Search results for "Spectroscopy"

showing 10 items of 10293 documents

Toxicological Impact of Rare Earth Elements (REEs) on the Reproduction and Development of Aquatic Organisms Using Sea Urchins as Biological Models

2022

The growing presence of lanthanides in the environment has drawn the attention of the scientific community on their safety and toxicity. The sources of lanthanides in the environment include diagnostic medicine, electronic devices, permanent magnets, etc. Their exponential use and the poor management of waste disposal raise serious concerns about the quality and safety of the ecosystems at a global level. This review focused on the impact of lanthanides in marine organisms on reproductive fitness, fertilization and embryonic development, using the sea urchin as a biological model system. Scientific evidence shows that exposure to lanthanides triggers a wide variety of toxic insults, includi…

Aquatic OrganismsCalcium uptakeReproductionOrganic ChemistryGadoliniumGeneral MedicineModels BiologicalCatalysisComputer Science ApplicationsInorganic Chemistrysea urchin embryo developmental biology reproductive toxicology rare earth elements lanthanides gadolinium gene expression echinopluteus calcium uptake.LarvaSea UrchinsAnimalsMetals Rare EarthGene expressionSettore BIO/06 - Anatomia Comparata E CitologiaPhysical and Theoretical ChemistrySea urchin embryonic developmentMolecular BiologyEcosystemSpectroscopyInternational Journal of Molecular Sciences
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Oxygenated Cembrene Diterpenes from Sarcophyton convolutum: Cytotoxic Sarcoconvolutum A–E

2021

The soft coral genus Sarcophyton contains the enzymatic machinery to synthesize a multitude of cembrene-type diterpenes. Herein, highly oxygenated cembrenoids, sarcoconvolutum A–E (1–5) were purified and characterized from an ethyl acetate extract of the red sea soft coral, Sarcophyton convolutum. Compounds were assemblies according to spectroscopic methods including FTIR, 1D- and 2D-NMR as well as HRMS. Metabolite cytotoxicity was tested against lung adenocarcinoma, cervical cancer, and oral-cavity carcinoma (A549, HeLa and HSC-2, respectively). The most cytotoxic compound, (4) was observed to be active against cell lines A549 and HSC-2 with IC50 values of 49.70 and 53.17 μM, respectively.

Aquatic Organismssarcoconvolutum A–EMagnetic Resonance Spectroscopy<i>Sarcophyton convolutum</i>StereochemistryQH301-705.5MetaboliteEthyl acetatePharmaceutical ScienceAntineoplastic AgentsArticleHeLaInhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundCell Line TumorDrug DiscoveryIc50 valuesAnimalsCytotoxic T cellBiology (General)CytotoxicityIndian OceanPharmacology Toxicology and Pharmaceutics (miscellaneous)cembrenoidschemistry.chemical_classificationbiologyChemistrySarcophyton<i>Sarcophyton convolutum</i>; sarcoconvolutum A–E; cembrenoids; cytotoxicitySarcophyton convolutumAnthozoabiology.organism_classificationEnzymecytotoxicityDiterpenesDrug Screening Assays AntitumorMarine Drugs
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( n ‐Bu 2 Sn) 2 O(CO 3 ): An active, robust and recyclable organotin(IV) for the direct synthesis of linear organic carbonates from carbon dioxide an…

2017

Organotin(IV) compounds are known to promote the direct synthesis of organic carbonates from carbon dioxide and alcohols. In the past, structural studies have highlighted that the carbonato moiety is a recurring ligand of tin species collected during CO2 pressurized reactions. In a mimetic approach and in order to achieve an available and recyclable precursor, the title compound (n-Bu2Sn)2O(CO3) (1) was prepared in a single step by reacting commercial di-n-butyltin dichloride with an aqueous solution of sodium carbonate. Compound 1 was characterized using infrared spectroscopy and thermogravimetric and elemental analyses. Multinuclear NMR investigations in solution were also conducted. Comp…

Aqueous solution010405 organic chemistryChemistryCarbonationInfrared spectroscopychemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundOrganic chemistryMoietyMethanolDimethyl carbonateSodium carbonateTinApplied Organometallic Chemistry
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Towards the understanding at the molecular level of the structured-water absorption and fluorescence spectra: a fingerprint of π-stacked water

2013

An intriguing absorption peak around ∼270 nm (4.59 eV) has been recurrently recorded in aqueous solutions of salts, sugars, amino acids, in the free-solute zone (exclusion zone) adjacent to various hydrophilic surfaces, as well as a transient in the conversion process of ice to water. The corresponding associated fluorescence has been observed in the interval 480–490 nm (2.58–2.53 eV). The spectroscopic features have been related to the presence of structured water but its nature remains incompletely understood. On the basis of high-level ab initio computations, the main absorption feature of structured water is assigned to the presence of two π-stacked ground-state water molecules, prefera…

Aqueous solutionAbsorption spectroscopyChemistryDimerBinding energyIntermolecular forceBiophysicsAnalytical chemistryCondensed Matter Physicschemistry.chemical_compoundExcited stateSinglet statePhysical and Theoretical ChemistryAbsorption (chemistry)Molecular BiologyMolecular Physics
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Theoretical electronic spectra of 2-aminopurine in vapor and in water

2006

The accurate quantum chemical CASSCF and CASPT2 methods combined with a Monte Carlo procedure to mimic solvation effects have been used in the calculation of the spectroscopic properties of two tautomers of 2-aminopurine (2AP). Absorption and emission spectra have been simulated both in vacuum and in aqueous environment. State and transition energies and properties have been obtained with high accuracy, leading to the assignment of the most important spectroscopic features. The lowest-lying 1 (,*) ( 1 La) state has been determined as responsible for the first band in the absorption spectrum and also for the strong fluorescence observed for the system in water. The combined approach used in …

Aqueous solutionAbsorption spectroscopyChemistryMonte Carlo methodSolvationAnalytical chemistryCondensed Matter PhysicsTautomerMolecular physicsAtomic and Molecular Physics and OpticsSpectral lineEmission spectrumPhysical and Theoretical ChemistryAbsorption (electromagnetic radiation)International Journal of Quantum Chemistry
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Photoassisted Oxidation of the Recalcitrant Cyanuric Acid Substrate in Aqueous ZnO Suspensions

2007

The photoassisted oxidative transformation of the highly recalcitrant cyanuric acid was examined in the liquid−solid regime at pH 3 and natural pH 7.5 under UV irradiation in oxygen- and ozone-saturated ZnO suspensions using ZnO as a photomediator. Loss of cyanuric acid was assayed by HPLC UV absorption spectroscopy, whereas intermediates and final products were determined by HPLC ion chromatography (IC), by MS techniques using an electrospray ionization mass spectrometer operated in the negative-ion mode, and by FT-IR spectroscopy. Final reaction products were CO2 gas and NO3- ions. The measure of nitrate in solution quantified the degree of mineralization of the substrate; its concentrati…

Aqueous solutionAbsorption spectroscopyElectrospray ionizationInorganic chemistryIon chromatographySubstrate (chemistry)Mass spectrometrySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyAdsorptionchemistryZnO photocatalyst cyanuric acidPhysical and Theoretical ChemistryCyanuric acidThe Journal of Physical Chemistry C
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Symbiosis between photoactive nanoparticles and their organic ligands.

2013

Photoactive spherical metal and semiconductor nanoparticles (NPs) are smart systems that exhibit unique properties, such as a high surface-to-volume ratio, a broad absorption spectrum and size-dependent properties. They are capped with a considerable number of ligands required to give rise to stable organic and aqueous NP colloidal solutions. In addition, the ligands can also be used to introduce functionality at the NP periphery. In this case, the NP could act as a 3D-scaffold, which would make a high local concentration of a functional moiety at the NP periphery possible, moreover, the photophysical properties of the NP could be tuned. The combined action of the organic capping and the in…

Aqueous solutionAbsorption spectroscopyLigandChemistryNanoparticleNanotechnologyGeneral MedicineLigandsBiochemistryMetalColloidMicroscopy Electron Transmissionvisual_artvisual_art.visual_art_mediumMoietyMoleculeNanoparticlesSpectrophotometry UltravioletPhysical and Theoretical ChemistryOrganic ChemicalsSymbiosisPhotochemistry and photobiology
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Converting p-terphenyl into a novel organo-catalyst for LED-driven energy and electron transfer photoreactions in water.

2021

p-Terphenyl is a potent photoredox catalyst under UV-irradiation. Aiming for more sustainable reaction conditions, we added two sulfonate groups to this key structure to achieve water solubility and incorporated an SO2-bridge thereby shifting the absorption spectrum towards the visible. The resulting photocatalyst shows unexpected triplet reactivity in several test reactions.

Aqueous solutionAbsorption spectroscopyMetals and AlloysGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundElectron transferSulfonatechemistryTerphenylMaterials ChemistryCeramics and CompositesPhotocatalysisReactivity (chemistry)Chemical communications (Cambridge, England)
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DNA fluorescence induced by polymethine cation pyrvinium binding

1991

Pyrvinium is a polymethine cation which shows interesting fluorescence emission and DNA binding properties. In diluted aqueous solution, pyrvinium pamoate induced a bright yellow fluorescence in kinetoplast DNA from Trypanosoma cruzi epimastigotes as well as in chicken erythrocyte nuclei under a wide range of excitations. No fading was observed after mounting in suitable media. Spectroscopic studies on pyrvinium solutions revealed bathochromic and hypochromic shifts in the absorption spectrum of its complex with DNA. A striking enhancement of pyrvinium fluorescence was found in solvents of high viscosity or after binding to DNA. Experimental results and the chemical structure of pyrvinium a…

Aqueous solutionAbsorption spectroscopyStereochemistryTrypanosoma cruziDNACell BiologyFluorescencePyrviniumPyrvinium Compoundschemistry.chemical_compoundSpectrometry FluorescencechemistryCationsKinetoplastBathochromic shiftBiophysicsAnimalsAnatomyBinding siteChickensDNAFluorescent DyesThe Histochemical Journal
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Influence of temperature on the synthesis of thiol-stabilized CdTe nanoparticles in aqueous solutions

2010

We have investigated the evolution of thiol-capped cadmium telluride nanocrystals prepared in aqueous solutions at low and room temperature followed by heating at 50–100 °C. The UV–visible absorption spectra, as well as transmission electron microscopy, atomic force microscopy, and dynamic light scattering observations made it possible to reveal differences in size and structure originating from different heating temperatures. It was shown that minimization of the nucleation process temperature provided formation of larger nanoparticles than at higher temperatures.

Aqueous solutionAbsorption spectroscopybusiness.industryChemistryNucleationNanoparticleSurfaces and InterfacesCondensed Matter PhysicsLight scatteringCadmium telluride photovoltaicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceOpticsChemical engineeringDynamic light scatteringTransmission electron microscopyMaterials ChemistryElectrical and Electronic Engineeringbusinessphysica status solidi (a)
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