Search results for "Infrared"

showing 10 items of 2110 documents

Premature aging in bone of fish from a highly polluted marine area

2015

Fish species have attracted considerable interest in studies assessing biological responses to environmental contaminants. In this study, the attention has been focussed on fishbone of selected fish species from a highly polluted marine area, Augusta Bay (Italy, Central Mediterranean) to evaluate if toxicant elements had an effect on the mineralogical structure of bones, although macroscopic deformations were not evident. In particular, an attempt was made to evaluate if bone mineral features, such as crystallinity, mineral maturity and carbonate/phosphate mineral content, determined by XR-Diffraction and FT-IR Spectroscopy, suffered negative effects due to trace element levels in fishbone,…

ChromiumMediterranean climatePremature agingAugusta Bay (Italy)XRDMineralogyAquatic ScienceOceanographyBone and Boneschemistry.chemical_compoundCalcification PhysiologicX-Ray DiffractionSpectroscopy Fourier Transform InfraredAnimalsBone mineralMaturity (geology)Body WeightWater PollutionFishesTrace elementCrystalline structure fishboneReproducibility of ResultsAging PrematureMercuryContaminationPollutionHydroxylapatiteFT-IRItalychemistryEnvironmental chemistryTrace elementEnvironmental scienceCarbonateBay
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[Cr(ddpd) 2 ] 3+ : A Molecular, Water‐Soluble, Highly NIR‐Emissive Ruby Analogue

2015

Bright, long-lived emission from first-row transition-metal complexes is very challenging to achieve. Herein, we present a new strategy relying on the rational tuning of energy levels. With the aid of the large N-Cr-N bite angle of the tridentate ligand ddpd (N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine) and its strong σ-donating capabilities, a very large ligand-field splitting could be introduced in the chromium(III) complex [Cr(ddpd)2](3+), that shifts the deactivating and photoreactive (4)T2 state well above the emitting (2)E state. Prevention of back-intersystem crossing from the (2)E to the (4)T2 state enables exceptionally high near-infrared phosphorescence quantum yields a…

ChromiumSubstitution reactionSpectroscopy Near-InfraredWaterchemistry.chemical_elementGeneral ChemistryBite anglePhotochemistryCatalysisMetalFluorescence intensityChromiumWater solubleIntersystem crossingSolubilityX-Ray DiffractionchemistryCoordination Complexesvisual_artvisual_art.visual_art_mediumPhosphorescenceAngewandte Chemie International Edition
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Detailed study of SNR G306.3–0.9 using XMM-Newton and Chandra observations

2016

Aims. We aim to study the spatial distribution of the physical and chemical properties of the X-ray emitting plasma of the supernova remnant (SNR) G306.3-0.9 in detail to obtain constraints on its ionization stage, the progenitor supernova explosion, and the age of the remnant. Methods. We used combined data from XMM-Newton and Chandra observatories to study the X-ray morphology of G306.3-0.9 in detail. A spatially resolved spectral analysis was used to obtain physical and geometrical parameters of different regions of the remnant. Spitzer infrared observations, available in the archive, were also used to constrain the progenitor supernova and study the environment in which the remnant evol…

Ciencias AstronómicasInfraredCiencias FísicasAstrophysics::High Energy Astrophysical PhenomenaISM [Infrared]FOS: Physical sciencesthermal [radiation mechanism]individual objects: SNR G306.3–0.9 [ISM]AstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics01 natural sciencesSpectral line//purl.org/becyt/ford/1 [https]ISM: individual objects: SNR G306.3IonizationISM [X-ray]0103 physical sciencesAstrophysics::Solar and Stellar AstrophysicsISM [X-rays]Radio continuum: ISMEjectaSupernova remnant010303 astronomy & astrophysicsISM: supernova remnantAstrophysics::Galaxy AstrophysicsISM: supernova remnantsPhysicsHigh Energy Astrophysical Phenomena (astro-ph.HE)Infrared: ISM010308 nuclear & particles physicssupernova remnants [ISM]Astronomy and AstrophysicsPlasma//purl.org/becyt/ford/1.3 [https]Astronomy and AstrophysicISM: individual objects: SNR G306.3–0.9ISM [Radio continuum]Radiation mechanisms: thermalX-rays: ISMindividual objects: G306.3-0.9 [ISM]Interstellar mediumAstronomíaSupernovathermal [Radiation mechanisms]Space and Planetary ScienceISM; ISM: individual objects: SNR G306.3; ISM: supernova remnants; Radiation mechanisms: thermal; Radio continuum: ISM; X-rays: ISM; Astronomy and Astrophysics; Space and Planetary Science [0.9; Infrared]0.9Astrophysics - High Energy Astrophysical PhenomenaCIENCIAS NATURALES Y EXACTAS
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Glucagon fibril polymorphism reflects differences in protofilament backbone structure

2010

Amyloid fibrils formed by the 29-residue peptide hormone glucagon at different concentrations have strikingly different morphologies when observed by transmission electron microscopy. Fibrils formed at low concentration (0.25 mg/mL) consist of two or more protofilaments with a regular twist, while fibrils at high concentration (8 mg/mL) consist of two straight protofilaments. Here, we explore the structural differences underlying glucagon polymorphism using proteolytic degradation, linear and circular dichroism, Fourier transform infrared spectroscopy (FTIR), and X-ray fiber diffraction. Morphological differences are perpetuated at all structural levels, indicating that the two fibril class…

Circular dichroismAmyloidProtein FoldingChemistryProtein StabilityCircular DichroismProteolytic enzymesmacromolecular substancesLinear dichroismFibrilGlucagonSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Protein Structure SecondaryCrystallographyX-Ray DiffractionStructural BiologySpectroscopy Fourier Transform InfraredSide chainFourier transform infrared spectroscopyProtein MultimerizationFiber diffractionMolecular BiologyProtein secondary structurePolymorphism Amyloid Glucagon Structural changesPeptide Hydrolases
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Spectroscopic and electrochemical study of interactions between DNA and different salts of 1,4-dihydropyridine AV-153

2020

1,4-dihydropyridines (1,4-DHP) possess important biochemical and pharmacological properties, including antimutagenic and DNA-binding activity. The latter activity was first described for water-soluble 1,4-DHP with carboxylic group in position 4, the sodium salt of the 1,4-DHP derivative AV-153 among others. Some data show the modification of physicochemical properties and biological activities of organic compounds by metal ions that form the salts. We demonstrated the different affinity to DNA and DNA-protecting capacity of AV-153 salts, depending on the salt-forming ion (Na, K, Li, Rb, Ca, Mg). This study aimed to use different approaches to collate data on the DNA-binding mode of AV-153-N…

Circular dichroismGuanine030303 biophysicsIntercalation (chemistry)Biophysicslcsh:MedicineCircular dichroismG-quadruplexBiochemistryMedicinal chemistryGeneral Biochemistry Genetics and Molecular BiologyNucleobase03 medical and health scienceschemistry.chemical_compoundCircular voltammetryMoleculeDenaturation (biochemistry)DNA bindingMolecular Biology14-dihydropyridines030304 developmental biologyAV-153 salts0303 health sciencesGeneral Neurosciencelcsh:RGeneral MedicineG-quadruplexeschemistryFourier-transformed infrared spectroscopySpectrofluorimetryGeneral Agricultural and Biological SciencesDNAPeerJ
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Confinement of chiral molecules in reverse micelles: FT-IR, polarimetric and VCD investigation on the state of dimethyl tartrate in sodium bis(2-ethy…

2008

Abstract The state of d and l -dimethyl tartrate confined within dry sodium bis(2-ethylhexyl) sulfosuccinate (AOT) reverse micelles dispersed in CCl 4 has been investigated by FT-IR spectroscopy, polarimetry, and vibrational circular dichroism (VCD). Measurements have been performed at 25 °C as a function of the solubilizate-to-surfactant molar ratio ( R ) at a fixed AOT concentration (0.158 M). The analysis of experimental data is consistent with the hypothesis that both enantiomers of dimethyl tartrate are mainly entrapped in the reverse micelles and located in proximity to the surfactant head-group region. The formation of this interesting self-organized chiral nanostructure involves som…

Circular dichroismInorganic chemistryInfrared spectroscopyTartrateMicellechemistry.chemical_compoundColloid and Surface ChemistryMonomerchemistryPulmonary surfactantVibrational circular dichroismPhysical chemistryEnantiomerDimethyl tartrate Sodium bis(2-ethylhexyl) sulfosuccinate Reverse micelles Chiral nanostructures FT-IR spectroscopy Vibrational circular dichroism Optical rotationColloids and Surfaces A: Physicochemical and Engineering Aspects
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Cytotoxic hydrophilic iminophosphorane coordination compounds of d8 metals. Studies of their interactions with DNA and HSA

2012

The synthesis and characterization of a new water-soluble N,N-chelating iminophosphorane ligand TPAN-C(O)-2-NC(5)H(4) (N,N-IM) (1) and its d(8) (Au(III), Pd(II) and Pt(II)) coordination complexes are reported. The structures of cationic [AuCl(2)(N,N-IM)]ClO(4) (2) and neutral [MCl(2)(N,N-IM)] M=Pd (3), Pt(4) complexes were determined by X-ray diffraction studies or by means of density-functional calculations. While the Pd and Pt compounds are stable in mixtures of DMSO/H(2)O over 4 days, the gold derivative (2) decomposes quickly to TPAO and previously reported neutral gold(III) compound [AuCl(2)(N,N-H)] 5 (containing the chelating N,N-fragment HN-C(O)-2-NC(5)H(4)). The cytotoxicities of co…

Circular dichroismMagnetic Resonance SpectroscopyStereochemistryPhosphoranesAntineoplastic AgentsBiochemistryMedicinal chemistryArticleCoordination complexInorganic ChemistryX-Ray DiffractionCell Line TumorSpectroscopy Fourier Transform InfraredmedicineHumansChelationSerum Albuminchemistry.chemical_classificationCisplatinLigandCircular DichroismIsothermal titration calorimetryDNANuclear magnetic resonance spectroscopyHuman serum albuminSpectrometry FluorescencechemistryMetalsCisplatinHydrophobic and Hydrophilic Interactionsmedicine.drugJournal of Inorganic Biochemistry
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Unconventional dihydrogen-bond interaction induced cyanide-bridged chiral nano-sized magnetic molecular wheel: synthesis, crystal structure and syste…

2019

A pair of cyanide-bridged 4d–3d heterobimetallic chiral macrocyclic enantiomeric magnetic complexes have been successfully assembled from the trans-dicyanoruthenium(III) building block [PPh4][Ru(Salen)(CN)2] (Salen = N,N-ethylenebis(salicylideneaminato)dianion) and [Mn((S,S/R,R)-Salcy)(H2O)2]ClO4 (Salcy = N,N′-(1,2-cyclohexanediylethylene)bis(salicylideneiminato)dianion) with the great help of the dihydrogen bond (DHB) interaction and characterized by elemental analysis, IR spectroscopy, circular dichroism (CD) and magnetic circular dichroism (MCD) spectroscopy. Single X-ray diffraction reveals that complex 1, {[Ru(Salen)(CN)2][R,R-Mn(Salcy)]}6·PPh3·6CH3CN·6CH3OH·12H2O, is a neutral dodecan…

Circular dichroismMaterials scienceMagnetismMagnetic circular dichroismInfrared spectroscopy02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCrystallographyMaterials ChemistryDihydrogen bond0210 nano-technologySpectroscopyGround stateJournal of Materials Chemistry C
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Sensing Chiral Drugs by Using CdSe/ZnS Nanoparticles Capped withN-Acetyl-L-Cysteine Methyl Ester

2013

Chiral quantum dots (QDs), differing in their core or shell size and, consequently, in their optical properties, were synthesized by the treatment of commercially available amine-capped quantum dots with methyl ester N-acetyl-L-cysteine (CysP). Interestingly, their colloidal methanol solutions remain stable for several months. Their NMR and IR spectra were in accordance with CysP binding to the QD surface through two anchoring groups; its thiolate (strongly bound) and the carbonyl group of its ester (weaker bound) group, whereas their circular dichroism (CD) spectra showed a new broad redshifted band, suggesting that the attachment to the QD surface modified the conformational equilibrium t…

Circular dichroismNaproxenStereochemistryInfrared spectroscopyIbuprofenSulfidesCatalysischemistry.chemical_compoundNaproxenQuantum DotsCadmium CompoundsmedicineSelenium CompoundsConformational isomerismChemistryCircular DichroismArylOrganic ChemistryEstersStereoisomerismGeneral ChemistryFluorescenceAcetylcysteineCrystallographySpectrometry FluorescenceFlurbiprofenPharmaceutical PreparationsKetoprofenZinc CompoundsQuantum dotEnantiomermedicine.drugChemistry - A European Journal
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Thermal aggregation and ion-induced cold-gelation of bovine serum albumin

2009

Protein cold-gelation has recently received particular attention for its relevance in bio and food technology. In this work, we report a study on bovine serum albumin cold-gelation induced by copper or zinc ions. Metal-induced cold-gelation of proteins requires two steps: during the first one, the heat treatment causes protein partial unfolding and aggregation; then, after cooling the solution to room temperature, gels are formed upon the addition of metal ions. The thermally induced behaviour has been mainly investigated through different techniques: Fourier transform infrared (FTIR) spectroscopy, circular dichroism, dynamic light scattering (DLS) and rheology. Data have shown that the agg…

Circular dichroismProtein FoldingTime FactorsLightMetal ions in aqueous solutionBiophysicsAnalytical chemistryViscoelasticityProtein Structure SecondaryIonDivalentDynamic light scatteringSpectroscopy Fourier Transform InfraredAnimalsScattering RadiationBovine serum albuminFourier transform infrared spectroscopychemistry.chemical_classificationbiologyChemistryCircular DichroismTemperatureSerum Albumin BovineGeneral MedicineElasticityKineticsZincbiology.proteinCattleRheologyCopperBovine serum albumin (BSA)Proteins aggregation Metal ions Cold-gelation
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