INFRARED SPECTRA AND THE STRUCTURES OF XANTHATES AND DIXANTHOGENS

1961 ◽  
Vol 39 (8) ◽  
pp. 1633-1637 ◽  
Author(s):  
M. L. Shankaranarayana ◽  
C. C. Patel

The infrared spectra of representative dialkyl dixanthogens and a few xanthates have been examined. All these compounds have two strong absorption bands in the regions 1140–1265 and 1010–1080 cm−1. On the basis of the shift of the bands with the changes in the substituents in the xanthic acid, the former band is assigned to the C=S group, while the latter to the CO group. Except in the ionic compounds, the canonical structure [Formula: see text] contributes very little to the structures of dixanthogens and covalent metal complexes.


1988 ◽  
Vol 42 (2) ◽  
pp. 242-247 ◽  
Author(s):  
Paul J. Brimmer ◽  
Peter R. Griffiths

The linearity of plots of the Kubelka-Munk function against concentration is investigated for weak and strong absorption bands in the spectrum of a typical organic analyte, caffeine. The linear region is extended when measurements are made with an off-axis optical geometry, in comparison to an in-line configuration. For the latter configuration, the linearity is improved when crossed polarizers are placed before and after the sample.



1986 ◽  
Vol 51 (1) ◽  
pp. 90-100 ◽  
Author(s):  
Soňa Vašíčková ◽  
Vladimír Pouzar ◽  
Ivan Černý ◽  
Pavel Drašar ◽  
Miroslav Havel

Infrared spectra of a series of compounds containing the CH3OCH2O- (MOM-O-) group have been studied. All the spectra exhibit three characteristic strong absorption bands due to coupled stretching vibrations of C-O-C-O-C grouping in the region 1 200 - 1 000 cm-1.



1967 ◽  
Vol 45 (24) ◽  
pp. 3199-3201 ◽  
Author(s):  
O. K. Srivastava ◽  
E. A. Secco

Infrared spectra of hexagonal Cd(OH)2, CdOHCl, and CdOHF, along with deuterated analogues CdODCl and CdODF, in the range 2.5–16 μ are reported for the first time. The effects of substituting a halogen for an OH group in Cd(OH)2 are (i) shift of OH stretching vibration to a lower frequency and (ii) appearance of strong absorption bands in the region 8–16 μ. All the observed bands in the deuterated analogues are displaced to lower frequencies with νH/νd ratios between 1.35–1.37. The spectra of CdOHCl and CdOHF show a high correlation with their zinc analogues and although both spectra appear consistent with a simple molecule of Cs or C1 symmetry, an alternate interpretation is given in terms of OH lattice vibrations.



1989 ◽  
Vol 213 ◽  
pp. 133-144 ◽  
Author(s):  
Carola Engelter ◽  
Graham E. Jackson ◽  
Cheryl L. Knight ◽  
David A. Thornton


1975 ◽  
Vol 6 (33) ◽  
pp. no-no
Author(s):  
H. OGOSHI ◽  
E. WATANABE ◽  
Z. YOSHIDA ◽  
J. KINCAID ◽  
K. NAKAMOTO


1974 ◽  
Vol 5 (8) ◽  
Author(s):  
P. V. KHADIKAR ◽  
R. L. AMERIA ◽  
M. G. KEKRE ◽  
S. D. CHAUHAN


1963 ◽  
Vol 16 (1) ◽  
pp. 93 ◽  
Author(s):  
RA Jones

The positions and intensities of the characteristic infrared absorption bands of the nucleus are recorded and discussed for thirty-five 2-monosubstituted pyrroles.



1953 ◽  
Vol 31 (4) ◽  
pp. 328-337 ◽  
Author(s):  
L. Breitman ◽  
E. W. R. Steacie

The infrared spectra of chloral, carbon tetrachloride, and chloroform have been determined between 1500 and 650 cm.−1 over a range of pressures in the gas phase. Absorption bands suitable for the quantitative analysis of binary and ternary mixtures of the components have been selected and their peak intensities shown to obey Beer's Law over the range of pressures studied. Ternary mixtures have been analyzed from the spectra with an accuracy of about 20%.The spectra of dichloromethane and methyl chloride have also been measured under comparable conditions.



Author(s):  
Hung-Yang Jain ◽  
Chih-Tsun Yang ◽  
Li-Kang Chu

The infrared spectrum of the simplest geminal diol, methanediol or methylene glycol (CH2(OH)2), was successfully probed in the gaseous hydration of formaldehyde. The observed absorption bands coincided with the anharmonic...



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