Search results for "Ft-IR"

showing 10 items of 48 documents

Caratterizzazione di sostanza organica disciolta mediante rilassometria NMR in modalità fast field cycling

2009

Settore AGR/13 - Chimica AgrariaNMR NMRD FT-IR DOM
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Synthesis, Characterization and in vitro antimicrobial activity of dialkyltin(IV)bis(fusidate) complexes.

2008

The complexation of one steroid antibiotic of the fusidane family, sodium fusidate [sodium 2-16-acetyloxy-3,11-dihydroxy-4,8,10,14-tetramethyl-2,3,4,5,6,7,9,11,12, 13,15,16-dodeca hydro-1H-cyclopenta[a]phenanthren-7-ylidene)-6-methyl-hept-5-enoate = (Nafus)], by dialkyltin(IV) has been studied by conventional technique as FT-IR, Mössbauer and NMR spectroscopies. Analytical data supported the general formula Alk2Sn(IV)fus2 (Alk = Me, Bu). Infrared spectral data of the complexes imply the presence of both uni- and bidentate, ester-type and bridging carboxylate group, respectively. On the basis of FT-IR and 119Sn Mössbauer spectroscopy, in both Me2Sn(IV)fus2 and Bu2Sn(IV)fus2, trigonal bipyram…

Settore CHIM/03 - Chimica Generale E InorganicaDialkyltin(IV) FT-IR Mössbauer NMR antimicrobial tests
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Organotin(IV)derivatives neurotoxicity and their modulation by Baclofen

2008

Several new diorganotin(IV) and triorganotin(IV) complexes with 4-amino-3- (4-chloro phenyl)]-butanoic acid ( = Baclofen) have been synthesized and their structure investigated both in the solid state and in solution phase through spectroscopic methods (FT-IR, Mössbauer, 1H and 13C NMR). According to experimental analytical data, the stoichiometry of the complexes has been proposed as R2SnBac2 and R3SnBac, respectively for diorganotin(IV) and triorganotin(IV) baclofen complexes. (Baclofen = HBac; R = Me, Bu, Ph).

Settore CHIM/03 - Chimica Generale E InorganicaOrganotin(IV) Baclofen Mossbauer FT-IR NMR
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Study of Confined 5-Aza[5]helicene in Ytterbium(III) Bis(2-ethylhexyl) Sulfosuccinate Reversed Micelles

2007

Some relevant physicochemical properties of 5-aza[5]helicene (H5) in solutions of ytterbium bis(2-ethylhexyl) sulfosuccinate (Yb(DEHSS)3) reversed micelles have been investigated by UV-vis-NIR, photoluminescence, and FT-IR techniques with the aim of emphasizing the role played by specific Yb(III)/H5 interactions and confinement effects as driving forces of its binding to reversed micelles, preferential solubilization site, and local photophysical properties. It has been found that the binding strength of 5-aza[5]helicene to reversed micelles, triggered by steric and orientational constrains as well as the water content, is mainly regulated by its interaction with the Yb(III) counterion. Mor…

Steric effectsYtterbiumPhotoluminescencechemistry.chemical_elementLIQUID-CRYSTALSPhotochemistryHeterocyclic Compounds 4 or More RingsMicellechemistry.chemical_compoundSpectroscopy Fourier Transform InfraredMaterials ChemistryWATEROrganic chemistryAOTYtterbiumPhysical and Theoretical ChemistryMicelleschemistry.chemical_classificationAza CompoundsSpectroscopy Near-InfraredCHIROPTICAL PROPERTIESSuccinatesSOLID-SOLID REACTIONSTATESurfaces Coatings and FilmsFT-IRSODIUM BIS(2-ETHYLHEXYL)SULFOSUCCINATEchemistryHeliceneSolubilizationSOLUBILIZATIONLUMINESCENCESpectrophotometry UltravioletCounterionThe Journal of Physical Chemistry B
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Adsorption of dissolved organic matter on clay minerals as assessed by infra-red, CPMAS 13C NMR spectroscopy and low field T1 NMR relaxometry

2011

Abstract Dissolved organic matter (DOM) is a very important environmental constituent due to its role in controlling factors for soil formation, mineral weathering and pollutant transport in the environment. Prediction of DOM physical–chemical properties is achieved by studying its chemical structure and spatial conformation. In the present study, dissolved organic matter extracted from compost obtained from the organic fraction of urban wastes (DOM-P) has been analysed by FT-IR, CPMAS 13C NMR spectroscopy and 1H T1 NMR relaxometry with fast field cycling (FFC) setup. While the first two spectroscopic techniques revealed the chemical changes of dissolved organic matter after adsorption eith…

T1 NMR relaxometryRelaxometryMineralCompostDOM; CPMAS 13C NMR; T1 NMR relaxometrySettore AGR/13 - Chimica Agrariaengineering.materialFT-IRchemistry.chemical_compoundMontmorilloniteAdsorptionchemistryGeochemistry and PetrologyEnvironmental chemistryDissolved organic carbonCPMAS 13C NMRengineeringOrganic chemistryKaoliniteDissolved organic matterRelaxometryClay mineralsDOMOrganic Geochemistry
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Insights into grafting of (3-Mercaptopropyl) trimethoxy silane on halloysite nanotubes surface

2020

Abstract Functionalization of halloysite nanotubes surface by using organosilanes is sensitive to the reaction conditions. Halloysite nanotubes (HNTs) were modified using (3-Mercaptopropyl) trimethoxy silane (MPTMS). The experiments were performed under different reaction conditions including, various solvents [Toluene, Tetrahydrofuran (THF), Ethanol, n-Hexane, 1,4 Dioxane and Acetonitrile], water content in the reaction media, volume of solvent, number of moles of silane and catalysts (triethyl amine, ammonia solution and tetra-ethoxy titanium). The elemental analysis, FT-IR analysis were used to identify the samples, which attained the highest percent of functionalization. SEM image and t…

Thermogravimetric analysisengineering.material010402 general chemistry01 natural sciencesBiochemistryHalloysiteOrganosilanesCatalysisInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryAcetonitrileTetrahydrofuranGrafting010405 organic chemistryOrganic ChemistryHalloysiteThermogravimetric analysisSilane0104 chemical sciencesFT-IRSolventchemistryChemical engineeringSEMNanoclayengineeringSurface modificationJournal of Organometallic Chemistry
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A new biodegradable and biocompatible hydrogel with polyaminoacid structure

2007

The preparation and physicochemical and biological characterization of a novel polyaminoacid hydrogel have been reported. The ,-poly(N-2- hydroxyethyl)-dl-aspartamide (PHEA) has been used as a starting polymer for a derivatization reaction with methacrylic anhydride (MA) to give rise to the methacrylate derivative named PHM. Photocrosslinking of PHM has been performed in aqueous solution at 313 nm and in the absence of toxic initiators. PHM-based hydrogel has been characterized by scanning electron microscopy, X-ray diffractometry, swelling measurements in aqueous media; the degradation of PHM-based hydrogel has been evaluated as a function of time in the absence or in the presence of ester…

Time FactorsBiocompatibilityCell SurvivalSurface PropertiesChemistry PharmaceuticalPharmaceutical ScienceMethacrylic anhydrideBiocompatible MaterialsMicroscopy Atomic ForceMethacrylateDosage formchemistry.chemical_compoundPolymethacrylic AcidsX-Ray DiffractionSpectroscopy Fourier Transform InfraredPolymer chemistryHumansTechnology PharmaceuticalDrug CarriersAqueous solutionHydrolysisEsterasestechnology industry and agricultureWaterHydrogelshydrogels FT-IRBlood ProteinschemistrySelf-healing hydrogelsDrug deliveryMicroscopy Electron ScanningK562 CellsPeptidesDrug carrierPorosityProtein BindingNuclear chemistryInternational Journal of Pharmaceutics
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Differences of stabilized organic carbon fractions and microbiological activity along Mediterranean Vertisols and Alfisols profiles

2010

This study examined the chemical and structural properties of humic substances and microbiological activity in order to verify differences in carbon dynamics along soil profiles in two Vertisols (Typic Haploxerert and Xeric Epiaquert) and two Alfisols (Mollic Haploxeralf and Ultic Haploxeralf) developed under Mediterranean climate in Italy. Humification parameters, thermal methods, including differential scanning calorimetry (DSC) and thermogravimetry (TG), together with Fourier transform infrared (FT-IR) and fluorescence spectroscopies were used to characterize humic acids (HA). Microbiological activity of soils was assessed by basal respiration, metabolic quotient (qCO2) and Cmic:Corg rat…

Total organic carbonChemistrySoil ScienceMineralogyVertisolHumusThermogravimetrySettore AGR/14 - PedologiaSoil pHEnvironmental chemistrySoil waterAlfisolSoil horizonVertisols Alfisols Microbial indices DSC TG FT-IR Fluorescence spectra Humic acidsGeoderma
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MULTIDISCIPLINARY STUDY FOR THE DATING AND THE RESTORATION OF THE SAN VITO WOODEN PULPIT OF MUSEO DIOCESANO OF PALERMO

2017

The aim of the present research is to investigate the execution techniques of San Vito wooden pulpit in the Museo Diocesano of Palermo and to provide helpful information to dating it in addition to technical, historical and artistic evaluations. In particular, this paper describes the application of analytical techniques (imaging diagnostics techniques, Scanning Electron Microscopy coupled with X-ray Energy Dispersive spectroscopy Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy and Fourier Transform Infrared Spectroscopy) to better understand the pulpit characteristics, both support and decoration, useful to plan and perform the correct restoration.

Wooden pulpit SEM-EDS FT-IR spectroscopy Museo Diocesano of Palermo
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Preparation and XAFS studies of organotin(IV) complexes with adenosine and related compounds and calf thymus DNA

2007

Complexes of adenosine and related compounds (adenosine-5’-monophosphate, adenosine-5’-triphosphate and pyridoxal-5-phosphate) with Bu2SnO and/or BuSnCl2 were prepared in the solid state. The compositions of the complexes were determined by standard analytical methods. It was found that the complexes contain the organotin(IV) moiety and the ligand in a ratio of 1:1. The FT-IR spectra demonstrated that Bu2SnO reacts with the D-ribose moiety of the ligands, while Bu2SnCl2 is coordinated to the deprotonated phosphate group. The basic part of the ligands does not participate directly in complex formation. Comparison of the experimental Mossbauer Δ (quadrupole splitting) values with those calcul…

XAFS organotin(IV) DNA Mossbauer FT-IRExtended X-ray absorption fine structureChemistryLigandStereochemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthQuadrupole splittingPollutionMedicinal chemistryAnalytical ChemistryX-ray absorption fine structureBond lengthDeprotonationNuclear Energy and EngineeringSettore CHIM/03 - Chimica Generale E InorganicaMössbauer spectroscopyMoietyRadiology Nuclear Medicine and imagingSpectroscopyJournal of Radioanalytical and Nuclear Chemistry
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