THE ELECTRONIC SPECTRA OF PF AND PF+

1962 ◽  
Vol 40 (7) ◽  
pp. 832-849 ◽  
Author(s):  
A. E. Douglas ◽  
M. Frackowiak
Keyword(s):  
High Resolution ◽  
Ground State ◽  
Electronic Spectra ◽  
Fine Structures ◽  
Vibrational Constants

Five band systems of PF and one of PF+ have been excited in a discharge through PF3 and have been photographed with a high resolution spectrograph. The rotational fine structures of a number of bands of each system have been analyzed and the rotational and vibrational constants determined. The principal constants for a 3Σ state of PF, which is believed to be the ground state, are ωe = 846.75 cm−1, Be = 0.5665 cm−1, re = 1.590 0 Å.

THE LYMAN BANDS OF MOLECULAR HYDROGEN

1959 ◽  
Vol 37 (5) ◽  
pp. 636-659 ◽  
Author(s):  
G. Herzberg ◽  
L. L. Howe
Keyword(s):  
High Resolution ◽  
Vibrational Level ◽  
Ground State ◽  
Molecular Hydrogen ◽  
Equilibrium Constants ◽  
Dissociation Limit ◽  
Vibrational Levels ◽  
State Formula ◽  
Single Formula ◽  
Vibrational Constants

The Lyman bands of H2 have been investigated under high resolution with a view to improving the rotational and vibrational constants of H2 in its ground state. Precise Bv and ΔG values have been obtained for all vibrational levels of the ground state. One or two of the highest rotational levels of the last vibrational level (v = 14) lie above the dissociation limit. Both the [Formula: see text] and ΔG″ curves have a point of inflection at about v″ = 3. This makes it difficult to represent the whole course of each of these curves by a single formula and therefore makes the resulting equilibrium constants somewhat uncertain. This uncertainty is not very great for the rotational constants for which we find[Formula: see text]but is considerable for the vibrational constants ωe and ωexe for which three-, four-, five-, and six-term formulae give results diverging by ± 1 cm−1. The rotational and vibrational constants for the upper state [Formula: see text] of the Lyman bands are also determined. An appreciable correction to the position of the upper state is found.

HIGH RESOLUTION RAMAN SPECTROSCOPY OF GASES: III. RAMAN SPECTRUM OF NITROGEN

1954 ◽  
Vol 32 (10) ◽  
pp. 630-634 ◽  
Author(s):  
B. P. Stoicheff
Keyword(s):  
Raman Spectroscopy ◽  
Raman Spectrum ◽  
High Resolution ◽  
Electronic Spectra ◽  
Second Order ◽  
Published Data ◽  
Rotational Spectrum ◽  
Rotational Constants ◽  
Vibrational Constants

The pure rotational spectrum and the Q branch of the 1–0 band of N2 were photographed in the second order of a 21 ft. grating. An analysis of the rotational spectrum yields the rotational constants[Formula: see text]The value of B0 together with the Bν values obtained from the electronic bands of N2 gives[Formula: see text]Revised values of the vibrational constants have also been calculated using the results of the present work and the published data on the electronic spectra.

Spectrum of AsS. I. Analysis of the A′2Π3/2–X2Π3/2 Band System

1971 ◽  
Vol 49 (10) ◽  
pp. 1249-1254 ◽  
Author(s):  
Midori Shimauchi
Keyword(s):  
High Resolution ◽  
Emission Spectrum ◽  
Ground State ◽  
Band System ◽  
Vibrational Analysis ◽  
Quartz Tube ◽  
Rotational Analysis ◽  
Vibrational Constants

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.

Absorption spectrum of the Mg2 molecule

1970 ◽  
Vol 48 (7) ◽  
pp. 901-914 ◽  
Author(s):  
W. J. Balfour ◽  
A. E. Douglas
Keyword(s):  
Absorption Spectrum ◽  
Excited State ◽  
High Resolution ◽  
Potential Energy ◽  
Dissociation Energy ◽  
Ground State ◽  
Potential Energy Curve ◽  
Energy Curve ◽  
Vibrational Constants

The absorption spectrum of the Mg2 molecule, which occurs in a furnace containing Mg vapor, has been photographed with a high resolution spectrograph. The rotational structures of the bands have been analyzed and the rotational and vibrational constants of the two states determined. The bands are found to arise from a 1Σ–1Σ transition between a very lightly bonded ground state and a more stable excited state. The R.K.R. potential energy curve of the ground state, which has a dissociation energy of 399 cm−1, has been determined. The more important constants of the ground state are ωe = 51.12 cm−1, ωexe = 1.64 cm−1, re = 3.890 Å and those of the upper state are ωe = 190.61 cm−1, ωexe = 1.14 cm−1, re = 3.082 Å.

THE SPECTRUM OF THE P2+ MOLECULE

1957 ◽  
Vol 35 (10) ◽  
pp. 1242-1249 ◽  
Author(s):  
N. A. Narasimham
Keyword(s):  
High Resolution ◽  
Discharge Tube ◽  
Hollow Cathode ◽  
Ground State ◽  
Band System ◽  
Hollow Cathode Discharge ◽  
Lower State ◽  
Vibrational Constants

Two band systems attributed to the P2+ molecule have been excited in a hollow cathode discharge tube. The first of these is a 2Π—2Π band system lying in the region 3400–3850 Å. The lower state of this system probably is the ground state of the P2+ molecule. The second system is a 2Σ—2Σ system lying in the region 3900–4400 Å. High resolution spectra of both the band systems have been analyzed and the rotational and vibrational constants determined.

Spectroscopic studies on toluene and some deuterated derivatives. II. Electronic spectra

1994 ◽  
Vol 72 (11-12) ◽  
pp. 1225-1235 ◽  
Author(s):  
Walter J. Balfour ◽  
Ram S. Ram
Keyword(s):  
Excited State ◽  
High Resolution ◽  
Ground State ◽  
Electronic Spectra ◽  
Spectroscopic Studies ◽  
Measured Data ◽  
Sequence Structure ◽  
State Information ◽  
Isotopic Species ◽  
Out Of Plane

The 266.7 nm absorption systems of toluene and seven deuterated isomers were observed at high resolution and analyses of their vibronic structure performed. All in-plane vibrations with ground-state frequencies less than 1000 cm−1 were identified from 0–1 hot bands. The frequencies agree well with data obtained from infrared and Raman studies. The corresponding vibrations were identified in the excited state. Information was also obtained on out-of-plane vibrations with ground-state frequencies less than 650 cm−1, since all of these are found to give sequence structure. A comparison of the measured data for the various isotopic species has enabled a consistent description of the excited state in toluene to be made. Problems associated with errors, ambiguities, and inconsistencies in previously published work have been addressed.

Ground state molecular parameters of phosphine, PH3, from the simultaneous analysis of the high-resolution infrared, microwave and submillimeterwave spectra

1985 ◽  
Vol 50 (11) ◽  
pp. 2480-2492 ◽  
Author(s):  
Soňa Přádná ◽  
Dušan Papoušek ◽  
Jyrki Kauppinen ◽  
Sergei P. Belov ◽  
Andrei F. Krupnov ◽  
...  
Keyword(s):  
Fourier Transform ◽  
High Resolution ◽  
Ground State ◽  
Unitary Transformation ◽  
Point Of View ◽  
Acoustic Detection ◽  
Molecular Parameters ◽  
Microwave Spectrometer ◽  
Fourier Transform Spectra ◽  
First Time

Fourier transform spectra of the ν2 band of PH3 have been remeasured with 0.0045 cm-1 resolution. Ground state combination differences from these data have been fitted simultaneously with the microwave and submillimeterwave data to determine the ground state spectroscopical parameters of PH3 including the parameters of the Δk = ± 3n interactions. The correlation between the latter parameters has been discussed from the point of view of the existence of two equivalent effective rotational operators which are related by a unitary transformation. The ΔJ = 0, +1, ΔK = 0 (A1 ↔ A2, E ↔ E) rotational transitions in the ν2 and ν4 states have been measured for the first time by using a microwave spectrometer and a radiofrequency spectrometer with acoustic detection.

ROTATIONAL ANALYSIS OF THE β BANDS OF PHOSPHORUS MONOXIDE

1959 ◽  
Vol 37 (2) ◽  
pp. 136-143 ◽  
Author(s):  
Nand Lal Singh
Keyword(s):  
Ground State ◽  
Band System ◽  
Electronic States ◽  
Rotational Analysis ◽  
Rotational Constants ◽  
Fine Structures ◽  
Π State

The fine structures of three of the β bands of PO which occur near 3200 Å have been analyzed. The analysis shows that the upper state of this band system is a 2Σ and not a 2Π state as previously believed. The rotational constants of both electronic states have been determined and it is found that the ground state constants, previously determined from the γ bands, are incorrect.

High resolution spectrum of GdO

1976 ◽  
Vol 54 (24) ◽  
pp. 2429-2434 ◽  
Author(s):  
B. R. Yadav ◽  
S. B. Rai ◽  
D. K. Rai
Keyword(s):  
High Resolution ◽  
Emission Spectrum ◽  
Visible Emission ◽  
High Resolution Spectrum ◽  
First Order ◽  
Isotopic Shifts ◽  
Vibrational Constants ◽  
Dc Arc

The visible emission spectrum of the GdO molecule has been produced in a DC arc source and has been photographed in the first order of a 10.6 m grating spectrograph. Bands are shown to have a six-headed structure and improved vibrational constants have been obtained in this study. Isotopic shifts have been calculated for the various isotopic molecules. Tentative suggestions regarding the nature of the transition have been made.

High-resolution Fourier-transform infrared spectroscopy of the Coriolis coupled ground state and ν7 mode of ketenimine

2011 ◽  
Vol 134 (23) ◽  
pp. 234306 ◽  
Author(s):  
Michael K. Bane ◽  
Evan G. Robertson ◽  
Christopher D. Thompson ◽  
Chris Medcraft ◽  
Dominique R. T. Appadoo ◽  
...  
Keyword(s):  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
High Resolution ◽  
Fourier Transform Infrared Spectroscopy ◽  
Ground State ◽  
Fourier Transform Infrared
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