Search results for "visual_art"

showing 10 items of 2987 documents

Studies on metal-drug complexes. Crystal structure and characterization of μ-sulfato bromazepam copper(II) complex

1987

Abstract The compound Cu(Bromazepam) SO 4 having been synthesized, its crystal structure shows distorted octahedral environment for the Copper(II) ion. Because of the long Cu-O(4) length (2.90 A), we can consider that there is a semicoordinative interaction with the sulfate group acting as tridentate bridging ligand. The structure is a polymeric chain where dimeric units are linked by the oxygen (C-O(5)) atom of the Bromazepam carbonyl group. The drug consequently acts as a tridentate ligand in this compound. The magnetic results show a very weak antiferromagnetic interaction.

chemistry.chemical_classificationBromazepamChemistryStereochemistrychemistry.chemical_elementBridging ligandCrystal structureBiochemistryCopperInorganic ChemistryMetalCrystallographyOctahedronvisual_artmedicinevisual_art.visual_art_mediumMoleculeInorganic compoundmedicine.drugJournal of Inorganic Biochemistry
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Synthesis and structural studies on Ni(II) dithiocarbamates : Exploring intramolecular Ni···H-C interactions

2017

Abstract Five new Ni(II) dithiocarbamates with NiS4, NiS2PN and NiS2PCl coordination spheres, viz. [Ni(bupmbzdtc)2] (1), [Ni(bupmbzdtc)(PPh3)(NCS)] (2), [Ni(bupmbzdtc)(PPh3)Cl] (3), [Ni(4-dpmpzdtc)(PPh3)Cl] (4) and [Ni(pbbzbudtc)(PPh3)(NCS)] (5), where bupmbzdtc = N-butyl(p-methylbenzyl)dithiocarbamato anion, 4-dpmpzdtc = 4-(diphenylmethyl)piperazinecarbodithioato anion, pbbzbudtc = N-(p-bromobenzyl)butyl-dithiocarbamato anion and PPh3 = triphenylphosphine, were synthesized and characterized by UV, IR, NMR and single crystal X-ray diffraction methods. Spectral results suggest a square planar geometry around the Ni(II) metal center for all the synthesized complexes. Single crystal X-ray stru…

chemistry.chemical_classificationC-H···Ni interaction010405 organic chemistryChemistryInorganic chemistrySolid-state010402 general chemistry01 natural sciencesNMR0104 chemical sciencesIonInorganic ChemistryMetalCrystallographydithiocarbamateIntramolecular forcevisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryDithiocarbamateX-ray structural analysisSingle crystalta116Polyhedron
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Anodic stripping voltammetric determination of heavy metals in solutions containing humic acids

1994

Various simultaneous effects of humic acids on the current and potential of differential pulse anodic stripping peaks of copper, lead, cadmium and zinc in weakly alkaline and acidic (pH 2) solutions have been investigated and interpreted with regard to metal complexation and the adsorption of humic acid on the mercury electrode. The applicability of the standard additions method for metal quantitation and the experimental conditions for UV-photolysis with a high-pressure mercury lamp have been examined in model as well as real water samples.

chemistry.chemical_classificationCadmiumInorganic chemistrychemistry.chemical_elementZincDropping mercury electrodeBiochemistryAnalytical ChemistryMercury (element)MetalAnodic stripping voltammetryAdsorptionchemistryvisual_artvisual_art.visual_art_mediumHumic acidFresenius' Journal of Analytical Chemistry
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Effect of ethylenediamine on the anodic stripping voltammetric determination of heavy metals in the presence of humic acid

1994

Ligand competition coupled with differential pulse anodic stripping voltammetry has been investigated for the determination of copper, lead and cadmium. Ethylenediamine displaces humic acid in its metal complexes forming kinetically labile compounds. It also eliminates interferences associated with the oxidation of copper. This enhances the sensitivity of the determination of the metals over a wide range of humic acid concentration (up to 30 mg/l). The procedure has been applied to the determination of heavy metals in a real water sample.

chemistry.chemical_classificationCadmiumStripping (chemistry)LigandInorganic chemistrychemistry.chemical_elementEthylenediaminecomplex mixturesBiochemistryCopperAnalytical ChemistryMetalAnodic stripping voltammetrychemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumHumic acidFresenius' Journal of Analytical Chemistry
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Sulfide mineral identification using laser-induced plasma spectroscopy

2003

Sulfide minerals in rock samples were identified with laser-induced plasma spectroscopy (LIPS) in the near vacuum ultraviolet spectral region. Reference spectra of pyrite, pyrrhotite, chalcopyrite, sphalerite, barite, calcite and dolomite were applied to classification of minerals in sulfur-bearing drill core samples. On the basis of the results mineral distributions in the sample were estimated. The potential of the LIPS method for in situ analysis is discussed.

chemistry.chemical_classificationCalciteMaterials scienceMineralSulfideChalcopyriteMechanical EngineeringMineralogyGeneral Chemistryengineering.materialGeotechnical Engineering and Engineering GeologySulfide mineralschemistry.chemical_compoundSphaleritechemistryControl and Systems Engineeringvisual_artengineeringvisual_art.visual_art_mediumPyritePyrrhotiteMinerals Engineering
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Effects of organic matter complexation on partitioning of transition metals into calcite: Cave-analogue crystal growth experiments

2022

We highlight the potential for first row transition metals to carry paleohydrological signals in speleothems, and argue that these metals constitute valuable proxies for climate reconstructions. Metal availability to speleothems is hypothesised to be restricted by organic complexation, which strongly limits the free ion activity of transition metals (Co2+, Ni2+ and Cu2+) in dripwater, thereby creating a kinetic overprint on metal concentrations and isotope ratios in speleothem calcite. This study presents the results of the first cave-analogue experiments of transition metal partitioning into calcite in the absence and presence of organic ligands. The Geological Microclimate (GeoMic) system…

chemistry.chemical_classificationCalcitegeographyAqueous solutiongeography.geographical_feature_categoryInorganic chemistryNitrilotriacetic acidSpeleothemF800Metalchemistry.chemical_compoundchemistryTransition metalGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumOrganic matterChelation
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Stabilization of immobilized cell systems using a modified metal surface, fructose polymer levan and a high cell concentration

1998

chemistry.chemical_classificationCellFructoseCell concentrationPolymerMetalchemistry.chemical_compoundmedicine.anatomical_structurechemistryChemical engineeringvisual_artvisual_art.visual_art_mediummedicineOrganic chemistry
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A chalcone-based highly selective and sensitive chromofluorogenic probe for trivalent metal cations

2015

[EN] Anew chalcone-based probe for the chromofluorogenic sens-ing of trivalent (Al3 +,Fe3+,Cr3+,Ga3+,In3+and As3 +)overmono-and divalent cationsand anionsisreported. In the presence of trivalent metal cations,the probe was able to displayaremarkable color change from yellow to colorless that wasclearly visible to the naked eye. Also, the initial strongyellowemission was gradually quenched and substituted by aweaklyshifted band.

chemistry.chemical_classificationChalconeQUIMICA INORGANICAGeneral ChemistryHighly selectivePhotochemistrysensorstrivalent cationsDivalentchalcone-based probeMetalchemistry.chemical_compoundchromofluorogenic sensingQUIMICA ORGANICAchemistryvisual_artQUIMICA ANALITICAvisual_art.visual_art_mediumNaked eyeanions
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Alkyl Complexes of Group 4 Metals Containing a Tridentate-Linked Amido−Cyclopentadienyl Ligand:  Synthesis, Structure, and Reactivity Including Ethyl…

1998

A series of group 4 metal complexes M(η5:η1:η1-C5Me4SiMe2NCH2CH2X)R2 (M = Ti; R = Me, CH2Ph; M = Zr, Hf; R = Me, Et, nPr, nBu, CH2Ph, CH2SiMe3, Ph) containing the tridentate-linked amido−tetramethy...

chemistry.chemical_classificationChemistryLigandOrganic ChemistryMedicinal chemistryCatalysisInorganic ChemistryMetalCyclopentadienyl complexEthylene polymerizationGroup (periodic table)visual_artvisual_art.visual_art_mediumOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryAlkylOrganometallics
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Cation and anion recognition characteristics of open-chain polyamines containing ethylenic and propylenic chains

2002

Abstract The interaction of the polyamines 4,7,10,13-tetraazahexadecane-1,16-diamine (L1) and 4,7,10-triazatridecane-1,13-diamine (L2) with H + , Cu 2+ , Zn 2+ , Co 2+ and the nucleotides ATP, ADP and AMP has been followed by NMR and potentiometric studies performed at 298.1 K in 0.15 mol dm −3 NaClO 4 . The influence of the different sequences of hydrocarbon chains and chelate rings present in the ligands on the values of the protonation constants, the stability of the metal ion complexes as well as in the co-ordination to nucleotides is analysed. The formation of mixed complexes has been investigated for the system Cu 2+ –L1–AMP.

chemistry.chemical_classificationChemistryPotentiometric titrationInorganic chemistryProtonationMedicinal chemistryIonInorganic ChemistryMetalHydrocarbonvisual_artMoleMaterials Chemistryvisual_art.visual_art_mediumChelationNucleotidePhysical and Theoretical ChemistryInorganica Chimica Acta
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