Search results for " aroma"

showing 10 items of 370 documents

Miscela binaria liquido ionico/[bmim][N3]: un mezzo efficace per la sintesi di arilazidi mediante SNAr

Settore CHIM/06 - Chimica Organicaionic liquids aromatic azides nucleophilic aromatic substitution
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Nanoparticelle di Ag-poliamminoCD come catalizzatori per la riduzione di nitrocomposti aromatici

2014

Sistemi nanoparticellari di Argento protetti con poliammino-beta-ciclodestrine sono stati preparati, caratterizzati, e impiegati come catalizzatori per la riduzione con boroidruro di sodio di una serie di nitrocomposti aromatici modello 1-8. Tale reazione costituisce una interessante alternativa rispetto ai metodi di riduzione più comuni (LiAlH4, Zn/HCl), che prevedono l’uso di condizioni di reazione piuttosto drastiche. La cinetica della reazione considerata è stata approfonditamente studiata al fine di chiarire il ruolo meccanicistico del catalizzatore. E’ stato trovato, infatti, che il processo risulta di ordine misto rispetto al substrato, e che le costanti cinetiche apparenti di reazio…

Settore CHIM/06 - Chimica Organicananoparticelle ciclodestrine nitrocomposti aromatici catalisi
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Photocatalytic process intensification by coupling with pervaporation

2011

The integration of photocatalysis with a membrane separation process, in particular pervaporation, permits the recovery of valuable intermediate compounds (aromatic aldehydes) while they are produced avoiding their further degradation in the reactive ambient. In this way the yield and the conversion are enhanced. The coupling of the two processes is straightforward and the integration is complete even maintaining pervaporation and photocatalysis in two separate apparatuses provided that the process stream is continuously recycled at a sufficiently high flow rate. Additional advantages are: higher degree of purification of the aldehyde in the powder-free product stream, semicontinuous produc…

Settore ING-IND/24 - Principi Di Ingegneria ChimicaChromatographyChemistrySettore ING-IND/25 - Impianti ChimiciAROMATIC ALDEHYDEPROCESS INTENSIFICATIONGeneral ChemistryCatalysisSeparation processVolumetric flow rateMembrane technologyPhotocatalysis Pervaporation Process ntensification Aromatic aldehydes Green chemistryChemical engineeringPERVAPORATIONYield (chemistry)Scientific methodPhotocatalysisDegradation (geology)PervaporationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTOCATALYSISGREEN CHEMISTRY
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Photocatalytic oxidation of aromatic alcohols to aldehydes in aqueous suspension of home prepared titanium dioxide: 2. Intrinsic and surface features…

2008

Some intrinsic electronic properties of home prepared (HP) TiO2 catalysts were investigated by diffuse reflectance spectroscopy and quasi-Fermi level measurements. These powders were used for carrying out the photocatalytic oxidation of benzyl alcohol to benzaldehyde and CO2 in water; the selectivity for aldehyde formation was enhanced by the addition of small amounts of ethanol, a typical hole trap. The values of band gap, valence band and conduction band edges are almost identical for all the HP samples in which anatase phase is predominant, whereas appreciable differences can be noticed for an HP sample containing high amount of rutile phase. A comparative ATR-FTIR study of the HP cataly…

Settore ING-IND/24 - Principi Di Ingegneria ChimicaIn situ ATR-FTIR analysisPhotocatalysis AT-FTIR TiO2 Aromatic alcohols Aliphatic alcohol Selective oxidationTiO2Selective oxidationPhotocatalysisAromatic alcoholsAliphatic alcohol
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Dibenzocycloheptatriene as end-group of Thiele and tetrabenzo-Chichibabin hydrocarbons

2020

The authors are grateful for the financial support from: MICIU/FEDER/AEI, Spain (PG2018-101181-B-I00, PGC2018-095808B-I00, MAT2016-80826-R, FIP-2018-HECTIC-PTM, Prometeo2019/076 and the "Severo Ochoa" Programme for Centres of Excellence in R & D; SEV-2015-0496), the European Research Council (ERC) (677023), DGR (Catalunya) (2017-SGR-918), and SNSF (Switzerland, TS., PZ00P2_174175). We thank the CSIRC-Alhambra and SciCore (Basel, Switzerland) for supercomputing facilities and the Servei de RMN, UAB, for instrument time.

SingletAggregation-induced emissionPolycyclic aromatic hydrocarbon010402 general chemistry01 natural sciencesCatalysisClosed-shellComputational chemistryMaterials ChemistrySinglet stateAggregation-induced emissionOpen shellchemistry.chemical_classification010405 organic chemistryChemistryDiradicalMetals and AlloysGeneral Chemistry3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnd-groupTerminal (electronics)Ceramics and CompositesPolycyclic aromatic-hydrocarbon
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Effect of rhamnolipids on microbial biomass content and biochemical parameters in soil contaminated with coal tar creosote

2019

AbstractThe objective of the present study was to compare the effect of rhamnolipids on the microbial biomass content and the activity of dehydrogenases (DHA), acid phosphatase (ACP), alkaline phosphatase (ALP), and urease (URE) in soil contaminated with two types of coal tar creosote: type C and type GX-Plus. The experiment was carried out on samples of sandy clay loam under laboratory conditions. Coal tar creosote was added to soil samples at a dose of 0 and 10 g·kg−1 DM, along with rhamnolipids at a dose of 0, 10, 100, and 1000 mg·kg−1 DM. The humidity of the samples was brought to 60% maximum water holding capacity, and the samples were incubated at 20°C. Microbial and biochemical param…

Soil testUreaseQH301-705.5polycyclic aromatic hydrocarbonsBiomass010501 environmental sciencescomplex mixtures01 natural sciencesGeneral Biochemistry Genetics and Molecular Biologylaw.inventionBioremediationbioremediationlawmedicineBiology (General)Coal tarsandy clay loampolycycli aromatic hydrocarbons0105 earth and related environmental sciencesGeneral Immunology and MicrobiologybiologyGeneral NeuroscienceAcid phosphatase04 agricultural and veterinary sciencessoil enzymatic activityCreosoteEnvironmental chemistryLoam040103 agronomy & agriculturebiology.protein0401 agriculture forestry and fisheriesGeneral Agricultural and Biological SciencesResearch Articlemedicine.drugOpen Life Sciences
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Reduced graphene oxide-based magnetic composite for trace determination of polycyclic aromatic hydrocarbons in cosmetics by stir bar sorptive dispers…

2020

This work describes a sensitive and rapid analytical method for trace determination of polycyclic aromatic hydrocarbons (PAHs) in cosmetic samples. The proposed method is based on stir bar sorptive-dispersive microextraction (SBSDME). A magnetic composite made of CoFe2O4 magnetic nanoparticles embedded into reduced graphene oxide sheets is used as sorbent phase. After the extraction, the target analytes are desorbed in toluene and then analyzed by gas chromatography-mass spectrometry (GC-MS). The main parameters involved in the extraction procedure (i.e., composite amount, extraction time and desorption time) were evaluated and optimized to provide the best extraction efficiency. The method…

SorbentCosmetics010402 general chemistryMass spectrometryFerric Compounds01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryMatrix (chemical analysis)Magneticschemistry.chemical_compoundLimit of DetectionPolycyclic Aromatic HydrocarbonsSolid Phase MicroextractionDetection limitChromatography010401 analytical chemistryOrganic ChemistryExtraction (chemistry)CobaltGeneral MedicineToluene0104 chemical sciencesLinear rangechemistryStandard additionGraphiteJournal of Chromatography A
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2020

Electrophilic (het)arenes can undergo reactions with nucleophiles yielding π- or Meisenheimer (σ-) complexes or the products of the SNAr addition/elimination reactions. Such building blocks have only rarely been employed for the design of enzyme inhibitors. Herein, we demonstrate the combination of a peptidic recognition sequence with such electrophilic (het)arenes to generate highly active inhibitors of disease-relevant proteases. We further elucidate an unexpected mode of action for the trypanosomal protease rhodesain using NMR spectroscopy and mass spectrometry, enzyme kinetics and various types of simulations. After hydrolysis of an ester function in the recognition sequence of a weakly…

StereochemistryCarboxylic acidmedicine.medical_treatmentPharmaceutical Science010402 general chemistry01 natural sciencesAnalytical ChemistryNucleophileNucleophilic aromatic substitutionDrug DiscoverymedicineEnzyme kineticsPhysical and Theoretical Chemistrychemistry.chemical_classificationProteasebiology010405 organic chemistryOrganic ChemistryActive siteCysteine proteaseMeisenheimer complex0104 chemical scienceschemistryChemistry (miscellaneous)biology.proteinMolecular MedicineMolecules
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Detoxication of carcinogenic fjord-region diol epoxides of polycyclic aromatic hydrocarbons by glutathione transferase P1-1 variants and glutathione.

1998

AbstractEpidemiological studies suggest that individuals differing in the expression of allelic variants of the human glutathione transferase (GST) Pi gene differ in susceptibility to chemical carcinogens such as polycyclic aromatic hydrocarbons (PAH). This study reports the catalytic efficiencies (kcat/Km) of two naturally occurring variants, GSTP1-1/I-105 and GSTP1-1/V-105, towards a series of fjord-region diol epoxides representing potent biologically active PAH metabolites, and two GSTP1-1 mutants with Ala105 and Trp105 in the active site. The results indicate that individuals who are homozygous for the allele encoding GSTP1-1/V-105 might be more susceptible to PAH carcinogenesis due to…

StereochemistryCarcinogenesisMutantBiophysicsPolycyclic aromatic hydrocarbonurologic and male genital diseasesBiochemistryCatalysischemistry.chemical_compoundStructure-Activity RelationshipStructural BiologyGeneticspolycyclic compoundsStructure–activity relationshipHumansGlutathione conjugationPolycyclic Aromatic HydrocarbonsMolecular BiologyGeneneoplasmsCarcinogenGlutathione Transferasechemistry.chemical_classificationbiologyMolecular StructureChemistryActive siteGenetic VariationBiological activityCell BiologyGlutathioneGlutathioneFjord regionPolycyclic aromatic hydrocarbonKineticsBiochemistryDiol epoxideHuman glutathione transferase P1-1Inactivation Metabolicbiology.proteinCarcinogensFEBS letters
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Regioselective substitution of 6,7-dichloroquinoline-5,8-dione: synthesis and X-ray crystal structure of 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dion…

2003

6,7-Dichloroquinoline-5,8-dione (1) was reacted with a number of 2-aminopyridine derivatives. Of the several possible products of this reaction, 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dione (6), produced by condensation and rearrangement, was obtained as the major product, and its structure was subsequently unambigously determined by X-ray crystallographic study. Ortho-quinones were produced via nucleophilic substitution at position C7, which was unexpected, considering that para-quinones were produced via C6 substitution in the reaction between compound 1 and ethyl acetoacetate in our previous work. Such unexpected nucleophilic substitution at C7 provides an effective, yet simple route, t…

StereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryMedicinal chemistryChemical synthesisInhibitory Concentration 50chemistry.chemical_compoundNucleophilic aromatic substitutionDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansMolecular BiologySubstitution reactionFluorenesMolecular StructureOrganic ChemistryQuinonesRegioselectivityStereoisomerismQuinonechemistryDoxorubicinEthyl acetoacetateQuinolinesMolecular MedicineAcid hydrolysisDrug Screening Assays AntitumorBioorganic & Medicinal Chemistry
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