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921.
铜(Ⅱ)-邻菲咯啉-(邻菲咯啉-5,6-二酮)络合物的合成及其同脱氧核糖核酸的作用 总被引:9,自引:0,他引:9
以邻菲咯啉(phen)、邻菲咯啉-5,6-二酮(dione)为配体首次合成了高氯酸邻菲咯啉-邻菲咯啉-5,6-二酮(Ⅱ)。用荧光光谱,摩尔比,粘度,MLCT减色效应,平衡常数以及荧光能量转移研究了各合物与鱼精子DNA的结合情况,证实了该络合物与DNA存在插入作用。基于络合物对DNA能量转移造成荧光量子产率比值(Φλ/Φ320)的降低,解释了不同波长激发光下,荧光发射峰在加入DNA后产生猝灭和增强两种绝然不同的现象。 相似文献
922.
The 1,2-diphcnylethyl radical and derivatives were generated from photolysis of tran-f-stilbene and its derivatives 1–13 with secondary amines as quenchers. The 1,2-diphenylelhyl radicals that escaped from the solvent cage were trapped by 2-methyl-2-nitrosopropane (MNP) and were detected by the HPLCEPR method. The yield of the spin adduct is greater for tertiary amines. The smaller yields of the spin adduct formed from secondary amines are ascribed to greater reactivities of the 1,2-diphenylethyl and dialkylamino radicals within the solvent cage. 相似文献
923.
Spectrophotometric method for the determination of phosphine (PH3) residues in coriander has been developed based on the reaction of phosphine with silver nitrate in 2% aqueous isopropanol. The yellow chromophore formed has an absorption maximum at 430 nm and the linear relation between the absorbances at 430 nm and the concentration of PH3 is obeyed in the range of 0.02 to 0.17 g. The method is sensitive with a detection limit of 0.008 g and can be applied for determination of 0.02 g/g residue in coriander. Recovery of added PH3 from a closed system ranges from 96 to 101%. 相似文献
924.
Earlier work by Lindenbaum and Boyd has demonstrated the important role of hydrophobic interactions involving the water solvent in determining the osmotic coefficients and properties of aqueous solutions of the tetraalkylammonium halides. Osmotic coefficients of solutions of tetramethyl-, tetraethyl-, tetrapropyl-, and tetrabutylammonium bromides in the more highly structured solvent D2O have now been determined by the gravimetric isopiestic method, using reference solutions of NaCl in D2O. The data were fitted to the Rush-Johnson and Pitzer equations. Satisfactory agreement with the results for aqueous solutions at comparable concentrations indicates that the solution chemistry of these quaternary ammonium bromides is not highly dependent on the degree of structure of the pure solvents. Supplementary data for mixtures of Me4NBr with Et4NBr, Pr4NBr, or Bu4NBr in both H2O and D2O are consistent with this conclusion.On leave 1980–82 from Banaras Hindu University, India 相似文献
925.
926.
G. G. Danagulyan G. A. Panosyan L. G. Sahakyan 《Chemistry of Heterocyclic Compounds》2007,43(8):996-1000
The interaction of the iodomethylates of pyrimidinyl-2-acetic acid derivatives with monosubstituted hydrazines, in addition
to the products of a Kost-Sagitullin rearrangement, leads also to N-substituted triazoles. The structure of the triazoles
was demonstrated by NOESY NMR experiments. The structure of the reaction products was determined on the basis of the response
observed in the spectra between the methyl group protons of the triazole ring and the spatially close proton of the substituent
in position 1 and a conclusion was drawn on the direction of the primary attack of nucleophile in the recyclization process
of the pyrimidinium salts into a 1,2,4-triazole.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1175–1179, August, 2007. 相似文献
927.
报道了一种快速、简便的同时测定食用香料麦芽酚、乙基麦芽酚光度法,方法基于在pH2.87的B R缓冲溶液中对麦芽酚和乙基麦芽酚两组分混合溶液进行光度测定,所得的重叠波谱数据用主成分回归法(PCR)、经典最小二乘法(CLS)和偏最小二乘法(PLS)等化学计量学方法进行处理,结果表明主成分回归法(PCR)的预报误差最小。对样品进行测定,获得了较好的定量分析结果。麦芽酚和乙基麦芽酚的线性范围均为1.0~20.0mg·L-1;检出限分别为0.4347和0 5589mg·L-1。 相似文献
928.
M. Yakup Arca Meltem Ylmaz Emine Yaln Gülay Bayramo
lu 《Journal of membrane science》2004,240(1-2):167-178
Poly(hydroxyethyl methacrylate), pHEMA, and a composite pHEMA/chitosan networks were synthesized in the membrane form via UV initiated photo-polymerisation in the presence of an initiator ,′-azoisobutyronitrile. Reactive Yellow 2 (RY-2) was covalently immobilised as a dye–ligand onto both membranes. The polarity and surface energy of the investigated membranes were determined by contact angle measurement. The incorporation of chitosan in the pHEMA networks produced more hydrophilic surface, as indicated by contact angle analysis. The binding characteristics of lysozyme, γ-globulins, human serum albumin (HSA) and bovine serum albumin (BSA) to pHEMA-RY-2 and pHEMA/chitosan-RY-2 affinity membranes have been investigated from aqueous solution and their dye–ligand free forms were used as control systems. When chitosan was incorporated in the pHEMA network as a cationic polymer led to higher adsorption capacity for the lysozyme. Selective adsorption behaviour was also observed in the case of pHEMA/chitosan-RY-2 membrane for the lysozyme. The non-specific adsorptions of the lysozyme on the pHEMA and pHEMA/chitosan membranes were about 1.9 and 7.2 mg/ml, respectively. These were negligible for all others investigated proteins. The lysozyme adsorption data was analysed using the first-order and the second-order models. The first-order equation in both affinity membrane systems is the most appropriate equation to predict the adsorption capacities of the adsorbents. The adsorption isotherms well fitted the combined Langmuir–Freundlich model. A theoretical analysis has been conducted to estimate the thermodynamic contributions (changes in enthalpy, entropy and Gibbs free energy) for the adsorption of lysozyme to both dye–ligand immobilised membranes. The adsorption capacities of both dye–ligand immobilised membranes increased with increasing the temperature while decreased with increasing the NaCl concentration. Both affinity membranes are stable when subjected to sanitization with sodium hydroxide after repeated separation–elution cycles. 相似文献
929.
LiMn2O4的湿法合成及锰的光度法测定研究 总被引:2,自引:0,他引:2
The LiMn2O4 spinel was prepared by wet method using Li2CO3, Mn(CH3COO)2·4H2O and CO2 as raw ma-terials. The products were measured by TG/DTA, XRD, IR. The results Showed that the sample calcined at 800℃ for 10h was well crystallized monophase product. The contents of Mn(Ⅲ) and Mn(Ⅳ) of LiMn2O4 spinel were determined simultaneously by spectrophotometric analysis with pyrophosphoric acid. 相似文献
930.
W. Yang H. Inoue T.Y. Chow H. Samura T. Saegusa 《Journal of Sol-Gel Science and Technology》1998,11(1):117-124
Au particles dispersed thin metal oxide films were prepared from precursor films containing HAuCl4 with H2S gas diffusion method. HAuCl4 was uniformly dissolved in the films as promoted by hydroxypropyl cellulose (HPC). The mechanism of the Au particle formation was studied. It was found that HAuCl4 was converted directly to Au metal particles upon contacting with H2S gas. Au particles generated by this method were characterized with small particle size, sharp size distribution and high volume fraction in the films. The surface plasma resonance absorption of Au particles shifted to longer wavelength when TiO2 component was introduced in the matrix. 相似文献