High resolution spectrum of NO2 loosely bound states: densities of states and long range forces

2001 ◽  
Vol 3 (12) ◽  
pp. 2268-2274 ◽  
Author(s):  
Sylvain Heilliette ◽  
Antoine Delon ◽  
Patrick Dupre´ ◽  
Re´my Jost
1972 ◽  
Vol 25 (2) ◽  
pp. 327 ◽  
Author(s):  
F Balkau ◽  
ML Heffernan

The analysis of the high resolution spectrum of benzothiophen in several solvents is reported. It is noted that the conditions are close to those leading to deceptively simple spectra, but under very high resolution sufficient lines could be resolved to give an unambiguous analysis. The inter-ring, long-range coupling constants, as well as their relative signs, could be determined from these spectra as a result of the strong coupling between protons.


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.


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.


2006 ◽  
Author(s):  
Duncan A. Robertson ◽  
David G. Macfarlane

2005 ◽  
Vol 71 (21) ◽  
Author(s):  
Zahirul Islam ◽  
D. Haskel ◽  
J. C. Lang ◽  
G. Srajer ◽  
X. Liu ◽  
...  

1975 ◽  
Vol 53 (13) ◽  
pp. 1980-1983 ◽  
Author(s):  
A. A. Chalmers ◽  
K. G. R. Pachler

The natural abundance 13C n.m.r. spectrum of 2-pyrone has been analyzed by the 13C–{1H} SPI technique. The magnitudes and signs of all long-range 13C,H couplings have been obtained and are compared with those of related compounds.


2003 ◽  
Vol 107 (51) ◽  
pp. 11347-11353 ◽  
Author(s):  
F. Rabilloud ◽  
D. Rayane ◽  
A. R. Allouche ◽  
R. Antoine ◽  
M. Aubert-Frécon ◽  
...  
Keyword(s):  

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