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991.
A. N. Veselkov L. N. Dymant S. S. Dreval' 《Theoretical and Experimental Chemistry》1987,23(3):346-350
The chemical shifts of the protons in the proflavine and acridine orange molecules in aqueous solution were measured by 1H NMR spectroscopy. The equilibrium constants for the association of the molecules and the chemical shifts of the protons in the monomers and associates were obtained from the concentration dependence of the proton chemical shifts. The most probable structures for the dimers of the dyes were calculated on the basis of the obtained chemical shifts, and a comparative analysis was made.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 23, No. 3, pp. 373–376, May–June, 1987. 相似文献
992.
The pathways in the microbiological transformation of pyridine and its derivatives (alkylpyridines, hydroxypyridines, pyridinecarboxylic acids, alkaloids, and condensed systems with a pyridine ring) under the influence of various microorganisms and several enzyme systems are examined. It is noted that oxidation, reduction, hydrolysis, and destruction of the aromatic ring are the most characteristic processes.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1299–1313, October, 1978. 相似文献
993.
Isothermal-thermogravimetric analyses were used to obtain kinetic data on the CFx decomposition. Weight of samplevs. time curves were obtained for compounds having stoichiometries CF0,61, CF0.96, CF1.08, and CF1.12 for several different temperatures over the range 450–650° and in both a nitrogen atmosphere and in vacuum. A small percentage of fluorine in the atmosphere was shown to strongly inhibit thermal decomposition.These experimental results were fit to various theoretical models and it was found that a satisfactory fit was obtained by use of the Avrami equation, -In(1–)=(kt)n, where is the extent of reaction,k is an apparent rate constant, andn is an apparent reaction order. The valuen=2.0 was indicated which corresponds to planar growth of the decomposed phase.This information was combined with analytical data for the gaseous and solid products of decomposition to formulate a detailed mechanism.
Abstracted in part from the Ph. D. thesis of Peter Kamarchik, Jr. Rice University, Houston, Texas, May, 1976.
This work was supported financially by the National Science Foundation, the U.S. Army Research Office (Durham), the National Aeronautics and Space Administration, and the Robert A. Welch Foundation. Liquid helium was provided under a grant from the Office of Naval Research. 相似文献
Zusammenfassung Isotherm-thermogravimetrische Analysen wurden durchgeführt um kinetische Daten über die Zersetzung von CFx zu erhalten. Probengewicht-Zeit-Kurven wurden für Verbindungen mit stöchiometrischen Verhältnissen von CF0.61, CF0.96, CF1.08 und CF1.12 bei verschiedenen Temperaturen im Bereich von 450° bis 650°, in Stickstoff sowie im Vakuum aufgenommen. Ein geringer Prozentsatz an Fluor in der Atmosphäre wirkte stark inhibierend auf die thermische Zersetzung.Diese Versuchsergebnisse wurden verschiedenen theoretischen Modellen angepasst und es wurde gezeigt, dass mit Hilfe der Avrami-Gleichung -In (1–)=(kt)n eine befriedigende Anpassung möglich ist, wobei =Ausmaß der Reaktion, k=scheinbare Geschwindigkeitskonstante undn=scheinbare Reaktionsordnung ist. Der angedeutete Wertn=2.0 entspricht einer planaren Zunahme der zersetzten Phasen.Diese Information wurde mit analytischen Daten der gasförmungen und festen Zersetzungsprodukte kombiniert um einen Mechanismus in allen Einzelheiten zu formulieren.
Résumé La TG isotherme a été utilisée pour obtenir des données cinétiques sur la décomposition de CFx. Les courbes donnant le poids de l'échantillon en fonction du temps ont été energistrées à différentes températures, entre 450 et 650°, en atmosphère d'azote et sous vide, sur des composés de composition CF0.61, CF0.96 et CF1.08. Un faible pourcentage de fluor dans l'atmosphèere s'est avéré inhiber considérablement la décomposition thermique.Ces résultats expérimentaux ont été confrontés à divers modèles mathématiques. On a trouvé un ajustement satisfaisant à l'aide de l'équation d'Avrami, -In (1–)=(kt)n, où es l'avancement de la réaction,k une constante de vitesse apparente etn un ordre de réaction apparent. La valeurn=2.0 correspond à une croissance dans le plan de la phase décomposée.Cette information a été combinée avec des données analytiques sur les produits de décomposition gazeux et solides, afin de formuler un mécanisme détaillé.
- CFx. — CF0.61, CF0.96, CF1.08 F1.12 450°–650°, , . . , -1(1–)= (kt)n, — , k — , n — . n=2, . , .
Abstracted in part from the Ph. D. thesis of Peter Kamarchik, Jr. Rice University, Houston, Texas, May, 1976.
This work was supported financially by the National Science Foundation, the U.S. Army Research Office (Durham), the National Aeronautics and Space Administration, and the Robert A. Welch Foundation. Liquid helium was provided under a grant from the Office of Naval Research. 相似文献
994.
J. Sztatisz S. Gál L. Fodor E. Pungor 《Journal of Thermal Analysis and Calorimetry》1977,12(3):351-360
The melting and crystallization of sorbitol were investigated with the DSC method and thermal microscopy. Sorbitol was found to have two crystalline modifications (confirmed by X-ray diffraction) with different melting points, while rapid cooling of molten sorbitol resulted in an amorphous form. The effect of inoculation on the crystallization of the melt was studied too. Powders of both crystalline modifications were used for this purpose. A new technological process for rapid crystallization of molten sorbitol has been worked out on the basis of the thermal analysis results. 相似文献
995.
Zh. M. Putieva L. G. Mzhel'skaya T. T. Gorovits E. S. Kondratenko N. K. Abubakirov 《Chemistry of Natural Compounds》1976,11(6):756-761
Summary Alternative structures for the acyloside chain of acanthophylloside B and C have been established.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 728–734, November–December, 1975. 相似文献
996.
L. Grosse und W. Klaus 《Fresenius' Journal of Analytical Chemistry》1972,259(3):195-203
Zusammenfassung Es werden allgemeine und qualitative Merkmale von Natrium-Carboxymethylcellulose, Methylcellulose und Hydroxyäthylcellulose sowie gravimetrische und titrimetrische Bestimmungsmöglichkeiten der wasserlöslichen Celluloseäther insbesondere im Zusammenhang mit dem Substitutionsgrad beschrieben.Verfahren zur Ermittlung der Viscosität von Lösungen, des Polymerisationsgrades und des Gelteilchengehaltes werden besprochen. Abschließend werden charakteristische Beispiele für das analytische Vorgehen bei Substanzgemischen gegeben, die nur einen geringen Anteil Celluloseäther enthalten.
Erweiterte und umgearbeitete Fassung eines Vortrages, gehalten am 28. 6. 1971 in Baden-Baden.
Frau Dr. G. Bartelmus, Analyt. Laboratorium der Fa. Kalle AG, sprechen wir an dieser Stelle unseren herzlichen Dank für wertvolle Beratung aus. 相似文献
Analysis of water-soluble cellulose ethers
General and qualitative characteristics of sodium carboxymethylcellulose, methylcellulose and hydroxyethylcellulose are presented and gravimetric and titrimetric methods for the determination of water-soluble cellulose ethers are described, especially with regard to the degree of substitution. Procedures for the measurement of the viscosity of solutions, of the degree of polymerisation and of the content of gel particles are discussed. Characteristic examples are presented for the treatment of mixtures containing only a small percentage of cellulose ethers.
Erweiterte und umgearbeitete Fassung eines Vortrages, gehalten am 28. 6. 1971 in Baden-Baden.
Frau Dr. G. Bartelmus, Analyt. Laboratorium der Fa. Kalle AG, sprechen wir an dieser Stelle unseren herzlichen Dank für wertvolle Beratung aus. 相似文献
997.
I. A. Ol'shevskaya V. Ya. Pochinok L. F. Avramenko 《Chemistry of Heterocyclic Compounds》1971,4(5):649-651
5-Azido-2-methylbenzthiazole, 6-azido-1, 2-dimethyl-, and 5-azido-2-methyl-1-phenylbenzimidazoles were prepared. By the reactions of these azides with alkyl halides the quaternary slats based on the cyanine dyes were obtained. 相似文献
998.
[reaction: see text] The enediamine tautomer of a variety of substituted amidine free bases reacts with nitric oxide (NO) to produce compounds containing a carbon-bound diazeniumdiolate [R1R2R3C-N(O)=NO-] functional group (previously called "nitrosohydroxylamines"). The new reaction has been shown to be quite general, although the nature of the products does vary. Amidines containing more than one replaceable hydrogen produce polydiazeniumdiolates as intermolecular salts, while those in which only one diazeniumdiolation can occur provide zwitterionic salts. These diazeniumdiolated amidines are shown to be useful NO donor compounds which undergo very slow spontaneous dissociation on dissolution in pH 7.4 phosphate buffer to produce mixtures of NO and nitrous oxide containing mostly NO. The most advantageous manifestation of the new discovery is the preparation of the monodiazeniumdiolated amidine zwitterions. Reaction of the medically relevant alpha-adrenergic agonists tetrahydrozoline and idazoxan produced monodiazeniumdiolated amidine zwitterions from which NO release was observed for up to 28 days and showed little sign of ending. The reaction should be applicable to a variety of pharmaceutical agents, including NO synthase inhibitors, antitumor agents, and antibacterials. 相似文献
999.
L. G. Shaidarova S. A. Ziganshina G. K. Budnikov 《Journal of Analytical Chemistry》2003,58(6):577-582
The electrocatalytic activity of ruthenium(IV) oxide incorporated into a carbon-paste electrode was studied in the oxidation of cysteine and cystine. The oxidation potentials of the amino acids decreased and the current peaks of their oxidation increased at a modified electrode as compared to an unmodified one. Procedures for the voltammetric determination of cysteine and cystine with the use of electrodes chemically modified with ruthenium(IV) oxide were proposed. 相似文献
1000.
F. De Meester J. M. Frre J. L. Piette P. Jacquemin L. Grooters G. Llabres S. Defays 《Journal of heterocyclic chemistry》1992,29(2):535-541
In an attempt to rationalize a synthesis of penicillin analogs modified at C(3), we have isolated the 3R(β)-carbinolamide derivative 4a. The trityl substituent on N(6′) seems to be responsible for the inversion of configuration which occurs at C(3) during the acid hydrolysis of the isocyanate intermediate. An hydrogen bond is formed on the β-face of the bell-shaped bicyclic skeleton between the N(6′)-nitrogen lone pair and the C(3) hydroxyl group. On standing, the carbinolamide analog slowly isomerizes to its expanded bicyclic isomer 4b , but the starting material may be easily recovered by treatment with acid. The postulated intermediate during isomerization, i.e., the open aldehyde form, does not accumulate. Substitutions of the hydroxyl group at C(3) lead to a variety of compounds with the biologically active 3S(α) configuration. These may be used to study the importance of the carboxyl group of penicillins in their interaction with β-lactamases at the molecular level. 相似文献