Identification of ν(N=N) in Metal Arylazo Complexes: The Infrared and Raman Spectra of some Arylazo Complexes of Rhodium(III)

1971 ◽  
Vol 49 (24) ◽  
pp. 3994-3996 ◽  
Author(s):  
G. W. Rayner-Canham ◽  
D. Sutton
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Isotopic Substitution ◽  
Infrared And Raman Spectra ◽  
Metal Ligand

The Raman and infrared spectra have been obtained for a series of rhodium-arylazo complexes RhCl2(PPh3)2(p-XC6H4N2) where X = H, F, Br, CF3, NO2, OCH3, NEt2. The N=N stretching frequency ν(N=N) has been unambiguously identified from its strong appearance in the Raman spectrum and from isotopic substitution studies using 15N. Trends in the value of ν(N=N) with the p-substituent X are discussed, in terms of the apparent degree of metal–ligand π-interaction.

Spectra and Structure of Silicon-Containing Compounds. XII. Infrared and Raman Spectra of Trimethylvinylsilane and Trimethyl-D9-vinylsilane

1980 ◽  
Vol 34 (1) ◽  
pp. 60-65 ◽  
Author(s):  
J. R. Durig ◽  
W. J. Natter ◽  
M. Johnson-Streusand
Keyword(s):  
Internal Rotation ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Isotopic Substitution ◽  
Infrared And Raman Spectra ◽  
Vibrational Assignment ◽  
Infrared Band ◽  
Frequency Shifts ◽  
Solid States ◽  
Barriers To Internal Rotation

The Raman spectra (0 to 3300 cm−1) of (CH3)3Si(CHCH2) and (CD3)3Si(CHCH2) in the gaseous, liquid and solid states have been recorded. The infrared spectra (20 to 3300 cm−1) of the same two compounds in the gaseous and solid states have also been recorded. A vibrational assignment based upon depolarization ratios, frequency shifts with isotopic substitution, infrared band contours, and group frequencies is proposed. The SiC3 torsion was observed at 55 and 50 cm−1 for the “light” and “heavy” molecules, respectively, and the barriers to internal rotation were calculated to be 0.73 kcal/mol and 0.64 kcal/mol for the light and heavy compounds, respectively. These results are compared to the corresponding data for similar molecules.

Vibrational spectra of mercury(II) and methylmercury(II) thiocyanates

1969 ◽  
Vol 22 (10) ◽  
pp. 2117 ◽  
Author(s):  
RPJ Cooney ◽  
JR Hall
Keyword(s):  
Raman Spectrum ◽  
Solid State ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Unit Cell ◽  
Infrared And Raman Spectra

The Raman spectra of Hg(SCN)2 in both the solid state and in solution have been recorded and interpreted in conjunction with the infrared spectra. For the solid state the Raman shifts for Hg-S stretching, S-C stretching, and C-N stretching are 270, 721, and 2112 cm-1 respectively. In diglyme solution the corresponding values are 278, 692, and 2139 cm- 1. The infrared and Raman spectra of CH3HgSCN in the solid state do not contain any coincidences which may indicate that the unit cell is centrosymmetric. The Raman spectrum of CH3HgSCN in CH3OH solution shows strong, sharp, polarized lines at 283, 540, 1186, and 2138 cm-1 which are attributed to Hg-S stretching, Hg-C stretching, CH3 deformation, and C-N stretching modes respectively.

Normal Coordinate Analysis of Benitoite (BaTiSi3O9) and its Constituent Ring

1992 ◽  
Vol 291 ◽  
Author(s):  
Charles C. Kim ◽  
M. I. Bell ◽  
D. A. McKeown
Keyword(s):  
Crystal Structure ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Normal Modes ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate ◽  
Structure Space ◽  
New Information ◽  
Atomic Interactions ◽  
Modes Of Vibration

ABSTRACTThe normal modes of vibration and their frequencies are calculated for benitoite, a mineral whose crystal structure (space group D23h) consists of three-membered silicate rings (Si3O9) linked by Ba+2 and Ti+4 ions. The calculation unambiguously assigns the normal modes to the lines in the Raman and infrared spectra and determines the atomic interactions. On the assumption that mode mixings and splittings due to inter-ring interactions are small, the normal frequencies of the isolated ring of C3h, symmetry are determined. The identification of normal modes characteristic of three-membered silicate rings may prove to be a valuable guide in the interpretation of the infrared and Raman spectra of amorphous silicates, potentially leading to new information on the ring statistics of these materials.

Illumination- and Annealing-Induced Changes in the Infrared and Raman Spectra of a-Si:H

2001 ◽  
Vol 664 ◽  
Author(s):  
L.-F. Arsenault ◽  
S. Lebiba ◽  
E. Sacher ◽  
A. Yelon
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Qualitative Agreement ◽  
Raman Signal ◽  
Infrared And Raman Spectra ◽  
Matrix Elements ◽  
Short Term ◽  
Phonon Peak ◽  
Induced Changes ◽  
Ir And Raman

ABSTRACTWe have investigated the changes, produced by light-soaking, in both the IR and Raman responses of the Si-Hn stretching peaks in the 2000-2100 cm−1 range. Our observations of the IR response are in qualitative agreement with those of Kong and co-workers [1]: that is, short-term light soaking produces an increase in the intensity of the signal and a simultaneous shift to lower frequency. In contrast, short-term light soaking decreases the total intensity of the Raman signal in the 2000-2100 cm−1 range, when normalized to the TO phonon peak at about 480 cm−1. In both cases, these modifications are reversed on annealing at 200° C. We suggest that these changes are attributable to alterations in the environments of the Si-Hn bonds, with the resultant transfer of intensity between IR and Raman matrix elements. Details of the evolution of the components of the Raman spectrum in the 2000-2100 cm−1 range are presented, and compared with IR changes in the same range.

Infrared and Raman Spectra of Spiropentane-H8

1972 ◽  
Vol 26 (5) ◽  
pp. 540-542 ◽  
Author(s):  
G. R. Burns ◽  
D. G. McGavin
Keyword(s):  
Low Temperature ◽  
Infrared Spectrum ◽  
Gas Phase ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Sufficient Information ◽  
Infrared And Raman Spectra ◽  
Calorimetric Data ◽  
Crystalline Films ◽  
Twist Mode

Infrared and Raman spectra have been measured for spiropentane-H8. Raman spectra for the liquid have enabled the b1 species ring twist to be assigned. Previous assignments of this mode were based on calorimetric data and on the assignment of a band in the infrared spectrum to a combination band involving the ring twist mode. Infrared spectra of low temperature crystalline films have provided sufficient information that, when taken with the Raman data and gas phase infrared spectra, we have assignments for all of the fundamental modes.

THE VIBRATIONAL SPECTRA OF SULPHURYL AND THIONYL HALIDES

1961 ◽  
Vol 39 (11) ◽  
pp. 2171-2178 ◽  
Author(s):  
R. J. Gillespie ◽  
E. A. Robinson
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Normal Modes ◽  
Infrared And Raman Spectra ◽  
Fundamental Frequencies

New assignments are proposed for the fundamental frequencies of SOF2, SOCl2, SO2Cl2, SO2F2, and SO2FBr, based on new measurements of the Raman spectrum of SO2Cl2 and previous measurements of the infrared and Raman spectra of these molecules. The fundamental frequencies of these molecules are found to be related to each other and to those of similar molecules when the normal modes are described in terms of characteristic vibrations of the SO, SO2, S(Hal), and S(Hal)2 groups.

FAR INFRARED AND RAMAN SPECTRA AND STRUCTURE OF DITHIOPHOSGENE

1964 ◽  
Vol 42 (9) ◽  
pp. 2107-2112 ◽  
Author(s):  
W. K. Busfield ◽  
M. J. Taylor ◽  
E. Whalley
Keyword(s):  
Raman Spectrum ◽  
Infrared Spectrum ◽  
Raman Spectra ◽  
Far Infrared ◽  
Infrared And Raman Spectra ◽  
Tentative Assignment

The infrared spectrum in the range 3000–50 cm−1 and the Raman spectrum of solutions of dithiophosgene have been obtained. There are no coincidences in the infrared and Raman spectra, and the only structure consistent with this and approximately tetrahedral carbon valencies is[Formula: see text]that is tetrachloro-1,3-dithietane, in which the ring is planar or nearly planar. A tentative assignment of the observed bands is given on the basis of D2h symmetry.

Spectra and Structure of Silicon-Containing Compounds. X. Infrared and Raman Spectra of Methoxytrimethylsilane and Methoxy-D3-Trimethylsilane

1978 ◽  
Vol 32 (5) ◽  
pp. 457-462 ◽  
Author(s):  
J. R. Durig ◽  
B. J. Streusand
Keyword(s):  
Solid State ◽  
Internal Rotation ◽  
Raman Spectra ◽  
Strong Mixing ◽  
Isotopic Substitution ◽  
Infrared And Raman Spectra ◽  
Vibrational Assignment ◽  
Torsional Mode ◽  
Frequency Shifts ◽  
Bending Mode

The infrared (20 to 3100 cm−1) and Raman (10 to 3100 cm−1) spectra of gaseous (CH3)3SiOCH3 and (CH3)3SiOCD3 have been recorded. The Raman spectra of both liquids and the infrared and Raman spectra of the “light” compound in the solid state have also been recorded. A vibrational assignment based upon depolarization ratios, frequency shifts with isotopic substitution, and group frequencies is proposed. The Si—O torsional mode was observed at 67 cm−1 which gives a barrier to internal rotation of 1.02 kcal/mol. Strong mixing of the Si—O—C bending mode with the C—Si—C bends is proposed. The CH3—O torsion was not observed.

scholarly journals Darstellung und Eigenschaften von cyclo-Nonaschwefeloxid (S9O) und von cyclo-Dekaschwefeloxid (S10O) [1] / Preparation and Properties of cyclo-Nonasulfuroxide (S9O) and of cyclo-Decasulfuroxide (S10O) [1]

1985 ◽  
Vol 40 (5) ◽  
pp. 594-600 ◽  
Author(s):  
Ralf Steudel ◽  
Torsten Sandow ◽  
Jürgen Steidel
Keyword(s):  
Acetic Acid ◽  
Raman Spectrum ◽  
Oxygen Atom ◽  
Raman Spectra ◽  
Carbon Disulfide ◽  
Methylene Chloride ◽  
Molar Ratio ◽  
Infrared And Raman Spectra ◽  
Cyclic Molecules ◽  
First Time

Abstract The homocyclic oxides S9O (m.p. 33 °C, dec.) and S10O (m.p. 51 °C, dec.) have been prepared by oxidation of the corresponding sulfur rings S9 and S10 , respectively, by trifluoroperoxy acetic acid (molar ratio 1:2-3) in a carbon disulfide/methylene chloride mixture. According to infrared and Raman spectra, both compounds contain an exocyclic oxygen atom. S9O and S10O decompose at 25 °C to give SO2 and a polysulfuroxide SnO with >10 but both can be stored at -78 °C without decomposition. The SS bond distances are discussed on the basis of the Raman spectra. In addition, the Raman spectrum of solid S9 has been recorded for the first time. It shows that S9 crystallizes as two allotropes (α-and β-S9) both consisting of cyclic molecules of either C1 or C2 symmetry with bond distances of between 203 and 209 pm.

INFRARED AND RAMAN SPECTRA OF CYANURIC FLUORIDE

1964 ◽  
Vol 42 (3) ◽  
pp. 690-695 ◽  
Author(s):  
James E. Griffiths ◽  
Donald E. Irish
Keyword(s):  
Raman Spectra ◽  
Infrared Spectra ◽  
Infrared And Raman Spectra ◽  
Polarization Measurements

Infrared spectra (250–2000 cm−1) and Raman displacements (Δv = 100–1800 cm−1) with qualitative polarization measurements are reported for cyanuric fluoride. All of the active fundamentals are assigned on the basis of a planar D3h model: a1′ = 1496, 999, 642; e′ = 1617, 1424, 1087, 576, 378; a2″ = 817, 436; e″ = 743 and 226 cm−1.

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