INFRARED SPECTRA OF XANTHATE COMPOUNDS: III. ORGANIC SOLVENT EFFECT ON THE C=S FREQUENCY

1961 ◽  
Vol 39 (9) ◽  
pp. 1783-1786 ◽  
Author(s):  
L. H. Little ◽  
G. W. Poling ◽  
J. Leja
Keyword(s):  
Absorption Band ◽  
Organic Solvent ◽  
Solvent Effect ◽  
Infrared Spectra ◽  
Characteristic Behavior ◽  
Band Assignment

The previously made absorption-band assignment (1) for the C=S stretching mode in xanthate-type compounds, 1020–1070 cm−1, has been confirmed by the characteristic behavior of the C=S dipole in a range of different solvents (Bellamy and Rogasch (2)).

Nature of the solvent effect in the infrared spectra of carbonyl compounds

1959 ◽  
Vol 1 (3) ◽  
pp. 19-22 ◽  
Author(s):  
M. Horák ◽  
J. Jonáš ◽  
J. Plíva
Keyword(s):  
Solvent Effect ◽  
Infrared Spectra ◽  
Carbonyl Compounds

The intensity of the absorption band in the infrared spectra of magnetized water and sodium oleate solutions

1970 ◽  
Vol 13 (4) ◽  
pp. 1332-1334
Author(s):  
M. A. Orel ◽  
I. V. Kagarlitskaya ◽  
I. V. Lapatukhin ◽  
R. A. Kabirova
Keyword(s):  
Absorption Band ◽  
Sodium Oleate ◽  
Infrared Spectra ◽  
Magnetized Water

Numerical estimation of the peak positions for the 1050-1300cm-1 absorption band due to an ester group in the infrared spectra.

1997 ◽  
Vol 46 (9) ◽  
pp. 695-702 ◽  
Author(s):  
Toshio OGAWA ◽  
Kenji HAYASHI ◽  
Satoshi OSAWA ◽  
Tetsuya KOYAMA
Keyword(s):  
Absorption Band ◽  
Infrared Spectra ◽  
Ester Group ◽  
Numerical Estimation

scholarly journals ON THE INFRARED ABSORPTION OF WATER AND HEAVY WATER IN CONDENSED STATES

1956 ◽  
Vol 34 (6) ◽  
pp. 798-808 ◽  
Author(s):  
Paul A. Giguère ◽  
K. B. Harvey
Keyword(s):  
Thin Films ◽  
Absorption Band ◽  
Water Molecule ◽  
Air Temperature ◽  
Heavy Water ◽  
Infrared Spectra ◽  
Infrared Absorption ◽  
Silver Chloride ◽  
Strong Absorption Band ◽  
Librational Mode

The infrared spectra (from 2 to 30 μ) of thin films of H2O and D2O were measured at various temperatures between 20 ° and −180 °C. A strong absorption band due to the librational mode of the water molecule has its maximum around 710 cm.−1 in the liquid. In ice it is shifted to 800 cm.−1 at −15 °C. and 850 cm.−1 at −170 °C. The corresponding D2O bands show the normal isotope shift. Thin films of water pressed between silver chloride plates could not be crystallized even at liquid air temperature as confirmed by their spectra, which were almost identical with those of the liquid.

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