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911.
The optically active methylphenyl-α-naphthylsilane racemises quickly in tetrahydrofuran in the presence of LiAlH4.Kinetic results show a different behaviour of the hydride depending on its concentration. Activation parameters have been obtained and mechanisms proposed.  相似文献   
912.
    
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Air regeneration of a coked silica-alumina catalyst for the synthesis of pyridines and picolines has been studied. The results are discussed in relation to changes in porosity and structure occuring during thermal treatment.
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913.
Acylquinoxalines     
The structure of 2,7-dimethyl-3-acetylquinoxaline was proved by conversion of it to 2,7-dimethyl-1,2,3,4-tetrahydroquinoxaline. 2,7-Dimethylquinoxaline and 2-methyl-3-acetyl-6-aminoquinoxaline were synthesized.See [1] for communication II.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1700–1701, December, 1972.  相似文献   
914.
The chemical reactions of size selected silicon cluster ions (containing up to 70 atoms) have been studied with a number of different reagents using injected ion drift tube techniques. Both kinetic and equilibrium measurements have been performed as a function of temperature, and the influence of cluster annealing on chemical reactivity explored. Unlike metal clusters, where bulk behavior appears to be approached with around 30 atoms, large silicon clusters (n up to 70) are much less reactive than bulk silicon surfaces. These results suggest that the clusters in the size range examined here are not small crystals of bulk silicon, but have compact, high coordination number structures with few dangling bonds.  相似文献   
915.
The system POCl3–NaAlCl4 was investigated by measuring the conductivity and the Raman and NMR spectra (27Al, 23Na and 31P) as a function of the mol fraction x of NaAlCl4 in POCl3. Additionally, Raman spectra of POCl3 solutions of NaFeCl4, LiAlCl4, LiFeCl4, and KAlCl4 were recorded. In solutions containing Li+ or Na+ ions a liquid to solid (or jelly) phase transition was observed under certain conditions, dependent on salt concentration and temperature. Observed changes in the Raman spectra of the electrolyte solutions in comparison to the pure solvent POCl3 demonstrate the existence of interactions. Clearly, the POCl3 eigenfrequencies and hence the molecules are pertubed. The formation of [M(POCl3)4]+ complexes (M = Li, Na) can be deduced from the Raman measurements. NMR investigations support this conclusion. For assigning of Raman spectra, (Li+, K+) cation and ([FeCl4]?, [SbCl6]?) anion substitutions were employed.  相似文献   
916.
The shifts of the stretching vibrations of the hydroxyl groups of phenol and pentachlorophenol during the formation of intermolecular hydrogen bonds with 2-thienyl phenyl ketones containing substituents in the benzene ring were measured. A correlation dependence between theD OH values and + substituent constants was established.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 482–485, April, 1974.  相似文献   
917.
A new spectrophotometric method was developed to determine vanadium using tannic acid as a complexing reagent to form a coloured reaction product which can easily be extracted by 1-pentanol in the presence of cetylpyridinium. The developed method can successfully be applied to determine trace levels of 10 ng/ml of vanadium in natural waters without any preconcentration step. It can also determine less than 1 mg/kg of vanadium in edible oils and petroleum products.  相似文献   
918.
The azo coupling of 2,5-diphenylpyrrole with arenediazonium chlorides has given previously unknown 3-arylazopyrroles and 4-phenylazo-3-phenylhydrazono-3H-pyrrole. The methylation and reductive acetylation of the anylazo derivatives have led to N-methylarylazo and acetylamino derivatives of 2,5-diphenylpyrrole. 3-Amino-2, 5-diphenylpyrrole has been obtained by the reduction of 3-p-chlorophenylazo-2,5-diphenylpyrrole. The aminomethylation of 2,5-diphenylpyrrole and its derivatives with bis(dialkylamino)methanes had led to aminomethyl derivatives.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5. pp. 612–615, May, 1986.  相似文献   
919.
The analysis of a coffee concentrate is described: 202 constituents have been identified, 154 of which for the first time. Some of these compounds are new chemicals; their synthesis is described. Most identifications are based upon mass spectrometry combined in many cases with IR. spectrometry and comparison with reference compounds. MS. and IR. data are given in detail. The analysis shows that a large number of minor constituents is present, many of which could not be identified.  相似文献   
920.
Zusammenfassung Es wird gezeigt, daß sich Insektizide auf der Basis der Ester der Thiophosphorsäure (E 605) aus biologischem Material mittels Wasser-dampfdestillation auf verhältnismäßig einfache Weise abscheiden lassen. Im Destillat erfolgt die Bestimmung nach Ausäthern und Lösen des Rückstandes in Äthanol durch Messen der Lichtabsorption im UV. Hierbei zeigt sich, daß die rechnerische Eliminierung der Störstoffe bei geringeren Konzentrationen der Ester leichter ist als bei hohen.Durch Messung der Lichtabsorption im IR läßt sich, genügende Konzentration vorausgesetzt, entscheiden, welcher Ester vorliegt.
Summary It was shown that insecticides based on the ester of thiophosphoric acid (E 605) can be separated in relatively simple fashion from biological material by means of steam distillation. The distillate is shaken out with ether and the residue dissolved in ethanol and the determination is accomplished by measuring the absorption in ultraviolet light. It was found that the computational elimination of the interfering materials is easier at lower concentrations of the ester than when higher concentrations are present. By measuring the light absorption in infrared, it is possible to decide which ester is present, provided the concentration is high enough.

Résumé On montre que les insecticides se séparent d'une manière relativement simple de l'élément biologique par un entraînement à la vapeur d'eau sur la base de l'ester de l'acide thiophosphorique (E 605). Le dosage s'effectue sur le distillat d'après l'épuisement à l'éther et la solubilité du résidu dans l'éthanol et la mesure de l'absorption lumineuse dans l'ultraviolet. On en déduit que l'élimination calculée de la substance gênante est plus facile pour les faibles concentrations de l'ester que pour les grandes. En mesurant l'absorption de la lumière dans l'infrarouge, on peut savoir de quel ester il s'agit pour des concentrations supposées suffisantes.
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