Search results for "Infrared"

showing 10 items of 2110 documents

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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Collisional Broadening of Rotational Lines in the Stimulated Raman Pentad Q-Branch of CD4

1992

Self- and argon-broadening coefficients are reported for a number of Raman Q-branch transitions in the nu(1) and nu(2) + nu(4) bands of (C-12)D4 at room temperature (296 K). The coefficients display a variation with j and with C exp n (symmetry species A, E, F) that is essentially independent of collision partner and which is similar to the j- and C exp n-dependence found in previous measurements of the IR line-broadening coefficients. The rotationally inelastic collision rates previously measured by Foy et al. (1988) for (C-13)D4 (V4 = 0, 1) in collision with (C-13)D4 or Ar account for only a part of the Raman broadening rate, suggesting possibly significant contributions to the linewidths…

DephasingInelastic collision02 engineering and technologyLORENTZ WIDTH01 natural sciencesLOW-TEMPERATURESSpectral linesymbols.namesakeNuclear magnetic resonance0103 physical sciencesSPECTRAStimulated ramanPhysicsTUNABLE-DIODE-LASERRadiationSPECTROSCOPY010304 chemical physicsINFRARED DOUBLE-RESONANCESpectral bands021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsSymmetry (physics)METHANE LINESCM-1 REGIONsymbolsSHIFT COEFFICIENTSAtomic physics0210 nano-technologyRaman spectroscopyENERGY-TRANSFER
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Flow injection near-infrared determination of ethanol in chloroform

1995

A simple and direct flow injection (FIA) procedure has been developed for the determination of the stabilizing agent ethanol in chloroform samples. The procedure is based on the use of the absorbance band of ethanol in the near-infrared (NIR) region at 2272 nm, measured in front of a reference sample of chloroform stabilized with amylene. The method developed provides a limit of detection of 0.0045% (v/v) and a dynamic range until 10% (v/v) with a typical variation coefficient of 0.4% for six independent analysis of a real sample containing approximately 1% (v/v) of ethanol. The sample injection frequency allowed by the method is 78 h−1.

Detection limitAbsorbancechemistry.chemical_compoundEthanolChloroformchemistryReference sampleNear-infrared spectroscopyAnalytical chemistryAlcoholBiochemistryDirect flowFresenius' Journal of Analytical Chemistry
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First‐Derivative Fourier‐Transform Infrared Determination of Oxadiazon in Commercial Herbicide Formulations

2008

Abstract A Fourier‐transform infrared (FTIR) method has been developed for the quantification of oxadiazon in herbicide formulations. The method involves the extraction of the active ingredient by sonication of the samples with CHCl3 and direct measurement of the peak area values in first‐order derivate spectra from 1770 cm−1 to 1774 cm−1 corrected with a baseline point located at 1950 cm−1 and after a 5‐point smoothing. A limit of detection (3 s) of 0.03 mg g−1 and a typical relative standard deviation (RSD) of 1.3% were found. Results obtained were comparable with those found by liquid chromatography with UV detection. The proposed method involves a 7‐times reduction in solvent consumptio…

Detection limitActive ingredientChromatographyChemistrySonicationExtraction (chemistry)Analytical chemistryAtomic and Molecular Physics and OpticsAnalytical ChemistrySolventsymbols.namesakeFourier transformsymbolsFourier transform infrared spectroscopySpectroscopySmoothingSpectroscopy Letters
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Determination of nitrogen in hydrolyzed protein formulations by continuous vapour phase FTIR.

2006

An on-line system with vapour generation (VG) and Fourier transform infrared (FTIR) spectrometric detection has been developed for the determination of free ammonium and organic nitrogen in agrochemical formulations containing hydrolyzed proteins. Commercial samples were digested, in batch mode, with sulphuric acid and the obtained solution was alkalinized on-line to transform the NH(4)(+) to NH(3) that was continuously monitored by FTIR. Free ammonium was determined in the same system after simple dilution of undigested samples with water. Different gas phase separators were assayed in order to introduce gaseous NH(3) into a home made IR gas cell of 10 cm pathlength, where the correspondin…

Detection limitAmmoniachemistry.chemical_compoundHydrolyzed proteinchemistryAnalytical chemistryInfrared spectroscopychemistry.chemical_elementAmmoniumFourier transform infrared spectroscopyNitrogenFourier transform spectroscopyAnalytical ChemistryTalanta
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Flow-injection determination of water in organic solvents by near-infrared spectrometry

1993

Abstract A flow-injection (FI) procedure was developed for the direct determination of water in organic solvents by using the O-H stretch absorbance band of water in the near-infrared (NIR) region. Dichloromethane was employed as a test solvent to study the influence of the flow parameters (carrier flow and sample injection volume) and time interval on the sensitivity and repeatability of the FI-NIR measurements. The developed procedure permits the determination of water in dichloromethane and isobutyl methyl ketone samples with limits of detection of 0.01 and 0.005% (v/v), respectively. Real and spiked samples of solvents were analysed by FI-NIR and accurate results were found. The method …

Detection limitAnalytical chemistryInfrared spectroscopyRepeatabilityContaminationBiochemistryAnalytical ChemistrySolventAbsorbancechemistry.chemical_compoundchemistryEnvironmental ChemistryWater contentSpectroscopyDichloromethaneAnalytica Chimica Acta
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Determination of carbonates in waters by on-line vapor generation FTIR

1998

Abstract An electrically heated gas-permeation unit (GPU) has been employed for the vapor-generation Fourier transform infrared (FTIR) determination of total carbonate in waters. The developed method is based on the simultaneous injection of 100 μ l sample and 100 μ l nitric acid in a two-channel manifold with a merging zone, which provides the generation of CO 2 through the GPU, heated at 90°C, from which CO 2 is swept by a stream of N 2 to a long-path infrared gas cell. Absorbance measurements were made in the range from 2500 to 2150 cm −1 and the corresponding flow injection recordings were obtained as a function of time. The areas of these peaks are interpolated in a calibration equatio…

Detection limitAqueous solutionChemistryInfraredAnalytical chemistryAbsorbancechemistry.chemical_compoundsymbols.namesakeFourier transformNitric acidCalibrationsymbolsFourier transform infrared spectroscopySpectroscopyVibrational Spectroscopy
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Fourier-transform infrared determination of nicotine in tobacco samples by transmittance measurements after leaching with CHCl3

1998

Abstract A new procedure is proposed for the FT-IR spectrometric determination of nicotine in tobacco. The method is based on the extraction of nicotine in CHCl 3 from tobacco samples, wetted with an aqueous solution of NH 3 (0.1 M), and the measurement of absorbance in the stopped-flow mode at 1316 cm −1 , using a spectral baseline correction established from 1334 to 1300 cm −1 . The procedure developed does not requires a complex sample preparation, and provides a limit of detection of 0.045 mg ml −1 nicotine, a sampling frequency of 3.3 h −1 and a coefficient of variation of 0.3% for five independent measurements of a tobacco sample with a nicotine content of 1.5% w/w. The accuracy of th…

Detection limitAqueous solutionChromatographyChemistryCoefficient of variationExtraction (chemistry)Analytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryAbsorbanceNicotinemedicineEnvironmental ChemistrySample preparationSpectroscopymedicine.drugAnalytica Chimica Acta
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The volatile inventory (F, Cl, Br, S, C) of magmatic apatite: An integrated analytical approach

2012

Abstract Apatite is ubiquitous in a wide range of magmatic rocks and its F–Cl–Br–S systematics can be used to decipher e.g., mixing processes within a magmatic complex and may give insights into fluid un-mixing and degassing processes during the emplacement and cooling of plutonic rocks. In this study, we analyzed a F-apatite (Durango, Mexico), a Cl-apatite (Odegarden, Norway) and apatites from five plutonic samples from the alkaline Mt. Saint Hilaire Complex (Canada) by means of Electron Microprobe Analysis (EPMA), Laser Ablation ICP-MS (LA-ICP-MS), Secondary Ion Mass Spectrometry (SIMS), pyrohydrolysis combined with ion chromatography, Fourier Transformed Infrared Spectroscopy (FTIR), Ins…

Detection limitBromineChemistryAnalytical chemistryInfrared spectroscopychemistry.chemical_elementGeologyElectron microprobeApatiteSecondary ion mass spectrometryGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumFourier transform infrared spectroscopyNeutron activation analysisChemical Geology
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Multicommutation Fourier transform infrared determination of benzene in gasoline

2004

A fully mechanized method to determine benzene in motor gasolines has been developed based on the use of Fourier transform infrared spectroscopy (FT-IR) and multicommutation. The flow network comprised a set of three-way solenoid valves and was controlled by means of a microcomputer furnished with an electronic interface and running by a software written in QUICK BASIC 4.5. The flow network and control software were designed to implement the multicommutation approach providing facilities to handle sample and reagent solutions, so that, sample dilution, external calibration and standard addition could be easily performed on-line. The method permits the direct determination of benzene without…

Detection limitChemistryDirect methodAnalytical chemistryInfrared spectroscopyBiochemistryFourier transform spectroscopyAnalytical Chemistrysymbols.namesakeFourier transformStandard additionsymbolsEnvironmental ChemistryGasolineFourier transform infrared spectroscopySpectroscopyAnalytica Chimica Acta
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