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941.
Summary The interaction of the herbicides diquat and paraquat with humic acid and the influence of various salts and pH on the strength of interaction was studied by charge-transfer chromatography. Interactions between humic acids and both herbicides, probably by complex formation, were confirmed; they were stronger with paraquat than with diquat. The complex formation makes the herbicides more hydrophilic, facilitating their movement on cellulose surface. Salts in the environment significantly decreased the strength of interaction, indicating the hydrophilic character of the interactive forces. The charge of the cation also influenced the strength of interaction whereas the effect of ion radii was negligible. The effect of pH was lower than that of salt concentration.  相似文献   
942.
Bromazepam, in the form of a cationic iron(II) chelate, can be determined spectrophotometrically at 588 nm with a limit of detection of ca. 10-6 M. When this chelate is ion-paired with perchlorate, it can be extracted into organic solvents such as 1,2-dichloroethane and 4-methyl-2-pentanone, and determined by atomic absorption spectrometry with a limit of detection of 1.5 × 10-5 M bromazepam at the iron resonance 248.3-nm line. Ion-pairs involving the Fe(II), Cu(II) and Co(II) chelates and perchlorate can be separated by h.p.l.c. using a C18 reverse-phase column and a mobile phase of 4:1 water—methanol, with a u.v. detector at 242 nm. This approach allowed for the determination of iron(II) ions in aqueous solution with a limit of detection of 10-8 M. The h.p.l.c. method could also be used to quantify bromazepam spiked in plasma in the concentration range 1–10 μg ml-1, following extraction of bromazepam from plasma and subsequent formation of the iron(II) ion-pair. Copper(II) forms a labile chelate with bromazepam in pH 4.8 acetate buffer which, when subjected to differential pulse voltammetry at the hanging mercury drop electrode, gives rise to a catalytic phenomenon which can be utilised for the determination of bromazepam in the concentration range 10-5–10-9 M.  相似文献   
943.
A flow system for the determination of d-glucose in undiluted whole blood, in which segmented sample injection and on-line dialysis are used to decrease the red cell volume fraction (haematrocrit) dependence, is described. Glucose is degraded enzymatically by means of immobilized glucose dehydrogenase. The nicotinamide coenzyme (NAD+) that is present in the solution is reduced in the enzymatic reaction and is reoxidized amperometically at 0 mV vs. Ag/AgCl on a graphite electrode, modified with phenoxazinium ion. The potential use of the system for clinical analysis is evaluated.  相似文献   
944.
The L3/L2 white-line intensity ratio in transition-metal oxides deviates widely from the statistical value of 2 : 1 but shows interesting systematics. In a series of oxides of a given metal, the ratio reaches a maximum for the d5 configuration (e.g. MnO) and a minimum for the d0 configuration (e.g. KMnO4). In a series of monoxides, sesquioxides and dioxides of different metals, the ratio is again a maximum at the d5 configuration and decreases as the configuration changes towards d0 or d10. Our results, obtained by electron energy-loss spectroscopy, carried out in an electron microscope, are interpreted on an atomic mechanism involving spin-spin coupling. According to this model, the L2 transition probability decreases in the progression d0 to d5 whereas the L3 transition probability decreases beyond d5.  相似文献   
945.
The automatic control of certain physical phenomena, such as temperature and speed of rotation, has long been commonplace. However, the means by which this form of control can be applied to a chemical process are not so obvious. A sensing system must be found to monitor the status of the particular chemical system.  相似文献   
946.
Nitroalkanes and their nitronate salts undergo α-arylation in good yield when treated with an aryllead triacetate in dimethyl sulfoxide.  相似文献   
947.
The state of mixed iron-tin oxide catalysts with a variable ratio of their metallic components has been studied by Mössbauer and ESCA spectroscopy. The results are compared with the activity of these catalysts in cyclohexane oxidation.
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948.
Tyson JF  West TS 《Talanta》1979,26(2):117-125
An apparatus has been built with which the intensity of a light-beam passing at grazing incidence over a platinum electrode can be monitored. The absorption of light which occurs during the electrolysis of dilute aqueous metal ion solutions has been studied as a function of a number of parameters including wavelength, potential difference and concentration. The theories of metal deposition and processes occurring at the electrode surface and in the diffusion layer have been examined and a mechanism for the production of the absorbing species in terms of increase in pH of the catholyte is proposed. The analytical potential of the technique is discussed.  相似文献   
949.
Summary The possible relation existing between RF values obtained by thin-layer chromatography for a group of anilines with connectivity indices proposed by Kier and Hall has been studied. Using multivariable regression the corresponding connectivity functions, selected for their respective correlation coefficients, standard deviations, Snedecor's F and Student's t were obtained. Regression analysis of the connectivity functions gives a correct prediction of the experimental elution sequence for this group of substances on silica gel stationary phases and various mobile phases of different polarity. The corresponding random and stability studies of the different prediction models selected were carried out, showing good stability and null randomness in all cases.  相似文献   
950.
Arylazides reacted with α amino-acrylonitriles 1 to produce 1-aryl-5-amino-triazoles, and with β amino-acrylonitriles 2 to give 1-aryl-4-cyanotriazoles. Kinetics showed the Hammett ρ to be > o and therefore, these reactions are controlled by LUMOazide-HOMOolefin interaction. Despite the captodative substitution in 1 and 2 (ΔΔ E~ 500 cal.M?1) does'nt agree with a diradical intermediate.  相似文献   
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