High-resolution spectrum of the ν1 fundamental band of isocyanic acid, HNCO

1990 ◽  
Vol 140 (2) ◽  
pp. 353-372 ◽  
Author(s):  
Koichi M.T. Yamada ◽  
Manfred Winnewisser ◽  
J.W.C. Johns
1975 ◽  
Vol 57 (3) ◽  
pp. 402-415 ◽  
Author(s):  
Michel Betrencourt ◽  
Mireille Morillon-Chapey ◽  
Claude Amiot ◽  
Guy Guelachvili

1981 ◽  
Vol 59 (10) ◽  
pp. 1313-1326 ◽  
Author(s):  
D. A. Steiner ◽  
S. R. Polo ◽  
T. K. McCubbin Jr. ◽  
K. A. Wishah

The ν1 fundamental band of DNCO has been observed for the first time under high resolution. The band origin for this deuterium–nitrogen stretching vibration is found to be at 2637.198 cm−1, rather distant from the previously reported value of 2634.9 cm−1. Eighteen subbands have been analyzed and term values for both ground and ν1 states with K up to 6 have been obtained. Effective rotational constants Bν and centrifugal distortion constants Dν and Hν have also been determined. Interaction is observed with the 2ν3 vibration which has a band origin around 2640 cm−1. Interesting perturbations are observed for the K = 0 and K = 4 levels of ν1.


Author(s):  
O.N. Ulenikov ◽  
E.S. Bekhtereva ◽  
Yu.V. Krivchikova ◽  
V.A. Zamotaeva ◽  
T. Buttersack ◽  
...  

1976 ◽  
Vol 54 (24) ◽  
pp. 2429-2434 ◽  
Author(s):  
B. R. Yadav ◽  
S. B. Rai ◽  
D. K. Rai

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.


2001 ◽  
Vol 3 (12) ◽  
pp. 2268-2274 ◽  
Author(s):  
Sylvain Heilliette ◽  
Antoine Delon ◽  
Patrick Dupre´ ◽  
Re´my Jost

1999 ◽  
Vol 72 (5) ◽  
pp. 844-853 ◽  
Author(s):  
Seiichi Kawahara ◽  
Saori Bushimata ◽  
Takashi Sugiyama ◽  
Chihiro Hashimoto ◽  
Yasuyuki Tanaka

Abstract A novel analytical method using high resolution 13C-NMR spectroscopy to study polymer latex, which is a heterogeneous system comprising polymer dispersoid and water, is described. The appropriate concentrations of surfactant and dried rubber content of a polybutadiene latex, which give the best spectrum, were found to be 1 w/v % and 10%, respectively. The half-widths of resonance peaks for the latex sample were almost identical to the half-widths obtained in solution, which were about one-third the width of those obtained using a solid sample of either a crosslinked or soluble polybutadiene. Nevertheless, the signal to noise ratio for the latex sample was slightly smaller than that for the solution sample. The values of spin-lattice relaxation time, T1, for the latex sample were similar to those for the solid sample. These demonstrate that the latex state C-NMR spectroscopy will be a powerful technique for structural characterization of crosslinked gels in the dispersoid because it gives a high resolution spectrum comparable to solution state spectroscopy, showing short T1 values corresponding to those for solid state C-NMR spectroscopy. High resolution latex state 13C-NMR spectroscopy was used to determine the concentrations of the various isomers of the polybutadiene in the dispersoid.


2009 ◽  
Vol 256 (2) ◽  
pp. 198-203 ◽  
Author(s):  
Chen-Lin Liu ◽  
Cheng-Liang Huang ◽  
Chi-Kung Ni ◽  
Nobukimi Ohashi ◽  
Jon T. Hougen

2012 ◽  
Vol 113 (11) ◽  
pp. 1250-1260
Author(s):  
V. Sironneau ◽  
P. Chelin ◽  
F. Kwabia Tchana ◽  
I. Kleiner ◽  
J. Orphal

2003 ◽  
Vol 28 (16) ◽  
pp. 1478 ◽  
Author(s):  
Sergei Churilov ◽  
Yogi N. Joshi ◽  
Joseph Reader

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