Search results for " aroma"

showing 10 items of 370 documents

On the Reaction of 3-Bromo-2-nitrobenzo[b]thiophene 13C-Labeled at C-2 with 3-(Trifluoromethyl)aniline:  A Preliminary Insight into a Nucleophilic Su…

1997

The results of the title reaction have furnished proofs against a rearrangement of the carbon-atom skeleton and for a nitro group shift in the relevant nucleophilic substitution.

Substitution reactionTrifluoromethylStereochemistryKornblum–DeLaMare rearrangementfungiOrganic Chemistrybehavioral disciplines and activitiesbody regionschemistry.chemical_compoundchemistryNucleophilic aromatic substitutionparasitic diseasesNitroNucleophilic substitutionThiopheneAcid hydrolysisThe Journal of Organic Chemistry
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On-Surface Synthesis of Dibenzohexacenohexacene and Dibenzopentaphenoheptaphene

2021

We report the on-surface synthesis and gas-phase theoretical studies of two novel nanographenes, namely, dibenzohexacenohexacene and dibenzopentaphenoheptaphene, using 8,8′-dibromo-5,5′-bibenzo[rst]pentaphene as a precursor. These nanographenes display a combination of armchair and zigzag edges, as shown by noncontact atomic force microscopy (nc-AFM), and their electronic properties are elucidated by density functional theory (DFT) calculations which reveal relatively low HOMO-LUMO energy gaps of about 1.75 eV.

Surface (mathematics)chemistry.chemical_classificationchemistry010405 organic chemistryComputational chemistryPolycyclic aromatic hydrocarbonPolycyclicaromatichydrocarbonOn-surfacesynthesisGeneral Chemistry010402 general chemistry01 natural sciencesNanographene0104 chemical sciencesBulletin of the Chemical Society of Japan
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Synthesis of Isoxazoline Derivatives through Boulton–Katritzky Rearrangement of 1,2,4-Oxadiazoles

2013

The base-induced rearrangement of 1,2,4-oxadiazoles into isoxazoline derivatives is reported. This represents the first example of a three-atom side-chain rearrangement that involves a saturated CCO side chain at C-3 of the oxadiazole. Nonaromatic 3-amino-isoxazoline derivatives are obtained in good yields. Interestingly, this reaction occurs through the rearrangement of aromatic oxadiazoles to form less stable bonds than those that are broken.

Synthetic methods Rearrangement Heterocycles AromaticitySettore CHIM/06 - Chimica Organica
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Asymmetric tandem reactions: New synthetic strategies

2010

The use of domino and multicomponent reactions in asymmetric synthesis is constantly increasing nowadays. This allows for the synthesis of complex molecules in a single synthetic sequence, usually with high atom economy. Herein, we report three examples of new asymmetric tandem reactions recently developed in our laboratories, giving rise to new families of enantiomerically enriched fluorinated and nonfluorinated heterocycles. Thus, 1,4-dihydropyridines (1,4-DHPs) bearing fluorinated substituents at C6 were assembled by means of a Hantzsch-type reaction; cyclic β-amino carbonyl derivatives were prepared using a cross-metathesis (CM)–intramolecular aza-Michael sequence; while fluorinated ind…

TandemChemistryGeneral Chemical EngineeringEnantioselective synthesisSequence (biology)General Chemistrycyclic beta-amino carbonyl compoundElectrophilic aromatic substitutionCombinatorial chemistryDominoNucleophilefluorinated beta-amino acidsAtom economyMoleculeOrganic chemistrytandem reactionsfluorinated dihydropyridinefluorinated indolines
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Influence of preparation conditions on the catalytic performance of mo/h-zsm-5 for methane dehydroaromatization

2021

[EN] Methane, the main component of natural gas, is an interesting source of chemicals and clean liquid fuels, and a promising alternative raw material to oil. Among the possible direct routes for methane conversion, its aromatization under non-oxidative conditions has received increasing attention, despite the low conversions obtained due to thermodynamic limitations, because of its high selectivity to benzene. Mo/H-ZSM-5, the first bifunctional zeolite-catalyst proposed for this reaction, is still considered as one of the most adequate and has been widely studied. Although the mono- or bifunctional nature of the MDA mechanism is still under debate, it is generally accepted that the Mo spe…

TechnologyQH301-705.5QC1-999Inorganic chemistryCatalysts preparation010402 general chemistry01 natural sciencesMethaneCatalysischemistry.chemical_compoundMo/ZSM-5General Materials ScienceBiology (General)Methane aromatizationZeoliteBifunctionalBenzeneQD1-999InstrumentationFluid Flow and Transfer Processes010405 organic chemistryTPhysicsProcess Chemistry and TechnologyGeneral EngineeringAromatizationCatalyst activationEngineering (General). Civil engineering (General)0104 chemical sciencesComputer Science ApplicationsChemistrychemistryZeolitesTA1-2040ZSM-5Selectivity
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On the use of ionic liquids as mobile phase additives in high-performance liquid chromatography. A review.

2015

The popularity of ionic liquids (ILs) has grown during the last decades in several analytical separation techniques. Consequently, the number of reports devoted to the applications of ILs is still increasing. This review is focused on the use of ILs (mainly imidazolium-based associated to chloride and tetrafluoroborate) as mobile phase additives in high-performance liquid chromatography (HPLC). In this approach, ILs just function as salts, but keep several kinds of intermolecular interactions, which are useful for chromatographic separations. Both cation and anion can be adsorbed on the stationary phase, creating a bilayer. This gives rise to hydrophobic, electrostatic and other specific in…

TetrafluoroborateHETEROCYCLIC AROMATIC-AMINESBiochemistryHigh-performance liquid chromatographyChlorideAnalytical Chemistrychemistry.chemical_compoundSilanol suppressionAdsorptionSOLUBILIZING ABILITIES[CHIM.ANAL]Chemical Sciences/Analytical chemistryPhase (matter)medicineEnvironmental ChemistryOrganic chemistryOptimisationSpectroscopyHALF-WIDTH PLOTSMechanisms of retentionOVERLOADED BAND PROFILESANALYTICAL-CHEMISTRYSILANOL-SUPPRESSING POTENCYHYDROCARBONACEOUS STATIONARY PHASESIntermolecular forceAdditivesHigh-performance liquid chromatographyIonic liquidsSilanolROOM-TEMPERATURERETENTION MECHANISMChemical engineeringchemistryRP-HPLCIonic liquidmedicine.drugAnalytica chimica acta
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Room Temperature Home Prepared TiO2 Rutile Used for Selective Photocatalytic Oxidation of Aromatic Alcohols to Aldehydes in Aqueous Medium

2009

TiO2 Aromatic alcohols Partial oxidation
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Titania Photocatalysts for Selective Oxidations in Water

2011

Heterogeneous photocatalysis by polycrystalline semiconductor oxides is an unconventional technology that has been mainly applied for the degradation of organic and inorganic pollutants in both the vapor and liquid phase. The application of photocatalysis in synthetic routes has also been researched in recent years, demonstrating its viability as an alternative route in organic chemistry. This work illustrates the main findings in the application of heterogeneous photocatalysis to the oxidation of organic compounds dissolved in water, free of any organic co-solvent. Two main aspects of the oxidative process have been studied: the first one is the partial oxidation of various mono-substitute…

TitaniumTiO2 photocatalysis selective oxidationsChemistryGeneral Chemical EngineeringInorganic chemistryWaterPhotochemical ProcessesHeterogeneous catalysisHydrocarbons AromaticCombinatorial chemistryCatalysisWater PurificationGeneral EnergyAlcoholsEnvironmental ChemistryGeneral Materials ScienceSettore CHIM/07 - Fondamenti Chimici Delle TecnologieOxidation-ReductionEnvironmental Restoration and RemediationWater Pollutants ChemicalChemSusChem
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Polycyclic aromatic hydrocarbons (PAHs) and their oxygen-containing derivatives (OPAHs) in soils from the Angren industrial area, Uzbekistan.

2009

We measured the concentrations and depth distribution (0-10, 10-20 cm) of 31 PAHs and 12 OPAHs in soils at eleven equidistant sampling points along a 20-km transect in the Angren industrial region (coal mine, power plant, rubber factory, gold mine), Uzbekistan to gain an insight into their concentrations, sources, and fate. Concentrations of all compounds were mostly much higher in the 0-10 cm than in the 10-20 cm layer except in disturbed soil close to the coal mine. Proximity to one of the industrial emitters was the main determinant of PAH and OPAH concentrations. The Sigma31PAHs concentrations correlated positively with the Sigma7 carbonyl-OPAH (r=0.98, p<0.01), Sigma5 hydroxyl-OPAH (r=…

TopsoilPersistent organic pollutantOpahbiologyChemistryHealth Toxicology and MutagenesisTrace elementIndustrial WasteSoil classificationGeneral MedicineUzbekistanToxicologybiology.organism_classificationPollutionSoil contaminationEnvironmental chemistrySoil waterSoil PollutantsPolycyclic HydrocarbonsPolycyclic Aromatic HydrocarbonsOxygen CompoundsEnvironmental MonitoringEnvironmental pollution (Barking, Essex : 1987)
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Photo-polymerized lauryl methacrylate monolithic columns for CEC using lauroyl peroxide as initiator

2009

Lauryl methacrylate (LMA)-ester based monolithic columns photo-polymerized using lauroyl peroxide (LPO) as initiator were prepared, and their morphological and CEC properties were studied. The composition of the polymerization mixture (i.e. ratios of monomers/porogenic solvents, 1,4-butanediol/1-propanol and LMA/crosslinker) was optimized. The morphological and chromatographic properties of LMA columns were evaluated by means of SEM pictures and van Deemter plots of PAHs, respectively. The polymerization mixture selected as optimal provided a fast separation of a mixture of PAHs with excellent efficiencies (minimum plate heights of 8.9-11.1 μm). Satisfactory column-to-column (RS D < 4.5%) a…

Van Deemter equationLipid PeroxidesChromatographyResolution (mass spectrometry)PhotochemistryClinical BiochemistryReproducibility of ResultsLauroyl peroxideBiochemistryAnalytical Chemistrychemistry.chemical_compoundMonomerchemistryPolymerizationCapillary ElectrochromatographyNitrilesMicroscopy Electron ScanningMethacrylatesAlkylbenzenesPolycyclic Aromatic HydrocarbonsLauryl methacrylateELECTROPHORESIS
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