Low-frequency Raman and far-infrared spectra of acetone/chloroform mixtures

1997 ◽  
Vol 15 (1) ◽  
pp. 61-67 ◽  
Author(s):  
T.S. Perova ◽  
D.H. Christensen ◽  
O. Faurskov Nielsen
1979 ◽  
Vol 32 (7) ◽  
pp. 1443 ◽  
Author(s):  
GA Bowmaker ◽  
L Tan

A number of different methods for preparing anionic Group 1B metal thiolate complexes have been investigated. The compounds [Me4N] [CU2(SMe)3] and [Et4N] [Ag5(SBut)6] are reported for the first time, and new methods for preparing the previously known compounds [Et4N] [Cu5(SBut)6], [Me4N]2 [CU5(SPh)7] and [Et4N]2 [Cu5(SPh)7] are described. The far-infrared spectra of the above compounds, and of CuSMe, CuSBut, AgSBut, [Me4N]2 [CU4(SPh)6] and [Me4N]2 [Ag5(SPh)7] have been obtained, and metal-sulfur stretching bands are assigned in the 150-350 cm-1 region. The low-frequency Raman spectra have also been obtained for some of these compounds. Possible structures for the new compounds are considered in the light of the low-frequency vibrational spectra.


1970 ◽  
Vol 24 (1) ◽  
pp. 16-20 ◽  
Author(s):  
J. R. Durig ◽  
D. J. Antion

The far-infrared spectra of thin films of NH4F and ND4F and the Raman spectra of polycrystalline samples of both compounds have been recorded at −170°C. Two low-frequency lattice vibrations were observed in each spectrum and these have been assigned as optical translations on the basis of their isotopic shift factors. Librational modes were not observed in any of the spectra.


1983 ◽  
Vol 61 (7) ◽  
pp. 1449-1452 ◽  
Author(s):  
Marek J. Wójcik ◽  
Czesława Paluszkiewicz

Infrared spectra of hydrogen-bonded methyl salicylate have been studied in the temperature range 173–293 K, in solutions of various concentrations (in CCl4) and in the gaseous state. Results show that the molecules form monomerie intramolecular hydrogen bonds in the solid, liquid, and gaseous state. Far-infrared spectra were recorded which give the wavenumber of low-frequency O … O mode used in theoretical reconstruction of the band connected with the O—H stretching vibration. The position and especially the width of this band are determined to a large extent by the influence of the environment.


1987 ◽  
Vol 36 (1) ◽  
pp. 846-849 ◽  
Author(s):  
G. A. Thomas ◽  
H. K. Ng ◽  
A. J. Millis ◽  
R. N. Bhatt ◽  
R. J. Cava ◽  
...  

1973 ◽  
Vol 27 (1) ◽  
pp. 22-26 ◽  
Author(s):  
S. M. Craven ◽  
F. F. Bentley ◽  
D. F. Pensenstadler

The low frequency infrared spectra from 450 to 75 cm−1 of seven oximes and five aldoximes have been recorded for pure samples and for dilute solutions in cyclohexane. An intense characteristic band is present in the solution spectra at 367 ± 10 cm−1. This characteristic band shifts to 275 ± 10 cm−1 in the spectra of the OD compounds. The 367 ± 10 cm−1 and 275 ± 10 cm−1 bands are assigned to OH and OD torsional vibrations. A comparison of the solution spectra with spectra of the solid samples indicated that the OH … N hydrogen bond stretch of oximes and aldoximes occurs in 300 to 200 cm−1 region. Strong bands also are present in 140 to 100 cm−1 region which are due to OH … N bending modes or perhaps lattice vibrations.


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