Search results for "Inorganic Chemical"

showing 10 items of 491 documents

Tetraiodoethynyl resorcinarene cavitands as multivalent halogen bond donors

2014

The first examples of iodoethynyl resorcinarene cavitands as rigid 3D halogen bond (XB) donor molecules are presented. These concave macrocycles form strong, RXB = 0.78–0.83, halogen bonds with dioxane oxygen, pyridine nitrogen and a bromide anion in tetraproropyl ammonium bromide resulting in deep cavity cavitand structures.

inorganic chemicalsHalogen bondChemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryResorcinarenePhotochemistryOxygenNitrogenCatalysis3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundBromidePolymer chemistryHalogenMaterials ChemistryCeramics and Compositesta116Chemical communications
researchProduct

Direct arylation of heteroaromatic compounds with congested, functionalised aryl bromides at low palladium/triphosphane catalyst loading.

2011

International audience; A new ferrocenyl triphosphane ligand associated to palladium was found to be an efficient catalyst for the direct coupling of highly congested, functionalised aryl bromides with a variety of heteroarenes. These coupling reactions can generally be performed by using a low-loading (0.1-0.5 mol%) of the catalyst. The present protocol tolerates important and useful functional groups, which allows for further elaboration into more sophisticated heterocyclic molecules. The straightforward arylation of heteroaromatic compounds with congested ortho-substituted aryl bromides may permit further convergent syntheses of diverse ligands, biologically active molecules and molecula…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisCoupling reactionCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundMoleculeOrganic chemistryEfficient catalystaryl bromidesheterocycles010405 organic chemistryChemistryLigandArylOrganic Chemistryferrocenyl polyphosphaneGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysispalladium0104 chemical sciencesC[BOND]H activationTriphosphanePalladium
researchProduct

<title>Micro-Raman scattering and infrared spectra of hemoglobin</title>

2008

Confocal micro-Raman and FT-IR spectroscopies have been used for detection of radiation influence of hemoglobin of patients examined by radio-isotopes diagnosis (Tc99m). After irradiation we observed some little changes of the Raman scattering bands which connected with out of plane porphyrine bending vibrations, also we observed additional band due to methemoglobin. Radiation of blood lead to the transition from hemoglobin (Fe2+) to methemoglobin (Fe3+) with a delocalization of iron from porphyrine plane. It was shown that FT-IR spectra indicate the radiation effects on hemoglobin.© (2008) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is per…

inorganic chemicalsScatteringChemistryAnalytical chemistryInfrared spectroscopyMethemoglobinSpectral lineFourier transform spectroscopysymbols.namesakeNuclear magnetic resonancesymbolsIrradiationHemoglobinRaman scatteringSPIE Proceedings
researchProduct

Surface Study of Pumice Supported Nickel Catalysts Used in the Hydrogenation of CO

1998

A series of pumice supported nickel catalysts used in the CO hydrogenation reaction were characterised by X-ray photoelectron spectroscopy. Qualitative and quantitative analysis of the XPS peaks have shown the effect of the calcination conditions on the chemical state of the nickel before hydrogenation and the particle size of the metal after reduction. Calcination at high temperature determined enrichment of sodium ions on the surface of the support and also on the metal particles. After exposure to the gas mixture CO/H2, formation of nickel carbides and other carbon species was checked. The correlation found between the surface atomic ratio Na/Si and the activity and selectivity of the ca…

inorganic chemicalsInorganic chemistrychemistry.chemical_elementlaw.inventionCatalysisMetalNickelChemical statechemistry.chemical_compoundchemistryX-ray photoelectron spectroscopylawvisual_artvisual_art.visual_art_mediumCalcinationAtomic ratioCarbon monoxide
researchProduct

Asymmetric [N–I–N]+halonium complexes in solution?

2020

Assessment of the solution equilibria of [bis(pyridine)iodine(I)]+ complexes by ESI-MS and NMR reveals the preference of iodine(I) to form complexes with a more basic pyridine. Mixtures of symmetric [bis(pyridine)iodine(I)]+ complexes undergo statistical ligand exchange, with a predominant entropic driving force favoring asymmetric systems. The influence of ligand basicity, concentration, temperature, and ligand composition is evaluated. Our findings are expected to facilitate the investigations, and the supramolecular and synthetic applications of halonium ions’ halogen bonds. peerReviewed

inorganic chemicals2019-20 coronavirus outbreakliuoksetLigandMetals and AlloysSupramolecular chemistrychemistry.chemical_elementliganditkompleksiyhdisteetGeneral ChemistryIodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonjodichemistry.chemical_compoundchemistryPyridineHalogenMaterials ChemistryCeramics and CompositesHalonium ionChemical Communications
researchProduct

Enhanced Permeability and Retention-like Extravasation of Nanoparticles from the Vasculature into Tuberculosis Granulomas in Zebrafish and Mouse Mode…

2018

The enhanced permeability and retention (EPR) effect is the only described mechanism enabling nanoparticles (NPs) flowing in blood to reach tumors by a passive targeting mechanism. Here, using the transparent zebrafish model infected with Mycobacterium marinum we show that an EPR-like process also occurs allowing different types of NPs to extravasate from the vasculature to reach granulomas that assemble during tuberculosis (TB) infection. PEGylated liposomes and other NP types cross endothelial barriers near infection sites within minutes after injection and accumulate close to granulomas. Although similar to 100 and 190 nm NPs concentrated most in granulomas, even similar to 700 nm liposo…

inorganic chemicalsEndotheliumGeneral Physics and Astronomy02 engineering and technologyPulmonary Artery010402 general chemistry01 natural sciencesPermeabilitylaw.inventionMiceConfocal microscopylawmedicineAnimalsGeneral Materials ScienceZebrafishTuberculosis PulmonaryMycobacterium marinumZebrafishLiposomeGranulomaMicroscopy ConfocalbiologyChemistryGeneral Engineeringtechnology industry and agriculture021001 nanoscience & nanotechnologybiology.organism_classificationExtravasation0104 chemical sciencesDisease Models Animalmedicine.anatomical_structurePermeability (electromagnetism)Drug deliveryBiophysicsMycobacterium marinumNanoparticles0210 nano-technology
researchProduct

Synergistic Anticancer Therapy by Ovalbumin Encapsulation-Enabled Tandem Reactive Oxygen Species Generation

2020

Abstract The anticancer efficacy of photodynamic therapy (PDT) is limited due to the hypoxic features of solid tumors. We report synergistic PDT/chemotherapy with integrated tandem Fenton reactions mediated by ovalbumin encapsulation for improved in vivo anticancer therapy via an enhanced reactive oxygen species (ROS) generation mechanism. O2 .− produced by the PDT is converted to H2O2 by superoxide dismutase, followed by the transformation of H2O2 to the highly toxic .OH via Fenton reactions by Fe2+ originating from the dissolution of co‐loaded Fe3O4 nanoparticles. The PDT process further facilitates the endosomal/lysosomal escape of the active agents and enhances their intracellular deliv…

inorganic chemicalsNanomedicines | Hot PaperOvalbuminmedicine.medical_treatmentRadicalsynergisticcisplatinPhotodynamic therapyAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisSuperoxide dismutasechemistry.chemical_compoundMicemedicineAnimalsHumansResearch Articleschemistry.chemical_classificationCisplatinReactive oxygen speciesOxidase testPhotosensitizing Agentsbiology010405 organic chemistryFenton reactionsDrug SynergismGeneral MedicineGeneral ChemistryhypoxicEndocytosis0104 chemical sciencesOvalbuminchemistryphotodynamic therapybiology.proteinBiophysicsMCF-7 CellsReactive Oxygen SpeciesNicotinamide adenine dinucleotide phosphatemedicine.drugResearch Article
researchProduct

Determination of copper, iron, molybdenum and silicon in hydrometallurgically roasted molybdenite concentrate solution by inductively coupled plasma …

1997

Abstract Inductively coupled plasma atomic emission spectrometry has been applied for the estimation of major constituents in molybdenite concentrate solutions produced by hydrometallurgical alkaline digestion. Copper, iron, molybdenum and silicon were considered as major constituents to be determined. Multiple linear regression was utilized for the control of matrix effects. Using simple acid-based standards, all the elements investigated could be determined with satisfactory results using an appropriate method of calculation.

inorganic chemicalsSiliconAnalytical chemistrychemistry.chemical_elementBiochemistryCopperAnalytical ChemistrychemistryMolybdenumMolybdeniteInductively coupled plasma atomic emission spectroscopyEnvironmental ChemistryInductively coupled plasmaSpectroscopyAtomic emission spectrometryAnalytica Chimica Acta
researchProduct

Enrichment and activation of smectite-poor clay

2011

A new method of smectite clay enrichment has been developed. The method is based on dispersing clay in a phosphate solution and sequential coagulation. The product of enrichment is characterized with X-ray powder diffraction, wavelength dispersive X-ray fluorescence spectrometry, differential thermal analysis and thermogravimetry. Sorption of methylene blue and hexadecylpyridinium bromide on raw and purified clays was studied.

inorganic chemicalsChemistryInorganic chemistryFluorescence spectrometrySorptionPhosphatecomplex mixturesThermogravimetrychemistry.chemical_compoundDifferential thermal analysisClay mineralsPowder diffractionMethylene blueNuclear chemistryIOP Conference Series: Materials Science and Engineering
researchProduct

CaCl2, Bisoxazoline, and Malonate: A Protocol for an Asymmetric Michael Reaction

2015

A mild protocol for the asymmetric Michael addition of dimethyl malonate to various α,β-unsaturated carbonyl compounds was developed. The salient feature of this methodology is that a cheap and environmentally friendly Lewis acid, CaCl2, was used as a catalyst. An aminoindanol- and pyridine-derived ligand provided in the presence of CaCl2 Michael adducts in moderate to high enantioselectivities. The scope of the reaction was demonstrated.

Bisoxazolineinorganic chemicalsAminoindanol010405 organic chemistryChemistryLigandOrganic ChemistryMalonateCaCl2macromolecular substances010402 general chemistrybehavioral disciplines and activities01 natural sciencesDimethyl malonatehumanities0104 chemical sciencesCatalysisAdductchemistry.chemical_compoundMalonateMichael reactionOrganic chemistryLewis acids and basesta116The Journal of Organic Chemistry
researchProduct