Search results for "Isostructural"

showing 10 items of 158 documents

Synthesis, structure and magnetic properties of iron (II), cobalt (II) and nickel (II) complexes of 2,6-bis(pyrazol-3-yl)pyridine and paramagnetic co…

2003

Abstract Iron (II), cobalt (II) and nickel (II) complexes of 2,6-bis(pyrazol-3-yl)pyridine (bpp) with [Cr(C2O4)3]3− have been prepared. They were characterised by single-crystal X-ray diffraction, magnetic susceptibility measurements and thermal gravimetric analyses. All three compounds are isostructural and they are formed by isolated [MII(bpp)2]2+ and [Cr(C2O4)3]3− complexes and free ClO4 −. As expected, only the salt [Fe(bpp)2]2[Cr(C2O4)3]ClO4·5H2O shows a thermal spin transition with transition temperature (T1/2) around 375 K that is correlated to the loss of water molecules.

ChemistryInorganic chemistrySpin transitionchemistry.chemical_elementMagnetic susceptibilityInorganic ChemistryNickelCrystallographyParamagnetismchemistry.chemical_compoundPyridineMaterials ChemistryMoleculePhysical and Theoretical ChemistryIsostructuralCobaltPolyhedron
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Trans-dicyanobis(acetylacetonato)ruthenate(III) as a precursor to build novel cyanide-bridged RuIII–MII bimetallic compounds [M=Co and Ni]

2006

Abstract The use of the mononuclear complex trans-[Ru(acac)2(CN)2]− as a ligand towards the preformed species [Ni2L(H2O)2Cl2], [Co(dmphen)](NO3)2, [Ni(dmphen)](NO3)2 and [Co(H2O)6](NO3)2 afforded the novel cyanide-bridged bimetallic compounds of formula [{Ru(acac)2(CN)2}{Ni2(L)(H2O)2}]{Ru(acac)2(CN)2}·2H2O (1), [{Ru(acac)2(CN)2}{Co(dmphen)(NO3)}]·H2O (2) and [{Ru(acac)2(CN)2}{Ni(dmphen)(NO3)}]·H2O (3) and [{Ru(acac)2(CN)2}2Co] (4) [Hacac = acetylacetone, dmphen = 2,9-dimethylphenanthroline and H2L = 11,23-dimethyl-3,7,15,19-tetrazatricyclo[19.3.1.19,13]hexacosa-2,7,9,11,13(26),14,19,21(25),22,24-decaene-25,26-diol]. Their syntheses, X-ray crystal structures and magnetic properties are repor…

ChemistryInorganic chemistrychemistry.chemical_elementCrystal structureRutheniumInorganic ChemistryCrystallographyNickelOctahedronMaterials ChemistryAntiferromagnetismPhysical and Theoretical ChemistryIsostructuralCobaltBimetallic stripCoordination Chemistry Reviews
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Why Do Chemically Similar Pharmaceutical Molecules Crystallize in Different Structures: A Case of Droperidol and Benperidol

2016

A detailed study of molecular conformation and intermolecular interactions in the experimental crystal structures and general trends observed in the Cambridge Structural Database as well as theoretical calculations were performed to identify the reason for the formation of different crystal structures of two chemically very similar pharmaceutical molecules benperidol and droperidol. The most important difference between both molecules was the weak intermolecular interactions formed by the central ring which therefore was responsible for the formation of different crystal structures. Cross-seeding experiments were performed to check the possibility for the formation of mutually isostructural…

ChemistryIntermolecular force02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsRing (chemistry)01 natural sciencesMolecular conformation0104 chemical sciencesBenperidolCrystallographymedicineMoleculeGeneral Materials ScienceIsostructural0210 nano-technologyDroperidolmedicine.drugCrystal Growth & Design
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Designing Solid Solutions of Enantiomers: Lack of Enantioselectivity of Chiral Naphthalimide Derivatives in the Solid State

2017

The enantiomers of a previously reported naphthalimide derivative are shown in this study to form a solid solution; furthermore, on the basis of the knowledge of solid solution structural aspects other naphthalimide derivatives have been synthesized and shown to lack the enantioselectivity in the solid state. The structural origin of solid solution formation is the same as observed in most of the cases in the literaturequasi-centrosymmetric structures form at nonracemic compositions where the most abundant enantiomer adjusts its conformation to mimic the absent one. Such solid solutions belong to the type showing some enantioselectivity. An extended single crystal X-ray diffraction study o…

ChemistryIntermolecular forceSolid-statechirality02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencessolid solutionsComputational chemistrycrystal engineerigOrganic chemistryGeneral Materials ScienceDensity functional theoryEnantiomerIsostructural0210 nano-technologyChirality (chemistry)Single crystalSolid solution
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Heterotrimetallic coordination polymers: {Cu(II)Ln(III)Fe(III)} chains and {Ni(II)Ln(III)Fe(III)} layers: synthesis, crystal structures, and magnetic…

2015

The use of the [Fe(III) (AA)(CN)4](-) complex anion as metalloligand towards the preformed [Cu(II) (valpn)Ln(III)](3+) or [Ni(II) (valpn)Ln(III) ](3+) heterometallic complex cations (AA=2,2'-bipyridine (bipy) and 1,10-phenathroline (phen); H2 valpn=1,3-propanediyl-bis(2-iminomethylene-6-methoxyphenol)) allowed the preparation of two families of heterotrimetallic complexes: three isostructural 1D coordination polymers of general formula {[Cu(II) (valpn)Ln(III) (H2O)3 (μ-NC)2 Fe(III) (phen)(CN)2 {(μ-NC)Fe(III) (phen)(CN)3}]NO3 ⋅7 H2O}n (Ln=Gd (1), Tb (2), and Dy (3)) and the trinuclear complex [Cu(II) (valpn)La(III) (OH2 )3 (O2 NO)(μ-NC)Fe(III) (phen)(CN)3 ]⋅NO3 ⋅H2O⋅CH3 CN (4) were obtained …

ChemistryLigandOrganic ChemistryInorganic chemistryGeneral ChemistryCrystal structureCatalysisMagnetizationchemistry.chemical_compoundBipyridineCrystallographyX-ray crystallographyMoleculeIsostructuralAcetonitrileChemistry (Weinheim an der Bergstrasse, Germany)
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Magnetostructural correlations in parallel square-planar halo-bridged copper(II) dimers. Part II: Structure and magnetic properties of [Cu2(terpy)2Br…

1987

Abstract The crystal and molecular structure of bis-μ- bromo-bis [(2,2′:6′,2″ - terpyridyl) copper (II) ] bis (hexafluorophosphate) has been determined from three dimensional single-crystal X-ray diffraction data, collected by counter techniques. The blue crystals belong to the monoclinic system, space group P21/a, with four formula units in a unit cell of dimensions a=20.40(2), b=13.35(2), c=6.453(8) A and β=97.74(9)°. The structure was solved using a refinement procedure and starting with the atomic positions of the isostructural complex [Cu(terpy)- Cl]2(PF6)2, to final agreement factors R=0.071 (Rw=0.077). The structure consists of dimeric molecules bridged by two bromine atoms. The coor…

ChemistryLigandStereochemistryCrystal structureMagnetic susceptibilityInorganic ChemistryBond lengthCrystallographychemistry.chemical_compoundSquare pyramidHexafluorophosphateMaterials ChemistryPhysical and Theoretical ChemistryIsostructuralCoordination geometryInorganica Chimica Acta
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Incommensurate nature of the multilayered molecular ferromagnetic metals based on bis(ethylenedithio)tetrathiafulvalene and bimetallic oxalate comple…

2004

The salt [ET]x[MnRh(ox)(3)].CH(2)Cl(2) (x = 2.526(1)) has been obtained and characterized. This paramagnetic metal is essentially isostructural to the ferromagnetic metal [ET]y[MnCr(ox)(3)].CH(2)Cl(2) (y approximately equal to 3) and provides a definite answer on the origin of the structural disorder present on such systems. As in the ferromagnetic analogue, this material shows high electrical conductivity at room temperature (13 S.cm(-1)) and metallic behavior.

ChemistryMineralogyOxalateInorganic ChemistryMetalParamagnetismchemistry.chemical_compoundCrystallographyFerromagnetismElectrical resistivity and conductivityvisual_artvisual_art.visual_art_mediumPhysical and Theoretical ChemistryIsostructuralBimetallic stripTetrathiafulvaleneInorganic chemistry
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Structural and conductivity studies in LiFeP 2 O 7 , LiScP 2 O 7 , and NaScP 2 O 7

2000

Structural studies of LiScP2O7 by Rietveld refinement confirm that this material is isostructural with LiFeP2O7 studied previously. However, NaScP2O7 shows a structure different from the structural types of the basic group of NaIMIIIP2O7 known thus far. Systematic ranges for the six structural types of AIMIIIP2O7 are presented in terms of ion radii sums and ratios. The framework of LiMP2O7 (M=Sc, Fe) has rather wide tunnels running along the crystallographic c-axis. This feature has determined our interest to check the ion conductivity in AIMIIIP2O7 (A=Li, Na; M=Sc, Fe). The bulk conductivity, however, is low in these compounds, 10−6–10−7 S/cm at 300 °C, as determined by impedance spectrosc…

ChemistryRietveld refinementInorganic chemistryAnalytical chemistrychemistry.chemical_elementConductivityCondensed Matter PhysicsElectrochemistryIonDielectric spectroscopyGroup (periodic table)ElectrochemistryGeneral Materials ScienceLithiumElectrical and Electronic EngineeringIsostructuralJournal of Solid State Electrochemistry
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On the Formation of Droperidol Solvates: Characterization of Structure and Properties

2014

A solvate screening and characterization of the obtained solvates was performed to rationalize and understand the solvate formation of active pharamaceutical ingredient droperidol. The solvate screening revealed that droperidol can form 11 different solvates. The analysis of the crystal structures and molecular properties revealed that droperidol solvate formation is mainly driven by the inability of droperidol molecules to pack efficiently. The obtained droperidol solvates were characterized by X-ray diffraction and thermal analysis. It was found that droperidol forms seven nonstoichiometric isostructural solvates, and the crystal structures were determined for five of these solvates. To b…

ChemistryStereochemistryGeneral ChemistryCrystal structureCondensed Matter PhysicsSolventCrystallographyLattice constantmedicineMoleculeGeneral Materials ScienceIsostructuralHydrateThermal analysisDroperidolmedicine.drugCrystal Growth & Design
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Influencing the Self‐Sorting Behavior of [2.2]Paracyclophane‐Based Ligands by Introducing Isostructural Binding Motifs

2020

Abstract Two isostructural ligands with either nitrile (Lnit) or isonitrile (Liso) moieties directly connected to a [2.2]paracyclophane backbone with pseudo‐meta substitution pattern have been synthesized. The ligand itself (Lnit) or its precursors (Liso) were resolved by HPLC on a chiral stationary phase and the absolute configuration of the isolated enantiomers was assigned by XRD analysis and/or by comparison of quantum‐chemical simulated and experimental electronic circular dichroism (ECD) spectra. Surprisingly, the resulting metallosupramolecular aggregates formed in solution upon coordination of [(dppp)Pd(OTf)2] differ in their composition: whereas Lnit forms dinuclear complexes, Liso…

Circular dichroismNitrileSupramolecular chemistry010402 general chemistry01 natural sciencesCatalysisself-sortingsupramolecular chemistrychemistry.chemical_compoundIsostructuralFull Paper010405 organic chemistryLigandOrganic ChemistryAbsolute configurationGeneral ChemistryNuclear magnetic resonance spectroscopyself-assemblyFull Papers0104 chemical sciencesCrystallographychemistrynitrile ligandsEnantiomerSupramolecular Chemistry | Hot Paperisonitrile ligandsChemistry (Weinheim an Der Bergstrasse, Germany)
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