Search results for "hydride"
showing 10 items of 322 documents
1966
Die spontane Autoxydation N,N-dialkylierter Arylamine verlauft langsam. Sie wird durch Essigsaure, Azoisobuttersauredinitril (AIBN), Kobaltverbindungen, Benzylchlorid und Essigsaureanhydrid beschleunigt. Essigsaureanhydrid uberfuhrt die als Inhibitoren sehr wirksamen, durch oxydative Entalkylierung entstandenen sek. Amine in die als Inhibitoren wirkungslosen N-Acetylderivate (Ausbeute bis 90%). Die bei der Autoxydation als Kettentrager wirksamen Aminohydroperoxyde I konnen (a) durch Kondensation in die Dialkylperoxyde II ubergefuhrt und (b) durch Triphenylphosphin desoxygeniert werden. Die Amindialkylperoxyde II lassen sich in Substanz aus den Autoxydationsansatzen isolieren. AIBN lost unte…
ChemInform Abstract: Reaction of 4-Acylaminomethylpyridine N-Oxides with Phenylbutazone in the Presence of Acetic Anhydride.
1988
ChemInform Abstract: The Mechanism of Formation of 3H,9H-Pyrano(3,4-b)indol-3-ones from 3- Indolalkanoic Acids.
2010
The mechanism of the formation of 1-methyl-3H,9H-pyrano[3,4-b]indol-3-one (4) from the corresponding 3-indolacetic acid 1 is discussed. The suggested mechanism is substantiated by the isolation of a stable intermediate 2 and its transformations in the presence of acetic anhydride and/or Lewis acids.
Über die homogene und heterogene acetylierung von polyformaldehyd. 28. Mitteilung über polyoxymethylene1
1966
Die Acetylierung der Endgruppen eines hochmoleckularen Polyoxymethylendiols mit Essigsaureanhydrid wurde bei 200°C in Substanz sowie bei 135°C in Losung und in Suspension untersucht. Die Umsetzung ist in homogenem Medium innerhalb kurzer Zeit praktisch vollstandig; bei 200°C erfolgt jedoch ohne Zusatz eines (tertiaren) Amins eine besonders starke Verminderung der Molekulargewichte und ein Verlust an Polymerem durch Bildung flussiger Oligo-oxymethylendiacetate. Eine fast quantitative Acetylierung ohne Molekulargewichtsverminderung ist durch Umsetzung bei 135°C in Losung unter Zusatz eines tertiaren Amins moglich. Die Veresterungsgeschwindigkeit bei 135°C ist in heterogenem Medium wesentlich …
Can Macroscopic Parameters, Such as Conversion and Selectivity, Distinguish between Different Cracking Mechanisms on Acid Catalysts?
1997
n-heptane cracking has been carried out for very short time periods on an established reaction mechanism which includes the following group of stream reactions on different zeolites: Initiation reactions (protolytic cracking), charge isomerization, chain isomerization, hydride transfer, β-scission–alkylation, desorption–adsorption, and hydrogen transfer–cyclization. It has been observed that a given experimental distribution of products can be explained by more than just one reaction scheme. This does not allow one to clearly distinguish the fraction of reactant which disappears via monomolecular initiation reactions with respect to bimolecular hydride transfer reactions.
A Series of Ultra-Efficient Blue Borane Fluorophores
2020
13 pags., 14 figs., 5 tabs.
Selective derivatisation of resorcarenes. Part 5. Acylation of tetrabenzoxazine derivatives
2000
The reaction of the tetrabenzoxazines 2 with acetic anhydride under mild conditions leads selectively and exclusively to the tetraamides 3 in which the oxazine rings are opened; their structure was deduced from their 1H NMR spectra and confirmed for one example by an X-ray single crystal structure analysis; acylation of the hydroxy groups was not observed.
Hydroxo Hydrido Complexes of Iron and Cobalt (Sn−Fe−Sn, Sn−Co−Sn): Probing Agostic Sn⋅⋅⋅H−M Interactions in Solution and in the Solid State
2000
Bis(toluene)iron 9 reacts with Lappert's stannylene [Sn[CH(SiMe3)2]2] (4) to form the paramagnetic bis-stannylene complex [[(eta6-toluene)Fe-Sn-[CH(SiMe3)2]2]2] (10). Compound 10 reacts with H2O to form the hydroxo hydrido complex [(eta6-C7H8)(mu-OH)(H)-Fe-[Sn[CH(SiMe3)2]2]2] (12) in high yield; its solid-state structure has been elucidated by X-ray and neutron diffraction analysis. In agreement with the 1H NMR results, 12 contains a hydridic ligand whose exact coordination geometry could be determined by neutron diffraction. The 1H and 119Sn NMR analysis of 12 suggested a multicenter Sn/Sn/H/Fe bonding interaction in solution, based on significantly large values of J(Sn,H,Fe) = 640+/-30 Hz…
Determination of alcohols in essential oils by liquid chromatography with ultraviolet detection after chromogenic derivatization
2013
Abstract An HPLC-UV method to determine compounds having a hydroxyl functional group in plant essential oils is developed. The sample is diluted with 1,4-dioxane and the analytes are derivatized with phthalic anhydride. The derivatives (phthalates hemiesters) are separated on a C8 column using an acetonitrile (ACN)/water gradient. Separation conditions were optimized using the DryLab® method development software. For the alcohols and phenols present in mint and rose essential oils, optimization led to a ca. 40 min gradient time and a column temperature of 8 °C. The alcohol and its derivatives were identified using HPLC with mass spectrometry (MS) detection. A large sensitivity enhancement w…
Reaction products and pathways in the selective oxidation of C-2-C-4 alkanes on MoVTeNb mixed oxide catalysts
2010
[EN] The catalytic properties of MoVTeNbO catalysts during the selective oxidation of short chain alkanes and olefins (C-2-C-4) have been comparatively studied The main reaction products have been ethylene from ethane acrylic acid from propane maim anhydride from n-butane and methacrolein from isobutane FTIR studies of the adsorption of the main reaction products i e olefins and aldehydes over MoVTeNbO catalyst has been carried out Accordingly the reaction pathway is explained on the basis of the characteristics of the alkane fed the stability and reactivity of both the intermediates and the reaction products and the nature of the catalytic sites involved in each reaction (C) 2010 Elsevier …