The Distortion Moment Microwave Spectrum of 12CH4 in the Ground Vibronic State

1975 ◽  
Vol 53 (19) ◽  
pp. 1791-1805 ◽  
Author(s):  
C. W. Holt ◽  
M. C. L. Gerry ◽  
I. Ozier

Seven Q branch transitions between 7.8 and 20 GHz have been observed in the distortion moment pure rotational spectrum of 12CH4 in its ground vibronic state. The spectrum was obtained using a conventional Stark modulated microwave spectrometer specially modified for the detection of very weak lines. From the frequencies of these seven transitions, along with the ortho–para splitting known for the (J = 2) state and two Q branch splittings measured earlier by infrared–microwave double resonance, we have determined the one quartic tensor distortion constant DT, the two sextic constants H4T and H6T, and the three octic constants L4T, L6T, and L8T. These are (in Hz): DT = (132 943.41 ± 0.71); H4T = −(16.9839 ± 0.0076); H6T = (11.0342 ± 0.0086); L4T = (20.27 ± 0.24) × 10−4; L6T = −(26.77 ± 0.35) × 10−4; L8T = −(30.0 ± 1.8) × 10−4. The errors are the standard deviations resulting from a least squares analysis. Estimates are also given of the absolute errors. These results consitute the first measurement of the octic distortion constants. The values for DT, H4T, and H6T are compared to earlier determinations. The theoretical considerations that affect the observation of these transitions are reviewed and a detailed description of the special experimental techniques used is given. The method of analysis is described. Finally, as an aid to other high resolution studies of methane and to possible astrophysical detection of the molecule, the Q branch splittings are tabulated up to J = 21.

1979 ◽  
Vol 57 (4) ◽  
pp. 593-600 ◽  
Author(s):  
R. H. Kagann ◽  
I. Ozier ◽  
G. A. McRae ◽  
M. C. L. Gerry

Ten pure rotational Q-branch transitions of the distortion moment spectrum of GeH4 have been measured between 9 and 23 GHz. They were observed in a conventional Stark modulated spectrometer modified to have a sensitivity of 1 × 10−11 cm−1. No Ge isotope splitting was observed in the spectrum. The spectrum was analysed in terms of a single set of six tensor centrifugal distortion constants DT, H4T, H6T, L4T, L6T, and L8T. The results were found to predict accurately transitions previously reported from infrared–microwave double resonance spectroscopy, and a complete analysis using both sets of data was carried out. The results are (in hertz): DT = 67 775.54 ± 0.86; H4T = −5.3827 ± 0.0055; H6T = 2.9693 ± 0.0019; L4T = (3.996 ± 0.088) × 10−4; L6T = −(4.122 ± 0.050) × 10−4; L8T = −(8.01 ± 0.14) × 10−4. The errors here are the standard deviations obtained from the least-squares analysis; estimates of the absolute errors are also given. For possible application in other high resolution studies, the constants have been used to calculate all tensor splittings for J ≤ 20.


1997 ◽  
Vol 52 (3) ◽  
pp. 293-294
Author(s):  
V. Storm ◽  
D. Consalvo ◽  
H. Dreizler

Abstract We report on the measurement and assignment of the benzonitrile-water complex rotational spectrum in the vi-bronic ground state. This study was facilitated by a newly constructed low frequency molecular beam Fourier trans-form microwave spectrometer.


2020 ◽  
Vol 10 (23) ◽  
pp. 8471
Author(s):  
Haoyang Tan ◽  
Miaoling Yang ◽  
Chenbo Huang ◽  
Shengwen Duan ◽  
Ming Sun ◽  
...  

The investigation on microwave spectrum of benzophenone was conducted with a recently constructed broadband chirped-pulse Fourier transform microwave spectrometer with a heating nozzle in the 2–8 GHz range. In this work, 138 b-type pure rotational transitions were assigned to bridge the measuring gap in the microwave region. The rotational constants for benzophenone were accurately determined by a combined microwave data fitting with frequency coverage between 2–14 GHz and have the following values: A = 1692.8892190(119) MHz, B = 412.6446602(43) MHz and C = 353.8745644(43) MHz.


1984 ◽  
Vol 62 (12) ◽  
pp. 1347-1360 ◽  
Author(s):  
Yasuki Endo ◽  
Shuji Saito ◽  
Eizi Hirota

The gas phase pure rotational spectrum of the chloromethyl radical, CH2Cl, has been observed for the first time in the millimetre wave region using a source frequency modulation microwave spectrometer equipped with a 1 m long free space absorption cell. The radical was generated by the reaction of CH3Cl with 2450-MHz microwave discharge products of CF4. The a-type R-branch transitions have been observed with resolved fine and hyperfine components for both the 35Cl and 37Cl isotopic species in the ground vibrational state. The small positive inertial defect. Δ0 = 0.0333 amu Å2, calculated from the rotational constants obtained for the 35Cl species indicates that the radical is planar in the ground vibronic state. The observed fine and hyperfine interaction constants are consistent with 2B1 symmetry, i.e., with the unpaired electron occupying a pπ orbital extending perpendicular to the molecular plane.


1976 ◽  
Vol 54 (11) ◽  
pp. 1094-1105 ◽  
Author(s):  
I. Ozier ◽  
R. M. Lees ◽  
M. C. L. Gerry

Eleven pure rotational Q-branch transitions have been observed between 8 and 25 GHz in the distortion moment spectrum of 28SiH4. The spectrometer used was a conventional Stark-modulated instrument modified to have a sensitivity of ~1 × 10−11 cm−1. From the eleven frequencies, values have been determined for the single quartic tensor distortion constant DT, the two sextic constants H4T and H6T, and the three octic constants L4T, H6T, and L8T. These are (in Hz): DT = (74 751.4 ± 1.6); H4T = −(6.044 ± 0.010); H6T = (2.598 ± 0.003); L4T = (46.5 ± 1.5) × 10−5; L6T = −(37.9 ± 0.8) × 10−5; L8T = −(76.6 ± 2.1) × 10−5. The errors here are the standard deviations obtained from a least squares analysis; estimates are also given of the absolute errors. For possible application in other high resolution studies of silane, the constants have been used to calculate all Q-branch splittings for J ≤ 20. The present results are compared to those obtained by double resonance methods by Kreiner and Oka; a definite identification has been found for one of their lines which had previously been tentatively assigned to another transition. The combination-differences data of Pierre, Guelachvili, and Amiot have been reanalysed on the basis of the current results to obtain improved values of the rotational constant and the quartic and sextic scalar distortion constants.


Dipolar modulation and phase interferometry, which are part of the class of high-resolution, double-resonance n.m.r. experimental techniques used to study solids, are examined in detail. A general theory of double-resonance interactions based on the heteronuclear dipolar Hamiltonian is presented. A number of experiments dealing with both heteronuclear and homonuclear dipolar modulation and selective dipolar difference spectra are discussed. These experiments are used to study hydrogen-bonded systems and catalytic systems. A simple theory explaining phase interferometry in n.m.r. is presented. Several phase interferometric experiments are also discussed. The motion and structure of 23 Na ions in β-alumina are examined with the use of this technique.


1985 ◽  
Vol 50 (11) ◽  
pp. 2480-2492 ◽  
Author(s):  
Soňa Přádná ◽  
Dušan Papoušek ◽  
Jyrki Kauppinen ◽  
Sergei P. Belov ◽  
Andrei F. Krupnov ◽  
...  

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.


1984 ◽  
Vol 49 (4) ◽  
pp. 805-820
Author(s):  
Ján Klas

The accuracy of the least squares method in the isotope dilution analysis is studied using two models, viz a model of a two-parameter straight line and a model of a one-parameter straight line.The equations for the direct and the inverse isotope dilution methods are transformed into linear coordinates, and the intercept and slope of the two-parameter straight line and the slope of the one-parameter straight line are evaluated and treated.


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