Search results for "Aniline"
showing 10 items of 259 documents
Formation rates and protonation constants of azo dyes in a sodium dodecylsulphate micellar solution.
1991
The effects of a sodium dodecylsulphate micellar solution on the coupling rates of several diazotizated arylamines with N-(1-naphthyl)-ethylenediamine and the shifts in the protonation constants of the corresponding azo dyes are quantitatively studied. Aniline, o-, m- and p-aminobenzoic acids, ethyl p-aminobenzoate and several sulphadrugs are used, and the relationships among the intensity of the effects and the molecular structure of the diazonium ions and the dyes are discussed. A single simplified procedure for the determination of all the substances at pH = 1.3 +/- 0.3, where coupling is quickly completed to directly produce the protonated form of the dyes, is established and applied to…
Unexpected formation of chroman-4-ones during the synthesis of 4-hydroxymethyl-2H-chromenes from 4-aryloxybut-2-yn-1-ols
1986
Abstract The unexpected formation of chroman-4-ones by refluxing 4-aryloxybut-2-yn-1-ols in diethylaniline has been studied, 4-hydroxymethyl-2H-chromene and chroman-4-carboxaldehyde derivatives being established as intennediates.
Modification of Polymer-Magnetic Nanoparticles by Luminescent and Conducting Substances
2014
The polymer encapsulated magnetic nanoparticles were obtained by suspension polymerization of styrene in the aqueous dispersion of magnetite. Functionalization of capsules was carried out by adsorp...
Lineare polyester mit carboxylendgruppen und deren bestimmung
1955
Durch Umsetzung von „alkoholischen” Bernsteinsaure-1,6-Hexandiol-Polyestern mit Bernsteinsaureanhydrid in Benzol werden kettenanaloge Polyester mit endstandigen Carboxylgruppen hergestellt. Die Titration dieser Carboxylgruppen ergibt Molgewichte bis ∼ 7 · 103. Mit Phenylisocyanat in indifferenten Losungsmitteln reagieren Polyesterdicarbonsauren unter Kettenverlangerung und Bildung von kettenstandigen Carbonsaureanhydridgruppen. Die Umsetzung der Polyester-dicarbonsauren in Phenylisocyanat ohne Verdunnungsmittel erfolgt kettenanalog unter Bildung von Carboxanilidendgruppen. Durch photometrische Anilinbestimmung nach der Hydrolyse konnen diese Endgruppen quantitativ bestimmt und Molgewichte b…
Biopartitioning micellar chromatography: An alternative high-throughput method for assessing the ecotoxicity of anilines and phenols
2007
An investigation of the use of the chromatographic retention (log k) as an in vitro approach for modelling the toxicity to Fathead Minnows of anilines and phenols is developed. A data set of 65 compounds with available experimental toxicity data was used. Log k data at three pH values were used for the compounds classification and two groups or 'MODEs' were identified. For one 'MODE' a quantitative retention-activity relationship (QRAR) model was calculated. Finally, it was used to estimate the toxicity to Fathead minnows of anilines and phenols for which experimental data are not available. These estimations were compared to those obtained from another toxicity (to Tetrahymena pyriformis) …
N-(tert-butoxycarbonylglycyl-alpha,beta-dehydrophenylalanylglycylphenylalanyl)-4-nitroaniline.
2000
In the crystal structure of the tetrapeptide Boc0–Gly1–ΔPhe2–Gly3–Phe4–p-NA (p-NA is para-nitroaniline), C33H36N6O8, there are two independent molecules differing in conformation in the asymmetric part of the unit cell. All the amino acids in the peptide are linked trans to each other. The torsion angles in the main chain of both molecules are close to the values of the type β-II turn. Two intramolecular and three intermolecular N—H⋯O hydrogen bonds stabilize the conformation of each of the molecules.
Thermogravimetric and calorimetric studies of water absorbed in polyaniline
1995
Abstract Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to study the behavior of residual water absorbed by an emeraldine base and a salt of chemically synthesized polyaniline (PANI—EB, PANI-ES). The matrix of PANI is shown to contain water molecules participating in both reversible and irreversible absorption. In its turn, the reversibly absorbed water consists of two components. The first component (WD 1 ) amounts to 5–7 wt.% and is removable from PANI-EB in a flow of dry nitrogen at room temperature. The second one (6–8 wt.%) of more strongly bonded water (WD 2 ) can be withdrawn from PANI-EB at temperatures from 70 to 150 °C depending on the measu…
Preparation of N,O-Aminals as Synthetic Equivalents of H2C=NAr and (H2C=NHAr)+ Ions: Neutral and Acid-promoted Transformations
1988
A general method for the synthesis of N,O-aminals derived from primary aromatic amines is described. The reactivity of these compounds under neutral and acidic conditions has been studied and the title compounds can be envisaged as general purpose H2C=NAr or (H2C=NHAr)+ equivalents. N,O-Aminals have been converted into perhydrotriazines by moderate heating and into bis(4-aminoaryl) methane derivatives or N-benzylarylamines, respectively when heated in acidic media with pH control. Reduction of N, O-acetals with sodium cyanoborohydride has revealed that the C-O bond is broken exclusively in acidic media.
Complex tauto- and rotamerism of 2-(R-phenyl)-1,2,3,4-tetrahydroquinazolines
2005
Detailed NMR spectral analysis of CDCl3 solutions of 2-(R-phenyl)-1,2,3,4-tetrahydroquinazolines reveals three or four tautomeric forms. Apart from 2-[(benzylideneamino)methyl]aniline, the other chain tautomeric forms are present only in minor quantities. In general, electron-donating substituents increase the contribution of all chain forms. Lowering the temperature of the CDCl3 solution of 2-(R-phenyl)-1,2,3,4-tetrahydroquinazolines decreases the content of the 2-[(benzylideneamino)methyl]aniline form. At the same time, the amount of the ring form increases. Opening of the tetrahydropyrimidine ring in 2-(R-phenyl)-1,2,3,4-tetrahydroquinazolines was found to be an endothermic process espec…
Dielektrische Relaxation und aromatischer Bindungszustand der Amino- und Hydroxylgruppe
1965
Bei funf Wellenlangen im Bereich von 60 cm bis 7 mm wurde in benzolischer Losung bei 20 °C die dielecktrische Absorption von Benzolderivaten gemessen, die Amino- oder Hydroxylgruppen enthalten. Danach erfolgt die elektrische Dipolorientierung bei N, N'-Dimethylanilin, Diphenylamin und ver wandten Molekulen in der Art, das die drei Bindungen des Stickstoffs uber die ebene Anordnung hinweg umklappen. Ebenso kann auch das Relaxationsverhalten von Anilin beschrieben werden. Voraussetzung fur diese Inversion ist die mesomere Wechselwirkung zwischen dem Stickstoff und einem aromatischen ϕ-Elektronen-system. Dagegen ergeben die Meswerte keinen Hinweis darauf, das bei der Hydroxylgruppe auch eine s…