Search results for "COMPOUND"

showing 10 items of 35174 documents

Densities, Refractive Indices, and Derived Excess Properties of the Binary Systems Toluene + Isooctane and Methylcyclohexane + Isooctane and the Tern…

2000

This paper reports mesurements of the densities and refractive indices of the binary systems toluene + isooctane and methylcyclohexane + isooctane and the ternary systems tert-butyl alcohol (TBA) + toluene + isooctane and tert-butyl alcohol (TBA) + methylcyclohexane + isooctane over the entire range of composition at 298.15 K. Excess molar volumes and changes of refractive indices were evaluated from the experimental data obtained. These derived properties were fitted to variable-degree polynomials. The experimental values of physical properties were compared with the values estimated by different methods.

tert-Butyl alcoholTernary numeral systemGeneral Chemical EngineeringButanolAnalytical chemistryAlcoholGeneral ChemistryToluenechemistry.chemical_compoundMolar volumechemistryOrganic chemistryBinary systemMethylcyclohexaneJournal of Chemical & Engineering Data
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N-[3-Methyl-1-phenyl-1-(1H-tetrazol-1-yl)butan-2-yl]acetamide

2016

In the molecule of the title compound, C14H19N5O, the dihedral angle formed between the tetrazole and phenyl rings is 68.39 (4)°. In the crystal, molecules are linked by N—H...N, C—H...N and C—H...O hydrogen bonds to form two-dimensional networks extending parallel to thebcplane.

tetrazolecrystal structureacetamidebiologyChemistryHydrogen bondPlane (geometry)StereochemistryGeneral MedicineCrystal structureDihedral angle010402 general chemistry010403 inorganic & nuclear chemistrybiology.organism_classification01 natural sciences0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographyhydrogen bondslcsh:QD901-999TetraTetrazolelcsh:CrystallographyAcetamideIUCrData
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Production and Properties of Starch Citrates—Current Research

2020

Starch modification by chemical reaction is widely used to improve the properties of native starch. Modified by citric acid, starch is characterized by specific properties resulting from the presence of citrate residues and as a result of cross-linking starch. The chemicals used for preparing starch citrates are safe for human health and the natural environment compared to the harsh chemicals used for conventional modifications. Starch citrates are traditionally produced by heating starch–citric acid mixtures in semi-dry conditions or by a heat moisture treatment. The conditions of the modification process (roasting temperature, heating time, citric acid dose) and the botanic source or geno…

the properties of starch citrateHealth (social science)food.ingredientStarchReview02 engineering and technologyPlant Sciencelcsh:Chemical technologyHealth Professions (miscellaneous)MicrobiologyChemical reactionCrystallinitychemistry.chemical_compound0404 agricultural biotechnologyfoodresistant citrate starchlcsh:TP1-1185Food scienceResistant starchRoastingchemistry.chemical_classificationMoisturestarchfood and beverages04 agricultural and veterinary sciences021001 nanoscience & nanotechnologymethods of starch citrification040401 food scienceEnzymechemistry0210 nano-technologyCitric acidFood ScienceFoods
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Formation of Si/SiO2 Luminescent Quantum Dots From Mesoporous Silicon by Sodium Tetraborate/Citric Acid Oxidation Treatment

2019

We propose a rapid, one-pot method to generate photoluminescent (PL) mesoporous silicon nanoparticles (PSiNPs). Typically, mesoporous silicon (meso-PSi) films, obtained by electrochemical etching of monocrystalline silicon substrates, do not display strong PL because the silicon nanocrystals (nc-Si) in the skeleton are generally too large to display quantum confinement effects. Here we describe an improved approach to form photoluminescent PSiNPs from meso-PSi by partial oxidation in aqueous sodium borate (borax) solutions. The borax solution acts to simultaneously oxidize the nc-Si surface and to partially dissolve the oxide product. This results in reduction of the size of the nc-Si core …

theranosticsMaterials sciencePassivationSiliconSilicon dioxideOxidechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencessilicon nanoparticles (SiNPs)Monocrystalline siliconlcsh:Chemistrychemistry.chemical_compoundporous silicon (PS)Silicic acidOriginal ResearchAqueous solutionGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemistryChemical engineeringchemistrylcsh:QD1-999photoluminescencebiomedical application0210 nano-technologyMesoporous materialFrontiers in Chemistry
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The Scope of Application of Macrocyclic Polyamines Beyond Metal Chelation

2019

International audience; Recent advances in the use of radiometals for both imaging and therapy has spurred on the development of an original chemistry that endows radionuclide-chelating molecular cages with ever sharper physicochemical properties. Macrocyclic polyamines (MPAs) such as cyclen and DOTA are among the most frequently encountered cages for the design of new radiotracers, owing to their versatile chemistry that makes them customizable molecular tools. The idea of using MPAs for alternative purposes has recently emerged, with an eye towards benefiting from their unique topology, versatility, symmetry and water-solubility. This review summarizes strategies that have been recently i…

theranosticsbioactive compounds[CHIM.ORGA]Chemical Sciences/Organic chemistrymolecular platform[CHIM.THER]Chemical Sciences/Medicinal ChemistrymultivalencypolyazamacrocyclesEuropean Journal of Organic Chemistry
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A library of monoalkenylsilsesquioxanes as potential comonomers for synthesis of hybrid materials

2018

In this paper we demonstrate a facile and efficient synthesis of monoalkenylsubstituted POSS compounds, i.e., R7(Si8O12)-alkenyl and R7(Si8O12)(OSiMe2)-alkenyl with a functional alkenyl group of chain length (from vinyl to dec-9-enyl, with or without additional –OSiMe2– spacer between the silsesquioxane core and alkenyl moiety) and with five types of inert groups (Et, iBu, iOc, Cy, Ph) at the POSS core. These compounds constitute a library of monosubstituted POSS systems, including thorough spectroscopic and thermal characteristics. These findings could be especially useful for material chemists applying the compounds as modifiers or comonomers for copolymerization reaction, e.g., with olef…

thermal propertiespolyhedral oligomeric silsesquioxanes02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesalkenylsubstituted silsesquioxanesthermal stabilitySilsesquioxane0104 chemical scienceschemistry.chemical_compoundChain lengthchemistryCopolymerOrganic chemistryMoietyPhysical and Theoretical Chemistry0210 nano-technologyHybrid materialJournal of Thermal Analysis and Calorimetry
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Thiazole Analogues of the Marine Alkaloid Nortopsentin as Inhibitors of Bacterial Biofilm Formation

2020

Anti-virulence strategy is currently considered a promising approach to overcome the global threat of the antibiotic resistance. Among different bacterial virulence factors, the biofilm formation is recognized as one of the most relevant. Considering the high and growing percentage of multi-drug resistant infections that are biofilm-mediated, new therapeutic agents capable of counteracting the formation of biofilms are urgently required. In this scenario, a new series of 18 thiazole derivatives was efficiently synthesized and evaluated for its ability to inhibit biofilm formation against the Gram-positive bacterial reference strains Staphylococcus aureus ATCC 25923 and S. aureus ATCC 6538 a…

thiazole derivativeAquatic OrganismsStaphylococcus aureusIndolesantibiotic resistanceSettore BIO/05 - ZoologiaPharmaceutical ScienceMicrobial Sensitivity TestsBacterial growthSettore BIO/19 - Microbiologia Generalemedicine.disease_cause01 natural sciencesArticlenortopsentinAnalytical ChemistryMicrobiologylcsh:QD241-441Inhibitory Concentration 50chemistry.chemical_compoundAlkaloidsAntibiotic resistancelcsh:Organic chemistryDrug DiscoverymedicinePhysical and Theoretical ChemistryThiazoleStrain (chemistry)010405 organic chemistryPseudomonas aeruginosamarine alkaloids analoguesAlkaloidOrganic ChemistryImidazolesBiofilmantibiofilm agentsSettore CHIM/08 - Chimica Farmaceuticamarine alkaloids analogueantibiofilm agent0104 chemical sciencesThiazoles010404 medicinal & biomolecular chemistrychemistryChemistry (miscellaneous)Staphylococcus aureusBiofilmsPseudomonas aeruginosathiazole derivativesMolecular MedicineMolecules
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Crystal structure and Hirshfeld surface analysis of (Z)-4-chloro-N′-(4-oxothiazolidin-2-ylidene)benzenesulfonohydrazide monohydrate

2018

The asymmetric unit of the title thiazole derivative containing a sulfonylhydrazinic moiety, C9H8ClN3O3S2·H2O, consists of two independent molecules and two water molecules. The central parts of the molecules are twisted as both the molecules are bent at both the S and N atoms. In the crystal, N—H...N, N—H...O, C—H...O and O—H...O hydrogen-bonding interactions connect the molecules, forming layers parallel to the ab plane. Two-dimensional fingerprint plots associated with the Hirshfeld surface show that the largest contributions to the crystal packing come from O...H/H...O (32.9%) and H...H (22.6%) interactions.

thiazole derivativecrystal structureCrystallography010405 organic chemistryHydrogen bondBent molecular geometryGeneral ChemistryCrystal structure010403 inorganic & nuclear chemistryCondensed Matter PhysicsHydrazide01 natural sciences0104 chemical sciencesCrystalchemistry.chemical_compoundCrystallographychemistryQD901-999hydrogen bondsMoietyHirshfeld surface analysisGeneral Materials SciencePhysics::Chemical PhysicsBenzeneDerivative (chemistry)Acta Crystallographica Section E: Crystallographic Communications
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Oxidation-responsive and "clickable" poly(ethylene glycol) via copolymerization of 2-(methylthio)ethyl glycidyl ether

2016

Poly(ethylene glycol) (PEG) is a widely used biocompatible polymer. We describe a novel epoxide monomer with methyl-thioether moiety, 2-(methylthio)ethyl glycidyl ether (MTEGE), which enables the synthesis of well-defined thioether-functional poly(ethylene glycol). Random and block mPEG-b-PMTEGE copolymers (Mw/Mn = 1.05-1.17) were obtained via anionic ring opening polymerization (AROP) with molecular weights ranging from 5 600 to 12 000 g·mol-1. The statistical copolymerization of MTEGE with ethylene oxide results in a random microstructure (rEO = 0.92 ± 0.02 and rMTEG E = 1.06 ± 0.02), which was confirmed by in situ 1H NMR kinetic studies. The random copolymers are thermorespon…

thioether-functional PEGoxidation-responsiveEpoxide02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryRing-opening polymerizationMicelleCatalysischemistry.chemical_compoundColloid and Surface ChemistryPolymer chemistryCopolymerMoiety2-(methylthio)ethyl glycidyl etherEthylene oxidepoly(ethylene glycol)sulfoniumGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesmulti-functional PEGMonomerchemistryPEOpolyetherthermoresponsive0210 nano-technologyEthylene glycol
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Protein tyrosine nitration and thiol oxidation by peroxynitrite-strategies to prevent these oxidative modifications.

2013

The reaction product of nitric oxide and superoxide, peroxynitrite, is a potent biological oxidant. The most important oxidative protein modifications described for peroxynitrite are cysteine-thiol oxidation and tyrosine nitration. We have previously demonstrated that intrinsic heme-thiolate (P450)-dependent enzymatic catalysis increases the nitration of tyrosine 430 in prostacyclin synthase and results in loss of activity which contributes to endothelial dysfunction. We here report the sensitive peroxynitrite-dependent nitration of an over-expressed and partially purified human prostacyclin synthase (3.3 μM) with an EC50 value of 5 μM. Microsomal thiols in these preparations effectively co…

thiol oxidationprotein tyrosine nitrationlcsh:Chemistrychemistry.chemical_compoundCytochrome P-450 Enzyme SystemSf9 CellsTyrosinelcsh:QH301-705.5Spectroscopychemistry.chemical_classification0303 health sciencesbiologySuperoxide030302 biochemistry & molecular biologyGeneral MedicineComputer Science ApplicationsIntramolecular OxidoreductasesBiochemistryThiolprostacyclin synthasesuperoxideOxidation-ReductionPeroxynitriteOxidative phosphorylationSpodopteraCatalysisArticleperoxynitriteNitric oxideProstacyclin synthaseInorganic Chemistry03 medical and health sciencesnitric oxideddc:570NitrationPeroxynitrous AcidAnimalsHumansSulfhydryl CompoundsPhysical and Theoretical ChemistryMolecular Biology030304 developmental biologyOrganic Chemistrynitric oxide; superoxide; peroxynitrite; protein tyrosine nitration; thiol oxidation; peroxynitrite scavengers; prostacyclin synthasechemistrylcsh:Biology (General)lcsh:QD1-999biology.proteinTyrosineCattleperoxynitrite scavengersProtein Processing Post-TranslationalInternational journal of molecular sciences
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