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Chandra Raju 《Czechoslovak Journal of Physics》1986,36(12):1350-1357
In this paper, we show that 2m
e
m
/(m
e
2
+m
2
= (g
V/g
A)
e
2
. From this expression, the Weinberg mixing parameter is shown to be 0·2254 or 0·2746. Assuming that the electron and muon neutrino masses are degenerate, we find thatm
v = (g
V/g
A)
e
2
. (m
e
m
)/M
WL, where MWL is the mass of the standard W± boson. The neutrino mass turns out to be 6·5 eV. The -neutrino mass is found to be about 81 MeV. The masses of c, t, s and b quarks are found to be respectively 1·7 GeV, 21·2 GeV, 0·57 GeV and 2·18 GeV by assumingm
d=m
u= 0·3 GeV. All these masses agree with other estimates except the b quark which has about half of its expected value. 相似文献
27.
. . 相似文献
28.
A. P. Gulea S. N. Spynu V. I. Tsapkov D. Poirier J. Roy 《Russian Journal of General Chemistry》2006,76(9):1458-1463
Isatin (L1) and N-methylisatin (L2) β-thiosemicarbazones react in ethanol with Cu(II) chloride and bromide in the presence of sulfanilamide (Streptocid, Sf1), N-acetylsulfanilamide (Sulfacyl, Sf2), Norsulfazole (Sf3), Aethazolum (Sf4), and Sulfadimesine (Sf5) to form coordination compounds Cu(Sf1–5)L1–2X2 · nH2O (X = Cl, Br; n = 2–5). All the complexes have a monomeric structure. Thiosemicarbazones L1 and L2 in these complexes are tridentate O,N,S ligands, and sulfanilamides Sf1–5 are monodentate ligands. Thermolysis of the substances involves the steps of dehydration (70–95°C) and complete decomposition (410–530°C). 相似文献
29.
Roy Edward Bruns Paul Martin Kuznesof James Elton Moore 《Journal of Molecular Structure》1975,29(2):211-223
CNDO molecular orbital calculations have been performed to analyze donor—acceptor interactions between molecular chlorine and benzene, toluene, mesitylene and hexamethylbenzene and the, as yet, unreported chlorine—hexafluorobenzene and carbon disulfide—benzene pairs. The stabilization energy and the dipole moment and its derivative (?p/?RCICI) calculated for the benzene—chlorine complex are in good agreement with the estimated experimental values. The trends in the experimental stabilization energies and the Cl-Cl vibrational frequencies with increasing methyl substitution appear to be well reproduced by the calculations. The charge transferred from the benzene donor is polarized toward the outer chlorine atom or sulfur atom. For hexafluorobenzene-chlorine the direction of electronic charge polarization is reversed from that of the benzene and methylbenzene complexes. The calculated results are discussed within the framework of Muliiken's simplified resonance theory for complexes. 相似文献
30.
l-(o-Carboxyphenyl)-3-hydroxy-3-methyltriazene is proposed as an excellent reagent for the spectrophotometric determination of iron(III) and titanium(IV), and also for the separation of titanium from a large quantity of iron as well as other cations and anions. Iron(III) forms an anionic violet 1:2 complex at pH 4.0–9.4, and a cationic green 1:1 complex at pH 1.5–2.0, with absorption maxima at 570 nm and 660 nm, respectively. The violet complex is quantitatively extracted in chloroform containing n-octylamine at pH 3.0–9.0. The green and the violet iron(III) complexes obey Beer's law, the respective optimal ranges being 8.9–35.8 and 3.9–11.2 p.p.m. The yellow titanium chelate extracted into chloroform (absorption maximum at 410 nm) between pH 1.0 and 3.5, can be re-extracted into concentrated sulphuric acid a violet colour being produced with absorption maximum at 530 nm. Beer's law is obeyed in the ranges 0.8–5.7 p.p.m. for the titanium complex in chloroform and 3.4–19.2 p.p.m. when extracted in concentrated sulphuric acid. Interferences from diverse ions are not severe. Procedures for the separation and determination of titanium in the presence of a large quantity of iron are given. The isolation of the iron(III) and vanadium(IV and V) complexes, and their properties, are described. 相似文献