene)carbohydrazide in Ni(II) complexes

2014

Abstract Versatile coordination behavior of a polydentate Schiff base ligand 1,5-bis(salicylidene)carbohydrazide (H3bsc) has been explored in Ni(II) complexes. [Ni(H3bsc)2](ClO4)2 (1)·H2O·3CH3CN is a bis chelate mononuclear complex of H3bsc in keto form, and [Ni4(H0.5bsc)2(O2CCMe3)3(CH3OH)4](2)·2H2O·2CH3OH is a tetranuclear complex of H3bsc with an unusual coordination. In 2, one phenolate group of the ligand coordinates in a monodentate way and the other coordinates in a μ2-bridging mode to the Ni(II) center. This unusual coordination mode of the ligand stabilizes the Ni(II) complex in a tetranuclear form where the carbonyl oxygen of the ligand exists in between keto and enol form of bond …

Schiff baseDenticityLigandStereochemistryCarbohydrazideEnolBond orderInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryMaterials ChemistryAntiferromagnetismChelationPhysical and Theoretical ChemistryInorganic Chemistry Communications
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Bis (μ-tetrazolato-NN′) bridged dinuclear nickel(II) Schiff base complexes: Tandem synthesis, structure and self assembly

2015

Abstract Two new bis(μ-tetrazolato-NN′) bridged dinuclear nickel(II) Schiff base complexes [Ni2L12(PTZ)2]·2(CH3)2SO·2.69H2O (1) and 2[Ni2L22(PTZ)2]·3H2O (2) (HL1 and HL2 are Schiff bases, HL1 = 2-((2-(dimethylamino)ethylimino)methyl)phenol, HL2 = 2-((2-(methylamino)ethylimino)methyl)-6-methoxyphenol and HPTZ is 5-pyrazinyltetrazole) have been synthesized via [3+2] cyclo-addition of 2-cyanopyrazine and sodium azide in presence of nickel(II) acetate tetrahydrate and the respective Schiff bases. The structures of the complexes are confirmed by single crystal X-ray diffraction analysis. Both complexes show fluorescence. The change in the denticity of the Schiff base blocking ligand is shown to …

Schiff baseDenticityTetrahydrateLigandStereochemistrySupramolecular chemistrychemistry.chemical_elementschiff base 15-pyrazinyltetrazolateInorganic Chemistrychemistry.chemical_compoundNickelchemistry3-dipolar cycloaddition13-Dipolar cycloadditionPolymer chemistryMaterials ChemistrySodium azidePhysical and Theoretical Chemistrydinuclearta116nickel(II)Polyhedron
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Synthesis, X-ray structure and magnetic properties of the azido adducts of quadridentate Schiff base manganese(III) complexes

2004

Abstract Two new azido derivatives of quadridentate Schiff base manganese(III) complexes have been synthesized and characterized structurally and magnetically. X-ray structure analysis revealed that both complexes viz. [Mn2(L1)2(N3)2] (1) and [Mn2(L2)2(N3)2] (2), where H2L1=N,N′-(1,1-dimethylethylene)-bis-(salicylaldiimine) and H2L2=bis(o-hydroxyacetophenone)-ethylenediimine exist as phenoxo-bridged dimer. The magnetic susceptibility of the complexes has been measured in the 5–300 K range. At room temperature the MnIII ions in complexes 1 and 2 possess an S=4 ground state. The global magnetic interaction in complex 1 is found to be ferromagnetic, while for complex 2 it is anti-ferromagnetic.

Schiff baseStereochemistryDimerchemistry.chemical_elementManganeseMagnetic susceptibilityAdductInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryMagnetochemistryMaterials ChemistryAzidePhysical and Theoretical ChemistryGround statePolyhedron
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Asymmetric bis-(μ1,1-azido) bridged dinuclear copper(II) complex with N2O donor Schiff base: synthesis, structure and magnetic study

2015

A copper(II) complex, [Cu2(L)2(N3)2] [where HL = 2-((3-(methylamino)propylimino)methyl)-6-methoxyphenol] has been synthesized and characterized by elemental analysis, IR, UV–vis and fluorescence spectroscopy, and single-crystal X-ray diffraction studies. The complex crystallizes in the trigonal space group R. The deprotonated tridentate Schiff base occupies three coordination sites of copper(II). The fourth coordination site is occupied by an azide. A symmetry-related azide from a different molecule coordinates with the fifth site of copper(II), thereby forming a double end-on azide-bridged centrosymmetric dimer. Variable temperature solid–state magnetic studies between 2 and 300 K were car…

Schiff baseStereochemistryDimerchemistry.chemical_elementschiff baseCopperchemistry.chemical_compoundCrystallographyMagnetizationCopper(II)Deprotonationchemistryfield-dependent magnetization studyantiferromagneticMaterials ChemistryMoleculeAntiferromagnetismAzidePhysical and Theoretical Chemistrydinuclearta116Journal of Coordination Chemistry
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Observation of novel oxygen⋯oxygen interaction in supramolecular assembly of cobalt(III) Schiff base complexes: a combined experimental and computati…

2015

Two mononuclear cobalt(III) Schiff base complexes with azide [Co(L)(N3)(L0 )] (1) and [Co(L)(N3)(L00)] (2) {where HL ¼ 1-((2-(diethylamino)ethylimino)methyl)naphthalene-2-ol, HL0 ¼ 2-hydroxy-1-naphthaldehyde and HL00 ¼ acetylacetone} have been synthesized and characterized by elemental analysis, IR and UV-Vis spectroscopy and single crystal X-ray diffraction studies. Both complexes show mononuclear structures with azide as terminal coligand. Structural features have been examined in detail that reveal the formation of interesting supramolecular networks generated through non-covalent forces including hydrogen bonding, C–H/H–C and C–H/p interactions. These interactions have been studied ener…

Schiff basekemianovel oxygenStereochemistryHydrogen bondGeneral Chemical EngineeringAcetylacetoneSupramolecular chemistrychemistry.chemical_elementGeneral ChemistrychemistrycobaltSupramolecular assemblychemistry.chemical_compoundCrystallographychemistryAzidekobolttiCobaltta116Natural bond orbitalRSC Advances: an international journal to further the chemical sciences
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Crystal and Molecular Structure and Stability of Isoniazid Cocrystals with Selected Carboxylic Acids

2013

Reaction of isoniazid with benzoic acid, sebacic acid, suberic acid, and cinnamic acid results in formation of cocrystals. Two polymorphs of isoniazid–suberic acid and two polymorphs of isoniazid–cinnamic acid cocrystals were isolated. Crystal structure analysis shows the presence of a pyridine–carboxylic acid synthon in the studied cocrystals. The hydrazide group of isoniazid participates in N–H···O and N–H···N hydrogen bond formation, producing different supramolecular synthons. The stability study of isoniazid cocrystals has been performed over a 22 week period. A comparison of melting points of isoniazid–dicarboxylic acid 2:1 cocrystals shows the decrease of melting point with an increa…

Sebacic acidHydrogen bondSynthonGeneral Chemistrybacterial infections and mycosesCondensed Matter PhysicsHydrazideCinnamic acidchemistry.chemical_compoundchemistryPolymer chemistryOrganic chemistryGeneral Materials ScienceSolubilitySuberic acidBenzoic acidCrystal Growth & Design
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Gelling and the collective dynamics in ferroelectric liquid crystals

2020

Dielectric spectroscopy has been applied to investigate the dynamic behaviour of a ferroelectric liquid crystal in the smectic C* and smectic A phases confined in gel matrices of a fibre like (1D) or platelet like (2D) structure. These gel matrices were obtained from semicarbazide or bis-acylurea derivatives, which self assemble because of their H-bonding motif. The confinement strongly influences the magnitude of the spontaneous polarization and the collective fluctuations of the director detected as the Goldstone-mode. It is thus possible to detect gelation by dielectric spectroscopy. By this method it was possible to follow the destruction and restoration of the gel structure induced by …

SemicarbazideMaterials scienceSelf assembleGeneral ChemistryCondensed Matter PhysicsFerroelectricityDielectric spectroscopySpontaneous polarizationchemistry.chemical_compoundCrystallographychemistryChemical physicsLiquid crystalCollective dynamicsSoft Matter
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Gelation of smectic liquid crystal phases with photosensitive gel forming agents.

2020

This paper studies the potential of 3 newly synthesized low molecular weight gelling agents (2 of them with azo groups) with the semicarbazide group as a H-bonding motif to gel the smectic phase of a commercial chiral smectic C material. To detect gelation two methods were used: the stabilization of the director pattern, which measures the interaction of the physical gel network with the LC-director, and the suppression of the onset of electrohydrodynamic instabilities, which measures the increase of viscosity. Special emphasis was put on the influence of the photochemical - isomerization of the gelling agents on gelation.From the stabilization of the director pattern an elastic component c…

SemicarbazidePhotoisomerizationChemistryGeneral ChemistryCondensed Matter PhysicsGel formingViscositychemistry.chemical_compoundChemical engineeringLiquid crystalPhase (matter)Organic chemistryElectrohydrodynamicsIsomerizationSoft matter
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A study of synergetic effect of ionic liquids and ultrasounds on the aryl azides formation

Settore CHIM/06 - Chimica OrganicaIonic liquids ultrasounds aryl azides
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