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991.
Résumé La méthyl-9-trihydroxy-2,3,7-fluorone-6 permet de déceler les ions de l'antimoine, en présence de tous autres cations et anions. Les conditions deph (ph = 4) sont à observer rigoureusement.Ce nouveau réactif est avantageusement utilisé dans la méthode d'analyse à la touche ou par empreinte.Les limites de sensibilité sont: en godet 0,2; sur papier gélatine 0,5; sur papier filtre 0,8.
Summary Methyl-9-trihydroxy-2,3,7-fluorone-6 is a reagent which allows to detect antimony ion in the presence of all the other cations and anions. Aph value of 4 must be strictly maintained.This new reagent can be advantageously applied for spot test and offprint analysis.Limits of identification: On the spot test plate 0,2; On gelatine paper 0,5; On filter paper 0,8.
Zusammenfassung Das Methyl-9-trioxy-2,3,7-fluoron-6 gestattet den Nachweis des Antimonions in Gegenwart aller anderen Kationen und Anionen. Dieph-Bedingungen (ph = 4) sind streng einzuhalten.Dieses neue Reagens läßt sich mit Vorteil zur Tüpfel- oder Abdruckanalyse verwenden.Erfassungsgrenzen: auf der Tüpfelplatte 0,2; auf Gelatinepapier 0,5; auf Filtrierpapier 0,8.相似文献
992.
R. M. Masagutov S. I. Spivak Z. Sh. Akhmadishin G. N. Kirichenko N. G. Grigorieva G. A. Tolstikov 《Reaction Kinetics and Catalysis Letters》1985,28(2):411-417
Kinetics of p-cumylphenol alkylation by isobutylene in the presence of 0.1–2 wt.% p-toluenesulfonic acid has been studied and a reaction scheme is suggested. The rate constants have been determined.
- 0,1–2 % . -. .相似文献
993.
Conclusions The esterification of amido- and ester-amidophosphites with 1-(2-thienyl)-2,2,2-trichloroethanol gave the l-(2-thienyl)-2,2,2-trichloroethyl dialkyl- and 1-(2-thienyl)-2,2,2-trichloroethyl alkylamidophosphites, which easily add sulfur or are oxidized to the corresponding thiophosphates and phosphates.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 182–187, January, 1981. 相似文献
994.
A number of ruthenium triphenylphosphine complexes catalyse the reduction of ketones to their corresponding alcohols in the presence of water. The most convenient catalyst precursors are carbonyl containing complexes which do not promote decarbonylation of the substrate. The hydrogenation of acetone with hydridochlorocarbonyltris(triphenylphosphine)ruthenium is first order with respect to the substrate concentration, the catalyst concentration, the hydrogen pressure and the water concentration. Turnover numbers up to 15,000 have been achieved with this catalyst. Other ketones are also reduced by RuHCl(CO)(PPh3)3 and the rate of the reaction is dependent on the nature of the substrate. 相似文献
995.
S. M. Danov V. A. Kolesnikov R. V. Efremov D. Yu. Mezhenin 《Russian Journal of Applied Chemistry》2005,78(4):680-682
The kinetics of dimethylamine hydroxyethylation at an ethylene oxide : dimethylamine : water molar ratio of 1 : 3 : (0.1–0.5) was studied in the temperature range 20–50°C. A kinetic model of the reaction, which adequately describes the experimental data, was suggested.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 4, 2005, pp. 687–689.Original Russian Text Copyright © 2005 by Danov, Kolesnikov, Efremov, Mezhenin. 相似文献
996.
The weak Lewis acid silicon tetrachloride can be activated by catalytic amounts of the chiral bisphosphoramide (R,R)-3 to form a highly reactive, chiral trichlorosilyl cation which is an extremely effective promoter of aldol addition reactions between aldehydes and silyl ketene acetals. The tert-butyldimethylsilyl ketene acetal of methyl acetate adds nearly instantaneously to aromatic and olefinic aldehydes as well as aliphatic aldehydes (albeit more slowly) with excellent enantioselectivity. The homologous tert-butyldimethylsilyl ketene acetal of tert-butyl propanoate adds with nearly exclusive anti diastereoselectivity to a similar range of aldehydes also with excellent enantioselectivity. The origin of the slower reaction rate with aliphatic aldehydes is revealed to be the formation of chlorosilyl ether adducts. 相似文献
997.
Rapid and sensitive silver-lipopolysaccharide staining using PhastSystem in fast horizontal polyacrylamide gel electrophoresis 总被引:1,自引:0,他引:1
A rapid and sensitive silver-lipopolysaccharide staining method has been developed by using PhastSystem. The total time of the procedure (including time of Phastgel electrophoresis) is within 2 h. It is at least 10 times faster than the previous reported methods and the sensitivity is also increased. 相似文献
998.
N. V. Myagkova G. R. Rakhmonberdiev Z. G. Sagdieva A. S. Sidikov 《Chemistry of Natural Compounds》1997,33(1):76-79
The thermodynamics of the mixing of water-soluble mixed cellulose esters with water has been studied. A dependence of the affinity of a water-soluble cellulose acetate for water on the nature of a new radical introduced into the macromolecule and the competing interaction of molecules of the same and different types has been shown. Thermodynamic analysis has demonstrated the dominating role of solvation among the various factors determining the interaction of cellulose acetomaleate and acetophthalate with a solvent. A fall in affinity in the cellulose aminoacetate-water system is due to the contribution of entropy effects, leading to an increase in the Flory-Huggins parameter.Tashkent Institute of Chemical Technology. Translated from Khimiya Prirodnykh Soedinenii, Vol. 33, No. 1, pp. 97–101, January–February, 1997. 相似文献
999.
El-Shazly RM Al-Hazmi GA Ghazy SE El-Shahawi MS El-Asmy AA 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,61(1-2):243-252
Several complexes of thiosemicarbazone derivatives with Ni(II) have been prepared. Structural investigation of the ligands and their complexes has been made based on elemental analysis, magnetic moment, spectral (UV-Vis, i.r., (1)H NMR, ms), and thermal studies. The i.r. spectra suggest the bidentate mononegative and tridentate (neutral, mono-, and binegative) behavior of the ligands. Different stereochemistries were suggested for the isolated complexes. The thermogravimetry (TG) and derivative thermogravimetry (DTG) have been used to study the thermal decomposition and kinetic parameters of some ligands and complexes using the Coats-Redfern and Horowitz-Metzger equations. The redox properties and stability of the complexes toward oxidation waves explored by cyclic voltammetry are related to the electron withdrawing or releasing ability of the substituent of thiosemicarbazone moiety. The samples displayed Ni(II)/Ni(I) couples irreversible waves associated with Ni(III)/Ni(II) process. 相似文献
1000.
Chiang MH Antonio MR Soderholm L 《Dalton transactions (Cambridge, England : 2003)》2004,(21):3562-3567
The ground state electronic properties of metal-exchanged Preyssler heteropolyoxoanions [M(n+)P(5)W(30)O(110)](n-15), in which the encapsulated M(n+) ions are the spherical, diamagnetic ions Na(+), Ca(2+), Sr(2+), Y(3+), La(3+) and Th(4+), are studied using a combination of electrochemical, optical, and NMR experiments. We have designed experiments that focus on the influence of the charge (n) of the encapsulated cations, which themselves have no redox response, and its effect upon the W-O framework MOs. As n increases, the cluster anions accept electrons into their LUMOs with increasing ease, and their lowest-energy LMCT bands reveal a corresponding blue shift, which is indicative of an increase of the LUMO-HOMO energy splitting with increasing n. (183)W NMR spectra are used to identify the atomic origin of the LUMO states, which are shown to be composed primarily of orbitals from the ring of 5 W atoms near M(n+). The cation charge correlates directly and linearly with the half-wave potentials of the first redox couples, the LMCT band energies, and the W chemical shifts. We have combined this suite of experimental results to construct an energy level diagram of the frontier MOs for the Preyssler cluster anions. In so doing, we provide a fundamental perspective that is not otherwise available on the cation's role with specific regard to the electronic behavior of the W-O orbitals. These results are expected to provide benchmarking information as theorists begin to study these large POM systems. 相似文献