THE RAMAN SPECTRA OF SOME POLYSULPHURYL CHLORIDES AND FLUORIDES

1961 ◽  
Vol 39 (11) ◽  
pp. 2179-2188 ◽  
Author(s):  
R. J. Gillespie ◽  
E. A. Robinson
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Characteristic Group ◽  
First Time

The Raman spectrum of disulphuryl chloride, S2O5Cl2, has been reinvestigated and the Raman spectra of S2O5F2, S2O5ClF, S3O8Cl2, S3O8F2, and the new compound S3O8ClF are reported for the first time. The vibrational spectra of these polysulphuryl halides are interpreted in terms of characteristic group frequencies by comparison with the vibrational spectra of simple sulphuryl compounds. The spectra are consistent with acyclic structures for the polysulphuryl halides.

Studies of the Jahn - Teller effect IV. The vibrational spectra of spin-degenerate molecules

1962 ◽  
Vol 255 (1050) ◽  
pp. 31-53 ◽  
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Physical Theory ◽  
Vibronic Coupling ◽  
Infra Red ◽  
Jahn Teller ◽  
Jahn Teller Effect ◽  
Active Vibration ◽  
Degenerate States

The physical theory necessary for interpreting the vibrational spectra of spin-degenerate molecules is developed in this paper. Particular attention is paid to those molecules whose behaviour is expected to be markedly different from that of both orbitally non-degenerate molecules and those with purely spatial degeneracy. These include certain Kramers degenerate molecules, whose Raman spectra are expected to contain reverse-polarized contributions, and also tetrahedral and octahedral molecules in fourfold degenerate states. The case of a fourfold degenerate octahedral molecule is investigated in the limits of strong vibronic coupling by one of the Jahn—Teller active vibrations (e g and t 2g ). It turns out that the forbidden t 2u vibration may be infra-red active, that the Raman spectrum may contain reverse-polarized contributions and that both infra-red and Raman spectra may contain strong progressions of bands involving multiple excitations of the vibronically active vibration.

Theoretical calculations of electronic Raman effects of the NO and O2 molecules

1970 ◽  
Vol 48 (14) ◽  
pp. 1664-1674 ◽  
Author(s):  
D. W. Lepard
Keyword(s):  
Raman Spectrum ◽  
Raman Spectra ◽  
Theoretical Calculations ◽  
Diatomic Molecules ◽  
Wave Functions ◽  
Rotational Structure ◽  
Intermediate Case ◽  
First Time

This paper presents a method for calculating the relative intensities and Raman shifts of the rotational structure in electronic Raman spectra of diatomic molecules. The method is exact in the sense that the wave functions used for the calculations may belong to any intermediate case of Hund's coupling schemes. Using this method, theoretical calculations of the pure rotational and electronic Raman spectrum of NO, and the pure rotational Raman spectrum of O2, are presented. Although a calculated stick spectrum for NO was previously shown by Fast et al., the details of this calculation are given here for the first time.

The Preparation and Low-Frequency Vibrational Spectra of Some Copper(I) and Silver(I) Alkane- and Arene-monothiolate Complexes

1979 ◽  
Vol 32 (7) ◽  
pp. 1443 ◽  
Author(s):  
GA Bowmaker ◽  
L Tan
Keyword(s):  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Low Frequency ◽  
Far Infrared ◽  
New Methods ◽  
Thiolate Complexes ◽  
New Compounds ◽  
First Time ◽  
Far Infrared Spectra

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.

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.

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.

Darstellung und Charakterisierung der Tetrabutylammoniumsalze von [Tc2Cl8]2-, [Tc2Cl8]3- und [Tc2Br8]2- Preparation and Characterization of the Tetrabutylammonium Salts of [Tc2Cl8]2-, [Tc2Cl8]3- und [Tc2Br8]2-

1980 ◽  
Vol 35 (7) ◽  
pp. 797-801 ◽  
Author(s):  
W. Preetz ◽  
G. Peters
Keyword(s):  
Electronic Spectrum ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
High Extent ◽  
First Time

The reduction of [TcCl6]2- with Zn in conc. HCl after evaporation and extraction of ZnCl2 by diethylether yields a red-brown product from which after dissolving in dilute HCl by a solution of (TBA)Cl in CH2Cl2 (TBA)2[Tc2Cl8] and (TBA)3[Tc2Cl8] can be extracted. The separation is achieved by the much better solubility of the green (TBA)2[Tc2Cl8] in acetone compared with that of the grey-blue (TBA)3[Tc2Cl8]. On treatment of (TBA)2[Tc2Cl8] dissolved in acetone with bromine-free conc. HBr carmine red (TBA)2[Tc2Br8] is obtained for the first time. The vibrational spectra are similar and can be assigned according to the assumed D4h-symmetry. In the Raman spectra of both octachloroditechnetates the intensive Tc-Tc-vibration (A1g) is observed at 307 cm-1, for (TBA)2[Tc2Br8] it is found at 323 cm-1 . The electronic spectrum of (TBA)2[Tc2Cl8] agrees to a high extent with that of the corresponding Re compound

Optical and Raman spectra of single crystals of perylene-TCNQ charge transfer complexes

1982 ◽  
Vol 60 (5) ◽  
pp. 588-595 ◽  
Author(s):  
A. D. Bandrauk ◽  
K. D. Truong ◽  
C. Carlone
Keyword(s):  
Raman Spectrum ◽  
Charge Transfer ◽  
Single Crystals ◽  
Raman Spectra ◽  
Optical Transmission ◽  
Charge Transfer Complexes ◽  
One Dimensional ◽  
Resonance Enhancement ◽  
First Time ◽  
Transmission And Reflection

Optical transmission and reflection measurements are reported for the quasi one dimensional solids perylene-TCNQ (P1T1) and (perylene)3-TCNQ (P3T1) in the region from 300 to 1200 nm. Raman spectra of single crystals of both compounds were obtained from 20 to 3000 cm−1. With 457.9 nm excitation, combinations and overtones of perylene are observed for the first time. A complete Raman spectrum of perylene and its deuterated homologue including librations is thus obtained via selective resonance enhancement of that molecule.

Vibrational Spectra and Normal Coordinate Analysis of Disulfuryl Difluoride S2O5F2 and Diselenonyl Difluoride Se2O5F2

1993 ◽  
Vol 58 (3) ◽  
pp. 517-529 ◽  
Author(s):  
Jiří Toužín ◽  
Miloš Černík
Keyword(s):  
Raman Spectrum ◽  
Force Field ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Room Temperature ◽  
Normal Coordinate Analysis ◽  
Normal Coordinate ◽  
Valence Force Field ◽  
Overlapping Bands

Raman spectra (1 600 - 100 cm-1) of liquid S2O5F2 and Se2O5F2 and infrared spectra of liquid and gaseous S2O5F2 were measured. A modified general valence force field was used for their interpretation by normal coordinate analysis. Refinement of the number of lines in the Raman spectrum of S2O5F2 by means of numerical separation of the overlapping bands led to the conclusion that liquid S2O5F2 consists at least of three rotamers at room temperature.

Structural study of chlorine pentafluoride in the condensed phases

1978 ◽  
Vol 56 (10) ◽  
pp. 1353-1357 ◽  
Author(s):  
M. Drifford ◽  
R. Rousson ◽  
J. M. Weulersse
Keyword(s):  
Raman Spectrum ◽  
Neutron Diffraction ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Room Temperature ◽  
Condensed Phases ◽  
Body Centered Cubic ◽  
X Ray ◽  
Solid Phases ◽  
Diffraction Patterns

Raman spectra of chlorine pentafluoride have been investigated in the condensed phases between room temperature and 4 K. X-Ray and neutron diffraction patterns were also recorded. The three solid phases previously described by nmr measurements have been characterised. Solid 1(161 K < T < 181 K) is body-centered cubic with a = 5.7 Å; its Raman spectrum is quite comparable with that of the liquid. Solid II (117 K < T < 161 K) is orthorhombic with a = 6.17 Å, b = 7.22 Å; c = 7.66 Å; according to the Raman spectra its structure seems to be similar to that of solid BrF5. The structure of solid III (T < 117 K) has not been determined; however, the vibrational spectra show that it is not very different from solid II.The analogy between the structures of the tri- and pentafluorides of chlorine and bromine is discussed.

Vibrational spectra of ammonium ammine-oxo-diperoxovanadate

1982 ◽  
Vol 47 (6) ◽  
pp. 1549-1555 ◽  
Author(s):  
Peter Schwendt ◽  
Miloslav Pisárčik
Keyword(s):  
Raman Spectrum ◽  
Bond Length ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Normal Coordinate Analysis ◽  
Wave Number ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate ◽  
Mass Model ◽  
Vibrational Coupling

Infrared and Raman spectra of solid NH4[VO(O2)2NH3], ND4[VO(O2)2ND3], 14/15NH4[VO(O2)214/15NH3] (about 50% 15N) and Raman spectrum of solution of NH4[VO(O2)2NH3] have been measured. Interpretation of the spectra was complemented by normal coordinate analysis in the approximation of point mass model (NH3). The results have shown that there exists coupling of vibrations of two V(O2) groups, which enables an explanation of differences between spectra of the mono- and diperoxo complexes. The vibrational coupling of VO and OO bonds within one V(O2) group probably causes small sensitivity of wave number of v(O-O) band to changes of d(O-O) bond length.

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