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61.
采用共沉淀法并通过改变焙烧温度制备了一系列具有不同晶相结构的La2Zr2O7催化剂,在微型固定床反应器上评价其甲烷氧化偶联反应性能,并利用XRD、Raman、CO2-TPD、XPS等表征手段,探究催化剂的物相结构、表面碱性以及表面氧物种的变化规律。结果表明,随着焙烧温度从700℃逐渐升高到1200℃,La2Zr2O7催化剂结晶度不断提高,晶相发生明显变化,从无定形结构逐渐向缺陷萤石结构过渡,最终转变成烧绿石结构。焙烧温度提高促使La2Zr2O7晶相转变过程中,催化剂表面的碱性强度减弱,中等碱性位数量以及具有催化活性的表面氧物种O22-和O2-的相对含量不断减少,致使催化剂的CH4转化率和C2+选择性不断降低。其中,无定形LZO-CP-700催化剂表现出最佳的甲烷氧化偶联反应性能。  相似文献   
62.
The reaction of cyano(cyclohexylidene)thioacetamide with cyanothioacetamide or malononitrile andN-methylmorpholine yieldsN-methylmorpholinium 6-amino-3,5-dicyano-1,4-dihydropyridine-4-spirocyclohexane-2-thiolate. Its structure was established based on the results of alkylation and X-ray structural analysis.Deceased.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2535–2540, October, 1996.  相似文献   
63.
Under the conditions studied for the synthesis of mesophase materials with alkylpyridinium halides an increase in the density of packing of these molecules in the encapsulated micelles was observed with an increase in the length of the alkyl radicals. The difference in the density of packing of these surface active reagents (SAR) depended to a considerable extent on the perfection of the hexagonal structure and the characteristic absorption properties of the mesophase materials of MCM-41 type.  相似文献   
64.
9-Methyl-3,3a,4,5-tetrahydro-6H-thieno[2,3-b]thiocino[4,5-c]isoxazole and 9-hydroxyimino-2-methyl-7-methylene-6, 7,8,9-tetrahydro-5H-thieno[2,3-b]thiocine have been prepared for the first time by the oxidation of 2--alkenylthio-3-thiophenecarbaldoximes with NaOCl. X-ray structural investigations of thieno[2,3-b]thiocine and 2-homomethallylthio-5-methyl-3-thiophenecarbaldoxime have been carried out.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1262–1266, July, 1993.  相似文献   
65.
The previously unknown 1-amino- and 3-aminonaphtho[1,2-d]imidazoles, 1-aminonaphtho[2,3-d]imidazole, 1-aminophenanthro[9,10-d]imidazole and the N-amino-N'-methylimidazolium picrates corresponding to them have been obtained by direct amination of a series of condensed imidazoles with O-picrylhydroxylamine. An X-ray structural investigation of 1-amino-3-methylnaphtho[1,2-d]imidazolium picrate showed that, in difference to 1-aminobenzimidazolium salts, a conformation exists in it in which the hydrogen atoms of the N-NH2 group are directed to the side of the meso carbon atom.  相似文献   
66.
Dynamic light scattering experiments in acid-catalyzed silica sols are discussed. It is shown that in spite of limited parameter accuracy and limited absolute knowledge of the particle sizes, the scattering data from various experiments are comparable with one another and give information about structural differences. Measurements at various angles indicate changes between non-spherical and nearly spherical particles and allow the estimation of gelling times before gelation.  相似文献   
67.
新鄂西香茶菜素为首次从抗癌中草药鄂西香茶菜[Rabdosia henryi (Hemsl) Hara]的叶子中分离得到的二萜化合物。前人曾从毛叶香茶菜[R. japonica (Burm. f)Hara]中分离出该化合物并依据光谱数据推测其结构(右图)。但其结晶学研究尚未见报道。为研究其立体结构及分子在晶体中的排布方式,我们对该化合物的晶体进行了X射线结构分析。  相似文献   
68.
The reaction of 2-diethylamino-3-diethylaminomethyl-1,3,2-benzoxazaphospholine with functionally substituted alcohols and phenols occurs with the cleavage of exocyclic P-N bond followed by N→P migration of the diethylaminomethyl group and formation of imidophosphonate dimers. A similar reaction with polyhydroxy compounds (diethylene glycol, glycerol) results in symmetrical and asymmetrical spirophosphoranes. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1781–1784, October, 1993.  相似文献   
69.
The potential of the structural analogy method in the topological studies of adamantane derivatives and analogs is demonstrated. The topological and structural characteristics of these compounds are calculated. Chromatographic retention indices were determined experimentally. Correlations between the topological indices and the physicochemical and chromatographic characteristics are investigated.  相似文献   
70.
Various melt-polymerizable bisimido-bisphthalonitrile polymer precursors were synthesized by the reaction of 4-aminophthalonitrile (4-APN) with bis(3,4-dicarboxyphenyl) dimethylsilane dianhydride (SIDA), 4,4′-hexafluoroisopropylidene diphthalic anhydride (6FDA), bis(3,4-dicarboxyphenyl)ether dianhydride (ODPA), and 3,3′, 4,4′-tetracarboxylichenzophen+ne dianhydride (BTDA) in an aprotic solvent. The synthesized monomers showed crystalline melting at 269 and 271°C. Elemental analysis, differential thermal analysis (DTA), infrared (IR), nuclear magnetic resonance (1H-NMR) and mass spectral studies were carried out to characterize the synthesized monomers. Thermogravimetric analysis (TGA) of the synthesized monomers showed their thermal stability at 410–400°C. A detailed study and NMR investigation of the first step of condensation reaction was carried out and indicated the formation of a transient charge transfer complex. Thermal cyclization of the formed intermediate, however, gave the required monomers. A preliminary study demonstrated that melt-polymerization of the synthesized monomers gave thermallystable, tough polymers.  相似文献   
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