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121.
Some gauge invariant atomic orbitals-coupled-perturbed Hartree-Fock (GIAO-CPHF) calculations were performed for seven indolizine derivatives and their monoprotonated forms. Chemical shift, molecular geometry, and charge distribution data are reported for each molecule. The calculations support the results of nuclear magnetic resonance (NMR) spectroscopy measurements showing that protonation occurs preferentially at N1. The good agreement between the calculated and observed 13C and 15N chemical shifts show that such calculations can be used for chemical shift assignment purposes. Cation structures and probable sites for electrophilic reaction or second protonation are also discussed. 相似文献
122.
本文使用涂金石墨管,自制氢化物石墨炉进样系统及连续流动氢化物发生器,直接测定了粮食,植物及水中的痕量汞。该法实用性强,线性范围宽,精密度好,准确度高。灵敏度为1.1ng/L,检出限(3σ)为0.8ng/L。 相似文献
123.
利用AFM和SNOM对淋巴细胞膜表面超微结构及其光学性质的初步研究 总被引:5,自引:0,他引:5
利用原子力显微镜(Atomic Force Microscopy,AFM)对淋巴细胞表面形貌进行了形态学的初步研究,观察到了其膜表面其他显微技术所不能发现的超微结构.同时也运用扫描近场光学显微镜(Scanning Near field Optical Microscopy,SNOM)对淋巴细胞进行成像,观察了其对光的透射、吸收等光学性质,并对两种成像方法进行了比较.研究发现:淋巴细胞膜表面凹凸不平,分布着大量直径几十到几百纳米不等的小颗粒;淋巴细胞中央部位有自发荧光现象.结果表明,AFM和SNOM可作为进一步探讨淋巴细胞的结构与功能关系的有力工具. 相似文献
124.
Three novel perylene polyimides (PPIs) containing p‐n diblock units were designed and synthesized for use in dye‐sensitized mesoporous TiO2 solar cells. They all dissolve in m‐cresol and N‐methyl‐2‐pyrrolidone (NMP). Their visible light absorption, electrochemical and photoelectrochemical properties were systematically studied. The polyimides have band gap energies of 2.16, 2.19 and 2.25 eV deduced from ultraviolet–visible absorption spectra, and electron affinity (Ea) and ionization potential (IP) of ?3.93 and 6.10 eV for PPI1, ?3.94 and 6.13 eV for PPI2, ?3.93 and 6.59 eV for PPI3, respectively, deduced from cyclic voltammogram. Experimental data show that introduction of 4,4′‐bisaminetriphenylamine cannot only greatly enhance optic‐electro conversion efficiency, but also enhance the dissolubility which in favorable for making the devices. The relationship of structure and properties of PPI is discussed and the mechanism of photocurrent generation is explained. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
125.
126.
Satchidanand S. Biswas Achamkulangara Sethumadhavan Pappu S. Murty 《Mikrochimica acta》1991,103(1-2):71-77
Inductively coupled plasma atomic emission spectrometry (ICP-AES) was employed to determine Y, Sm, Eu, Gd, Dy, Ho and Er in high purity terbium oxide. Terbium oxide was dissolved in 0.5 mol/l HNO3 and nebulized into the plasma generated by a 56 MHz RF generator at 1.5 kW output power. Using a Jobin-Yvon 1-m Czenry-Turner high resolution, high dispersion scanning monochromator, lines mutually interference-free as well as free of interference from the matrix Tb were chosen for the seven analytes. A set of standards containing the analytes in the concentration range 0.01–1.0 gmg/ml with 1 mg/ml Tb was used for calibration. It was necessary to apply background correction to the gross analyte line intensities in order to obtain linear calibration plots for the analytes. 相似文献
127.
本文制定了N_2O-C_2H_2焰原子吸收光谱直接测定Sm-Eu-Gd富集物中Sm、Eu和Gd的分析方法。采用氧化镧溶液作为缓冲剂消除干扰提高灵敏度。此法不需要复杂的分离过程。方法简便、快速、成本低、适合工厂采用。 相似文献
128.
A batch of sulphydryl cotton microcolumns was prepared and charged with a mixed Hg standard solution (methyl-, ethyl- and inorganic Hg, 10 g l–1 as Hg, 3 ml) and stored at 4 °C in a light-tight box. At regular time intervals over a 4 month period microcolumns were removed and Hg species were quantified by gas chromatography microwave-induced plasma atomic emission spectrometry (after elution, extraction and derivatization steps). It was found that analyte recoveries for methyl- and inorganic Hg were quantitative over the 4 month period while ethyl-Hg species appeared to be stable for up to 2 months. 相似文献
129.
Masataka Hiraide Kennich Ishikawa Zuo Sheng Chen Hiroshi Kawaguchi 《Mikrochimica acta》1994,117(1-2):7-13
Coprecipitation first with magnesium hydroxide, next with tin(IV) hydroxide is developed for the determination of traces of beryllium in sea-water. To a 200-ml sample is added a sodium hydroxide solution to form magnesium hydroxide at pH 11.5, on which beryllium is quantitatively coprecipitated. The precipitate is separated by centrifugation and dissolved in 2 ml of 12 mol/l hydrochloric acid. The resulting solution (ca. 10 ml) is mixed with 2 mg of tin (IV) carrier and the pH is adjusted to 5.0 to collect the beryllium on tin (IV) hydroxide, leaving magnesium ions in the solution. The tin (IV) hydroxide is centrifuged, dissolved in 0.1 ml of 5 mol/l hydrobromic acid, and then diluted to 1 ml with water. Magnesium is so added as to be 500 g/ml for increasing the sensitivity about four times, and the beryllium in the solution is determined by graphite furnace atomic absorption spectrometry. The experiments with synthetic seawater samples showed that pg — g amounts of beryllium can be coprecipitated on the metal hydroxides and beryllium at the low ng/1 level can be determined with reasonable precision (RSD < 10%). The detection limit of the proposed method is 0.5 ng/l of beryllium in seawater. 相似文献
130.
Moreno-Cid A Yebra MC Cancela S Cespón RM 《Analytical and bioanalytical chemistry》2003,377(4):730-734
Iron was extracted on-line from solid meat samples by a simple and rapid continuous ultrasound-assisted extraction system (CUES). The CUES is connected to a flow injection manifold, which allows the on-line flame atomic absorption spectrometric determination of iron. A Plakett–Burman design was used for the optimisation of the CUES. The method achieved a total sampling frequency of 11 samples per hour with a relative standard deviation for the complete procedure of 0.4%. The detection limit was 0.6 g g–1 (dry mass) for a sample amount of 30 mg. Accurate results were obtained by measuring the certified reference materials BCR-186 (pig kidney) and BCR-184 (bovine muscle). The analytical procedure was applied to different real meat samples with satisfactory results. 相似文献