Application of Laser-Excited Raman Spectroscopy to Organic Chemistry I. Raman Spectra of Some Acyclic Monoterpenes

1969 ◽  
Vol 23 (6) ◽  
pp. 610-615 ◽  
Author(s):  
Stanley K. Freeman ◽  
Dana W. Mayo

Laser-Raman spectra of 12 acyclic terpenoids has been recorded. Assignments were made for stretching mode vibrations of carbon-carbon double bonds by comparison with infrared spectra. The results of intensity and depolarization studies are discussed.

1975 ◽  
Vol 29 (4) ◽  
pp. 337-344 ◽  
Author(s):  
G. E. Walrafen ◽  
J. Stone

The utility of Raman spectroscopy as a means of characterizing the properties of pure and doped fused silica has been investigated. Laser-Raman spectra were obtained by forward scattering from solid optical fibers ∼35 to 85 m in length using 514.5 nm excitation with an “image slicer” and a Cary model 81 instrument. Clad and unclad fibers of fused silica and doped fibers having SiO2-GeO2 and SiO2-GeO2-B2O3 cores were examined. Raman spectra were also obtained from bulk samples of glasses, including pure GeO2, pure B2O3, and various compositions of SiO2-GeO2, SiO2-B2O3, and SiO2-GeO2-B2O3. The addition of dopants to fused silica was found to alter the Raman spectrum both by the appearance of new bands, roughly proportional to dopant concentration and not common either to the fused silica or to the dopant alone, and by the marked alteration of other Raman bands, which is indicative of changes in the local intermolecular order. Thus, addition of GeO2 produces new Raman bands at ∼675 and ∼1000 cm−1; and of B2O3, new bands at ∼940 and ∼1350 cm−1. Addition of GeO2 and/or B2O3 weakens the relatively sharp Raman lines near 485 and 600 cm−1 (and a similar but small effect was also noted with increasing OH content). GeO2 and B2O3 together also produce observable narrowing of the broad intense 440 cm−1 Raman contour. These spectral effects are interpreted, respectively, in terms of a decrease in the concentrations of [Formula: see text] and [Formula: see text] defects produced by dopant addition and of a concomitant reordering of the silica structure. Raman spectroscopy thus appears to be a useful optical technique for elucidating the properties of dopants that have been especially chosen for good optical transmission and hence are not easily detectable by absorption measurements.


1979 ◽  
Vol 33 (1) ◽  
pp. 41-45 ◽  
Author(s):  
David A. Stephenson ◽  
Richard J. Blint

A technique for rapid acquisition and computer processing of Raman signals is described for probing premixed laminar hydrocarbon-air flames using laser Raman spectroscopy. Temperatures can be determined to within ±50°K by fitting the observed N2 spectrum at any point in the flame. Fits to the spectra of O2, CO, H2, and CO2 are used to measure their mole fractions at the calculated N2 temperature. For the remaining polyatomic species, the total area under the peak is the primary measure of their concentration.


1977 ◽  
Vol 31 (1) ◽  
pp. 30-35 ◽  
Author(s):  
P. J. Trotter

Raman spectra of a number of azo dye structures have been analyzed. In azonaphthol and azopyrazol dyes, hydroxyazo to keto-hydrazone tautomerizations, [Formula: see text] were observed in aqueous basic and acidic media. Observations of azo and ring vibrations, as well as hydrazone (C=N plus C=0) bands, were made. It was noted that the azo-anions (examined at pH 12) convert to the protonated neutral hydrazone (keto) form in aqueous acid (run at pH 2). Infrared spectra were used to confirm the presence of the C=0 group in keto-tautomeric forms.


1972 ◽  
Vol 50 (10) ◽  
pp. 1596-1600 ◽  
Author(s):  
J. Hubert ◽  
P. C. Kong ◽  
F. D. Rochon ◽  
T. Theophanides

Zeise's salt, anhydrous and monohydrate, has been prepared by a new method similar to the original method used by Zeise. The infrared and laser Raman spectra of the anhydrous Zeise's salt together with the infrared spectra of the deutero and bromo analogs, are reported and discussed. The vibrational spectra are interpreted in terms of a cyclopropane-like ring structure, obtained by the insertion of the platinum atom into the double bond.


1970 ◽  
Vol 48 (20) ◽  
pp. 3117-3123 ◽  
Author(s):  
A. M. Qureshl ◽  
F. Aubke

The infrared spectra from 4000–250 cm−1 and the laser Raman spectra of NOAsF6, NO2AsF6, N2F3AsF6, F2NOAsF6, NOSbF6, NO2SbF6, N2F3Sb2F11, and F2NOSb2F11 are recorded. Eight of the nine fundamentals expected for the N2F3+ cation can be observed and are tentatively assigned. The vibrational spectra of the MF5 adducts are in agreement with an ionic formulation; however, the mutual exclusion rule for infrared and Raman active vibrations appears to be relaxed and one of the fundamentals v5 [F2g] is split into a doublet in almost all cases.


1982 ◽  
Vol 60 (17) ◽  
pp. 2216-2221 ◽  
Author(s):  
Michel Manfait ◽  
Alain J. P. Alix ◽  
Jacqueline Delaunay-Zeches ◽  
Théophile Theophanides

The laser Raman spectra of the hydroxo-bridged platinum(II) complexes, di-μ-hydroxo-bis(diammine) platinum(II)-nitrate [(NH3)2Pt(OH)2Pt(NH3)2](NO3)2, and isotopic derivatives involving the atoms H/D and 16O/18O are recorded in the solid state in the range 0–4000 cm−1. The infrared spectra of the complexes are recorded in KBr pellets in the range 200–4000 cm−1. Assignments of the different lines for the nitrate ion, the ammonia molecules, the hydroxo groups, and the square planar skeleton vibrations of the complex and its isotopic analogs are given.


1977 ◽  
Vol 31 (6) ◽  
pp. 515-518 ◽  
Author(s):  
Dwaine M. Thomas

The Raman spectra of various concentrations of dimethylnitrosamine in water have been measured. The lowest concentration detected was 10 mg/l. Instrumental parameters were varied to optimize the signal response.


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