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21.
Zusammenfassung Die Oberfl?chenspannungen der Systeme: 1. Wasser/propionsaures Natrium mit verschiedenen Alkoholen; 2. Wasser/buttersaures
Natrium mit verschiedenen Alkoholen; 3. Wasser/crotonsaures Natrium mit verschiedenen Alkoholen und 4. Wasser/caprylsaures
Natrium mit verschiedenen Alkoholen wurden gemessen, und die Ergebnisse werden im Sinne der in früheren Arbeiten (3, 4) ver?ffentlichten
Hypothese diskutiert.
übersetzt von Dr. K, Jaeckel (Marburg/L.)
Wir danken Herrn Dr. A. Chatterji, Head of the Chemistry Department, für sein Entgegenkommen. Einer von uns (J. M.) dankt dem Scientific Research Grants Committee für ein Stipendium zur Durchführung der Arbeit. 相似文献
Summary The surface tension of the systems (1) water-sodium propionate and different alcohols, (2) water-sodium butyrate and different alcohols, (3) water-sodium crotonate and different alcohols and (4) water-sodium caprylate and different alcohols has been determined and the results have been discussed on the basis of the hypothesis suggested in previous papers (3, 4).
übersetzt von Dr. K, Jaeckel (Marburg/L.)
Wir danken Herrn Dr. A. Chatterji, Head of the Chemistry Department, für sein Entgegenkommen. Einer von uns (J. M.) dankt dem Scientific Research Grants Committee für ein Stipendium zur Durchführung der Arbeit. 相似文献
22.
M. S. Marthas S. G. Amin H. P. S. Chawk Ajay K. Bose 《Journal of heterocyclic chemistry》1978,15(4):601-604
A convenient synthesis of α-hydroxy-β-lactams has been devised that involves the annelation of an inline with benzyloxyacetyl chloride and triethylamine and subsequent hydrogenolysis in the presence of palladium on carbon. In most cases a cis-β-lactam was obtained. A thioimidate can also be used as the imino component in the annelation reaction but the hydrogenolysis step fails. The annelation of the appropriate thiazoline to a 6-epi-penicillin derivative occurred much more readily with benzyloxyacetyl chloride than with azidoacetyl chloride. 相似文献
23.
S. P. Mushran A. K. Bose J. N. Tiwari 《Monatshefte für Chemie / Chemical Monthly》1976,107(4):1021-1027
N-bromosuccinimide oxidation of cyclopentanone in acidic media in presence of mercuric acetate has been made. A zero order dependance to N-bromosuccinimide and a first order dependence to cyclopentanone and hydrogen ion concentration has been observed. Ionic strength, mercuric acetate and succinimide has negligible effect while methanol addition has a positive effect. Various rate parameters have been computed and 1,2-cyclopentanedione identified as the end product. A suitable mechanism in confirmity with the above observations has been proposed.With 2 Figures 相似文献
24.
Bose D Martinavarro-Domínguez A Gil-Agustí M Carda-Broch S Durgbanshi A Capella-Peiró ME Esteve-Romero J 《Biomedical chromatography : BMC》2005,19(5):343-349
A micellar liquid chromatographic (MLC) procedure was developed for the clinical monitoring of imipramine and its active metabolite, desipramine. The determination of these highly hydrophobic substances was carried out after direct injection of the serum samples using a mobile phase composed of 0.15 m SDS--6% (v/v) pentanol buffered at pH 7, pumped at 1.5 mL/min into a C(18) column (250 x 4.6 mm), and electrochemical detection at 650 mV. Using this MLC method, calibration was linear (r > 0.995) and the limits of detection (ng/mL) were 0.34 and 0.24 for imipramine and desipramine, respectively. Repeatabilities and intermediate precision were tested at three different concentrations in the calibration range and a CV (%) below 2.2 was obtained. In this MLC procedure, the serum is determined without treatment, thus allowing repeated serial injections without changes in retention factors, and reducing the time and consumables required to carry out the pretreatment process. The assay method can be applied to the routine determination of serum imipramine and its metabolite in therapeutic drug monitoring. 相似文献
25.
The ionisation efficiencies of N2O vs. CO2 as well as their ratios were measured in detail introducing clean N2O and CO2 into the electron impact ion source of an isotope ratio mass spectrometer. Changes in the ionisation efficiency ratio (IER) were found for different electron energy settings and compared with the ratios of literature ionisation cross-section values for pure N2O and CO2. To establish the influence of mixtures of N2O and CO2 in a mass spectrometer, artificial air mixtures were prepared by mixing different amounts of N2O and CO2 from well-calibrated spike cylinders with CO2-free air. The mixing ratios varied from 8-512 ppb for N2O and from 328-744 ppm for CO2. With these mixtures the effects of varying N2O concentrations on apparent CO2 isotope ratios in air samples were determined. After applying a mass balance correction the delta13C results were consistent within small error margins. The data seemed almost independent from a particular choice for the IER of N2O vs. CO2 in the correction algorithm. For delta18O a small effect of the ionisation efficiency ratio of N2O vs. CO2 was found. Several sets of calculations were made varying the IER between 0.88 and 0.62. The dependence of delta18O was the smallest with an adopted IER of 0.68-0.72 in the mass balance correction equation for isotopic analysis of CO2 in air. For high-precision measurements of the CO2 stable isotope ratios in air samples a careful assessment of the mass spectrometer performance is necessary. Different ion sources, even different ion source settings, alter the IER of N2O vs. CO2 which is used in the N2O correction algorithm. Preferably, the specific mass spectrometric behaviour should be established with clean N2O/CO2 mixtures or with air mixtures covering a larger range of N2O concentrations. 相似文献
26.
Thiourea and its organic derivatives and thiosemicarbazide are determined in water, methanol or glacial acetic acid medium by reaction with an excess of iodine trichloride in the presence of mercuric chloride. The reaction is complete in 15 min. The excess of iodine trichloride is evaluated by adding potassium iodide and titrating the liberated iodine with thiosulphate. A variety of organic thioureas can be determined with an average accuracy and precision of 0.2%. 相似文献
27.
Summary From the study of the electrical conductance of the systems: Water-0.2N sodium salts of fatty acids and Butanol-I containing
different amounts of free acids, it has been concluded that two types of micelles exist in such systems. Above 50% Butanol-I
concentration lipophilic hydromicelles exist, whereas below 50% Butanol-I concentration hydrophilic oleomicelles are formed.
It has also been observed that the concentration at which the change in the micelle structure takes place depends on the chain
length of the soap. The conductance of the solutions of all the systems goes on decreasing with the increase in Butanol-I
concentration as well as with the increase in the chain length of the soap. The results are in agreement with viscosity and
surface tension results obtained in the previous communications.
Zusammenfassung Aus Untersuchungen der elektrischen Leitf?higkeit eines Systems: Wasser/0,2 n Natriumsalze der Fetts?uren und Butanol-I, das verschiedene Betr?ge an freien S?uren enth?lt, wurde auf die Anwesenheit von zwei verschiedenen Mizelltypen in solchen Systemen geschlossen. Bei Konzentrationen von mehr als 50% Butanol-I existieren lipophile Hydromizellen, w?hrend unterhalb 50% Butanol-I hydrophile ?lmizellen gebildet werden. Es wurde beobachtet, da? die Konzentration bei der der Strukturwechsel der Mizellen stattfindet, von der Kettenl?nge der Seife abh?ngt. Die Leitf?higkeit der L?sungen aller Systeme beginnt abzunehmen mit der Zunahme der Konzentration von Butanol-I, wie auch mit dem Wachsen der Kettenl?nge der Seife. Die Ergebnisse sind in übereinstimmung mit den früher erhaltenen bei Untersuchungen von Viskosit?t und Oberfl?chenspannung.相似文献
28.
29.
Synthetic organic reactions have been conducted under microwave irradiation in open vessels in unaltered domestic microwave ovens. Reaction times vary from a few seconds for sub-milligram reactions to about 15 minutes for reactions carried out on a scale of hundreds of grams. Promising results have been obtained for several condensations, as well as the Bischler-Napieralski reaction, the Wolff-Kishner reduction, free radical dehalogenation reactions, and other standard synthetic operations. Rapid catalytic transfer hydrogenation using ammonium formate as the source of hydrogen has been conducted at about 100-130 °C under microwave irradiation. Meaningful, safe and inexpensive synthetic experiments for undergraduate and pre-college students have been developed and tested. The MORE chemistry techniques make it possible to use simple apparatus and very short reaction times. Commercial microwave ovens are now essential equipment in our research and teaching laboratories [1-3]. These ovens are relatively inexpensive, easy to move from one laboratory and set up in another, and safe to operate. Glass, plastics, and ceramics are essentially transparent to microwaves whereas many organic compounds are dipolar in nature and absorb microwave energy readily. We have found that untraditional experimental arrangements are possible for conducting a wide variety of organic reactions in open vessels inside domestic microwave ovens. Depending on the quantity of reactants, most reactions (on a scale of milligrams to several grams) can be completed in minutes instead of hours. One important element of our “Microwave-induced Organic Reaction Enhancement” (MORE) chemistry is the proper choice of a microwave energy transfer agent as the reaction medium. 相似文献
30.
ESCA and ESR studies on TMI incorporating alumina-boria catalyst systems for CO conversion show the presence of carbidic phase and no valence change of the incorporated copper in the spent catalyst. 相似文献