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931.
Multinuclear magnetic resonance data for the title compounds are presented and discussed. The intramolecular coordination observed in the solid state is shown to be retained in solution. The best probes for the presence or absence of pentacoordination at tin are provided by the various tin-element coupling constants, although chemical shifts are in some cases also informative. A selenium-proton correlated spectrum indicated that the coupling constant 1J(Sn,Se) has a positive sign. 相似文献
932.
Effect of methanol dilution on H-ZSM-5 zeolite deactivation in the process of light olefin formation
A. .A. Cichowlas P. T. Wierzchowski L. W. Zatorski 《Reaction Kinetics and Catalysis Letters》1986,32(2):341-346
Conversion of methanol in the presence of H2O, O2, H2, CO, CO2 and He was studied at 733 K on H-ZSM-5 zeolite. The effect of diluent on the selectivity to light olefins and resistance to coking of H-ZSM-5 were observed. Among the diluents studied only water exerts a promoting effect on prolonged activity of the catalyst. Some explanations of the deactivation process are given.
H2O, O2, H2, CO, CO2 He H-ZSM-5 733K. H-ZSM-5. . .相似文献
933.
T. S. Martins J. R. Matos G. Vicentini P. C. Isolani 《Journal of Thermal Analysis and Calorimetry》2005,82(1):77-82
Summary Rare earth picrate (RE) complexes with L-lysine (Lys) were synthesized and characterized. Elemental analysis (CHN), EDTA titrations and thermogravimetry data suggest
a general formula RE(pic)3·2Lys·2H2O, where RE=La-Lu (without Pm) and Y, pic=picrate). IR spectra suggest that Lys is coordinated to the central ion through the nitrogen of the α-amino group. Parameters
obtained from the absorption spectrum of the Nd compound indicated that the metal-ligand bonds are essentially electrostatic.
Emission spectrum and biexponential behavior of the luminescence decay of the Eu compound suggest the existence of polymeric
species. Thermogravimetric/derivative thermogravimetric (TG/DTG) and differential scanning calorimetry (DSC) curves of all
complexes are very similar, with five events. The final products are the corresponding rare earth oxides and their X-ray diffraction
patterns are identical to the calcinated oxides.</o:p> 相似文献
934.
Photoconversion of lutetium diphthalocyanine and interpretation of its electronic absorption spectra
V. G. Maslov T. P. Prokof'eva A. N. Sidorov 《Theoretical and Experimental Chemistry》1990,25(5):564-568
When frozen solutions of lutetium diphthalocyanine (LuPC2) in a mixture of methylene chloride with trichloroethylene are irradiated by UV light, monocations of LuPC2 form. The photoreaction is slowed and ceases in an early stage apparently due to the reversibility of the photoconversion in this system. The reduced form of LuPC2 (its monoanions) are completely converted into the neutral form of LuPC2 during irradiation. When this photoconversion is carried out in a frozen solution, the electronic absorption bands in the spectrum of the LuPC2 formed are displaced in comparison to the bands of the original substance under the same conditions, posibly due to the difference between the structures of the solvation shells. An interpretation of the electronic absorption spectrum of LuPC2 in the 300–1600-nm region has been given on the basis of the scheme of the molecular orbitals of sandwich phthalocyanine dimer with one -electronic vacancy.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 25, No. 5, pp. 614–618, September–October, 1989.We express our thanks to P. N. Moskalev for supplying the preparations of MIIIPC2. 相似文献
935.
Condensation of aryl- and aroylhydrazines and thiosemicarbazide with 2-diphenylphosphinoyloxybenzaldehyde results in formation of the corresponding hydrazones and thiosemicarbazone. The products give rise to conformational equilibrium between rotational and Z,E isomers, which is strongly displaced toward the E,E',Z' isomer and is determined by the nature of substituent in the hydrazine fragment. 相似文献
936.
T. Katsuki 《Russian Chemical Bulletin》2004,53(9):1859-1870
The recent development of asymmetric Baeyer—Villiger oxidation of prochiral and racemic ketones is briefly summarized, focusing on the regio- and stereocontrol of the oxidation attained by regulating the stereoelectronic demand in the step of rearrangement of the Criegee intermediate.Based on the report presented at the International Conference Modern Trends in Organoelement and Polymer Chemistry dedicated to the 50th anniversary of the A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences (Moscow, May 30–June 4, 2004).Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1784–1794, September, 2004. 相似文献
937.
Catalytic nitrobenzene oxidation of lignins 总被引:1,自引:0,他引:1
A. F. Gogotov N. A. Rybal'chenko T. I. Makovskaya V. A. Babkin 《Russian Chemical Bulletin》1996,45(12):2854-2857
Alkaline nitrobenzene oxidation of hardwood and softwood lignins in the presence of redox and phase-transfer catalysts was studied. The selectivity of oxidation of lignins increased by 1.7 to 1.9 times. A possible mechanism of catalysis is discussed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 3004–3007, December, 1996. 相似文献
938.
Institute of the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh
Soedinenii, No. 6, pp. 899–900, November–December, 1993. 相似文献
939.
Ya. S. Yakhyaev S. N. Khadzhiev T. M. Gairbekov S. E. Spiridonov 《Reaction Kinetics and Catalysis Letters》1986,30(2):263-268
The effect of hydrothermal treatment of decationized superhigh-silica zeolite on the mechanism of n-hexane conversion has been studied. It has been established that thermosteam modification sharply decreases the cracking activity and increases the selectivity to aromatization reactions. Zeolite acidity markedly decreases, but its crystal structure does not become amorphous.
-. . .相似文献
940.