Search results for " inorganic"

showing 10 items of 796 documents

Superparamagnetic recoverable flowerlike Fe3O4@Bi2O3 core–shell with g-C3N4 sheet nanocomposite: synthesis, characterization, mechanism and kinetic s…

2019

In the present research study, a simple method was developed for the synthesis of three-dimensional flowerlike Fe3O4@Bi2O3 core–shell with g-C3N4 sheet nanocomposites. The X-ray diffraction, Fourier transform infrared spectroscopy, scanning electronic microscopy, transmission electron microscope, vibrating sample magnetometer, dynamic laser scattering analyzer and UV–Vis diffuse reflection spectroscopy were employed for the characterization of structure, purity and morphology of the resultant samples. The degradation of indigo carmine as a model of organic dye pollutant is applied for photo-catalytic activity. The parameters which are affecting the efficiency of various parameters, such as;…

010302 applied physicsDiffractionNanocompositeMaterials scienceKineticsAnalytical chemistryElectronCondensed Matter Physics01 natural sciencesAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialsflowerlike Fe3O4@Bi2O3 core-shell g-C3N4 superparamagnetic photocatalysischemistry.chemical_compoundIndigo carminechemistryTransmission electron microscopySettore CHIM/03 - Chimica Generale E Inorganica0103 physical sciencesSettore CHIM/07 - Fondamenti Chimici Delle TecnologieElectrical and Electronic EngineeringFourier transform infrared spectroscopySuperparamagnetism
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Carbonyl compounds of Tc, Re, and Bh: Electronic structure, bonding, and volatility.

2018

Calculations of molecular properties of M(CO)5 and MH(CO)5, where M = Tc, Re, and Bh, and of the products of their decomposition, M(CO)4 and MH(CO)4, were performed using density functional theory and coupled-cluster methods implemented in the relativistic program suits such as ADF, DIRAC, and ReSpect. The calculated first M—CO bond dissociation energies (FBDEs) of Bh(CO)5 and BhH(CO)5 turned out to be significantly weaker than those of the corresponding Re homologs. The reason for that is the relativistic destabilization and expansion of the 6d AOs, responsible for weaker σ-forth and π-back donations in the Bh compounds. The relativistic FBDEs of M(CO)5 have, therefore, a Λ-shape behavior …

010304 chemical physicsGeneral Physics and Astronomychemistry.chemical_elementBohriumInteraction modelElectronic structure010403 inorganic & nuclear chemistry01 natural sciencesBond-dissociation energy0104 chemical sciencesAdsorptionchemistry0103 physical sciencesMoleculePhysical chemistryDensity functional theoryPhysical and Theoretical ChemistryVolatility (chemistry)The Journal of chemical physics
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Determination of the chemical warfare agents Sarin, Soman and Tabun in natural waters employing fluorescent hybrid silica materials

2017

[EN] A novel mesoporous silica material containing boron-dipyrromethene (BODIPY) moieties (I) is employed for the detection of nerve agent simulants (NASs) and the organophosphate nerve or chemical warfare agents (CWAs) Sarin (GB), Soman (GD), and Tabun (GA) in aqueous environments. The reactive BODIPY dye with an optimum positioned hydroxyl group undergoes acylation reactions with phosph(on)ate substrates, yielding a bicyclic ring. Due to aggregation of the dyes in water, the sensitivity of the free dye in solution is very low. Only after immobilization of the BODIPY moieties into the silica substrates is aggregation inhibited and a sensitive determination of the NASs diethyl cyanophosphon…

010402 general chemistry01 natural sciencesFluorescence detectionchemistry.chemical_compoundQUIMICA ANALITICAMaterials ChemistrymedicineOrganic chemistryReactivity (chemistry)Electrical and Electronic EngineeringInstrumentationNerve agentTabunAqueous solutionQuenching (fluorescence)010405 organic chemistryChemistryQUIMICA INORGANICAMetals and AlloysMesoporous silicaCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDiethyl chlorophosphateNerve agent simulantsMesoporous silica materialsBODIPYmedicine.drugNuclear chemistry
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Exploring the Chemoselectivity towards Cysteine Arylation by Cyclometallated Au III Compounds: New Mechanistic Insights

2020

To gain more insight into the factors controlling the efficient cysteine arylation by cyclometalated Au(III) complexes, the reaction between selected gold compounds and different peptides was investigated by high‐resolution liquid chromatography electrospray ionization mass spectrometry (HR‐LC‐ESI‐MS). The deducted mechanisms of C–S cross‐coupling, also supported by density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations, evidenced the key role of secondary peptidic gold binding sites in favouring the process of reductive elimination.

010405 organic chemistryChemistryElectrospray ionizationOrganic Chemistrycyclometallated gold complexes010402 general chemistryMass spectrometry01 natural sciencesBiochemistryCombinatorial chemistryMolecular mechanicsReductive elimination0104 chemical sciencesddc:cysteine arylationGold CompoundschemoselectivitySettore CHIM/03 - Chimica Generale E InorganicapeptidesMolecular MedicineDensity functional theoryChemoselectivityMolecular BiologyCysteinemass spectrometry
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Recent progress in the application of fluorinated chiral sulfinimine reagents

2018

Abstract The development of synthetic methodology allowing for a strategic incorporation of fluorine into target compounds is in a high demand in many areas of the chemical and pharmaceutical industries. In this regard, application of fluorinated chiral sulfinimine reagents, in particularly, N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimine, is one of the most general and practical approaches for preparation of compounds containing pharmacophoric fluoro-amino-keto/hydroxy moieties. This article provides a timely and comprehensive overview of the recent synthetic applications of fluorinated chiral sulfinimine reagents for asymmetric synthesis of fluoro-containing polyfunctional amino-compound…

010405 organic chemistryChemistryOrganic ChemistryEnantioselective synthesisAsymmetric synthesisFluoro-imineAmino compounds010402 general chemistry01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesInorganic ChemistrySulfinimineReagentEnvironmental ChemistryPhysical and Theoretical ChemistryAmino compounds; Asymmetric synthesis; Fluoro-imine; Sulfinimine; Biochemistry; Environmental Chemistry; Physical and Theoretical Chemistry; Organic Chemistry; Inorganic ChemistryJournal of Fluorine Chemistry
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Self-assembled Pt2L2 boxes strongly bind G-quadruplex DNA and influence gene expression in cancer cells

2017

Supramolecular Pt(ii) quadrangular boxes bind native and G-quadruplex DNA motifs in a size-dependent fashion. Three Pt molecular squares of distinct size show biological activity against cancer cells and heavily influence the expression of genes known to form G-quadruplexes in their promoter regions. The smallest Pt-box displays less activity but more selectivity for a quadruplex formed in the c-Kit gene.

010405 organic chemistryChemistrySupramolecular chemistryBiological activity010402 general chemistryG-quadruplex01 natural sciencesMolecular biology0104 chemical sciencesSelf assembledCell biologyInorganic Chemistrychemistry.chemical_compoundG-quadruplex PlatinumSettore CHIM/03 - Chimica Generale E InorganicaGene expressionCancer cellheterocyclic compoundsGeneDNADalton Transactions
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2017

The title compound, C12H9BrN2O3, was prepared in two steps from 2-chloro-3-nitropyridine. The nitrobiaryl unit is twisted, with dihedral angles of 35.4 (5)° between the nitro substituent and the pyridine ring to which it is bound, and 51.0 (5)° between the nitro group and the benzene ring. In the crystal, the molecules are connectedviaC—H...O hydrogen bonds, forming strands along theb-axis direction.

010405 organic chemistryHydrogen bondSubstituentCrystal structureDihedral angle010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundchemistryPyridineNitroBenzeneIUCrData
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2016

The title compound, C32H48O8P2S2, was prepared by the nickel-catalyzed reaction of bis(5-bromothienyl)dipropoxybenzene and triisopropyl phosphite. The thiophene rings are inclined to the benzene ring by 14.6 (2) and 25.3 (3)°. One propyloxy group is disordered. Four hydrogen bonds connect the molecules, which are arranged in ribbons parallel to thebcplane.

010405 organic chemistryStereochemistryHydrogen bondGeneral MedicineCrystal structure010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesPhosphonateMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundchemistryThiopheneBenzeneIUCrData
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Annually resolved δ13Cshell chronologies of long-lived bivalve mollusks (Arctica islandica) reveal oceanic carbon dynamics in the temperate North Atl…

2011

Abstract The ability of the ocean to absorb carbon dioxide is likely to be adversely affected by recent climate change. However, relatively little is known about the spatiotemporal variability in the oceanic carbon cycle due to the lack of long-term, high-resolution dissolved inorganic carbon isotope ( δ 13 C DIC ) data, especially for the temperate North Atlantic, which is the major oceanic sink for anthropogenic CO 2 . Here, we report shell carbon isotope values ( δ 13 C shell ), a potential proxy for δ 13 C DIC , of old-grown specimens of the long-lived bivalve mollusk, Arctica islandica . This paper presents the first absolutely dated, annually resolved δ 13 C shell record from surface …

010504 meteorology & atmospheric sciences010502 geochemistry & geophysicsOceanography01 natural sciencesCarbon cycleSuess effectSclerochronologySclerochronology14. Life underwaterArctica islandicaEcology Evolution Behavior and Systematics0105 earth and related environmental sciencesEarth-Surface ProcessesPolar frontStable carbon isotope ratiobiologyOcean currentOceanic Suess effectPaleontologybiology.organism_classificationDissolved inorganic carbonOceanographyCarbon dioxide13. Climate actionIsotopes of carbon[SDE]Environmental SciencesOceanic carbon cycleGeology
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Applicability and consequences of the integration of alternative models for CO<sub>2</sub> transfer velocity into a process-based lake mo…

2019

Abstract. Freshwater lakes are important in carbon cycling, especially in the boreal zone where many lakes are supersaturated with the greenhouse gas carbon dioxide (CO2) and emit it to the atmosphere, thus ventilating carbon originally fixed by the terrestrial system. The exchange of CO2 between water and the atmosphere is commonly estimated using simple wind-based parameterizations or models of gas transfer velocity (k). More complex surface renewal models, however, have been shown to yield more correct estimates of k in comparison with direct CO2 flux measurements. We incorporated four gas exchange models with different complexity into a vertical process-based physico-biochemical lake mo…

0106 biological sciences010504 meteorology & atmospheric sciences010604 marine biology & hydrobiologyEddy covariancechemistry.chemical_elementAtmospheric sciences01 natural sciences6. Clean waterCarbon cycleAtmospherechemistry.chemical_compoundWater columnchemistryTotal inorganic carbon13. Climate actionGreenhouse gasCarbon dioxideEnvironmental scienceCarbonEcology Evolution Behavior and Systematics0105 earth and related environmental sciencesEarth-Surface ProcessesBiogeosciences
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