Search results for "Crystal"

showing 10 items of 22886 documents

3,4′,5,5′-Tetramethoxy-2′-methylbiphenyl-4-ol

2019

The asymmetric unit of the title compound, C17H20O5, contains two independent molecules, A and B, with similar geometries [dihedral angles between the phenyl rings = 56.19 (8) and 54.98 (7)°, respectively]. Intramolecular O—H...O hydrogen bonds occur in both molecules. In the crystal, the A molecules form [1\overline{1}0] chains linked by O—H...O hydrogen bonds from the hydroxyl group to one of the methoxy O atoms. The B molecules form O—H...O hydrogen bonds to the hydroxyl O atoms of the A molecules and thus act as fixed spacers between the chains of molecule A. Some weak C—H...O contacts are also present.

inorganic chemicalsbiaryl systemcrystal structurebiology010405 organic chemistryHydrogen bondMeth-Crystal structureDihedral angle010402 general chemistrybiology.organism_classification01 natural scienceshumanities0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographychemistryGroup (periodic table)cross-couplinglcsh:QD901-999Tetralcsh:CrystallographyPhysics::Chemical PhysicsIUCrData
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Halogen bonding and host–guest chemistry between N-alkylammonium resorcinarene halides, diiodoperfluorobutane and neutral guests

2019

Single crystal X-ray structures of halogen-bonded assemblies formed between host N-hexylammonium resorcinarene bromide (1) or N-cyclohexylammonium resorcinarene chloride (2), and 1,4-diiodooctafluorobutane and accompanying small solvent guests (methanol, acetonitrile and water) are presented. The guests’ inclusion affects the geometry of the cavity of the receptors 1 and 2, while the divalent halogen bond donor 1,4-diiodooctafluorobutane determines the overall nature of the halogen bond assembly. The crystal lattice of 1 contains two structurally different dimeric assemblies A and B, formally resulting in the mixture of a capsular dimer and a dimeric pseudo-capsule. 1H and 19F NMR analyses …

inorganic chemicalscapsuleDimerHalideFluorine-19 NMRCrystal structurelcsh:QD241-441kemialliset sidoksetchemistry.chemical_compoundlcsh:Organic chemistryBromidesupramolekulaarinen kemiahost-guest chemistryhost–guest chemistrylcsh:ScienceHost–guest chemistryta116Biochemistry Biophysics and Structural BiologyX-ray crystallographyresorcinarene saltsHalogen bondChemistryOrganic ChemistryResorcinareneChemistryCrystallographyhalogen bondinglcsh:Qröntgenkristallografiadimeric assembliesBeilstein Journal of Organic Chemistry
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Pressure- and temperature-induced valence tautomeric interconversion in a o-dioxolene adduct of a cobalt-tetraazamacrocycle complex

2001

An electronic switch at the molecular level has been realized by using a class of ionic compounds of the formula [Co(L)(diox)]Y (L = tetraazamacrocyclic ligand, Y = mononegative anion). Such compounds undergo temperature- and pressure-induced intramolecular one-electron transfer equilibria. The transition temperature of interconversion varies with the nature of the counterions Y (Y = PF6, BPh4, I). Surprisingly the effect of the anion on the transition temperature is not only governed by its volume but also by its coulombic interaction.

inorganic chemicalschemistry.chemical_classificationQuantitative Biology::BiomoleculesValence (chemistry)Transition temperatureOrganic ChemistryIonic bondingGeneral ChemistryPhotochemistryTautomerCatalysisAdductElectron transferCrystallographychemistryIntramolecular forceCondensed Matter::Strongly Correlated ElectronsPhysics::Chemical PhysicsCounterion
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Synthesis, characterization and antimicrobial activity of palladium(II) complexes with some alkyl derivates of thiosalicylic acids: Crystal structure…

2012

Abstract S-Alkyl (R = benzyl, methyl, ethyl, propyl and butyl) derivatives of thiosalicylic acid and the corresponding palladium(II) complexes were prepared and their structures were proposed on the basis of infrared, 1H and 13C NMR spectroscopy. The cis geometrical configurations of the isolated complexes were proposed on the basis of an X-ray structural study of the bis(S-benzyl-thiosalicylate)–palladium(II), [Pd(S-bz-thiosal)2] complex. Antimicrobial activity of the tested compounds was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 26 species of microorganisms. The tested ligands, with a few exceptions, sho…

inorganic chemicalschemistry.chemical_classificationThiosalicylic acidbiologyStereochemistrychemistry.chemical_elementCrystal structurebiology.organism_classificationAntimicrobialMedicinal chemistryAspergillus fumigatusInorganic Chemistrychemistry.chemical_compoundMinimum inhibitory concentrationchemistryMaterials ChemistryPhysical and Theoretical ChemistryAntibacterial activityta116AlkylPalladiumPolyhedron
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Crystal structure of a 1:1 salt of 4-amino­benzoic acid (vitamin B10) with pyrazinoic acid

2018

The paper reports the crystal structure of novel salt of 4-amino­benzoic acid (Vitamin B10) with pyrazinoic acid.

inorganic chemicalscrystal structure4-amino­benzoic acidmelting pointStackingchemical and pharmacologic phenomena02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesCocrystalResearch Communicationslcsh:ChemistryCrystalchemistry.chemical_compoundPyrazinoic acidpyrazinoic acid4-Aminobenzoic acidsaltGeneral Materials ScienceBenzoic acidHydrogen bondChemistryorganic chemicalshemic and immune systemsGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicshydrogen bonding0104 chemical sciencesCrystallography4-aminobenzoic acidlcsh:QD1-9990210 nano-technologyActa Crystallographica Section E: Crystallographic Communications
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Crystal structure of hydrocortisone 17-butyrate

2014

In the title compound, C25H36O6, the two central cyclohexane rings exhibit a chair conformation. The terminal cyclohexene and cyclopentane rings are in half-chair and envelope conformations (with the C atom bearing the methyl substituent as the flap), respectively. The methyl group of the butyrate chain is disordered over two orientations, with a refined occupancy ratio of 0.742 (6):0.258 (6). Intramolecular O—H...O and C—H...O hydrogen bonds are observed. In the crystal, molecules are linked by O—H...O hydrogen bonds into chains running parallel to theaaxis.

inorganic chemicalscrystal structureCrystallographyHydrogen bondCyclohexane conformationeducationGeneral ChemistryButyrateCrystal structureCondensed Matter PhysicsBioinformaticsData ReportshumanitiesCrystalchemistry.chemical_compoundCrystallographychemistryQD901-999Atomhydrogen bondshydro­cortisone derivativehydrocortisone derivativeGeneral Materials Sciencepharmacological activityMethyl groupActa Crystallographica Section E
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Crystal structure ofN-(tert-butoxycarbonyl)glycyl-(Z)-β-bromodehydroalanine methyl ester [Boc–Gly–(β-Br)(Z)ΔAla–OMe]

2014

In a de­hydro­amino acid with a C=C bond between the α- and β-C atoms, the amino acid residues are linked trans to each other and there are no strong intra­molecular hydrogen bonds. The torsion angles indicate a non-helical conformation of the mol­ecule.

inorganic chemicalscrystal structureStereochemistryeducationCrystal structurebehavioral disciplines and activitiesResearch CommunicationsSteric repulsionlcsh:Chemistrychemistry.chemical_compoundde­hydro­amino acidβ-bromo­dehydro­alaninedehydroamino acidnon-helical conformationGeneral Materials Science[beta]-bromo­dehydro­alanineAmino acid residuehealth care economics and organizationsQuantitative Biology::BiomoleculesDipeptideChemistryHydrogen bondGeneral Chemistryhydrogen bondingCondensed Matter Physicshumanitieslcsh:QD1-999β-bromodehydroalanineAlanine methyl esterActa Crystallographica Section E Structure Reports Online
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Crystal structure of diethyl 2-amino-5-{4-[bis-(4-methyl-phen-yl)amino]-benzamido}-thio-phene-3,4-di-carboxyl-ate.

2019

The title compound forms a head-to-head centrosymmetric dimer, involving a pair of inter­molecular N—H⋯O hydrogen bonds. It also forms two intra­molecular bonds between its amine and amide and the ester carbonyl groups.

inorganic chemicalscrystal structureintra- and intermolecular bondingThio-hydrogen-bonded dimerCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistryResearch Communicationslcsh:Chemistrychemistry.chemical_compoundAmideGeneral Materials SciencePhene010405 organic chemistryHydrogen bondRegioselectivityGeneral ChemistryCondensed Matter Physics3. Good health0104 chemical scienceslcsh:QD1-999chemistryintra- and inter­molecular bondingAmine gas treatingActa crystallographica. Section E, Crystallographic communications
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Structural Characterization of Surfactant-Coated Bimetallic Cobalt/Nickel Nanoclusters by XPS, EXAFS, WAXS, and SAXS

2011

Cobalt nickel bimetallic nanoparticles were synthesized by changing the sequence of the chemical reduction of Co(II) and Ni(II) ions confined in the core of bis(2-ethylhexyl)phosphate (2)., and Ni(DEHP)(2). The reduction was carried out by mixing, sequentially or contemporaneously, fixed amounts of n-heptane solution of Co(DEHP)2 and Ni(DEHP)2 micelles with a solution of sodium borohydride in ethanol at a fixed (reductant)/(total metal) molar ratio. This procedure involves the rapid formation of surfactant-coated nanoparticles, indicated as Co/Ni (Co after Ni), Ni/Co (Ni after Co), and Co + Ni (simultaneous), followed by their slow separation as nanostructures embedded in a sodium bis(2-eth…

inorganic chemicalsendocrine systemMaterials sciencechemistry.chemical_elementNanoparticleNanoclustersMetalSodium borohydridechemistry.chemical_compoundX-ray photoelectron spectroscopyNANOPARTICLESPARTICLESBimetallic Cobalt/Nickel Nanoclusters. XPS. EXAFS. WAXS. SAXS.GOLDPhysical and Theoretical ChemistryBimetallic stripMICELLESSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyNickelGeneral Energychemistryvisual_artNANOPARTICLES; PARTICLES; GOLD; MICELLESvisual_art.visual_art_mediumCobaltNuclear chemistry
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Heterogeneous fenton oxidation using magnesium ferrite nanoparticles for ibuprofen removal from wastewater: optimization and kinetics studies

2020

In this study, the catalytic properties of Fenton-like catalyst based on magnesium ferrite nanoparticles for IBP degradation were examined. Structural and morphological studies showed the low crystallinity and mesoporous structure for the catalyst obtained via a glycine-nitrate method. The influences of catalyst dosage, oxidant concentration, and solution pH on the pollutant degradation were investigated. The pseudo-first-order model describes kinetic data, and under optimal condition (catalyst dose of 0.5 g L-1, H2O2 concentration of 20.0 mM, and pH of 8.0), apparent rate constant reached 0.091 min-1. It was shown that Fenton reaction was mainly induced by iron atoms on the catalyst surfac…

inorganic chemicalshapetusMaterials scienceArticle SubjectKineticsNanoparticlejätevesi02 engineering and technology010501 environmental sciences01 natural sciencesCatalysisCrystallinitykatalyytitReaction rate constantT1-995General Materials ScienceTechnology (General)jäteveden käsittely0105 earth and related environmental sciencesvedenpuhdistusmagnesium ferrite ; ibuprofen removal ; fenton oxidationlääkeaineet021001 nanoscience & nanotechnologyibuprofeeniWastewaterChemical engineeringnanohiukkasetLeaching (metallurgy)0210 nano-technologyMesoporous material
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