Search results for "Fourier Transform Infrared"

showing 10 items of 598 documents

FT-IR spectroscopic investigation of bacterial cell envelopes from Zymomonas mobilis which have different surface hydrophobicities

2013

Abstract Changes in the cell envelope composition of bacteria Zymomonas mobilis 113S which resulted in varied cell surface hydrophobicity (CSH) were examined using FT-IR-spectroscopy and conventional methods of biochemical analysis. Significant differences in all analyses were detected between hydrophilic and hydrophobic compounds in the envelopes of Z. mobilis . A significant positive linear relationship ( P Z. mobilis and the ratio of absorbance band intensities assigned to the CH 2 and CH 3 vibrations from lipids as well as the asymmetric and symmetric stretching vibrations of these methylene and methyl groups. Differences were also seen between the ratio of band absorbances arising from…

chemistry.chemical_classificationbiologyStereochemistrybiology.organism_classificationZymomonas mobilisAbsorbancechemistry.chemical_compoundCrystallographychemistryAmideCell envelopeMethyleneFourier transform infrared spectroscopySpectroscopySpectroscopyAlkylVibrational Spectroscopy
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FTIR TENTATIVE CHARACTERIZATION OF HUMIC ACIDS EXTRACTED FROM ORGANIC MATERIALS

2001

Turkish humic acids, extracted from different materials, were characterized by their infrared spectra and by means of acidity measurements. The information obtained is of great interest to ascertain the nature and origin of humic acid samples.

chemistry.chemical_classificationchemistryInorganic chemistryHumic acidInfrared spectroscopyFourier transform infrared spectroscopycomplex mixturesSpectroscopyAtomic and Molecular Physics and OpticsAnalytical ChemistryCharacterization (materials science)Spectroscopy Letters
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MbCO embedded in trehalosyldextrin matrices: thermal effects and protein-matrix coupling

2010

Saccharide-based biopreservation is widely studied because of its scientific importance and possible technological outcomes for food and pharmaceutical industries. Ternary protein/saccharide/water systems have been extensively exploited to model the characteristics of the in vivo biopreservation process. A tight, water dependent, protein–matrix coupling has been shown to occur in various simple saccharide amorphous matrices, which is stronger in trehalose. The efficiency as bioprotectant of trehalose has been ascribed to this tight coupling, since the appearance of damages on biological structures will more involve structural variations of the surrounding matrix. Here we present, as an appl…

chemistry.chemical_classificationdenaturationBiophysicsInfrared spectroscopyTrehaloseBioengineeringApplied Microbiology and BiotechnologyTrehaloseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Analytical ChemistryAmorphous solidchemistry.chemical_compoundMatrix (mathematics)chemistryChemical engineeringOrganic chemistryDenaturation (biochemistry)DextrinFourier transform infrared spectroscopyTernary operationMbCOdextrinInfrared spectroscopyFood ScienceSettore CHIM/02 - Chimica Fisica
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H-NMR and FT-IR study of the state of melatonin confined in membrane models: location and interactions of melatonin in water free lecithin and AOT re…

2004

The state of melatonin confined either in dry lecithin or bis(2-ethylhexyl) sulfosuccinate sodium salt (AOT) reversed micelles has been investigated by H-NMR and FT-IR spectroscopies as a function of the melatonin to surfactant molar ratio (R). The analysis of experimental results leads to hypothesize that, independently of R and the surfactant nature and as a consequence of anisotropic melatonin/surfactant interactions, melatonin is totally solubilized in reversed micelles and mainly located by opportune orientation in the nanodomain constituted by the surfactant head groups. The absence of significant spectral changes related to the protons linked to the first carbon atoms of surfactant a…

chemistry.chemical_classificationendocrine systemfood.ingredientOrganic ChemistryPhotochemistryMicelleLecithinlcsh:QD241-441MelatoninfoodMembranelcsh:Organic chemistrychemistryPulmonary surfactantmedicineProton NMRFourier transform infrared spectroscopyhormones hormone substitutes and hormone antagonistsAlkylmedicine.drugArkivoc
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NMR and Infrared Spectroscopies of C-S-H and Al-Substituted C-S-H Synthesised in Alkaline Solutions

1998

(C,N)-(S,A)-H samples have been synthesised from mixes of different CaO/SiO2 and AI(OH)3/SiO2 ratios in stirred suspensions in more or less concentrated soda solutions. The stoichiometry and spectroscopic characteristics of samples have been studied by FTIR, 27A1 and 29Si MAS NMR spectroscopies. The structural changes induced by substitutions have been discussed on the basis of the dreiketten structure of the tobermorite silicate chains.

chemistry.chemical_compoundCrystallographychemistryInfraredTobermoriteFourier transform infrared spectroscopySilicateStoichiometry
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Simple New Method for the Preparation of La(IO<sub>3</sub>)<sub>3</sub> Nanoparticles

2020

We present a cost- and time-efficient method for the controlled preparation of single phase La(IO3)3 nanoparticles via a simple soft-chemical route which takes a matter of hours, thereby providing an alternative to the common hydrothermal method which takes days. Nanoparticles of pure α-La(IO3)3 and pure δ-La(IO3)3 were synthesised via the new method depending on the source of iodate ions, thereby demonstrating the versatility of the synthesis route. The crystal structure, nanoparticle size-dispersal and chemical composition were characterised via angle- and energy-dispersive powder X-ray diffraction, scanning electron microscopy and Fourier-transform infrared spectrosco…

chemistry.chemical_compoundMaterials sciencechemistryChemical engineeringScanning electron microscopeInfrared spectroscopyNanoparticleCrystal structureFourier transform infrared spectroscopyIodateHydrothermal circulationIon
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Non-covalent graphene nanobuds from mono- and tripodal binding motifs.

2017

Graphene nanobuds were prepared via the non-covalent anchoring of C60-based molecules endowed with one or three pyrene units, respectively. TGA, FTIR, UV-Vis and TEM investigations confirmed the formation of nanohybrids. For the two molecular derivatives, striking differences were determined in their interaction with graphene or carbon surfaces by Raman, cyclic voltammetry and molecular mechanics calculations, revealing the important role of pyrene adsorption in modulating the electronic properties of the nanohybrids.

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysislaw.inventionsymbols.namesakechemistry.chemical_compoundAdsorptionlawMaterials ChemistryOrganic chemistryMoleculeFourier transform infrared spectroscopyGrapheneMetals and Alloystechnology industry and agricultureQuímica orgánicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistryCeramics and CompositessymbolsPyreneCyclic voltammetry0210 nano-technologyRaman spectroscopyCarbonChemical communications (Cambridge, England)
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Temperature-Induced Structural Transitions in the Gallium-Based MIL-53 Metal–Organic Framework

2013

We report a structural and thermodynamic investigation of the phase behavior of Ga(OH,F)-MIL-53, a gallium-based metal–organic framework (MOF) having the MIL-53 topology containing 0.7 wt % fluorine bonded to the metal. Despite some small structural differences, especially for the hydrated form, the overall physical chemistry behavior of Ga(OH,F)-MIL-53 is very similar to standard fluorine free Ga-MIL-53 material. A combination of in situ X-ray diffraction, in situ Fourier transform infrared spectroscopy, differential scanning calorimetry, and heat capacity measurements allowed us to establish that Ga(OH,F)-MIL-53 under vacuum (i.e., the empty material) exhibits two stable phases: a nonporo…

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesHeat capacityMetalDifferential scanning calorimetryPhase (matter)[CHIM] Chemical Sciences[CHIM]Chemical SciencesPhysical and Theoretical ChemistryGalliumFourier transform infrared spectroscopyComputingMilieux_MISCELLANEOUS[CHIM.MATE] Chemical Sciences/Material chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryCrystallographyGeneral Energychemistryvisual_artvisual_art.visual_art_mediumFluorinePhysical chemistryMetal-organic framework0210 nano-technology
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Conformational investigation of α,β‐dehydropeptides. XV: N‐acetyl‐α,β‐dehydroamino acid N ′N ′‐dimethylamides: conformational properties from infrare…

2005

The FTIR spectra were analysed in the region of the nu(s)(N-H), AI(C=O) and nu(s)(Calpha=Cbeta) bands for a series of Ac-DeltaXaa-NMe2, where DeltaXaa = DeltaAla, (Z)-DeltaAbu, (Z)-DeltaLeu, (Z)-DeltaPhe and DeltaVal, to determine a predominant solution conformation of these alpha,beta-dehydropeptide-related molecules. Measurements were taken in CCl4, DCM and MeCN solutions. In the same way, spectra of saturated analogues Ac-Xaa-NMe2, where Xaa = Ala, Abu, Leu, Phe and Val, were investigated. To help interpret the spectroscopic results, conformational maps were calculated by the B3LYP/6-31+G** method. Also, the relative energies of all conformers of the dehydro compounds in vacuo as well as…

conformationStereochemistryProtein ConformationαPeptideamide/π(Ph) interactionBiochemistrySpectral linechemistry.chemical_compoundStructural BiologyAmideDrug DiscoverySpectroscopy Fourier Transform InfraredSide chainMoleculeC5 hydrogen bondFourier transform infrared spectroscopysolute/solvent interactionMolecular BiologyConformational isomerismβ‐dehydroamino acidsPharmacologychemistry.chemical_classificationChemistryHydrogen bondOrganic ChemistryGeneral MedicineModels TheoreticalAmidestheoretical IR frequenciesFTIR spectroscopyMolecular Medicinedensity functional theory calculationsPeptidesJournal of Peptide Science
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Conformational investigation of α,β‐dehydropeptides Part VI. Molecular and crystal structure of benzyloxycarbonylglycyl‐(Z )‐dehydrophenylalanine

1994

The structure of a peptide containing C-terminal dehydrophenylalanine, Z-Gly-(Z)-delta Phe (C19H18N2O5, MW = 354) was determined from single-crystal X-ray diffraction data. Needle-shaped crystals were grown from a 1:1 mixture of methanol-acetone in the monoclinic space group P2(1) with a = 14.717(4), b = 4.941(2), c = 12.073(4) A, beta = 103.72(4) degrees; V = 852.86(8) A3, Z = 2 and Dc = 1.32 g cm-3. The structure was solved by direct methods using SHELXS-86 and refined to a final R-index of 0.032 for 1714 observed reflections. The peptide adopts a conformation folded at the glycine residue, and principal torsion angles are omega 0 = -167.6(2) degrees, phi 1 = -71.8(3) degrees, psi 1 = -31…

conformationdehydropeptidehydrogen bondProtein ConformationChemistryHydrogen bondhelical conformersIntermolecular forceDipeptidesCrystal structuredehydrophenylalanineBiochemistryZ‐Gly‐(Z )‐APheCrystallographyProtein structureX-Ray DiffractionIntramolecular forceSpectroscopy Fourier Transform InfraredX-ray crystallographyMoleculeinfrared spectroscopyX‐ray structure analysisMonoclinic crystal systemInternational Journal of Peptide and Protein Research
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