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E. Matsinos J. Guy E. Simopoulou W. Venus P. Allport M. Berggren M. Calicchio T. Coghen A. M. Cooper-Sarkar O. Erriquez N. Giannakopoulos G. T. Jones P. Marage M. M. Mobayyen D. R. O. Morrison S. O'Neale M. A. Parker J. Sacton R. A. Sansum N. Schmitz G. W. Van Apeldoorn K. Varvell A. Vayaki H. Wachsmuth W. Wittek BEBC WA Collaboration 《Zeitschrift fur Physik C Particles and Fields》1989,44(1):79-87
Backward proton and pion production is studied in ν and \(\bar v\) charged current interactions in neon. The results are compared with other experiments and theory. The complete backward proton data is compatible with protons produced by reinteractions in the nucleus. However in events with only one proton, muon variables appear correlated to those for the backward proton, as expected by the two-nucleon correlation model. 相似文献
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Dorris Heiligmann und L. Acker 《Fresenius' Journal of Analytical Chemistry》1955,144(4):291-294
Ohne Zusammenfassung 相似文献
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Differential pulse polarographic methods for determination of corticosteroids in multicomponent and complex pharmaceutical preparations are described. The influence of other reducible common components of such preparations and excipients on the height of the reduction peaks of corticosteroids and the accuracy of the results was investigated, as well as the interference of excipients by adsorption processes at the electrode or at solid particles of the preparations. In the procedures developed, variations in composition of the supporting electrolyte according to the lipophilicity of the preparation, and the use of standard additions, produce results quickly and reliably. Standard deviations vary from 0.8 to 2.8%. 相似文献
47.
R. Meij D.J. Stufkens K. Vrieze W. Van Gerresheim C.H. Stam 《Journal of organometallic chemistry》1979,164(3):353-370
Each of the compounds [MCl(Pr3)2(ArylNSO)] (M = RhI, IrI; R = i-Pr, Cy: Aryl = C6H5, 4-MeC6H4, 4-ClC6H4, 2,4,6-Me3C6H2 appears to exist as two isomers both in the solid state and in solution. The molecular and single crystal structure of one of the isomers of [RhCl(P-i-Pr)3)2(4-Me6H4NSO)] shows that the N-sulfinylaniline ligand is in the cis-configuration and coordinated to the rhodium atom via the sulfur-atom. The ligand lies in a plane which includes the rhodium atom and is in agreement with the Rh-S distance of 2.10 Å. IR results of the compounds (solid and solutions), 21P NMR data and 15N NMR of a 15N labelled compound, which yielded a 103Rh15N coupling constant of 15.5 Hz, show that in the second isomer the N-sulfinylaniline ligand is probably bonded to the metal atom via the π-NS bond.The ratio of the metal-π-NS bonded isomer and the metal-S bonded isomer decreases in the order Aryl = 4-ClC6H4 > C6H5 > 4-MeC6H4; R = i-Pr > Cy and M = Rh > Ir. The interconversion of the two isomers is intramolecular and becomes observable on the 31P NMR time scale at about 40° C for M = Rh.In the case of [Ir(P-i-Pr3)2(4-MeC6H4NSO)], cyclometallation of the sul- finylaniline is observed via the ortho-carbon atom, whereas cyclometallation via P-i-Pr3 is observed when the ortho-positions are blocked by methyl groups, e.g. when L = 2,4,6-Me3C6H2NSO. 相似文献
48.
The diagnostic value of an interpretation system for vibrational spectra has been investigated in relation to the number of structural units the system can cope with. For five structural units the correlated wavenumber intervals are derived from three infrared and three Raman files by the CRISE program. The interpretative value of each interval in relation to the intensity threshold is discussed. For most intervals a decrease is found on increasing the number of structural units. 相似文献
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Microwave induced delayed phosphorescence (MIDP) measurements have been performed in the 00 bands of the phosphorescence spectrum of benzene dissolved in two phases of cyclohexane. From the relative radiative rates for decay of the three zero-field levels it is concluded that on the average the symmetry of the electronic structure is lower than D2h. In the monoclinic low temperature stable phase of cyclohexane (phase II) the structure is approximately antiquinoidal, and in the metastable phase III it is approximately quinoidal. 相似文献