Vibrational Analysis for a New CuCl Band System Excited by Active Nitrogen

1938 ◽  
Vol 54 (7) ◽  
pp. 497-498 ◽  
Author(s):  
Sidney Bloomenthal
1983 ◽  
Vol 37 (6) ◽  
pp. 545-552 ◽  
Author(s):  
John Kishman ◽  
Eric Barish ◽  
Ralph Allen

A predominantly blue “active nitrogen” afterglow was generated in pure flowing nitrogen or in air by using a dielectric discharge at pressures from 1 to 20 Torr. The afterglow contains triplet state molecules and vibrationally excited ground state molecules. These species are produced directly by electron impact without the formation and recombination of nitrogen atoms. The most intense emission is the N2 second positive band system. The N2 first positive and N2+ first negative systems are also observed. The spectral and electrical properties of this discharge are discussed in order to establish guidelines for the analytical use of the afterglow for chemiluminescence reactions. The metastatic nitrogen efficiently transfers its energy to atomic and molecular species which are introduced into the gas phase and these excited species emit characteristic radiation. The effects of electrothermal atomization of Zn and the introduction of gaseous species (e.g., NO) on the afterglow are described.


1972 ◽  
Vol 50 (12) ◽  
pp. 1402-1408 ◽  
Author(s):  
S. M. Japar

The 2800 Å band system of p-dibromobenzene has been photographed under high resolution and an extended vibrational analysis has been carried out. The analysis is not inconsistent with the assignment of the system to a 1B2u ← 1Ag transition, by analogy with other p-dihalogenated benzenes. The observed spectrum can be explained in terms of a number of strong type-B vibronic bands and a considerably smaller number of type-A vibronic bands. The extensive sequence structure is adequately accounted for, and can be related to observations on other halogenated benzene molecules. Thirteen ground state and nine excited state fundamental vibrational frequencies have been assigned.


1966 ◽  
Vol 20 (4) ◽  
pp. 359-380 ◽  
Author(s):  
John C.D. Brand ◽  
Denis R. Williams ◽  
Thomas J. Cook

In 1917 Lord Rayleigh and Prof. A. Fowler observed that when the vapour of a carbon compound is introduced into the afterglow of active nitrogen, the two CN systems—the so-called "red" and "violet" systems—are developed, but their appearance in this source is strikingly different from the more familiar appearance of the same bands in the carbon arc in air. The "violet" system as ordinarily observed in the arc, comprises the four well-known groups of bands which degrade towards the further ultra-violet from prominent heads at λλ 4606, 4216, 3883 and 3590 respectively, and four groups of weaker bands, the so-called "tail" bands, degrading towards the red. The modifications of the λ 4216 and λ 3883 groups are shown in figs. 4 and 5 of Plate 6, in Rayleigh and Fowler's paper. The description of these modifications will be much facilitated by reference to Table I, which shows the wave-lengths and wave-numbers of the band-heads, and the initial and final vibrational quantum numbers ( n', n" ) for the bands, as well as other particulars to which frequent reference will be made later. The modifications are conveniently described as two effects:— First Effect.—In the typical case of the λ 4216 ( n" - n' = +1) group in the afterglow, there is a modified development of the lines of the first (0, 1) and the third (2, 3) bands, and a partial suppression of the heads of the second (1, 2) and fourth (3, 4) bands. The lines near the head of the (0, 1) band in the afterglow are apparently identical with lines in the corresponding part of the same band in the arc, but at a short distance, about 9 A. U., from the head there is a conspicuous gap of about 3 A. U., beyond which the lines recover in intensity and overrun the weakened (1, 2) head. The (2, 3) band, though not nearly so strong as the (0, 1), shows a similar gap and regain of intensity, its lines over-running the weakened (3, 4) head. A similar effect occurs in the λ 3883 ( n" - n' = 0) group.


1971 ◽  
Vol 49 (10) ◽  
pp. 1249-1254 ◽  
Author(s):  
Midori Shimauchi

The emission spectrum of the AsS radical, excited in a quartz tube by a 2450 MHz oscillator, was photographed on a high resolution spectrograph from 2450 to 6900 Å. Seven bands around 6000 Å showing clear rotational structures were chosen for the first rotational analysis of the AsS spectrum. The bands were found to arise from a 2Π3/2–2Π3/2 transition. The rotational and vibrational constants of the two states derived from the present work are consistent with the previous vibrational analysis of the A′2Π3/2–X2Π3/2 system. The constants of the upper doublet component of the ground state, X2Π3/2, are ωe = 562.40 cm−1, ωexe = 2.02 cm−1, re = 2.0216 Å; the constants of the A′2Π3/2 state are ΔG′(1/2) = 403.37 cm−1, ν0,0 = 18 621.21 cm−1, re = 2.2500 Å.


1966 ◽  
Vol 44 (2) ◽  
pp. 337-352 ◽  
Author(s):  
R. A. Durie

Observation by the author (Durie 1951) of a well-developed band system in the emission from an iodine–fluorine flame provided the first evidence for the existence of iodine monofluoride (IF), the last of the six possible diatomic inter-halogen compounds to be detected. The spectrum, which lies in the region 4 300 to 7 600 Å, has since been photographed under high resolution using a 21-ft concave grating spectrograph. The rotational structure of the bands is shown to be consistent with an A3Π0+ → X1Σ transition in the IF molecule. A rotational and vibrational analysis of the bands has been carried out and the molecular constants evaluated for IF. The results are as follows:[Formula: see text]The present evidence relating to the value of the dissociation energy of IF is discussed.


1975 ◽  
Vol 53 (20) ◽  
pp. 2321-2325 ◽  
Author(s):  
J. A. Coxon ◽  
W. E. Jones ◽  
K. V. Subbaram

Twenty-three new violet degraded bands in the region λ 4100–4700 Å have been observed in emission from a microwave discharge through beryllium chloride and flowing xenon at total pressures near 200 Torr. The band system is attributed to the A2Π–X2Σ+ transition of the new molecule BeXe+. Approximate molecular constants are reported from the vibrational analysis. The observation and assignment of this spectrum of BeXe+ confirm our recent results on the BeAr+ and BeKr+ molecules, for which it was proposed that the ion-induced dipole interaction was largely responsible for the ground state binding energies.


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