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991.
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Jingfei Luan Zhigang Zou Minghui Lu Guoyou Luan Yanfeng Chen 《Research on Chemical Intermediates》2006,32(1):31-42
In2BiTaO7 was synthesized using the solid-state reaction method and its photocatalytic properties were investigated. The results of
powder X-ray diffraction (XRD) indicated that the compound crystallizes in the pyrochlore-type structure, cubic system with
space group Fd-3m. The lattice parameter is 10.6972(1) ?. In addition, the compound shows strong optical absorption in the
visible region (λ > 420 nm) and the band gap of In2BiTaO7 was estimated to be about 2.47 eV. For the photocatalytic reaction, H2 or O2 evolution was observed from CH3OH/H2O or AgNO3 solution respectively with In2BiTaO7 as the photocatalyst under visible light irradiation, indicating that In2BiTaO7 is responsive to visible light for splitting water. Furthermore, the catalyst remained photoactive in the wavelength range
up to 510 nm. Photocatalytic degradation of methylene blue (MB) dye over the compound was further investigated under visible
light irradiation. The results showed that complete removal of aqueous MB could be achieved after irradiation for 135 min
over In2BiTaO7. Furthermore, under visible light irradiation In2BiTaO7 showed markedly higher catalytic activity compared to P-25 for MB photocatalytic degradation. 相似文献
994.
[formula: see text] S-Nitrosoglutathione oxidized 4-substituted Hantzsch 1,4-dihydropyridines in CH3CN/H2O or CH3CN/phosphate aqueous buffer solution to give aromatic products in various yields. 相似文献
995.
利用双缩脲试剂,在可见光区建立了N-磷酰化二肽、二肽以及磷酰化多肽的分光光度定量分析方法。在经典的双缩脲分光光度法的实验条件下,观察到N-磷酰化二肽、二肽与双缩脲试剂的复合物的最大吸收波长均为620nm及N-磷酰基对二肽有很强的增色作用。 相似文献
996.
Simultaneous determination of triterpene saponins in ginseng drugs by high-performance liquid chromatography 总被引:3,自引:0,他引:3
A HPLC method for the simultaneous determination of 11 triterpene saponins with four-type aglycones (protopanaxadiol, protopanaxatriol, ocotillol and oleanolic acid types) in Ginseng drugs was developed and validated. Using a gradient of acetonitrile and 10 mM K-phosphate buffer (pH 5.80) as the mobile phase and UV detection at 196 nm, more than 18 ginsenosides with different aglycones were separated satisfactorily within 60 min. The detection limits (signal/noise> or =3) were 0.1 microg for ginsenosides Rb1, Rc, Rd, Re and Rg1, chikusetsusaponin III, and notoginsenoside R2, 0.2 microg for gisenoside Ro and chikusetsusaponin IVa, 0.3 microg for chikusetsusaponin IV, and 3 microg for majonoside R2. The calibration curve of each saponin had a correlation coefficient close to 1. Intra- and interday precisions were less than 2.1% (n=5) and 3.3% (n=15), respectively. The recovery rates of extraction were in the range of 96.4-102.7% for all ginsenosides. By adopting this method, the determinations of 11 ginsenosides in three Ginseng drugs derived from Panax ginseng, Panax vietnamensis var. fuscidiscus and Panax japonicus (Japan) were achieved. 相似文献
997.
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999.
M. A. Yurovskaya A. Z. Afanas'ev S. L. Druzina Yu. G. Bundel' 《Chemistry of Heterocyclic Compounds》1989,25(6):667-672
The introduction of bulky alkyl substituents (iso-Pr,tert-Bu) into any positions of the starting 3-nitropyridinium salt only increases the reaction time and decreases the yields of the corresponding alkylindoles somewhat.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 805–810, June, 1989. 相似文献
1000.