Search results for "ALK"

showing 10 items of 4314 documents

A kinetic study of the basic hydrolysis of 2-phenylethyl nitrite in the presence of borate buffer and β-cyclodextrin

2002

The kinetics of the hydrolysis of 2-phenylethyl nitrite have been studied in basic aqueous solutions (borate buffer) in the absence and presence of β-cyclodextrin. The observed kinetic trends show that the hydrolysis reaction consists of at least three subsequent processes. The first is a fast acid-base reaction between the boron atom of boric acid and oxygen atom of the alkyl nitrite. The second one should be the nucleophilic attack of hydroxyl ion on the alkyl nitrite. The last process could be referred to as a combination of transfer of hydrogen acid to a water molecule followed by ruptures of nitrogen-oxygen and boron-oxygen bonds. The effect of β- cyclodextrin on each process is also d…

inorganic chemicalschemistry.chemical_classificationAqueous solutionCyclodextrinOrganic ChemistryKineticsInorganic chemistryMedicinal chemistrylcsh:QD241-441Boric acidchemistry.chemical_compoundHydrolysislcsh:Organic chemistryNucleophilechemistryNitriteAlkylArkivoc
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On the effect of the nature of counterions on the self-assembly of polyoxyethylene alkyl ether carboxylic acids

2020

In this contribution, we investigate the effect of the type of counterion on the properties of dilute solutions of polyoxyethylene alkyl ether carboxylic acids. Two different surfactants, presenting an oleic acid alkyl chain and on-average five and nine ethylene oxide units, and terminated by a weakly anionic carboxymethyl group were studied. The surfactants were gradually ionized with sodium hydroxide, arginine, and choline hydroxide. The solutions properties were probed by light scattering, electrophoretic mobility, density and sound velocity measurements, as well as by small-angle neutron scattering. To our initial surprise, no specific effect arising from the nature of the counterion co…

inorganic chemicalschemistry.chemical_classificationEthylene oxideCharge density02 engineering and technologyGeneral ChemistryNeutron scattering010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundPulmonary surfactantchemistrySodium hydroxideCounterion condensationSurfactantPolymer chemistryCounterion0210 nano-technologyAlkylSettore CHIM/02 - Chimica FisicaSoft Matter
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Magnetic Core–Shell Nanoparticles as Carriers for Olefin Dimerization Catalysts

2013

We report the covalent support of functionalized nickel complexes on magnetic core–shell hybrid particles γ-Fe2O3/SiO2. Two completely different ways of connecting the particle with these nickel complexes were carried out. The first approach used the hydrosilylation method between the alkene-substituted nickel complex and a silane. In a second approach, the particles were connected with the complexes by means of click chemistry (copper-catalyzed Huisgen 1,3-dipolar cycloaddition). For this purpose, the nickel complexes were substituted with an alkyne moiety. Transmission and scanning electron microscopies, energy-dispersive X-ray diffraction, and FTIR spectroscopy were the methods employed …

inorganic chemicalschemistry.chemical_classificationHydrosilylationNanoparticleAlkynechemistry.chemical_elementPhotochemistryCycloadditionCatalysisInorganic Chemistrychemistry.chemical_compoundNickelchemistryotorhinolaryngologic diseasesClick chemistryMoietyEuropean Journal of Inorganic Chemistry
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Synthesis, characterization and antimicrobial activity of palladium(II) complexes with some alkyl derivates of thiosalicylic acids: Crystal structure…

2012

Abstract S-Alkyl (R = benzyl, methyl, ethyl, propyl and butyl) derivatives of thiosalicylic acid and the corresponding palladium(II) complexes were prepared and their structures were proposed on the basis of infrared, 1H and 13C NMR spectroscopy. The cis geometrical configurations of the isolated complexes were proposed on the basis of an X-ray structural study of the bis(S-benzyl-thiosalicylate)–palladium(II), [Pd(S-bz-thiosal)2] complex. Antimicrobial activity of the tested compounds was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 26 species of microorganisms. The tested ligands, with a few exceptions, sho…

inorganic chemicalschemistry.chemical_classificationThiosalicylic acidbiologyStereochemistrychemistry.chemical_elementCrystal structurebiology.organism_classificationAntimicrobialMedicinal chemistryAspergillus fumigatusInorganic Chemistrychemistry.chemical_compoundMinimum inhibitory concentrationchemistryMaterials ChemistryPhysical and Theoretical ChemistryAntibacterial activityta116AlkylPalladiumPolyhedron
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Divergent reactivity of nucleophilic 1-bora-7a-azaindenide anions

2017

The reactions of 1-bora-7a-azaindenide anions, prepared in moderate to excellent yields by reduction of the appropriate 1-bora-7a-azaindenyl chlorides with KC8 in THF, with alkyl halides and carbon dioxide were studied. With alkyl halides (CH2Cl2, CH3I and BrCH(D)CH(D)tBu), the anions behave as boron anions, alkylating the boron centre via a classic SN2 mechanism. This was established with DFT methods and via experiments utilizing the neo-hexyl stereoprobe BrCH(D)CH(D)tBu. These reactions were in part driven by a re-aromatization of the six membered pyridyl ring upon formation of the product. Conversely, in the reaction of the 1-bora-7a-azaindenide anions with CO2, a novel carboxylation of …

inorganic chemicalschemistry.chemical_classificationanionit010405 organic chemistryHalidechemistry.chemical_element010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryNucleophilechemistryCarboxylation13. Climate actionbooriSN2 reactionReactivity (chemistry)Boronboronta116anionsAlkyl
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Thieme Chemistry Journals Awardees – Where Are They Now? Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

2017

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

inorganic chemicalschemistry.chemical_classificationmolybdenum pentachloridedisulfides010405 organic chemistryArylOrganic Chemistrychemistry.chemical_elementMolybdenum pentachloride010402 general chemistryoxidative coupling01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMolybdenumReagentcross-couplingOrganic chemistryOxidative coupling of methaneC–S bond formationAlkylSynlett
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Reaction of 2-acetyltetralone with some esters of benzoic acid

1986

In order to investigate the pharmacological screening of a number of pyran-4-ones their synthesis by cyclization with sulphuric acid of the corresponding 1,3,5-triketones has been carried out with high yields. In the course of preparation of the latter the reaction of 2-acetyltetralone with some esters of benzoic acid derivatives has been studied and in particular, for a number of them, an interesting nucleophilic substitution of a chlorine atom with an alkoxy group on a benzenic nucleus has been evidenced.

inorganic chemicalschemistry.chemical_compoundBicyclic moleculechemistryOrganic ChemistryChlorine atomAlkoxy groupNucleophilic substitutionTriketoneOrganic chemistryAcid hydrolysisSulfuric acidBenzoic acidJournal of Heterocyclic Chemistry
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ChemInform Abstract: Reaction of 2-Acetyltetralone with Some Esters of Benzoic Acid.

1987

In order to investigate the pharmacological screening of a number of pyran-4-ones their synthesis by cyclization with sulphuric acid of the corresponding 1,3,5-triketones has been carried out with high yields. In the course of preparation of the latter the reaction of 2-acetyltetralone with some esters of benzoic acid derivatives has been studied and in particular, for a number of them, an interesting nucleophilic substitution of a chlorine atom with an alkoxy group on a benzenic nucleus has been evidenced.

inorganic chemicalschemistry.chemical_compoundChemistryChlorine atomAlkoxy groupNucleophilic substitutionOrder (group theory)General MedicineMedicinal chemistryBenzoic acidChemInform
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Friedel-Crafts catalytic alkylations using rare earth-based mineral supports

1998

Abstract Rare earth halides supported on mineral supports (K10 montmorillonite and silica) were investigated as catalysts for Friedel-Crafts alkylations. This project concerns the replacement of the widely used Lewis acid AlCl3 in Friedel-Crafts reactions by environmentally friendly catalysts in that they circumvent the production of aluminum waste. The catalytic activity of these heterogeneous catalysts was established in a series of alkylations of aromatic compounds.

inorganic chemicalsintegumentary systemHalideGeneral ChemistryAlkylationHeterogeneous catalysisEnvironmentally friendlyCatalysischemistry.chemical_compoundMontmorillonitechemistryOrganic chemistryLewis acids and basesFriedel–Crafts reactionComptes Rendus de l'Académie des Sciences - Series IIC - Chemistry
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Formation of nanosized strontium substituted hydroxyapatites

2012

Incorporation of specific elements into calcium phosphates offers the combination of a bioactive material and a therapeutic effect. This is important for improving the integration of implants as well as treating medical conditions. Strontium is a suitable candidate and displays the ability to stimulate bone growth and reducing bone resorption. This study investigated the formation of strontium carbonated hydroxyapatite nanoparticles from an amorphous phase. Crystallization of carbonated hydroxyapatite occurred at 585 o C, but samples with an intended 25% and 75% replacement of calcium with strontium crystallized at 624 o C. Heat treatment at the crystallization temperature revealed that str…

inorganic chemicalsmusculoskeletal diseasesBone growthAlkaline earth metalStrontiumMaterials scienceMatériauxMineralogychemistry.chemical_elementCalciumHeat treatmentApatiteHydroxyapatiteNanocrystalslaw.inventionchemistryChemical engineeringStrontiumlawvisual_artCalcium Compoundsvisual_art.visual_art_mediumHydroxyapatitesCrystallizationIOP Conference Series: Materials Science and Engineering
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