Search results for " inorganic"

showing 10 items of 796 documents

Preparation and structural characterization of organotin(IV) complexes with ligands containing a hetero {N} atom and a hydroxy group or hydroxy and c…

2005

AbstractTwenty-two n-butyltin(IV) and t-butyltin(IV) complexes of ligands containing an –OH (–C@O) group or –OH and –COOHgroups and an aromatic {N} donor atom were prepared by metathetical reactions. On the basis of the FT-IR and Mo¨ssbauer spec-troscopic data, molecular structures were assigned to these compounds. The binding sites of the ligands were identified by means ofFT-IR spectroscopic measurements, and it was found that in most cases the organotin(IV) moiety reacts with the phenolic form ofthese ligands. In the complexes with –OH and –COOH functions, the –COOH group is coordinated to the organotin(IV) centres in amonodentate manner. The 119 Sn Mo¨ssbauer and the FT-IR studies suppor…

2-MERCAPTOPYRIDINEStereochemistryMossbauer spectroscopyMETAL COMPLEXESchemistry.chemical_elementorganotin(IV)3-HYDROXYPYRIDINEBiochemistryMedicinal chemistryInorganic Chemistry2-HYDROXYPYRIDINEGroup (periodic table)Mössbauer spectroscopyMaterials ChemistryMoietyCRYSTAL-STRUCTURERAMAN-SPECTRAPhysical and Theoretical ChemistryBinding siteFourier transform infrared spectroscopyChemistryOrganic ChemistryX-ray diffraction DICARBOXYLIC-ACIDSFT-IRMODELTrigonal bipyramidal molecular geometryTINSettore CHIM/03 - Chimica Generale E InorganicaX-ray crystallographyTinOrganotin(IV)FT-IRMössbauer spectroscopyX-ray diffractionJournal of Organometallic Chemistry
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Keggin heteropolyacid supported on BN and C3N4: Comparison between catalytic and photocatalytic alcohol dehydration

2020

The Keggin heteropolyacid (HPA), H3PW12O40 (PW12) has been supported on commercial boron nitride (BN) and two types of home prepared carbon nitride (C3N4). The supported PW12 was used in the gas-solid (photo)catalytic 2-propanol dehydration reaction to give propene at atmospheric pressure and temperatures in the range 70–120 °C and resulted more active than the pristine PW12. Reaction rate increased by increasing the temperature. Noticeably, the propene formation rate was higher by irradiating the catalytic system. The PW12/BN material resulted more active than PW12/C3N4. The acidity of the HPA cluster accounts for the catalytic role, whereas both the acidity and the redox properties of the…

2-Propanol dehydration Heteropolyacid Keggin Photocatalysis PolyoxometalateMaterials scienceInorganic chemistry02 engineering and technology01 natural sciencesRedoxCatalysisReaction ratePropenechemistry.chemical_compoundPhotocatalysi0103 physical sciences2-Propanol dehydrationGeneral Materials ScienceKegginCarbon nitride010302 applied physicsPolyoxometalateMechanical EngineeringHeteropolyacid021001 nanoscience & nanotechnologyCondensed Matter PhysicsDehydration reactionchemistrySettore CHIM/03 - Chimica Generale E InorganicaMechanics of MaterialsBoron nitridePhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technology
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Anilato-based multifunctional molecular materials

2018

En esta Tesis presentamos varias series de compuestos moleculares basados en el ligando anilato (anilato = C6O4X22- = 2,5-disustituida-3,6-dihidroxi-1,4-benzoquinona) y diferentes átomos metálicos incluyendo metales de los bloques s, p, d y f. En el capítulo uno presentamos la síntesis y caracterización de nuevas sales precursoras, basadas en el ligando anilato, con fórmula general A3[M(C6O4X2)3]; (MIII = Fe, Cr y Ga; X = Cl, Br and NO2). Hemos usado diferentes cationes A+ (A = K+, [PPh3Et]+, [PPh3Pr]+, [PBu4]+, [NBu4]+, [NHep4]+, [PPh4]+ y K+, compuestos 1-20) para estudiar el papel que juega la forma y el tamaño del catión en la estructura y simetría de las correspondientes sales. Este es…

220208 - MAGNETISMOMaterial multifuncionalPolímero de coordinación220608 - ESTRUCTURA MOLECULAROrdenamiento magnéticoSingle Molecule Magnet221005 - ELECTROQUIMICA230300 - QUIMICA INORGANICAMagnetismoTransición de espínLuminiscencia
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An experimental search for a correlation between outdoor 222Rn concentration and 210Pb activity in air particulate samples

2018

This work was aimed to search for a correlation between outdoor 222Rn air concentration and 210Pb activity in particulate samples collected on a filter. The existence of a correlation could support the hypothesis that both 222Rn and its long-lived product 210Pb are embedded into the same air masses and undergo the same air transport phenomena. Lead-210 activity was determined by means of gamma ray spectrometric measurement carried out a few days after the sampling whereas 222Rn concentration was measured through a commercial monitor. Experimental tests allowed to obtain a weak correlation between 222Rn and 210Pb air concentration as a preliminary result due to high uncertainties of outdoor …

222Rn 210Pb air filtration atmospheric particulate gamma-ray spectrometry222RnSettore ING-IND/20 - Misure E Strumentazione Nucleariair filtrationParticulates010403 inorganic & nuclear chemistry01 natural sciences0104 chemical sciencesCorrelationatmospheric particulateNuclear Energy and Engineeringgamma ray spectrometryEnvironmental chemistrylcsh:QC770-798Environmental sciencelcsh:Nuclear and particle physics. Atomic energy. RadioactivitySafety Risk Reliability and Quality210PbNuclear Technology and Radiation Protection
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A dual channel sulphur-containing a macrocycle functionalised BODIPY probe for the detection of Hg(II) in a mixed aqueous solution

2018

We report herein the synthesis and chromo-fluorogenic behaviour of a new probe 1 containing a boron-dipirromethene (BODIPY) unit electronically connected with a dithia-dioxa-aza macrocycle. Acetonitrile and water-acetonitrile 95:5 v/v solutions of the probe showed an ICT band in the visible zone and are nearly non-emissive. When acetonitrile was used as solvent, addition of Hg(II) and trivalent metal cations induced an hypsochromic shift of the absorption band and moderate emission enhancements. A highly selective response was obtained when using competitive media such as wateracetonitrile 95:5 v/v. In this case only Hg(II) induced a hypsochromic shift of the absorption band and a marked em…

:Ciências Químicas [Ciências Naturais]BodipyHeterocyclesColorimetric sensor010402 general chemistryPhotochemistry01 natural sciencesCatalysisMetalchemistry.chemical_compoundSynthesisQUIMICA ORGANICABODIPYMaterials ChemistryFluorimetric sensorDetection in aqueous solutionAcetonitrileDual channel chemosensorCrown etherchemistry.chemical_classificationAqueous solutionScience & Technology010405 organic chemistryChemistryOptical chemosensorQUIMICA INORGANICAWaterGeneral ChemistryMercuryCiências Naturais::Ciências QuímicasFluorescence3. Good health0104 chemical sciencesAbsorption bandvisual_artHg (II)Coordinationvisual_art.visual_art_mediumHypsochromic shiftfluorescenceBODIPYCrown ether
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Synthesis, Structural Analysis, Fiber Formation and Preliminary Anticancer Characterization of the Organotin Polyether from Dibutyltin Dichloride and…

2012

The organotin polyether derived from reaction of dibutyltin dichloride and 2,5-dimethyl-3-hexyne-2,5-diol was rapidly synthesized employing classical interfacial polymerization in 65% yield and a chain length of 360 units. IR results are consistent with the polyether structure. Bands characteristic of the formation of the Sn-O are present and bands characteristic of the Sn-Cl are absent. F MALDI MS results in the low mass range gives ion fragment clusters to five units. Isotopic abundance matches for tin are consistent with its presence in these ion fragment clusters. In the high mass range ion fragment clusters to greater than 300 units are found. The products offer outstanding inhibition …

AMPICILLINMALDI MSORGANOMETALLIC POLYMERSanomalous fiber formationANTIVIRAL ACTIVITYSettore CHIM/05 - Scienza E Tecnologia Dei Materiali PolimericiCONTAINING POLYMERSOrganotin polyetherCONDENSATIONtin-containing polymerF MALDI MSSettore CHIM/03 - Chimica Generale E InorganicaNORFLOXACININTERFACIAL TECHNIQUEanticancer drugdibutyltin dichlorideMATRIXPOLYESTERS25-dimethyl-3-hexyne-25-diol
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Interaction of Cd(II) and Ni(II) terpyridine complexes with model polynucleotides: A multidisciplinary approach

2016

Two metal complexes of 2,2′:6′,2′′-terpyridine (terpy), i.e. Cd(terpy)Cl2 and Ni(terpy)Cl2·3H2O, have been prepared and extensively characterized. The interaction of Cd(terpy)Cl2 with synthetic DNA models, poly(dA-dT)·poly(dA-dT) (polyAT) and poly(dG-dC)·poly(dG-dC) (polyGC), has been studied by CD, fluorescence and UV-vis electronic absorption spectroscopy at several metal/polynucleotide–phosphate ratios and for different NaCl concentrations. All the experimental results indicate an intercalative mechanism of interaction. The optimized geometry of the cadmium complex intercalated between the sixth and seventh base pairs of (AT) and (GC) dodecanucleotide duplexes, obtained by quantum mechan…

Absorption spectroscopyGeneral Chemical EngineeringInorganic chemistryIntercalation (chemistry)chemistry.chemical_element010402 general chemistry01 natural sciencesMetalchemistry.chemical_compoundDNA-bindingChemical Engineering (all)SpectroscopyDNA-binding; circular-dichroism; chelate complexes010405 organic chemistryChemistry (all)chelate complexesGeneral Chemistry0104 chemical sciencesNickelCrystallographycircular-dichroismchemistryOctahedronPolynucleotideSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumTerpyridine
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DNA-binding of zinc(II) and nickel(II) salphen-like complexes extrapolated at 1 M salt concentration: Removing the ionic strength bias in physiologic…

2020

Abstract The DNA-binding of two salphen-like metal complexes of nickel(II) (1) and zinc(II) (2) was investigated in different ionic strength solutions by absorption spectroscopy. The data analysis allowed us to obtain the values of their extrapolated DNA-binding constant in physiological conditions, with DNA-binding strength in the order Ni > Zn, and to give relative weight to the electrostatic and non-electrostatic contributions to their DNA-interaction.

Absorption spectroscopyInorganic chemistryStatic ElectricitySalt (chemistry)chemistry.chemical_elementRelative weightZincPhenylenediaminesSodium Chloride010402 general chemistry01 natural sciencesBiochemistryInorganic ChemistryMetalchemistry.chemical_compoundIonic strengthCoordination ComplexesNickelSalphenchemistry.chemical_classification010405 organic chemistryChemistrySpectrum AnalysisOsmolar ConcentrationDNA0104 chemical sciencesNickelZincIonic strengthSettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumUV–visible absorptionDNAJournal of Inorganic Biochemistry
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No change in apolipoprotein AI metabolism when subcutaneous insulin infusion is replaced by intraperitoneal insulin infusion in type 1 diabetic patie…

2006

In type 1 diabetic patients, the replacement of subcutaneous insulin infusion by intraperitoneal insulin infusion restores the normal physiological gradient between the portal vein and the peripheral circulation, which is likely to modify HDL metabolism. This stable isotope kinetic study was designed to compare HDL apolipoprotein (apo) AI metabolism in seven type 1 diabetic patients first treated by continuous subcutaneous insulin infusion by an external pump and then 3 months after the beginning of intraperitoneal insulin infusion by an implantable pump. Glycaemic control was comparable under subcutaneous and intraperitoneal insulin infusion (HbA1c=7.34+/-0.94% versus 7.24+/-1.00%, NS). HD…

AdultMalemedicine.medical_specialtyApolipoprotein Bmedicine.medical_treatmentCarbon Compounds InorganicSulfidesAdministration Cutaneouschemistry.chemical_compoundInsulin Infusion SystemsDiabetes mellitusInternal medicinemedicineHumansInsulinInfusions ParenteralPancreatic hormoneType 1 diabetesTriglyceridebiologyApolipoprotein A-Ibusiness.industryCholesterolInsulinMetabolismMiddle Agedmedicine.diseaseKineticsEndocrinologyDiabetes Mellitus Type 1chemistrybiology.proteinFemaleCardiology and Cardiovascular MedicinebusinessLipoproteins HDLAtherosclerosis
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Effect of TiO2 and Al2O3 Addition on the Performance of Chitosan/Phosphotungstic Composite Membranes for Direct Methanol Fuel Cells

2023

Composite chitosan/phosphotungstic acid (CS/PTA) with the addition of TiO2 and Al2O3 particles were synthesized to be used as proton exchange membranes in direct methanol fuel cells (DMFCs). The influence of fillers was assessed through X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, liquid uptake, ion exchange capacity and methanol permeability measurements. The addition of TiO2 particles into proton exchange membranes led to an increase in crystallinity and a decrease in liquid uptake and methanol permeability with respect to pristine CS/PTA membranes, whilst the effect of the introduction of Al2O3 particles on the characteristics of membranes is almost the op…

Al2O3; DMFC; TiO2; chitosan; hybrid membranes; inorganic filler; methanol permeability; phosphotungstic acid; power density; proton exchange membraneProcess Chemistry and TechnologyAl<sub>2</sub>O<sub>3</sub>power densityinorganic fillerFiltration and SeparationSettore ING-IND/23 - Chimica Fisica Applicataphosphotungstic acidAl2O3TiO2Chemical Engineering (miscellaneous)chitosanhybrid membranesmethanol permeabilityTiO<sub>2</sub>DMFCproton exchange membraneMembranes
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