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921.
A. N. Kost L. N. Khaimov Yu. Dzhurakulov K. Kh. Khaidarov L. D. Lebedeva A. L. Kotov 《Chemistry of Heterocyclic Compounds》1975,11(11):1263-1266
2-Substituted or 2,2-disubstituted 4,6-dioxo-1,3-dioxanes, which are analogs of Meldrum's acid and were obtained by reaction of malonic acid with acetic anhydride and the appropriate carbonyl compound in the presence of sulfuric acid, exist in solution preferably in a single form according to the PMR and 13C NMR spectral data. Fluctuation of the CH2 group is not observed. The mass spectra are characteristic and are distinguished by splitting out of the carbonyl compound from the molecular ion or successive splitting out of CO2 and ketene molecules. The Meldrum acid analogs do not affect plant growth but have a depressive effect on the central nervous system of animals and low toxicity.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1482–1486, November, 1975. 相似文献
922.
923.
E. S. Domnina G. G. Skvortsova N. P. Glazkova M. F. Shostakovskii 《Chemistry of Heterocyclic Compounds》1967,2(3):283-286
The reaction of indole with acetylene under pressure is investigated. It is shown that under the action of KOH in aqueous dioxane at 220° C, N-vinylindole C10H9N is formed in 66% yield, and that this compound undergoes free radical and cationic polymerization. 相似文献
924.
925.
A technique for following the hydrolysis of pyromellitic acid dianhydride (PMDA) by differential thermal analysis (DTA) is described. On exposure of PMDA to moisture, an endothennic peak is initiated between 190 and 200 degrees . As the degree of hydrolysis increases, this peak becomes more intense and shifts to higher temperatures. The formation of pyromellitic acid (PMA) during the hydrolysis of PMDA can be determined qualitatively by DTA. 相似文献
926.
E. Steinnes 《Fresenius' Journal of Analytical Chemistry》1969,247(1-2):23-27
Summary A non-destructive neutron-activation method for the determination of samarium in rocks, based on activation with epithermal neutrons, is described. By this means the formation of153Sm, as compared to most interfering radionuclides, is considerably higher than by thermal neutron activation. The precision of the method is 2–3% in the range of 3–25 ppm, and the sensivity is about 0,1 ppm. Results are presented for some standard rocks. The influence of other rare earth nuclides on the measurement of the 41 KeV X-ray of153Sm has been investigated.
Zerstörungsfreie Bestimmung von Samarium in Gesteinen durch Aktivierungsanalyse mit epithermischen Neutronen
Zusammenfassung Die Bildung von153Sm ist hierbei im Vergleich zu den meisten störenden Radionukliden beträchtlich größer als bei der Aktivierung mit thermischen Neutronen. Die Präzision des Verfahrens beträgt 2–3% im Bereich von 3–25 ppm, die Empfindlichkeit etwa 0,1 ppm. Für einige Standardgesteine werden die Ergebnisse angeführt. Der Einfluß anderer Nuklide Seltener Erden auf die Messung der 41 keV Röntgenstrahlung von153Sm wurde untersucht.相似文献
927.
B. Brocklehurst R.S. Dixon E.M. Gardy V.J. Lopata M.J. Quinn A. Singh F.P. Sargent 《Chemical physics letters》1974,28(3):361-363
Excited state formation by ion recombination in solutions of fluorene in squalene has been studied by pulse radiolysis at the center of a large electromagnet. The products of the slower part of the ion recombination are affected by an applied magnetic field. The fluorescence yield increases by a factor of about 1.5 whereas the triplet yield decreases. 相似文献
928.
Conclusions A study was made of the kinetics of the alkaline hydrolysis of some phenyl esters of phosphorus acids. An estimate was made of the contribution made by the induction effect and the p–d conjugation of the phenoxyl group to the free activation energy of the alkaline hydrolysis of the investigated esters.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2794–2796, December, 1972. 相似文献
929.
930.
É. K. Orlova V. A. Zagorevskii I. D. Tsvetkova 《Chemistry of Heterocyclic Compounds》1970,6(9):1088-1091
Reaction of 4, 4-dichloroflavine (I) with sulfurylchloride affords 2, 3, 3, 4, 4-pentachloroflavan (II). Hydrolysis of II gives 2-hydroxy-3, 3-dichloro-4-flavanone (III), while alcoholysis with aqueous alcohols yields 2-alkoxy-3,3-dichloro-4-flavanones (IVa, b). Treatment of III with SOCl2 gives 2,3,3-trlchloro-4-flavanone (V), which with caustic alkali or sodium ethoxide is converted into o-(1-phenyl-2, 2-dichlorovinyloxy)benzoic acid (VIc) or its ethyl ester (VIb), respectively.For Part XLII, see [7].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1167–1170, September, 1970. 相似文献