Search results for "X-ray"

showing 10 items of 4234 documents

Exchange coupling across the cyanide bridge: structural and DFT interpretation of the magnetic properties of a binuclear chromium(III) complex.

2006

The reaction of [Cr(CN)6]3− with a mixture of trans-[Cr(cyclam)(OH)2]Cl, [Cr(cyclam)(OH)Cl]Cl and [Cr(cyclam)Cl2]Cl affords the cyanide bridged dimer, trans-[HO–Cr(cyclam)–NC–Cr(CN)5]−. The tetraphenylphosphonium salt of the anion crystallizes in space group P21/n and shows a bent arrangement of the Cr1–CN–Cr2 unit with the Cr1–CN bond angle at 166.9° and CN–Cr2 at 160.32°. The Cr2–O bond, trans to the hexacyanide fragment, is very short at 1.902 A. Two dimers are held together by two hydrogen bonds connecting the Cr2–OH group of each dimer with one of the NH groups of the cyclam ligand of an adjacent molecule, leading to an almost linear configuration. These dimers of dimers get packed par…

ChromiumCyanidesChemistryHydrogen bondLigandCyanideDimerInorganic chemistryCrystallography X-RayMagnetic susceptibilityInorganic ChemistryCrystallographychemistry.chemical_compoundMagneticsMolecular geometryCyclamMoleculeDalton transactions (Cambridge, England : 2003)
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The chemistry of Cr(VI) adsorption on to poly(p-phenylenediamine) adsorbent

2019

Abstract Water pollution due to industrial processes has necessitated and spurred robust research into the development of adsorbent materials for remediation. Polyphenylenediamines (PPD) have attracted significant attention because of their dual cationic and redox properties. They are able to reduce Cr(VI) to Cr(III) in solution. Interrogation of the chemical processes involved in the Cr(VI) adsorption on para-PPD was primarily by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FT-IR) spectroscopy. It was confirmed that the underlying oxidation of the amino groups to imines during the reduction of Cr(VI) to Cr(III) was irreversible. This process occurred at both acidi…

ChromiumEnvironmental Engineering02 engineering and technologyPhenylenediamines010402 general chemistry01 natural sciencesRedoxWater PurificationAdsorptionX-ray photoelectron spectroscopySpectroscopy Fourier Transform InfraredChelationSpectroscopyWater Science and Technologychemistry.chemical_classificationAqueous solutionCationic polymerizationPolymerHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical scienceschemistryAdsorption0210 nano-technologyWater Pollutants ChemicalNuclear chemistryWater Science and Technology
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Premature aging in bone of fish from a highly polluted marine area

2015

Fish species have attracted considerable interest in studies assessing biological responses to environmental contaminants. In this study, the attention has been focussed on fishbone of selected fish species from a highly polluted marine area, Augusta Bay (Italy, Central Mediterranean) to evaluate if toxicant elements had an effect on the mineralogical structure of bones, although macroscopic deformations were not evident. In particular, an attempt was made to evaluate if bone mineral features, such as crystallinity, mineral maturity and carbonate/phosphate mineral content, determined by XR-Diffraction and FT-IR Spectroscopy, suffered negative effects due to trace element levels in fishbone,…

ChromiumMediterranean climatePremature agingAugusta Bay (Italy)XRDMineralogyAquatic ScienceOceanographyBone and Boneschemistry.chemical_compoundCalcification PhysiologicX-Ray DiffractionSpectroscopy Fourier Transform InfraredAnimalsBone mineralMaturity (geology)Body WeightWater PollutionFishesTrace elementCrystalline structure fishboneReproducibility of ResultsAging PrematureMercuryContaminationPollutionHydroxylapatiteFT-IRItalychemistryEnvironmental chemistryTrace elementEnvironmental scienceCarbonateBay
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Reduction of ferricytochrome c catalyzed by optically active chromium(III) complexes

2009

The reduction rates of horse heart ferricytochrome c by amalgamated zinc or by electrolysis at fixed potential on a mercury pool as the cathode have been measured in a buffered solution at pH 7.5 by absorption spectrophotometry. In both cases, the reaction was strongly accelerated by the presence of the optically active complexes Lambda-[Cr(III)((S,S)-promp)H(2)O](+) (H(2)promp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(S)-proline]), Delta-[Cr(III)((R,R)-alamp)H(2)O](+) (H(2)alamp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(R)-alanine]) and Lambda-[Cr(III)((S,S)-alamp)(H(2)O)(2)](+). These were shown to undergo reversible one-electron reduction to the corresponding labile chromium(…

ChromiumModels MolecularAbsorption spectroscopyInorganic chemistrychemistry.chemical_elementZinc010402 general chemistryCrystallography X-Ray01 natural sciencesMedicinal chemistryCatalysislaw.inventionCatalysisInorganic ChemistryChromiumchemistry.chemical_compoundlawElectrochemistryOrganometallic CompoundsAnimals[CHIM.COOR]Chemical Sciences/Coordination chemistryHorsesPhysical and Theoretical ChemistryMethyleneComputingMilieux_MISCELLANEOUSElectrolysisMolecular Structure010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryCytochromes cSelective catalytic reductionHeart0104 chemical sciences3. Good healthKineticschemistryCyclic voltammetryOxidation-Reduction
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Ferromagnetic coupling and magnetic anisotropy in oxalato-bridged trinuclear chromium(iii)-cobalt(ii) complexes with aromatic diimine ligands

2010

Two novel heterotrinuclear chromium(III)-cobalt(II) complexes of formula {[Cr(III)(bpy)(ox)(2)](2)Co(II)(Me(2)bpy)}.2H(2)O (1) and {[Cr(III)(phen)(ox)(2)](2)Co(II)(Me(2)bpy)}.1.5H(2)O (2) [ox = oxalato, bpy = 2,2'-bipyridine, Me(2)bpy = 6,6'-dimethyl-2,2'-bipyridine, and phen = 1,10-phenanthroline] have been synthesized using the "complex-as-ligand/complex-as-metal" strategy. The X-ray crystal structure of 2 consists of neutral oxalato-bridged Cr(III)(2)Co(II) bent entities formed by the coordination of two anionic [Cr(III)(phen)(ox)(2)](-) complexes through one of their oxalato groups toward a cationic cis-[Co(II)(Me(2)bpy)](2+) complex. The three tris(chelated), six-coordinated metal atom…

ChromiumModels MolecularOxalatesMolecular StructureChemistryStereochemistrySupramolecular chemistryStereoisomerismCobaltCrystal structureCrystallography X-RayLigandsMagnetic susceptibilityInorganic ChemistryMagneticsCrystallographyMagnetic anisotropyIntramolecular forceOrganometallic CompoundsAnisotropyAntiferromagnetismMolecular orbitalIminesDiimineDalton Trans.
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[Cr(ddpd) 2 ] 3+ : A Molecular, Water‐Soluble, Highly NIR‐Emissive Ruby Analogue

2015

Bright, long-lived emission from first-row transition-metal complexes is very challenging to achieve. Herein, we present a new strategy relying on the rational tuning of energy levels. With the aid of the large N-Cr-N bite angle of the tridentate ligand ddpd (N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine) and its strong σ-donating capabilities, a very large ligand-field splitting could be introduced in the chromium(III) complex [Cr(ddpd)2](3+), that shifts the deactivating and photoreactive (4)T2 state well above the emitting (2)E state. Prevention of back-intersystem crossing from the (2)E to the (4)T2 state enables exceptionally high near-infrared phosphorescence quantum yields a…

ChromiumSubstitution reactionSpectroscopy Near-InfraredWaterchemistry.chemical_elementGeneral ChemistryBite anglePhotochemistryCatalysisMetalFluorescence intensityChromiumWater solubleIntersystem crossingSolubilityX-Ray DiffractionchemistryCoordination Complexesvisual_artvisual_art.visual_art_mediumPhosphorescenceAngewandte Chemie International Edition
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Noninvasive evaluation of the celiac trunk and superior mesenteric artery with multislice CT in patients with chronic mesenteric ischaemia.

2008

This study sought to assess the role of multislice computed tomography (MSCT) in patients with suspected chronic mesenteric ischaemia (CMI). Forty-five patients (29 men; mean age 68) underwent MSCT angiography of the abdomen for suspected CMI (main clinical finding: postprandial abdominal pain). The scan protocol was detectors/collimation 16/0.75 mm; feed 36 mm/s; rotation time 500 ms; increment 0.4 mm; 120-150 mAs and 120 kVp. A volume of 80 ml of contrast material was administered through an antecubital vein (rate 4 ml/s), followed by 40 ml of saline (rate 4 ml/s). Images were analysed on the workstation with different algorithms (axial image scrolling, multiplanar reconstructions, maximu…

Chronic mesenteric ischaemiaAdultMalemedicine.medical_specialtychemical and pharmacologic phenomenacomplex mixturesAbdominal anginaCeliac ArteryIschemiaMesenteric Artery Superiormedicine.arteryparasitic diseasesMSCT angiographymedicineHumansRadiology Nuclear Medicine and imagingIn patientMesenterycardiovascular diseasesSuperior mesenteric arteryMSCT angiography Chronic mesenteric ischaemia Abdominal anginaAbdominal anginaNeuroradiologyAgedAged 80 and overmedicine.diagnostic_testbusiness.industryUltrasoundAngiographynutritional and metabolic diseasesInterventional radiologyGeneral MedicineMiddle Agedbacterial infections and mycosesChronic mesenteric ischaemiaTrunkdigestive system diseasessurgical procedures operativecardiovascular systemFemaleRadiologyCOMPUTED TOMOGRAPHYmedicine.symptombusinessTomography X-Ray Computedtherapeutics
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Pauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. Influence of the alkene on the regioselectivity.

2014

Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.

Ciclització (Química)EthyleneHydrocarbons FluorinatedStereochemistryNorbornadieneQuímica organometàl·licaPharmaceutical ScienceAlkynetrifluoromethylalkynesCrystallography X-RayArticlecyclopentenonesAnalytical ChemistryRing formation (Chemistry)cycloadditionslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryNorbornenechemistry.chemical_classificationPauson-Khand reactionTrifluoromethylMolecular StructureAlkenePauson–Khand reactionOrganic ChemistryRegioselectivityStereoisomerismCobaltEthylenesNorbornaneschemistryOrganometallic chemistryChemistry (miscellaneous)AlkynesregioselectivityMolecular MedicineMolecules (Basel, Switzerland)
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Detailed study of SNR G306.3–0.9 using XMM-Newton and Chandra observations

2016

Aims. We aim to study the spatial distribution of the physical and chemical properties of the X-ray emitting plasma of the supernova remnant (SNR) G306.3-0.9 in detail to obtain constraints on its ionization stage, the progenitor supernova explosion, and the age of the remnant. Methods. We used combined data from XMM-Newton and Chandra observatories to study the X-ray morphology of G306.3-0.9 in detail. A spatially resolved spectral analysis was used to obtain physical and geometrical parameters of different regions of the remnant. Spitzer infrared observations, available in the archive, were also used to constrain the progenitor supernova and study the environment in which the remnant evol…

Ciencias AstronómicasInfraredCiencias FísicasAstrophysics::High Energy Astrophysical PhenomenaISM [Infrared]FOS: Physical sciencesthermal [radiation mechanism]individual objects: SNR G306.3–0.9 [ISM]AstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics01 natural sciencesSpectral line//purl.org/becyt/ford/1 [https]ISM: individual objects: SNR G306.3IonizationISM [X-ray]0103 physical sciencesAstrophysics::Solar and Stellar AstrophysicsISM [X-rays]Radio continuum: ISMEjectaSupernova remnant010303 astronomy & astrophysicsISM: supernova remnantAstrophysics::Galaxy AstrophysicsISM: supernova remnantsPhysicsHigh Energy Astrophysical Phenomena (astro-ph.HE)Infrared: ISM010308 nuclear & particles physicssupernova remnants [ISM]Astronomy and AstrophysicsPlasma//purl.org/becyt/ford/1.3 [https]Astronomy and AstrophysicISM: individual objects: SNR G306.3–0.9ISM [Radio continuum]Radiation mechanisms: thermalX-rays: ISMindividual objects: G306.3-0.9 [ISM]Interstellar mediumAstronomíaSupernovathermal [Radiation mechanisms]Space and Planetary ScienceISM; ISM: individual objects: SNR G306.3; ISM: supernova remnants; Radiation mechanisms: thermal; Radio continuum: ISM; X-rays: ISM; Astronomy and Astrophysics; Space and Planetary Science [0.9; Infrared]0.9Astrophysics - High Energy Astrophysical PhenomenaCIENCIAS NATURALES Y EXACTAS
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SHOCK-CLOUD INTERACTION AND PARTICLE ACCELERATION IN THE SOUTHWESTERN LIMB OF SN 1006

2014

The supernova remnant SN 1006 is a powerful source of high-energy particles and evolves in a relatively tenuous and uniform environment despite interacting with an atomic cloud in its northwestern limb. The X-ray image of SN 1006 reveals an indentation in the southwestern part of the shock front and the H I maps show an isolated (southwestern) cloud, having the same velocity as the northwestern cloud, whose morphology fits perfectly in the indentation. We performed spatially resolved spectral analysis of a set of small regions in the southwestern nonthermal limb and studied the deep X-ray spectra obtained within the XMM-Newton SN 1006 Large Program. We also analyzed archive H I data, obtain…

Ciencias FísicasAstrophysics::High Energy Astrophysical PhenomenaHadronSynchrotron radiationAstrophysicsSpectral lineISM: cloudIndentationSupernova remnantISM: individual objects (SN 1006)acceleration of particleISM: supernova remnantAstrophysics::Galaxy Astrophysicsacceleration of particlesPhysicssupernova remnants X-rays: ISM [ISM]Astronomy and AstrophysicsX-rays: ISMShock (mechanics)Particle accelerationAstronomíaSpace and Planetary Scienceindividual objects: SN 1006 [ISM]clouds [ISM]CIENCIAS NATURALES Y EXACTASFermi Gamma-ray Space Telescope
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