High-Resolution Vibrational Spectra of Furazan II. The B1 Fundamental ν 11 at ~ 1175 cm–1 from Fourier-Transform Infrared Spectroscopy

1992 ◽  
Vol 47 (3) ◽  
pp. 499-506 ◽  
Author(s):  
Otto L. Stiefvater

Abstract The high-resolution FT-IR spectrum of the A-type fundamental ν11 of furazan ( C2H2N20) has been recorded and analysed against the background of rotational information from DRM microwave spectroscopy to yield the band origin as ν110= 1175.3377 + 0.0001 cm-1 . The combined use of microwave (MW) and FT-IR data gives this band origin with a statistical uncertainty of σ= 10-6cm-1 and leads to a refinement of the rotational constants of the state ν11 = 1 over those derivable from either MW or FT-IR data alone

1993 ◽  
Vol 48 (4) ◽  
pp. 605-612 ◽  
Author(s):  
Otto L. Stiefvater

Abstract With prior information on vibrationally excited states from DRM microwave spectroscopy, two B-type high-resolution FT-IR bands of furazan were examined to yield the band origins v03 = 1316.2254 cm-1 and v04 = 1036.1689 cm-1 with an estimated absolute uncertainty of ±0.0001 cm-1 . The rotational and distortion constants of both fundamental states were refined by the combination of rotational with rovibrational data in the least-squares fits of the bands.


1993 ◽  
Vol 48 (5-6) ◽  
pp. 692-698
Author(s):  
Otto L. Stiefvater ◽  
Stefan Klee

Abstract The band origin of the A1 mode v2 , which represents the symmetrical stretching vibration of the two C = N bonds of furazan, has been determined from the high-resolution FT-IR band as v20 = 1418.4724± 0.0001 cm-1. The rotational parameters of this excited state, as determined in a preceding DRM microwave study, have been confirmed and their precision was raised through the combined fit of microwave data and of some 2500 rovibrational transitions.The use of conjugate low-J Q-branch lines for the determination of the origin of a B-type IR band of an asymmetric rotor is illustrated.


2011 ◽  
Vol 134 (23) ◽  
pp. 234306 ◽  
Author(s):  
Michael K. Bane ◽  
Evan G. Robertson ◽  
Christopher D. Thompson ◽  
Chris Medcraft ◽  
Dominique R. T. Appadoo ◽  
...  

2020 ◽  
Vol 13 (1) ◽  
pp. 183-199 ◽  
Author(s):  
Yirui Zhang ◽  
Yu Katayama ◽  
Ryoichi Tatara ◽  
Livia Giordano ◽  
Yang Yu ◽  
...  

Carbonate oxidation via dehydrogenation on LiNi0.8Co0.1Mn0.1O2 at voltages as low as 3.8 VLi was revealed by in situ FT-IR measurements.


2012 ◽  
Vol 9 (1) ◽  
pp. 253-259 ◽  
Author(s):  
Hamid Najib ◽  
Siham Hmimou ◽  
Hicham Msahal

The high-resolution Fourier transform infrared spectrum of nitrogen trifluoride NF3has been studied in the v1+ v4perpendicular band region around 1523 cm−1. All experimental data have been refined applying various reduction forms of the effective rovibrational Hamiltonian developed for an isolated degenerate state of a symmetric top molecule. The v1= v4= 1 excited state of the14NF3oblate molecule was treated with models taking into account ℓ- andk-type intravibrational resonances. Parameters up to sixth order have been accurately determined and the unitary equivalence of the derived parameter sets in different reductions was demonstrated.


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