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991.
YuYingFENG XiaoTianGU JiaHongZHOU JianChunBAO GangLI TianHongLU 《中国化学快报》2004,15(12):1505-1508
New Ge/SiO2 glasses have been synthesized by heating the GeO2/SiO2 dry gels under H2 gas at 700℃. The resulting fluorescence spectra show that this kind of Ge/SiO2 glasses emit strong photoluminescence at 392 nm (3.12 eV), medium strong photoluminescence at 600 nm (2.05 eV) and weak photoluminescence at 770 nm (1.60 eV) respectively. Possible photoluminescence mechanisms are also discussed based on the results of X-ray diffraction (XRD) and X-ray photoelectron spectra (XPS). 相似文献
992.
Ibrahim Isildak Murat Yolcu Omer Isildak Nadir Demirel Giray Topal Halil Hosgoren 《Mikrochimica acta》2004,144(1-3):177-181
Two diaza-crown ether compounds were synthesized and evaluated as Ag+-selective carriers in polyvinylchloride (PVC) membrane electrodes of solid-state type. The all-solid-state PVC membrane electrode based on N,N-Dibenzyl-dibenzo-diaza-18-crown-6 exhibited a super-Nernstian response (75±10mV per decade) over the concentration range of 1×10–1 to 7×10–6M of Ag+ ion and a detection limit of 3×10–6M, at a wide range of pH (pH 4–7). The response time of the electrode was fast (less than 10s), and it can be used for three months without any significant deviation in potential. The proposed all-solid-state PVC membrane electrodes revealed high selectivity toward Ag+ ion with respect to alkali, alkaline earth, heavy and transition metal ions. A flow-through cell of all-solid-state PVC membrane Ag+-selective electrode based on N,N-Dibenzyl-dibenzo-diaza-18-crown-6 has also been prepared and applied for flow-injection analysis of Ag+ ion in solution. 相似文献
993.
Lanying?Yang Yi?Zhang Qingqi?Chen Jin Shi?MaEmail author 《Monatshefte für Chemie / Chemical Monthly》2004,135(2):223-229
Summary. 1-(Dipyrrin-2-yl)-1-(dipyrrin-3-yl)methane, the N-confused analog of biladiene-ac, is prepared by condensation of 2,3-dipyrromethane with two molecules of 2-formylpyrrole in dichloromethane in the presence of hydrogen bromide. Self-assembly of the ligand with Zn(II) in dichloromethane and methanol offers a dinuclear dimeric complex with a ligand:metal ratio of 2:2. X-Ray crystal structure analysis reveals two ligands bound through a head-to-tail pattern to two zinc centers to form a severely distorted helical conformation, which has the shape of a rectangle. 相似文献
994.
Chlorosulfonyl isocyanate adds to α-pinene in concerted fashion to give the unrearranged N-chlorosulfonyl-β-lactam 2 (75%). Thermolysis of cycloadduct 2 affords the rearranged N-chlorosulfonyl-γ-lactam 6 (60%) via a sequence of transient carbonium ions (45). Reductive hydrolysis of 2 and 6 gave, respectively, the NH-β-lactam 3 (70%) and the NH-γ-lactam 7 (70%). Proof of structure of the rearranged γ-lactams 6 and 7 are provided, respectively, by X-ray crystallographic analysis and the application of the Eu(dpm)3 NMR shift reagent. 相似文献
995.
Yu. G. Budnikova A. G. Kafiyatullina Yu. M. Kargin O. G. Sinyashin 《Russian Chemical Bulletin》2003,52(7):1504-1511
Electrochemical reduction of cobalt(ii) complexes containing -acceptor ligands (L = bpy, Ph2Ppy) proceeds through three consecutive reversible steps: one-electron transfer to form a more stable CoIL complex, transfer of two electrons at more negative potentials to form an anionic [NiL]– complex, and reduction of the ligand to the radical anion. The stability of the cobalt complexes with different ligands decreases in the series Ph2Ppy > Ph3P > bpy. 相似文献
996.
DFT Study on the (S)-Proline-catalyzed Direct Aldol Reaction between Acetone and 4-Nitrobenzaldehyde
1 INTRODUCTION Aldol reaction, one of the most important C–C bond-formation reactions, is widely utilized in orga- nic synthesis[1]. Extensive efforts have been donated to the development of catalytic stereo-selective va- riants of this reaction[2]. However, the direct aldol reaction between unmodified carbonyles would be the most attractive synthetic alternative. Proline-catalyzed intermolecular direct aldol reac- tion between acetone and 4-nitrobenzaldehyde was first reported by List… 相似文献
997.
Thi Thanh-Tâm Nguyên Claude Delseth Jean-Pierre Kintzinger Pierre-Alain Carrupt Pierre Vogel 《Tetrahedron》1980,36(19):2793-2797
Natural-abundance 17O-NMR spectra of 7-oxanorbornane exo-3-oxatricyclo [3.2.1.02.4]octane and their unsaturated derivatives (endo cyclic and exocyclic double bonds) have been measured. Linear correlation laws were observed for of these ethers/corresponding hydrocarbons. The “cyclization shifts” for δo in ethers were not correlated by the “cyclization shifts” for δc of the corresponding hydrocarbons. 相似文献
998.
氟化锶/氧化钕催化剂的甲烷氧化偶联性能及其吸附氧物种的原位FTIR光谱研究龙瑞强,万惠霖,赖华龙,蔡启瑞(厦门大学化学系固体表面物理化学国家重点实验室,厦门,361005)关键词甲烷氧化偶联,氟化锶/氧化钕,吸附氧物种近年来,甲烷氧化偶联(OCM)的... 相似文献
999.
Filiz Taneri Tamer Güneri Zolt%aacute;n Aigner Michael Kata 《Journal of inclusion phenomena and macrocyclic chemistry》2002,44(1-4):257-260
Highly-soluble cyclodextrin derivatives, such as hydroxypropyl--cyclodextrin(HP--CD) and methyl--cyclodextrin (MEB), were tested as solubilizingagents for ketoconazole, with the aim of improving the physicochemical andbiopharmaceutical properties of this lipophilic imidazole antifungal agent. Productswere prepared in four molecular ratios by physical mixing, kneading and spray-dryingmethods. The kneaded products in a ratio of 1:2 and the spray-dried products exhibitedthe highest dissolution rates. The phase solubility diagrams of ketoconazole with thesecyclodextrins at 25 °C in water and in simulated intestinal medium wereconstructed. A solubility diagram of AL type was obtained with HP--CD, and one of AP type with MEB. The complexes were characterized by thermal methods(DSC, TG, DTG and DTA). Multicomponent systems were prepared with tartaric acid.The effects of water-soluble polymers, e.g., polyvinylpyrrolidone, on the aqueous solubility of ketoconazole were investigated. Particle size distribution, surface area, partition coefficient, heat of dissolution and wettability studies were also carried out. The formation of inclusion complexes was observed by means of thermoanalytical studies. 相似文献
1000.
Kozhevnikov I. S. Kovalev V. L. Rusinov O. N. Chupakhin 《Chemistry of Heterocyclic Compounds》2001,37(9):1136-1140
3-R-6-Phenyl-1,2,4-triazine 4-oxides react with cyclic -diketones (dimethylbarbituric acid, dimedone, and indan) in both acidic (substrate activation) and basic conditions (nucleophile activation) with formation of H-adducts, intermediates in the nucleophilic substitution of hydrogen (SN
H) in 3-R-5-Nu-4-hydroxy-6-phenyl-4,5-dihydro-1,2,4-triazines. Oxidative aromatisation of these intermediates or auto-aromatisation of acylated (benzoyl chloride) at the NOH -adducts with elimination of benzoic acid gave the corresponding substituted 1,2,4-triazine 4-oxides or 1,2,4-triazines. 相似文献