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1.
Summary Experiments and simulations prove that correlation chromatography can greatly reduce the disadvantage of a non-linear response of the chromatographic column. A factor that has been accepted as being an important source of error in correlation or multiplex chromatography, has been shown not to be. Separations affected, improve dramatically when correlation chromatography is used, and a substantial amount of correlation noise only arises when there is a large difference in separation between a conventional chromatogram and a correlogram.A model has been developed for simulating these nonlinearities. It is shown that, especially for correlation chromatography, the simulation results match the practical measurements very well. 相似文献
2.
Pascher W. Den Besten J. H. Caprioli D. Leijtens X. Smit M. van Dijk R. 《Optical and Quantum Electronics》2003,35(4-5):453-464
Based on a rigorous vectorial analysis, a fast travelling-wave Mach–Zehnder modulator is modelled and designed. The cross-section of the semiconductor layer stack and the lossy electrodes are carefully modelled using the method of lines in order to investigate propagation characteristics, velocity and losses. This yields an accurate microwave and optical field distribution to explain the behaviour of the component. In order to enhance the modulation efficiency, design curves are derived and the cross-sectional dimensions for minimum microwave loss are determined. The loss of the optimized modulator agrees very well with small-signal measurements up to 40 GHz and HFSS simulations. The layerstack of the fabricated device is suitable for integration with InP multi-wavelength lasers. 相似文献
3.
For a series of substituted arylsulfenyl chlorides the stereochemistry of AdE-reactions with a series of substituted Z- and E-β-deuterostyrenes has been elucidated. Non-stereospecific reaction was observed only for the pair 2,4-dinitrobenzenesulfenyl chloride-p-methoxystyrene; for all the other reactants the reaction proceeded in a strictly stereospecific manner. 相似文献
4.
Chekmarev DS Lazareva MI Zatonsky GV Maskaev AV Caple R Smit W 《The Journal of organic chemistry》2002,67(23):7957-7967
Data on the selectivity of the Lewis acids induced transformations of the title compounds are presented, and the routes leading to formation of products containing either cyclohexane or 1,3-diene units are described. 相似文献
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7.
Conclusions The decomposition of the complex obtained in the reaction of pivaloyl tetrafluoroborate with norcarane and its 1-methyl and 1-phenyl derivatives by water gives 1-hydroxy-3-pivaloyl derivatives of cyclohexanes and the corresponding unsaturated ketones. The hydride decomposition of the same complex leads to derivatives of 6-oxabicyclo[3.2.1]octane.For preliminary report see [1].Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2512–2518, November, 1976. 相似文献
8.
1. | From MNDO quantum chemical calculations, opening of the episulfonium ion ring by neutral nucleophiles X (X=NH3 and HCN) and related SN2 reactions of protonated methylthiol (PMT) with X proceed through formation of pre-reaction complexes in which X is coordinated either at the reacting C atom or (only in opening of episulfonium ion rings) at the center of the C-C bond. |
2. | In their electronic structure, the transition states for the reactions are reminiscent of a carbocation simultaneously reacting with the attacking and the leaving nucleophilic fragments (X S). |
3. | Opening of episulfonium ion rings proceeds slightly more easily (Ea 10–12 kcal/mole) than substitution in PMT (Ea 22–25 kcal/mole). The ease of ring opening for episulfonium ions is due to the large exothermicity of the reaction and the lower internal activation barrier compared with SN2 reactions in PMT. |
9.
A two-step synthesis was proposed for the tetracyclic triquinane bis-enone from two monocyclic precursors. The bis-enone obtained is a structural fragment of retigeranic acid.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1908–1910, August, 1990. 相似文献
10.
The -arylthioalkylation of 2-methoxy-1,3-butadiene is regiospecific at the alkoxy-substituted C=C bond, giving 6-arylthioalk-1-en-3-ones.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2036–2040, September, 1990. 相似文献