Search results for "Fate"

showing 10 items of 765 documents

CCDC 921191: Experimental Crystal Structure Determination

2013

Related Article: Pilar Amo-Ochoa, Simone S. Alexandre, Samira Hribesh, Miguel A. Galindo, Oscar Castillo, Carlos J. Gómez-García, Andrew R. Pike, José M. Soler, Andrew Houlton, Ross W. Harrington, William Clegg, Félix Zamora|2013|Inorg.Chem.|52|5290|doi:10.1021/ic400237h

(2-amino-9-pentofuranosyl-9H-purine-6-thiolato)-bis(2-amino-9-pentofuranosyl-19-dihydro-6H-purine-6-thione)-cobalt(iii) sulfate trihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Oxoanion binding to a cyclic pseudopeptide containing 1,4-disubstituted 1,2,3-triazole moieties

2016

A macrocyclic pseudopeptide 3 is described featuring three amide groups and three 1,4-disubstituted 1,2,3-triazole units along the ring. This pseudopeptide was designed such that the amide NH groups and the triazole CH groups converge toward the cavity, thus creating an environment well suited for anion recognition. Conformational studies in solution combined with X-ray crystallography confirmed this preorganisation. Solubility of 3 restricted binding studies to organic media such as 5 vol% DMSO/acetone or DMSO/water mixtures with a water content up to 5 vol%. These binding studies demonstrated that 3 binds to a variety of inorganic anions in DMSO/acetone including chloride, nitrate, sulfat…

010405 organic chemistryChemistryStereochemistryDimerOrganic ChemistryTriazoleoxoanion bindings010402 general chemistry01 natural sciencesBiochemistryChlorideMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundpseudopeptidesStability constants of complexesAmidemedicineMoleculePhysical and Theoretical ChemistrySulfateSolubilityta116medicine.drugOrganic & Biomolecular Chemistry
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High-Pressure Behavior of Nickel Sulfate Monohydrate: Isothermal Compressibility, Structural Polymorphism, and Transition Pathway

2020

Single crystals of synthetic nickel sulfate monohydrate, α-NiSO4·H2O (space-group symmetry C2/c at ambient conditions), were subject to high-pressure behavior investigations in a diamond-anvil cell up to 10.8 GPa. By means of subtle spectral changes in Raman spectra recorded at 298 K on isothermal compression, two discontinuities were identified at 2.47(1) and 6.5(5) GPa. Both transitions turn out to be apparently second order in character, as deduced from the continuous evolution of unit-cell volumes determined from single-crystal X-ray diffraction. The first structural transition from α- to β-NiSO4·H2O is an obvious ferroelastic C2/c–P1̅ transition. It is purely displacive from a structur…

010405 organic chemistryChemistrychemistry.chemical_element010402 general chemistry01 natural sciencesArticle0104 chemical sciencesInorganic ChemistryNickelchemistry.chemical_compoundPolymorphism (materials science)High pressureCompressibilityPhysical chemistryPhysical and Theoretical ChemistrySulfateInorganic Chemistry
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Computational Study of the Effect of Glyoxal–Sulfate Clustering on the Henry’s Law Coefficient of Glyoxal

2014

We have used quantum chemical methods to investigate the molecular mechanism behind the recently reported ( Kampf , C. J. ; Environ. Sci. Technol . 2013 , 47 , 4236 - 4244 ) strong dependence of the Henry's law coefficient of glyoxal (C2O2H2) on the sulfate concentration of the aqueous phase. Although the glyoxal molecule interacts only weakly with sulfate, its hydrated forms (C2O3H4 and C2O4H6) form strong complexes with sulfate, displacing water molecules from the solvation shell and increasing the uptake of glyoxal into sulfate-containing aqueous solutions, including sulfate-containing aerosol particles. This promotes the participation of glyoxal in reactions leading to secondary organic…

010504 meteorology & atmospheric sciences010501 environmental sciences01 natural scienceschemistry.chemical_compoundComputational chemistryPressureMoleculeOrganic chemistryComputer SimulationPhysical and Theoretical ChemistrySulfateEquilibrium constant0105 earth and related environmental sciencesAerosolsAqueous solutionAtmosphereSulfatesAqueous two-phase systemWaterGlyoxalHenry's lawSolvation shellModels ChemicalchemistrySolventsGlyoxalThe Journal of Physical Chemistry A
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Aerosol Chemistry Resolved by Mass Spectrometry: Linking Field Measurements of Cloud Condensation Nuclei Activity to Organic Aerosol Composition.

2016

Aerosol hygroscopic properties were linked to its chemical composition by using complementary online mass spectrometric techniques in a comprehensive chemical characterization study at a rural mountaintop station in central Germany in August 2012. In particular, atmospheric pressure chemical ionization mass spectrometry ((-)APCI-MS) provided measurements of organic acids, organosulfates, and nitrooxy-organosulfates in the particle phase at 1 min time resolution. Offline analysis of filter samples enabled us to determine the molecular composition of signals appearing in the online (-)APCI-MS spectra. Aerosol mass spectrometry (AMS) provided quantitative measurements of total submicrometer or…

010504 meteorology & atmospheric sciencesAnalytical chemistryAtmospheric-pressure chemical ionizationGeneral Chemistry010501 environmental sciencesMass spectrometry01 natural sciencesAerosolchemistry.chemical_compoundchemistryEnvironmental ChemistryAerosol mass spectrometryCloud condensation nucleiSulfateChemical compositionMass fraction0105 earth and related environmental sciencesEnvironmental sciencetechnology
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ATR–FTIR Spectral Analysis and Soluble Components of PM10 And PM2.5 Particulate Matter over the Urban Area of Palermo (Italy) during Normal Days and …

2019

Several epidemiological studies have shown a close relationship between the mass of particulate matter (PM) and its effects on human health. This study reports the identification of inorganic and organic components by attenuated total reflectance-Fourier-transform infrared spectroscopy (ATR-FTIR) analysis in PM10 and PM2.5 filters collected from three air quality monitoring stations in the city of Palermo (Sicily, Italy) during non-Saharan dust events and Saharan events. It also provides information on the abundance and types of water-soluble species. ATR-FTIR analysis identified sulfate, ammonium, nitrate, and carbonate matter characterized by vibrational frequencies at 603, 615, 670, and …

010504 meteorology & atmospheric sciencesHealth Toxicology and Mutagenesissaharan dust eventsPM10 and PM2.5Infrared spectroscopychemistry.chemical_elementlcsh:Medicine[SDU.STU]Sciences of the Universe [physics]/Earth Sciencesionic soluble components010501 environmental sciencesMineral dust01 natural sciencesionic soluble componentSaharan dust eventPM<sub>10</sub> and PM<sub>2.5</sub>Absorbancechemistry.chemical_compound11. SustainabilitySulfate0105 earth and related environmental sciencesparticulate mattersirocco windsPM 10 and PM 2.5lcsh:RPublic Health Environmental and Occupational HealthSettore GEO/07 - Petrologia E PetrografiaParticulatesSettore GEO/08 - Geochimica E Vulcanologiachemistry13. Climate action[SDU]Sciences of the Universe [physics]Environmental chemistryCarbonateClay mineralsCarbonATR-FTIRInternational Journal of Environmental Research and Public Health
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New insights on secondary minerals from Italian sulfuric acid caves

2018

Sulfuric acid minerals are important clues to identify the speleogenetic phases of hypogene caves. Italy hosts ~25% of the known worldwide sulfuric acid speleogenetic (SAS) systems, including the famous well-studied Frasassi, Monte Cucco, and Acquasanta Terme caves. Nevertheless, other underground environments have been analyzed, and interesting mineralogical assemblages were found associated with peculiar geomorphological features such as cupolas, replacement pockets, feeders, sulfuric notches, and sub-horizontal levels. In this paper, we focused on 15 cave systems located along the Apennine Chain, in Apulia, in Sicily, and in Sardinia, where copious SAS minerals were observed. Some of the…

010504 meteorology & atmospheric sciencesHypogeneQH301-705.5cave minerals speleothem sulfuric acid cave secondary mineralsSettore GEO/04 - Geografia Fisica E GeomorfologiahypogeneGeochemistrySpeleothem010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundCavesulfuric acid caverising watersBiology (General)speleothem0105 earth and related environmental sciencesEarth-Surface Processescave mineralsgeographyCave sulfateSettore GEO/06 - MineralogiaQE1-996.5geography.geographical_feature_categorycave sulfatesSulfuric acidRising waterGeologyhypogene rising waters Apennine Chain mineralogy cave sulfateschemistryApennine Chainmineralogysecondary mineralsGeologyInternational Journal of Speleology
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Evidence for marine biogenic influence on summertime Arctic aerosol

2017

International audience; We present vertically-resolved observations of aerosol composition during pristine summertime Arctic background conditions. The methansulfonic acid (MSA)-to-sulfate ratio peaked near the surface (mean 0.10), indicating a contribution from ocean-derived biogenic sulfur. Similarly, the organic aerosol (OA)-to-sulfate ratio increased towards the surface (mean 2.0). Both MSA-to-sulfate and OA-to-sulfate ratios were significantly correlated with FLEXPART-WRF-predicted airmass residence time over open water, indicating marine influenced OA. External mixing of sea salt aerosol from a larger number fraction of organic, sulfate and amine-containing particles, together with lo…

010504 meteorology & atmospheric sciencesmethanesulfonic acidchemistry.chemical_element010501 environmental sciencesAtmospheric sciences01 natural sciencesMethanesulfonic acidArctic aerosolchemistry.chemical_compoundmarine organic aerosolCloud condensation nucleiSulfateSea salt aerosol0105 earth and related environmental sciences[SDU.OCEAN]Sciences of the Universe [physics]/Ocean Atmosphereaerosol mass spectrometrySulfurArctic summerAerosolGeophysicsArcticchemistry13. Climate actionGeneral Earth and Planetary SciencesAerosol mass spectrometryEnvironmental sciencesecondary organic aerosol
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Volcanic climate forcing preceding the inception of the Younger Dryas: Implications for tracing the Laacher See eruption

2021

Climatic warming from the last glacial maximum to the current interglacial period was punctuated by a similar to 1300 years long cold period, commonly referred to as the Younger Dryas (YD). Several hypotheses have been proposed for the mechanism triggering the abrupt inception of the YD, including freshwater forcing, an extra-terrestrial impact, and aerosols from volcanic eruptions. Here, we use synchronised sulphate and sulphur records from both Greenland and Antarctic ice cores to reconstruct volcanic forcing between 13,200-12,800 a BPGICC05 (years before 1950 CE on the Greenland Ice Core Chronology 2005; GICC05). This continuous reconstruction of stratospheric sulphur injections highligh…

010506 paleontologyArcheologyYounger Dryas010504 meteorology & atmospheric sciences530 PhysicsCIRCULATIONIce cores; Laacher See eruption; Sulphate; Volcanic radiative forcing; Younger DryasSULFURForcing (mathematics)01 natural sciencesVolcanic radiative forcingANTARCTIC ICE-CORESOCEANIce coreCHRONOLOGYYounger Dryas550 Earth sciences & geologyEcology Evolution Behavior and Systematics0105 earth and related environmental sciencesGlobal and Planetary Changegeographygeography.geographical_feature_categoryGeologyLast Glacial MaximumRECORDWAIS DIVIDESulphateRadiative forcingGREENLANDLaacher See eruptionVolcano13. Climate actionIce coresClimatologySYNCHRONIZATIONInterglacialClimate modelSULFATEGeologyQuaternary Science Reviews
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Hydrothermalism in the Tyrrhenian Sea: Inorganic and microbial sulfur cycling as revealed by geochemical and multiple sulfur isotope data

2011

15 pages; International audience; The Palinuro volcanic complex and the Panarea hydrothermal field, both located in the Tyrrhenian Sea (Italy), are associated with island arc magmatism and characterized by polymetallic sulfide mineralization. Dissolved sulfide concentrations, pH, and Eh measured in porewaters at both sites reveal a variable hydrothermal influence on porewater chemistry. Multiple sulfur isotopic measurements for disseminated sulfides (CRS: chromium reducible sulfur) extracted from sediments at Palinuro yielded a broad range in δ34S range between −29.8 and +10.2‰ and Δ33S values between+0.015 and+0.134‰. In contrast, sediments at Panarea exhibit a much smaller range in δ34SCR…

010506 paleontologySulfide[SDE.MCG]Environmental Sciences/Global ChangesGeochemistrychemistry.chemical_elementDisproportionationengineering.material010502 geochemistry & geophysics01 natural sciencesHydrothermal circulationchemistry.chemical_compoundδ34S[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryMassive sulfide complexGeochemistry and PetrologyHydrothermalism14. Life underwaterMultiple sulfur isotopesSulfate0105 earth and related environmental scienceschemistry.chemical_classificationgeographygeography.geographical_feature_categorySulfur cyclingGeology[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/GeochemistrySulfur[ SDE.MCG ] Environmental Sciences/Global ChangeschemistryVolcano13. Climate actionengineeringPyriteGeologyChemical Geology
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