Search results for "Spectrophotometry"

showing 10 items of 644 documents

Partitioning study of polycyclic aromatic hydrocarbons between water and some selected water-insoluble phases

2007

An investigation on the partitioning of naphthalene and phenanthrene between water and some water-insoluble phases has been carried out by Uv-vis-NIR spectrophotometry. The analysis of the experimental results emphasized the role of intermolecular interactions and structural features of the hosting phases as driving forces of the partitioning of these polycyclic aromatic hydrocarbons. The critical comparison of the resulting distribution constants allowed to evaluate the potentials of some extracting phases to set up sensitive analytical methods and/or effective environment remediation technologies.

DNA-ADDUCTSEXTRACTIONSpectroscopy Near-Infraredmedicine.diagnostic_testEnvironmental remediationChemistryMUTATIONSIntermolecular forcetechnology industry and agricultureWaterWater insolublePhenanthreneSensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundSolubilityEnvironmental chemistrySpectrophotometrySOLUBILIZATIONmedicinePolycyclic CompoundsSpectrophotometry UltravioletGeneral Environmental ScienceNaphthalene
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Comparison of conventional twist drill protocol and piezosurgery for implant insertion: an ex vivo study on different bone types.

2015

Objective The aim of this ex vivo study was to compare implant insertion procedures using piezosurgery and conventional drilling in different qualities of bone. Implant bed preparation time, generated heat, and primary implant stability were analyzed. Material and methods Fresh ex vivo porcine bone block samples (cancellous, mixed, and cortical bone) were obtained. The bone quality was quantified by ultrasound transmission velocity (UTV). Each bone sample received three implants of the same diameter using each of the techniques of piezosurgery and conventional twist drills. Time for preparation was taken and the temperature while performing the osteotomy was measured using infrared spectros…

Dental InstrumentsMaterials scienceSpectrophotometry InfraredSwinemedicine.medical_treatmentDentistryIn Vitro TechniquesOsteotomy03 medical and health sciences0302 clinical medicinemedicineAnimalsPiezosurgery030223 otorhinolaryngologyPiezosurgeryDental ImplantsDrillbusiness.industryDental Implantation Endosseous030206 dentistryDental instrumentsOsteotomyResonance frequency analysismedicine.anatomical_structureTorqueCortical boneImplantOral SurgerybusinessCancellous boneBiomedical engineeringClinical oral implants research
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Acetazolamide-M(II) [M(II) = Co(II), Ni(II), Cu(II)] complexes with ethylamine, diethylamine, triethylamine, and potassium hidroxide

1991

Abstract Complexes of Co(II), Ni(II), and Cu(II) with dideprotonated Acm are synthesized and characterized. Acm acts as bidentate ligand through the N-sulfonamido atom and the N-thiadiazole atom except for K6CoAcm4·6H2O in which Acm behaves as monodentate through the N-sulfonamido atom.

DenticityDiethylaminesPotassium CompoundsPotassiumInorganic chemistrychemistry.chemical_elementLigandsBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNickelEthylaminesHydroxidesmedicineTriethylamineDiethylamineChemistrySpectrophotometry AtomicCobaltAcetazolamideSpectrophotometryPotassiumEthylamineAcetazolamideCoppermedicine.drugJournal of Inorganic Biochemistry
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Synthetic, structural and biochemical studies of polynuclear platinum(II) complexes with heterocyclic ligands.

2008

"Non-classical" di- and trinuclear Pt(II) complexes with polydentate nitrogen ligands; ionic [(PtCl(2))(2)(tptz)(2)(mu-PtClNCPh)]Cl (1) [tptz =2,4,6-tris(2-pyridyl)-1,3,5-triazine], [(PtCl(2))(2)(bptz)(2)(mu-Pt)]Cl(2) (2) [bptz = 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine] and neutral [(PtCl(2))(2)(tptz)(2)(mu-PtCl(2))](H(2)O)(4) (3), [(PtCl(2))(2)(mu-tppz)](CHCl(3)) (4) [tppz = 2,3,5,6-tetra(2-pyridyl)pyrazine] complexes, have been prepared and structurally characterized. The neutral tptz and tppz complexes present three and two separate PtCl(2) moieties, respectively, in a cis position, presumably acting in a bifunctional mode towards DNA; the cationic tptz and bptz complexes contain monofuncti…

DenticityMagnetic Resonance SpectroscopyPyrazineSpectrophotometry InfraredStereochemistryCell SurvivalCytotoxicitychemistry.chemical_elementPlatinum CompoundsLigandsChemical synthesisPolydentate nitrogen ligandchemistry.chemical_compoundHeterocyclic CompoundsCell Line TumorDrug DiscoveryHumansBifunctionalPharmacologyMolecular StructureLigandOrganic ChemistryCationic polymerizationBiological activityGeneral MedicinechemistryPolynuclear platinum complexeSettore CHIM/03 - Chimica Generale E InorganicaPlatinumEuropean journal of medicinal chemistry
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Mononuclear Perfluoroalkyl-Heterocyclic Complexes of Pd(II): Synthesis, Structural Characterization and Antimicrobial Activity

2020

Two mononuclear Pd(II) complexes [PdCl2(pfptp)] (1) and [PdCl2(pfhtp)] (2), with ligands 2-(3-perfluoropropyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfptp) and 2-(3-perfluoroheptyl-1-methyl-1,2,4-triazole-5yl)-pyridine (pfhtp), were synthesized and structurally characterized. The two complexes showed a bidentate coordination of the ligand occurring through N atom of pyridine ring and N4 atom of 1,2,4-triazole. Both complexes showed antimicrobial activity when tested against both Gram-negative and Gram-positive bacterial strains.

Denticityperfluoroalkyl heterocyclic ligandsSpectrophotometry InfraredStereochemistryProton Magnetic Resonance SpectroscopyPharmaceutical ScienceMicrobial Sensitivity TestsSettore BIO/19 - Microbiologia GeneraleRing (chemistry)Analytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryAnti-Infective AgentsHeterocyclic CompoundsDrug DiscoveryPyridinemononuclear palladium complexesSettore BIO/06 - Anatomia Comparata E CitologiaPhysical and Theoretical ChemistrytriazolesFluorocarbonsantimicrobial activityBacteriaChemistryLigandCommunicationnarcosisOrganic ChemistrySettore CHIM/06 - Chimica OrganicaDNAAntimicrobialSettore CHIM/03 - Chimica Generale E InorganicaChemistry (miscellaneous)Molecular MedicinePalladiumPlasmidsMolecules
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Influence of the differentiation system on the analytical parameters for the spectrophotometric determination of clonazepam in urine

1991

Abstract Electronic and mathematical differentiation of the ultraviolet visible spectra were compared from the study of the analytical parameters of the direct determination of clonazepam in urine samples. Third-order derivative spectra were used. The mathematical differentiation provides higher sensitivity, a lower limit of detection, and better accuracy and precision than the electronic one. The use of a diode array instrument provides lower sensitivity than that found using a conventional spectrometer; however, the limit of detection obtained in both cases is of the same order.

Detection limitAccuracy and precisionChromatographymedicine.diagnostic_testSpectrometerChemistryAnalytical chemistryUrineDiode arrayAnalytical ChemistrySpectrophotometrymedicineSensitivity (control systems)SpectroscopyDerivative spectroscopyMicrochemical Journal
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Ionic liquid-based single-drop microextraction followed by liquid chromatography-ultraviolet spectrophotometry detection to determine typical UV filt…

2009

Abstract A user-friendly and inexpensive ionic liquid-based single-drop microextraction (IL-SDME) procedure has been developed to preconcentrate trace amounts of six typical UV filters extensively used in cosmetic products (i.e., 2-hydroxy-4-methoxybenzophenone, isoamyl 4-methoxycinnamate, 3-(4′-methylbenzylidene)camphor, 2-ethylhexyl 2-cyano-3,3-diphenylacrylate, 2-ethylhexyl 4-dimethylaminobenzoate and 2-ethylhexyl 4-methoxycinnamate) from surface water samples prior to analysis by liquid chromatography-ultraviolet spectrophotometry detection (LC-UV). A two-stage multivariate optimization approach was developed by means of a Plackett–Burman design for screening and selecting the significa…

Detection limitAnalyteChromatographyCentral composite designmedicine.diagnostic_testAnalytical chemistryRepeatabilityAnalytical Chemistrychemistry.chemical_compoundchemistryIonic strengthSpectrophotometryIonic liquidmedicineSample preparationTalanta
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High-performance liquid chromatographic determination of spironolactone and its major metabolite canrenone in urine using ultraviolet detection and c…

1994

A rapid and simple column liquid chromatographic method involving a column-switching system for the determination of spironolactone and its main metabolite canrenone in urine is described. Purification and concentration was performed using an Hypersil ODS-C18, 30 microns (20 x 2.1 mm I.D.) pre-column. The most polar urinary compounds were removed by washing the pre-column with water, and the analytes were subsequently switched to a LiChrospher RP C18, 5 microns (125 x 4 mm I.D.) analytical column and separated by means of an acetonitrile-water mobile-phase. Under the proposed conditions, the extraction efficiency was approximately 100% over the 0.5-10.0 micrograms/ml concentration range. Th…

Detection limitAnalyteChromatographyChemistryMetaboliteExtraction (chemistry)General ChemistryUrineSpironolactoneHigh-performance liquid chromatographychemistry.chemical_compoundCanrenonemedicineHumansIndicators and ReagentsSpectrophotometry UltravioletCanrenoneQuantitative analysis (chemistry)Chromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical applications
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Determination of hydroxytyrosol and tyrosol by liquid chromatography for the quality control of cosmetic products based on olive extracts

2014

An analytical method for the simultaneous determination of hydroxytyrosol and tyrosol in different types of olive extract raw materials and cosmetic cream samples has been developed. The determination was performed by liquid chromatography with UV spectrophotometric detection. Different chromatographic parameters, such as mobile phase pH and composition, oven temperature and different sample preparation variables were studied. The best chromatographic separation was obtained under the following conditions: C18 column set at 35°C and isocratic elution of a mixture ethanol: 1% acetic acid solution at pH 5 (5:95, v/v) as mobile phase pumped at 1 mL min(-1). The detection wavelength was set at …

Detection limitAnalyteChromatographyIsocratic elutionPlant ExtractsClinical BiochemistryPharmaceutical ScienceCosmeticsRepeatabilityPhenylethyl AlcoholRaw materialAnalytical ChemistryTyrosolchemistry.chemical_compoundchemistryLimit of DetectionOleaDrug DiscoveryHydroxytyrosolSpectrophotometry UltravioletSample preparationSpectroscopyChromatography LiquidJournal of Pharmaceutical and Biomedical Analysis
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