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Line spectrum appearance

A — P transition, shown in Figure 7.10(b), has six components. As with doublet states the multiplet splitting decreases rapidly with L so the resulting six lines in the spectrum appear, at medium resolution, as a triplet. For this reason the fine structure is often called a compound triplet. [Pg.222]

Because there is an equal probability that a given unpaired electron will have a quantum number of or —j, radicals cause two lines or groups of lines to appear on an electronic spectrum, and are sometimes referred to as doublets. [Pg.239]

Absorption of ultraviolet and visible radiation in organic molecules is restricted to certain functional groups (chromophores) that contain valence electrons of low excitation energy (Figure 4). The spectrum of a molecule containing these chromophores is complex. This is because the superposition of rotational and vibrational transitions on the electronic transitions gives a combination of overlapping lines. This appears as a continuous absorption band. [Pg.80]

Consequently, the second line should appear at 102.6 nm in the absorption spectrum. [Pg.180]

Because the electrons lie in definite orbitals the value of AE and the frequency of light absorbed will also have definite values. The frequency of the absorbed light will be associated with a particular line in the spectrum. So the spectrum of the compound will have a large number of lines corresponding to the large number of excited states. So the lines will appear as a band and they will give colour to the definite parts of the spectrum. [Pg.217]

Present M sbauer Studies of Natural Pyroxenes and Olivines. Table IX gives the major element chemical compositions of the silicate minerals examined in this study. Table X compares the Mossbauer parameters of these minerals, while Figures 9-13 show representative Mossbauer spectra. Fayalite (Figure 9) is the only olivine in this group. The two lines are, however, somewhat broadened (0.35 and 0.39 mm./ sec.) compared with the width of natural iron foil lines observed with our source (0.24 mm./sec.) and suggest the near coincidence of two quadrupole-split doublets resulting from Mi and M2 sites. Analysis of this "two-line spectrum into a four-line spectrum in the manner described by Evans et al (11) could possibly yield parameters for the two iron sites, but this was not undertaken since both lines appear symmetric. The "two-line quadrupole splitting of 2.78 mm./sec. is somewhat smaller... [Pg.75]

The g-value of the methyl radical whose centre of ESR spectrum appears at 329.4 mT in a spectrometer operating at 9-233 G. Hz (h = 6-627 x 1034 Js, electron Bohr Magneton = 9-27 X 1024 JTl) is. The number of lines in the ESR spectrum of this methyl radical predicated ... [Pg.174]

A six- or four-line ESR spectrum that can be fitted to a triplet spin Hamiltonian is strong evidence that the species in the sample embodies two unpaired electron spins. Support for the presence of a triplet spin system often can be found in the weak Ams = 2 line, which appears at one-half the field strength of the center of gravity of the Ams = 1 six-line pattern. This nominally forbidden Amj = 2 resonance results when the ESR spectrometer field and frequency produce a micro-wave quantum of energy just sufficient to jump the gap between the uppermost and lowermost triplet substates, that is, a transition over two quantum levels. [Pg.173]

We have shown that the radiant flux spectrum, as recorded by the spectrometer, is given by the convolution of the true radiant flux spectrum (as it would be recorded by a perfect instrument) with the spectrometer response function. In absorption spectroscopy, absorption lines typically appear superimposed upon a spectral background that is determined by the emission spectrum of the source, the spectral response of the detector, and other effects. Because we are interested in the properties of the absorbing molecules, it is necessary to correct for this background, or baseline as it is sometimes called. Furthermore, we shall see that the valuable physical-realizability constraints presented in Chapter 4 are easiest to apply when the data have this form. [Pg.54]

T. Melville noted in 1752 that sodium colours the flame of alcohol yellow, and A. S. Marggraf used this as a test to distinguish sodium from potassium salts. With an ordinary one-prism spectroscope, the spectrum appears with a single yellow fine corresponding with the D-line of the solar spectrum. This line really consists of two lines of wave-length 5896 and 5890. The emission spectrum of sodium shows many other lines of feeble intensity. In a salted Bunsen s flame, practically... [Pg.463]

The atomic lines in the spectrum appear as vertical lines or peaks due to the nature of the transition involved. That is, in molecules an electronic transition is usually accompanied by simultaneous changes in the molecule vibrational and rotational energy levels sometimes all the three energy types may change... [Pg.5]


See other pages where Line spectrum appearance is mentioned: [Pg.10]    [Pg.10]    [Pg.110]    [Pg.1569]    [Pg.513]    [Pg.37]    [Pg.278]    [Pg.166]    [Pg.195]    [Pg.324]    [Pg.87]    [Pg.285]    [Pg.420]    [Pg.268]    [Pg.37]    [Pg.96]    [Pg.2]    [Pg.232]    [Pg.135]    [Pg.123]    [Pg.179]    [Pg.39]    [Pg.124]    [Pg.262]    [Pg.242]    [Pg.40]    [Pg.553]    [Pg.212]    [Pg.357]    [Pg.177]    [Pg.58]    [Pg.59]    [Pg.463]    [Pg.464]    [Pg.467]    [Pg.168]    [Pg.240]    [Pg.217]    [Pg.151]    [Pg.8]   
See also in sourсe #XX -- [ Pg.212 , Pg.212 , Pg.213 ]

See also in sourсe #XX -- [ Pg.212 , Pg.212 , Pg.213 ]

See also in sourсe #XX -- [ Pg.222 , Pg.223 , Pg.225 ]




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Line spectrum

Spectrum line spectra

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