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31.
32.
用降解法合成了未见报道的标题配合物.通过化学分析、ICP和TG曲线确定了其化学式为K10H3[Y(SiW9Mo2O39)2];利用IR、XRD、183W-NMR、循环伏安等手段对其结构进行了表征.结果表明,杂多阴离子为α-型Keggin结构.采用稀土多元渗的方法对配合物进行了气相热扩渗,ICP和XPS测试表明,微量的稀土元素La,Sm和Dy可以渗入到配合物的体相,并与组分元素发生键合作用;导电性的测试结果表明,室温扩渗后,试样的电导率提高了约104倍,有望成为具有实际应用的固体电解质. 相似文献
33.
The hydrothermal syntheses of the alkali metal molybdenum bronzes from starting solids (HxMoO3) with structural affinities to the desired products were investigated. Single-phase potassium blue and red bronzes were prepared by the hydrothermal treatments at around 430 K, and characterized by powder X-ray diffraction, IR spectroscopy, and SEM. The formation processes of these two bronzes during the hydrothermal treatments were found to differ. The blue bronze was formed by a structure-inheriting solid-state route from HxMoO3 with x<0.3, whereas the red bronze was formed for x>0.3 through a solution dissolution/deposition route via the formation of MoO3+MoO2. 相似文献
34.
E. V. Chubarova D. G. Samsonenko H. G. Platas F. M. Dolgushin A. V. Gerasimenko M. N. Sokolov Z. A. Starikova M. Yu. Antipin V. P. Fedin 《Journal of Structural Chemistry》2004,45(6):1004-1013
Compounds of trigonal cluster chloroaqua complexes with cucurbit[8]uril were synthesized by slowly evaporating HCl solutions of chalcogenides heterometallic cubane cluster complexes of molybdenum and tungsten with cucurbit[8]uril in air; the complexes were characterized by X-ray diffraction analysis: (H3O)8[Mo3S4(H2O)2.5Cl6.5]2Cl(PdCl4)·(C48H48N32O16)· 29H2O (a = 13.3183(17) Å, b = 13.7104(18) Å, c = 18.225(3) Å; α = 80.263(3)°, β = 77. 958(3)°, γ = 87.149(4)°, V = 3207.4(7) Å3, space group P
, Z = 1, ρ(calc) = 1.900 g/cm3), (H3O)4 [Mo3S4(H2O)3Cl6]2·(C48H48N32O16)3·68H2O (a = 21.413(6) Å, c = 49.832(10) Å; γ = 120°, V = 19788(8) Å3, space group R
, Z = 3, ρ(calc) = 1.695 g/cm3), (H3O)6 [Mo3S4(H2O)3Cl6]2Cl2·(C48H48N32O16)·12H2O (a = 15.881(2) Å, b = 17.191(2) Å, c = 23.276(4) Å; β = 98.865(15)°, V = 6278.7(15) Å3, space group P21/c, Z = 2, ρ(calc) = 1.638 g/cm3), [W3S4(H2O)5Cl4]2·(C48H48N32O16)3·35H2O (a = 21.038(3) Å; α = 61.20(1)°, V = 6762.0(14) Å3, space group R
, Z = 1, ρ(calc) = 1.582 g/cm3). The [Mo3S4(H2O)3Cl6]2− anion complex was isolated as three geometrical isomers.Original Russian Text Copyright © 2004 by E. V. Chubarova, D. G. Samsonenko, H. G. Platas, F. M. Dolgushin, A. V. Gerasimenko, M. N. Sokolov, Z. A. Starikova, M. Yu. Antipin, and V. P. Fedin__________Translated from Zhurnal Strukturnoi Khimii, Vol. 45, No. 6, pp. 1049–1058, November–December, 2004. 相似文献
35.
ZheLi DangLi WeiHuang KechangXie 《天然气化学杂志》2005,14(2):115-118
The Cu-Mo/ZSM-5 catalysts with different Cu/Mo ratios were prepared by wet impregnation method, and their catalytic performance for selective catalytic reduction of NOx was studied. The results showed that Cu-Mo/ZSM-5 is a very effective catalyst for NOx catalytic reduction with ammonia, especially when Cu/Mo molar ratio is about 1.5. It not only exhibited the extremely high catalytic activity, but also showed good stability for 02. The bulk phase structure of Cu-Mo/ZSM-5 catalysts was determined by XRD technique, and the results indicated that there is a maximum dispersion for Cu species when Cu/Mo molar ratio is 1.5, and an interaction between Cu and Mo along with HZSM-5 may be present in Cu-Mo/ZSM-5, which may possibly result in a special structure favorable for the catalytic reduction of NOx over Cu-Mo/ZSM-5 catalyst. 相似文献
36.
含氮宾的两个三核羰基铁簇合物是由[Et_3NH][HFe_3(CO)_(11)]与C_6H_5NCO在苯中反应获得。应用四园衍射仪测定了H_2Fe_3(N-C_6H_5)(CO)_9(Ⅰ)和Fe_3(N-C_6H_5)(μ_3-CO)(CO)_9(Ⅱ)的晶体结构。晶体数据为:C_(15)H_7NO_9Fe_3(Ⅰ),空间群P2_1/a,a=18.343(2),b=9.072(1),c=11.451(1)(?),β=102.03(1)°,V=1863.7(?)~3,Z=4,D_c=2.143g/cm~3;C_(16)H_5NO_(10)Fe_3(Ⅱ),空间群P2_1/c,a=8.634(1),b=13.026(1),c=17.642(2)(?),β=97.68(1)°,V=1966.3(?)~3,Z=4,D_c=1.820g/cm结构系用直接法解出,最后R_(Ⅰ)因子为0.033,R_(Ⅱ)因子为0.027。测定结果表明,(Ⅰ)和(Ⅱ)分子均具有C_s对称性,且三个Fe原子共面,呈近似等边三角形结构。(Ⅰ)中面桥N原子以不对称方式与三个Fe原子成键;(Ⅱ)中面桥羰基以不对称方式与三个Fe原子键连。Fe-N和Fe-C键长分别在1.896-1.938(?)和2.006-2.110(?)之间。 相似文献
37.
Prochiral alkenes, aldehydes, and ketones constitute the most frequently used starting materials for enantioselective organic syntheses. Protocols often involve chiral binding agents or Lewis acids that can give two diastereomeric adducts, the ratios of which are measures of chiral recognition. With π adducts, the diastereomers differ in the enantioface of the C?C or O?C group bound to the Lewis acid. This review provides the first comprehensive analysis of such equilibria and related binding phenomena with chiral transition metal Lewis acids. An extensive body of data from the authors' laboratory for complexes of the pyramidal rhenium fragment [(η5?C5H5)Re(No)(PPh3)]+ ( I ) affords particular insight. Literature data for other complexes are also summarized. A general model for chiral recognition based upon the relative steric properties of four quadrants is presented. This enables binding selectivities to be individually and rationally optimized for different classes of ligands. Electronic effects are also identified and correlated with specific structural properties. Relationships between binding equilibria, reactivity, and product configurations are discussed. 相似文献
38.
39.
S. Stupnikova E. Petushkova D. Muceniece V. Lūsis 《Chemistry of Heterocyclic Compounds》2007,43(1):41-49
The recyclization of 1,4-dihydropyridines in aqueous-alcoholic hydrochloric acid medium proceeds with cleavage of a C-N bond
and pyridine ring opening. Cyclohexenone derivatives are formed as a result of the subsequent intramolecular crotonic condensation
of the acyclic intermediate. The leaving carbonyl substituents depart simultaneously with recyclization, depending on the
acidity of the reaction medium.
Dedicated to Prof. Dr. E. Lukevics on the occasion of his 70th birthday.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 49–58, January, 2007. 相似文献
40.
担载于ZrO2上的Ru3(CO)12-Fe(CO)9混合簇的红外光谱表明,Ru3(CO)12以Ru(CO)2O2表面络合物存在.混合族在真空中随温度升高而发生脱羰基作用,500℃左右羰基完全脱掉;以Al2O3为载体者其羰基不易脱除,升高温度出现多种羰基带.混合簇中的Fe2-(CO)9极易脱羰基.担载混合簇在Ar气中进行TPDE时,低温时以脱羰基为主,高于150℃时发生表面歧化反应而生成CO2;在H2气中,低温时仍以脱羰基为主,高于150℃时发生表面加氢反应而生成CH4.混合簇的脱羰基和表面反应能力与Ru/Fe比及载体有关.担载混合簇在CO加氢反应中以Ru(CO)2O2和分散Fe存在,还出现-CHx多种表面物种. 相似文献