Relative Intensity Measurements in Microwave Spectroscopy

1963 ◽  
Vol 34 (8) ◽  
pp. 901-907 ◽  
Author(s):  
Alan S. Esbitt ◽  
E. Bright Wilson
1990 ◽  
Vol 45 (9-10) ◽  
pp. 1131-1143
Author(s):  
Otto L. Stiefvater

Abstract The pure rotation spectra of molecules in 25 vibrationally excited states of perdeuterated furazan, C2D2N2O, have been studied by double resonance modulation (DRM) microwave spectroscopy. Twelve of these spectra have been correlated, -on the basis of relative intensity measurements under DRM -, with fundamental vibrations as previously established by IR spectroscopy. Rotational parameters for these 12 fundamental levels are reported, and the contributions to the effective rotational constants and to the inertia defect of the ground state of d2 -furazan have been determined for 10 modes of vibration.


1975 ◽  
Vol 29 (5) ◽  
pp. 386-389 ◽  
Author(s):  
Arthur K. Covington ◽  
Jennifer M. Thain

A new technique is described for obtaining quantitative relative intensity measurements, in the study of solution equilibria by laser-Raman spectroscopy, without the necessity for adding an internal standard to the sample. A rotating cylindrical double cell with separate compartments for sample and reference is used to superimpose the Raman spectra of sample and reference and hence avoid any uncertainties arising from the displacement of the equilibrium by reference substance addition.


1972 ◽  
Vol 5 (4) ◽  
pp. 1587-1591 ◽  
Author(s):  
J. H. McCrary ◽  
L. V. Singman ◽  
L. H. Ziegler ◽  
L. D. Looney ◽  
C. M. Edmonds ◽  
...  

1973 ◽  
Vol 51 (4) ◽  
pp. 529-532 ◽  
Author(s):  
R. Kewley

The microwave spectrum of cyclohexene sulfide (7-thiabicycIo[4,1,0]heptane) has been investigated in the 26.5–40 GHz region. R-branch lines due to both a- and c-type transitions have been assigned for the ground vibrational state and for the first excited states of the ring bending and ring twisting modes. From relative intensity measurements the frequencies of these two modes are estimated as: vbend = 115 ± 20 cm−1 and vtwist = 200 ± 60 cm−1. The rotational constants for the ground vibrational state are (in MHz): A = 3512.086 ± 0.010, B = 2057.969 ± 0.003, and C = 1623.023 ± 0.003. These values are consistent with a twisted half chair structure for the heavy atom skeleton of cyclohexene sulfide, similar to that of cyclohexene oxide.


2010 ◽  
Vol 3 (5) ◽  
pp. 1287-1305 ◽  
Author(s):  
T. Vlemmix ◽  
A. J. M. Piters ◽  
P. Stammes ◽  
P. Wang ◽  
P. F. Levelt

Abstract. Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) is a technique to measure trace gas amounts in the lower troposphere from ground-based scattered sunlight observations. MAX-DOAS observations are especially suitable for validation of tropospheric trace gas observations from satellite, since they have a representative range of several kilometers, both in the horizontal and in the vertical dimension. A two-step retrieval scheme is presented here, to derive aerosol corrected tropospheric NO2 columns from MAX-DOAS observations. In a first step, boundary layer aerosols, characterized in terms of aerosol optical thickness (AOT), are estimated from relative intensity observations, which are defined as the ratio of the sky radiance at elevation α and the sky radiance in the zenith. Relative intensity measurements have the advantage of a strong dependence on boundary layer AOT and almost no dependence on boundary layer height. In a second step, tropospheric NO2 columns are derived from differential slant columns, based on AOT-dependent air mass factors. This two-step retrieval scheme was applied to cloud free periods in a twelve month data set of observations in De Bilt, The Netherlands. In a comparison with AERONET (Cabauw site) a mean difference in AOT (AERONET minus MAX-DOAS) of −0.01±0.08 was found, and a correlation of 0.85. Tropospheric-NO2 columns were compared with OMI-satellite tropospheric NO2. For ground-based observations restricted to uncertainties below 10%, no significant difference was found, and a correlation of 0.88.


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