Search results for "Catalysis"

showing 10 items of 5944 documents

Photocatalytic oxidation of aromatic alcohols to aldehydes in aqueous suspension of home-prepared titanium dioxide

2008

Abstract Oxygenated aqueous suspensions of home-prepared (HP) and commercial TiO2 catalysts were used in a batch photoreactor for carrying out the oxidation of benzyl alcohol (BA) and 4-methoxybenzyl alcohol (MBA) under different operative conditions. HP catalysts were synthesized from TiCl4 and underwent a hydrolysis treatment of different times under mild conditions. The textural characterization of catalysts was carried out with XRD, SEM observations, BET surface area and porosity measurements. For both alcohols the main oxidation products were the corresponding aromatic aldehydes and CO2. The HP catalysts exhibited selectivity values towards the aldehyde production up to 28% (BA convers…

chemistry.chemical_classificationProcess Chemistry and TechnologyButanolAlcoholAldehydeCatalysisCatalysischemistry.chemical_compoundchemistryBenzyl alcoholAlcohol oxidationOrganic chemistryMethanolPartial oxidationApplied Catalysis A: General
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Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
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SiO2-supported vanadium magnesium mixed oxides as selective catalysts for the oxydehydrogenation of short chain alkanes

2001

Abstract Unsupported and SiO 2 -supported VMgO mixed oxides catalysts have been prepared, characterized and tested in the oxidation of propane, n -butane and propylene. Mg-vanadates are observed by XRD, IR and Raman spectroscopy in both pure and supported VMgO catalysts, although the effective Mg/V ratio, in the VMgO phases formed, depends on the silica content. Since SiO 2 reacts partially with MgO during the calcination step, forming Mg 2 SiO 4 , the effective Mg/V ratio depends on the silica content. In this sense, pyro -Mg 2 V 2 O 7 is mainly formed on supported catalysts with Mg/V atomic ratios lower than 4, while ortho -Mg 3 V 2 O 8 is observed on supported catalysts with Mg/V atomic …

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryVanadiumchemistry.chemical_elementButaneCatalysisCatalysisPropenechemistry.chemical_compoundHydrocarbonchemistryPropaneAtomic ratioPartial oxidationApplied Catalysis A: General
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Translocation of enzymes into a mesoporous MOF for enhanced catalytic activity under extreme conditions

2019

Translocation of protease into mesoporous MIL-101-NH2 results in enhanced catalytic activity, excellent recyclability and tolerance to competing enzymes.

chemistry.chemical_classificationProtease010405 organic chemistrymedicine.medical_treatmenteducationfungiQuímica organometàl·licaGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryhumanities0104 chemical sciencesEnzyme catalysisCatalysisChemistryEnzymechemistryBiocatalysismedicineBiocompositeMesoporous material
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Enzyme molecular mechanism as a starting point to design new inhibitors: a theoretical study of O-GlcNAcase.

2011

O-Glycoprotein 2-acetamino-2-deoxy-β-d-glucopyranosidase (O-GlcNAcase) hydrolyzes O-linked 2-acetamido-2-deoxy-β-d-glucopyranoside (O-GlcNAc) residues from post-translationally modified serine/threonine residues of nucleocytoplasmic protein. The chemical process involves substrate-assisted catalysis, where two aspartate residues have been identified as the two key catalytic residues of O-GlcNAcase. In this report, the first step of the catalytic mechanism used by O-GlcNAcase involving substrate-assisted catalysis has been studied using a hybrid quantum mechanical/molecular mechanical (QM/MM) Molecular Dynamics (MD) calculations. The free energy profile shows that the formation of the oxazol…

chemistry.chemical_classificationProtonStereochemistryClostridium perfringensOxazolineMolecular Dynamics Simulationbeta-N-AcetylhexosaminidasesSurfaces Coatings and FilmsCatalysisSubstrate SpecificitySerinechemistry.chemical_compoundHydrolysisMolecular dynamicsEnzymechemistryMaterials ChemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThreonineEnzyme InhibitorsOxazolesThe journal of physical chemistry. B
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Bistetrazine-Cyanines as Double-Clicking Fluorogenic Two-Point Binder or Crosslinker Probes

2018

Fluorogenic probes can be used to minimize the background fluorescence of unreacted and nonspecifically adsorbed reagents. The preceding years have brought substantial developments in the design and synthesis of bioorthogonally applicable fluorogenic systems mainly based on the quenching effects of azide and tetrazine moieties. The modulation power exerted by these bioorthogonal motifs typically becomes less efficient on more conjugated systems; that is, on probes with redshifted emission wavelength. To reach efficient quenching, that is, fluorogenicity, even in the red range of the spectrum, we present the synthesis, fluorogenic, and conjugation characterization of bistetrazine-cyanine pro…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryChemistryOrganic ChemistryPeptideGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesFluorescenceCombinatorial chemistryCatalysis0104 chemical sciencesTetrazinechemistry.chemical_compoundCovalent bondAzideBioorthogonal chemistryChemistry - A European Journal
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Influence of Several Effectors on the Structure-Activity Relationship of Spleen Phosphodiesterase

1993

The influence of Mg(II) and organic solvents on the structure-activity relationship of spleen phosphodiesterase II was analyzed using UV and fluorescence spectroscopies. An increase in the RNase activity found in the presence of Mg(II) was related to the enzyme-Mg(II) interaction detected by UV spectroscopy. In the fluorescence spectra of phosphodiesterase strong hypochromic and bathochromic effects were observed when RNA was present at a concentration (52 μg ml−1) of the same magnitude as the concentration that inhibits the activity (Ki = 40 μg ml−1). The strong quenching observed in the presence of RNA shows the importance of large dynamic and static quenching of the Trp residues of the e…

chemistry.chemical_classificationQuenching (fluorescence)ChemistryPhosphodiesteraseBiochemistryFluorescenceCatalysisFluorescence spectroscopyUltraviolet visible spectroscopyEnzymeBiochemistryBathochromic shiftBiophysicsDenaturation (biochemistry)General Agricultural and Biological SciencesBiotechnologyBiocatalysis
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Photocatalysis within Hyperbranched Polyethers with a Benzophenone Core

2008

Quenching and product studies have been performed to demonstrate the suitability of hyperbranched polyethers with a tetrafunctionalized benzophenone core as photocatalysts. The triplet photosensitized transformation of an unsaturated diazo compound has been used as the model reaction. The polymer with highest molecular weight led to a similar product distribution even after several catalytic cycles, which evidences its excellent photostability under prolonged irradiation time. We attribute this to the stabilizing effect of the hyperbranched polymer shell.

chemistry.chemical_classificationQuenching (fluorescence)Organic ChemistryEtherPolymerPhotochemistryProduct distributionCatalysischemistry.chemical_compoundchemistryPolymer chemistryBenzophenonePhotocatalysisDiazoThe Journal of Organic Chemistry
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New insights into the water-solubilization of thiol-sensitive fluorogenic probes based on long-wavelength 7-hydroxycoumarin scaffolds

2014

Abstract The synthesis and photophysical properties of novel water-soluble phenol-based fluorophores derived from 3-benzothiazolyl-7-hydroxycoumarin and emitting in the range 485–631 nm are described. Further conversion into thiol-sensitive fluorogenic probes through the chemical modification of their hydroxyl group was next investigated. Depending on the type of thiol-reactive quenching moiety used (2,4-dinitrobenzenesulfonyl ester, 2,4-dinitrophenyl ether or benzoquinone-type Michael acceptors) and the water-solubilizing group(s) pre-introduced into the coumarin core, dramatic differences in the thiol-induced fluorescence activation of these pro-fluorophores under physiological conditions…

chemistry.chemical_classificationQuenching (fluorescence)[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringChemical modificationEther[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.THER]Chemical Sciences/Medicinal ChemistryPhotochemistryCoumarinFluorescence[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryThiolPhenolMoietyComputingMilieux_MISCELLANEOUS[CHIM.CHEM]Chemical Sciences/CheminformaticsDyes and Pigments
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Diastereodivergent Synthesis of Fluorinated Cyclic β(3)-Amino Acid Derivatives.

2015

The ability of 2-p-tolylbenzyl carbanions to behave as a source of chiral benzylic nucleophiles has been shown in its reaction with fluorinated imines. The process takes place with high levels of stereocontrol, rendering the corresponding amines as single diastereoisomers. Subsequent cross-metathesis followed by intramolecular aza-Michael reaction makes the synthesis of fluorinated homoproline derivatives bearing three stereogenic centers possible. Furthermore, the selectivity of the cyclization process can easily be tuned up in a diastereodivergent manner simply by changing the reaction conditions.

chemistry.chemical_classificationReaction conditionsHydrocarbons FluorinatedMolecular StructureProlineOrganic ChemistryDiastereomerBiochemistryCatalysisAmino acidStereocenterchemistryNucleophileIntramolecular forceOrganic chemistryPhysical and Theoretical ChemistryAmino AcidsSelectivityCarbanionOrganic letters
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