Zusammenfassung Eine Reihe von Hydroxybenzylbenzimidazolen wurde durch Kondensation verschiedener aromatischer o-Diamine mit Brommandelsäuren unter Verwendung von 6n-HCl als Kondensationsmittel hergestellt. Für die Substituenten in der Benzolhälfte wurden die Stellungen 4(7)-, 5(6)-, 5,6- oder 4,6(5,7)- ge-wählt; der Phenylrest der Hydroxybenzylhälfte trägt ein Bromatom in der o- oder p-Stellung. Die Darstellung der o-Brom-mandelsäure wird beschrieben.
A series of hydroxybenzylbenzimidazoles has been synthesized by condensing various aromatic o-diamines with bromomandelic acids using 6 N hydrochloric acid as condensing agent. o-Phenylene diamines to yield benzimidazoles substituted at positions 4(7)-, 5(6)- or 4,6(5,7)- were selected; the phenyl group of the hydroxybenzyl moiety carries a bromo substituent in the o- or p-position. The preparation of o-bromomandelic acid is described in some detail.
We prove some a priori estimates in dimension for equations of type prescribed scalar curvature. In the particular case of the unit sphere we give an estimation of the constant c in the inequality . To cite this article: S. Skander Bahoura, C. R. Acad. Sci. Paris, Ser. I 341 (2005).相似文献
N-Glycosides of Asn and homologues have been synthesized starting from hexafluoroacetone-protected -activated Asp, Glu, and Aad derivatives and glycosylamines. The synthetic value of the new building blocks was demonstrated by the concise incorporation of N-glycosylated Asn, Gln, and Aad -amides into glycopeptides. 相似文献
Structural Chemistry - A combined experimental and theoretical study is presented to predict and analyze the inhibition efficiency and adsorption mechanism of 4-aminobenzoic acid molecule for... 相似文献
Conducting polypyrrole (PPy)/C (Vulcan XC-72) composite materials were synthesized by chemical polymerization method. These
materials were used as matrix to support platinum nanoparticles, which were produced by the carbonyl chemical route. For the
same catalyst loading (50 μg cm−2), it was observed that the nature of the composite strongly influences the electrochemical activity of nanoparticulated platinum
toward the oxygen reduction reaction in acid medium. The variation of the PPy/C ratio determines the so-called substrate effect
for electrocatalysis.
Dedicated to Prof. Dr. Teresa Iwasita on the occasion of her 65th birthday in recognition of her numerous contributions to
interfacial electrochemistry. 相似文献
Amino-acyl-quinoxalinone yellow dyes are cyclised analogues of the yellow azomethine dyes developed for, and still used in, silver halide colour photography. Unlike image azomethine dyes, which are rapidly deactivated in their excited states by torsion about the azomethine bond, amino-acyl-quinoxalinone dyes have an interesting photophysics because torsion is not possible due to their cyclised structure. We report results from studies on singlet and triplet state properties, and singlet oxygen yields, of the yellow dye, 7-diethylamino-3-(2,2-dimethyl-propionyl)-5-methyl-1-phenyl-1H-quinoxalin-2-one, in polar and nonpolar solvents. The dye photophysics is characterised by a weak fluorescence, with a solvent dependent emission yield (ΦF?≈?0.002–0.004), and short singlet state lifetime (τexpt?≈?20–50 ps), both increasing by a factor of ≈2 in going from polar acetonitrile to non-polar dioxane as solvent. DFT ZINDO calculations show a transition involving significant electron transfer from the diethyl-amino group into the carbonyl region of the molecule. In solution, in the presence of oxygen, the triplet state decays almost exclusively by oxygen quenching, and singlet oxygen is produced in high yield (Φ??≈?0.5–0.55). The triplet state absorbs across the 450–750 nm region with maxima around 480 and 650 nm, and moderate molar absorption coefficients (ca. 6000–8000 M?1 cm?1). In a glass at 77 K, triplet decay gives a red phosphorescence, with λmax?≈?640–650 nm, and a ?≈?0.25 s lifetime. If singlet oxygen yields are a good indication of triplet yields, then internal conversion and intersystem crossing occur with roughly equal efficiency.
Crystal structure of Li2HPO3,H2O was determined by single-crystal X-Ray diffraction analysis at 173(2) K. It crystallizes in the monoclinic system (P21/c) with the parameters: a = 5.0322(9) ?, b = 8.9795(17) ?, c = 17.088(4) ?, β = 92.672(16)° and Z = 8. The structure was refined to R = 0.0237 and ωR = 0.0650 for 1449 reflexions. The framework of Li2HPO3, H2O can be described as layers perpendicular to the crystallographic c axis. The structure contains two types of Li-tetrahedrons. In one kind each O atom belongs to one HPO3 group, while in the second kind one apex is an O from water. A network of hydrogen bonds interactions insures the connection
between the layers. 相似文献
A new hybrid phosphate, (C6H5NH3)[ZnCl(HPO3)], has been synthesized and its structure characterized from single-crystal X-ray diffraction. The title compound crystallizes
in the orthorhombic space group Pbca (n. 61) with the unit-cell parameters: a = 9.8635(2) ?, b = 9.4516(10) ?, c = 22.2430(4) ?, Z = 8 and V = 2,073.62(6) ?3. The final R factors were R/ωR = 0.0361/0.0924. Its framework might be described as a layered structure with two (010)-parallel cationic and anionic layers.
The IR spectrum of this phase shows characteristic bands of phosphite and anilinium groups. 相似文献
In this paper, the approximate controllability of neutral stochastic fractional differential equations involving nonlocal initial conditions is studied. By using Sadovskii’s fixed point theorem with stochastic analysis theory, we derive a new set of sufficient conditions for the approximate controllability of semilinear fractional stochastic differential equations with nonlocal conditions under the assumption that the corresponding linear system is approximately controllable. Finally, an application to a fractional partial stochastic differential equation with nonlocal initial condition is provided to illustrate the obtained theory. 相似文献