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排序方式: 共有608条查询结果,搜索用时 15 毫秒
1.
Hideaki Murasugi Dr. Shohei Kumagai Dr. Hiroaki Iguchi Prof. Dr. Masahiro Yamashita Dr. Shinya Takaishi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(42):9885-9891
Crystal structures of a series of organic–inorganic hybrid gold iodide perovskites, formulated as A2[AuII2][AuIIII4] [A=methylammonium (MA) ( 1 ) and formamidinium (FA) ( 2 )], A′2[I3]1−x[AuII2]x[AuIIII4] [A′=imidazolium (IMD) ( 3 ), guanidinium (GUA) ( 4 ), dimethylammonium (DMA) ( 5 ), pyridinium (PY) ( 6 ), and piperizinium (PIP) ( 7 )], systematically changed depending on the cation size. In addition, triiodide (I3−) ions were partly incorporated into the AuI2− sites of 3 – 7 , whereas they were not incorporated into those of 1 and 2 . Such a difference comes from the size of the organic cation. Optical absorption spectra showed characteristic intervalence charge-transfer bands from AuI to AuIII species, and the optical band gap increased as the size of the cation became larger. 相似文献
2.
Keigo Fugami Takashi Nishikata Masayuki Kameyama 《Journal of organometallic chemistry》2003,687(2):567-569
Palladium-catalyzed reaction between 1-alkenyltin trichlorides and norbornene resulted in stereoselective formation of 3-alkylidenepentacyclo[9.2.1.5,81.1,110.2,1004,9]pentadecane instead of an expected simple alkenylstannylation product. Generation of trichlorostannane and its decomposition product, tin(II) chloride, was confirmed by trapping it with methyl propiolate and norbornene and analysis of the reaction by 119Sn NMR, respectively. 相似文献
3.
Abdul Majid Jim Tunney Steve Argue Mike Post 《Journal of Sol-Gel Science and Technology》2004,32(1-3):323-326
We have investigated the synthesis of perovskite-type SrFeOx (2.5 x 3.0) using three preparative methods: sol-gel, mechanochemical processing and solid state reactions at high temperature of the corresponding oxides. The sample obtained after calcination of the gel from sol-gel method, contained the least amount of strontium carbonate impurity. The amount of strontium carbonate impurity decreased with the increase in calcination temperature. Perovskites obtained have been characterized by X-ray diffraction (XRD) and nitrogen adsorption isotherms. Samples obtained from three methods have been compared with respect to calcination temperature, crystallite size and specific surface area.Issued as NRCC No. 46479. 相似文献
4.
R. Bontchev K. Cheshkova D. Mehandjiev J. Darriet 《Reaction Kinetics and Catalysis Letters》1998,63(1):121-127
The catalytic activity of Ba2Ru0.67Bi1.33O6, Ba2RuBiO6, Ba3Ru2BiO9 and BaRuO3 towards NO-decomposition prior to and after treatment with NH3 has been studied. About 100% degree of conversion has been achieved at 400°C for samples with the highest percentage of hexagonal
stacking in their crystal structures. It has been shown that the active sites are units of two or three face-sharing [RuO6] octahedra in which a strong Ru−Ru interaction takes placevia the common faces. 相似文献
5.
G. N. Pirogova R. I. Korosteleva N. M. Panich T. A. Lagutina Yu. V. Voronin 《Russian Chemical Bulletin》1994,43(4):551-554
The catalytic activity of MIMIIO3] perovskite-type complex oxides (MI = La, Y, Nd, Yb; MII = Co, Mn, Ni) in the oxidation of CO, propylene, benzene, ethylbenzene,o-xylene, and ethyl acetate was investigated. The Co-containing catalysts were shown to be more active in the oxidation than the Mn-containing catalysts. A relationship between the catalytic and adsorption properties was established.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 602–605, April, 1994. 相似文献
6.
Stefan G Ebbinghaus 《Journal of solid state chemistry》2004,177(3):817-823
Single crystals of the new compound La1.2Sr2.4RuO7, an oxide related to the hexagonal perovskites, were grown from a BaCl2 flux. The structure was solved by single crystal X-ray diffraction. La1.2Sr2.4RuO7 crystallizes in the space group with a=5.760(1) Å and c=18.273(3) Å. It is one of the rare examples of oxides with isolated RuO6-octahedra. The structure consists of alternating layers of RuO6-octahedra and trigonal (La,Sr)O6-prisms. These prisms are capped by one additional oxygen ion, which occupies a distorted position within the (La,Sr)O6-layers. La1.2Sr2.4RuO7 is the second member of the general [A2O][AnBn−1O3n] family of hexagonal perovskites with n=2 and the first ruthenate possessing this structure. XANES investigations, bond valence sum calculations and magnetic measurements show that ruthenium takes the oxidation state +5. Although the ruthenium ions have quite long distances, a medium strong antiferromagnetic interaction between these paramagnetic centers was observed. 相似文献
7.
Dean C. Luehrs Richard E. Brown Kalpana A. Godbole 《Journal of solution chemistry》1989,18(5):463-469
A linear free energy relationship was found betweenv
max, the energy of the absorption maximum of chloride, bromide, or iodide ion in various solvents, and the solvatochromic parameter which is a measure of the hydrogen bond donor ability of the solvent. The relationships are: for chloride,v
max=6.99+50.16 kK; for bromide,v
max=5.52+45.20 kK; for iodide,v
max=5.02+40.33 kK. The correlation ofv
max for iodide ion with gave a larger correlation coefficient and smaller standard deviation than a correlation with the E
T
(30) parameter of Dimroth. From the values ofv
max for iodide ion and the solvated electron in liquid ammonia at 25°C, these correlations indicate a preliminary value of 0.00 for the parameter of liquid ammonia. This had not been reported before and is lower than expected from a general knowledge of the physical and chemical properties of liquid ammonia but is consistent with a more detailed consideration and recent gas phase measurements of hydrogen bond donor strength. 相似文献
8.
S. Colonna S. De Rossi M. Faticanti I. Pettiti P. Porta 《Journal of molecular catalysis. A, Chemical》2002,180(1-2):161-168
ZrO2-supported La, Co oxide catalysts with different La, Co loading (2, 6, 8, 12 and 16 wt.% as LaCoO3) were prepared by impregnation of tetragonal ZrO2 with equimolar amounts of La and Co citrate precursors and calcination at 1073 K. The catalysts were characterized by X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS), and BET specific surface area determination. Catalytic CO oxidation was performed at 298–800 K. XRD revealed the presence of tetragonal zirconia with traces of the monoclinic phase. LaCoO3 perovskite was also detected for loading higher than 6%. XAS experiments suggested that at high loading LaCoO3 and Co3O4 were formed, while at low loading, La, Co oxide species interacting with support, and hard to be structurally defined, prevailed. The catalysis study evidenced that the catalytic activity was due to segregated and highly dispersed cobalt oxide species. 相似文献
9.
Summary The dependence of the chloride distribution coefficient on the co-ion of solutions of different alkali fluorides, MF, up to 11M is tested on the strongly basic anion-exchange resin AG1-X10. Under the same experimental conditions the distribution coefficient decreases in the following order for M+: Na+>K+>Rb+>Cs+. This can be explained by the different co-ion-chloride interactions. The consequence of this interaction for a chromatographic separation of chloride is shown with 5M KF and CsF solutions, used as eluants. Depending on the fluoride concentration, the distribution coefficient passes through a minimum value to increase again at higher electrolyte concentration. The non-exchange electrolyte in the resin phase is responsible for this effect. In addition, the bromide and the iodide distribution coefficients up to 10M KF solutions are determined. One results is that the selectivity coefficient between halide ions increases at higher electrolyte concentrations. 相似文献
10.
固体氧化物电解池是一种高效、环境友好型的能量转换器件,可以直接将电能转化为化学能. 本文介绍了近年来作者课题组在固体氧化物电解池直接用于CO2还原的研究进展,并以阴极材料为主着重讨论了金属陶瓷电极和混合导电型钙钛矿氧化物电极的研究工作,最后展望了未来固体氧化物电解池直接电解CO2的研究思路和方向. 相似文献