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161.
采用50~200nm同步辐射光,对CH2Br2的光电离过程进行了研究,根据测定的母体离子及其碎片离子出现势,得到二溴甲烷的绝热电离势为10.23±0.01eV,并获得了离子的生成焓,解离能及键能等热力学数据,分析了碎片离子的光解离电离通道。 相似文献
162.
Ai Jun HOU Hui YANG Bei JIANG Qin Shi ZHAO Yan Ze LIU Zhong Wen LIN Han Dong SUN Laboratory of Phytochemistry Kunming Institute of Botany Chinese Academy of Sciences Kunming Department of Phytochemistry Henan College of Traditional Chinese 《中国化学快报》2000,11(9)
In continuation of our research on diterpenoids in the Isodon species, several newcompounds"' were obtained from the leaves oflsodon xerophilus (C. Y. Wu et H. W. Li)H. Hara (Labiatae), a perennial shrub native to Yunnan province. Further fractionation ofthe EtOAc extract led to the isolation of tWo new enl-kauranoids, xerophilusin E (l) andxerophilusin F (2). This paper deals with the structUral elucidation of the newcompounds.Xerophilusin E (l), a minor constitUent, was obtained as p… 相似文献
163.
Niu CG Gui XQ Zeng GM Guan AL Gao PF Qin PZ 《Analytical and bioanalytical chemistry》2005,383(2):349-357
A fluorescence ratiometric sensor for pH determination is described in this paper. The sensor incorporated the pH-sensitive
dye meso-5,10,15,20-tetra-(4-allyloxyphenyl)porphyrin (TAPP) as an indicator and a pH-insensitive dye N-(2-methacryloxyethyl)benzo[k,l]thioxanthene-3,4-dicarboximide (MBTD), a benzothioxanthene derivative, as a reference for fluorescence ratiometric measurement.
To prevent leakage of the dyes, both were photocopolymerized with acrylamide, hydroxyethyl methacrylate, and triethylene glycol
dimethacrylate on the silanized glass surface. The reproducibility and response time of the prepared sensor were sufficient.
Most common coexisting inorganic ions and organic compounds did not interfere with pH sensing. In the acidic pH range from
1.5 to 5.0 the fluorescence intensity ratio of the two dyes varied linearly as a function of pH. The sensing membrane was
found to have a lifetime of at least one month. The sensor was applied to the analysis of waste water and artificial samples. 相似文献
164.
165.
A novel mode of affinity chromatography (AC) based on an open tubular capillary column (OTAC) is demonstrated. The OTAC column is prepared by immobilizing Cibacron blue F3GA onto the inner surface of a 50-microm-i.d. capillary column. The AC experiment is performed on a capillary electrophoresis instrument by using its pressure system as the driving force. Bovine serum albumin and lysozyme (Lys) are successfully separated with stepwise gradient elution. The relative standard deviation (RSD) for the elution time of the retained Lys is 0.08%, and good repeatability of its peak area and peak height with an RSD value lower than 2.12% for 10 consecutive runs is observed. The loading capacity and detection limit for the retained Lys are approximately 36 ng and 8.6 ng, respectively. It is also found that the amount of protein adsorbed is unaffected by the flow rate of the loading buffer, and OTAC can be used for the fast determination of biopolymers. Some of the advantages of OTAC over conventional modes of open tubular capillary liquid chromatography are that the detection sensitivity and loading capacity of a sample can be greatly improved, because the relatively large inner diameter of the capillary can be adopted and the whole capillary column can be used to adsorb the solute in OTAC. 相似文献
166.
A highly sensitive and selective catalytic adsorptive cathodic striping procedure for the determination of trace germanium is presented. The method is based on adsorptive accumulation of the Ge(IV)‐gallic acid (GA) complex onto a hanging mercury drop electrode, followed by reduction of the adsorbed species. The reduction current is enhanced catalytically by addition of vanadium(IV)‐EDTA. The optimal experimental conditions include the use of 0.03 mol/L HClO4 (pH1.6), 6.0×10?3 mol/L GA, 3.0×10?3 mol/L V(IV), 4.0×10?3 mol/L EDTA, an accumulation potential of ?0.10 V(vs. Ag/AgCl), an accumulation time of 120 s and a differential pulse potential scan mode. The peak current is proportional to the concentration of Ge(IV) over the range of 3.0×10?11 to 1.0×10?8 mol/L and the detection limit is 2×10?11 mol/L for a 120 s adsorption time. The relative standard deviation at 5.0×10?10 mol/L level is 3.1%. No serious interferences were found. The method was applied to the determination of germanium in ore, mineral water and vegetable samples with satisfactory results. 相似文献
167.
12种道地中药中无机元素的含量测定 总被引:1,自引:0,他引:1
报道了用X射线荧光分析法测定的12种道地中药,98个不同产地样品中的Fe、Cu、Zn、Mn、Sr、Ca、K含量。结果表明,不同种属,不同产地,不同品种中药元素量存在差异,不同加工方法影响中药中元素含量,同种中药中元素分布模式也不同。 相似文献
168.
169.
Xiang Qin LIN Liang Dong FENG Hao ZHANG 《中国化学快报》2006,17(4):493-495
A setup for recording surface tension curves at a mercury drop during potential scanning is designed based on photo-sensitive detection system. Surface tension spectrum at Hg drop can be recorded by voltammetric study. A Yb(III)-NO2- catalytic reduction system was used for characterization. The simple, sensitive technique can be expected to provide fresh information on molecular interactions at electrode surfaces. 相似文献
170.
Tseng CM Dyakov YA Huang CL Mebel AM Lin SH Lee YT Ni CK 《Journal of the American Chemical Society》2004,126(28):8760-8768
Photoisomerization and photodissociation of aniline and 4-methylpyridine at 193 nm were studied separately using multimass ion imaging techniques. Photofragment translational energy distributions and dissociation rates were measured. Our results demonstrate that more than 23% of the ground electronic state aniline and 10% of 4-methylpyridine produced from the excitation by 193 nm photons after internal conversion isomerize to seven-membered ring isomers, followed by the H atom migration in the seven-membered ring, and then rearomatize to both methylpyridine and aniline prior to dissociation. The significance of this isomerization is that the carbon, nitrogen, and hydrogen atoms belonging to the alkyl or amino groups are involved in the exchange with those atoms in the aromatic ring during the isomerization. 相似文献