Preparation, Infrared and Raman Spectra, and Stereochemistries of Pentacoordinate Trimethylphosphine Complexes, MX4•P(CH3)3 and MX4•P(CD3)3 where M = Ge or Sn and X = Cl or Br

1973 ◽  
Vol 51 (16) ◽  
pp. 2697-2709 ◽  
Author(s):  
D. K. Frieson ◽  
G. A. Ozin
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Axial Ligand ◽  
Axial Position ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate ◽  
X Ray ◽  
Trigonal Bipyramidal ◽  
Equatorial Ligand

The 1:1 adducts MX4•PMe3 (M = Ge or Sn; X = Cl or Br) are prepared by recrystallization of the respective 1:2 complexes from excess MX4 acceptor. Solid state infrared and Raman Spectra and X-ray powder photographs suggest that these adducts are all trigonal bipyramidal with the ligand in an axial position. Normal coordinate calculations in C3v symmetry (axial ligand) and Cs symmetry (equatorial ligand) support this assignment. The rather high ν(MP) frequencies indicate unusually strong metal–phosphorus donor bonds in these compounds.

Vibration spectra of sulphur tetranitride

1981 ◽  
Vol 46 (11) ◽  
pp. 2613-2619 ◽  
Author(s):  
Jiří Toužín
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Normal Coordinate Analysis ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate ◽  
Vibration Spectra

Available data on infrared and Raman spectra of S4N4 in solid state and solutions have been verified and completed. On the basis of normal coordinate analysis an attempt has been made to define with more precision the interpretation of vibration spectra of this compound given in earlier reports.

Vibrational spectra of aquadioxotetra; peroxodivanadates(V) M2[V2O2(O2)4(H2O)]·xH2O (M = N(CH3)4, Cs)

1990 ◽  
Vol 55 (6) ◽  
pp. 1485-1490 ◽  
Author(s):  
Peter Schwendt ◽  
Milan Sýkora
Keyword(s):  
Raman Spectra ◽  
Vibrational Spectra ◽  
Normal Coordinate Analysis ◽  
Force Constants ◽  
Infrared And Raman Spectra ◽  
Empirical Correlations ◽  
Normal Coordinate ◽  
Bond Lengths ◽  
Stretching Vibrations

The infrared and Raman spectra of M2[V2O2(O2)4(H2O)]·xH2O and M2[V2O2(O2)4(D2O)]·xD2O (M = N(CH3)4, Cs) were measured. In the region of the vanadium-oxygen stretching vibrations, the spectra were interpreted based on normal coordinate analysis, employing empirical correlations between the bond lengths and force constants.

scholarly journals Infrared and Raman Spectra of Chloral, and Normal Coordinate Analyses of Acetaldehyde, Fluoral, Chloral, and Bromal.

1971 ◽  
Vol 25 ◽  
pp. 813-832 ◽  
Author(s):  
G. Hagen ◽  
Kjeld Schaumburg ◽  
Karl-Axel Wilhelmi ◽  
A. A. Lindberg ◽  
Inger Lagerlund ◽  
...  
Keyword(s):  
Raman Spectra ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate

The Vibrational Spectrum and Urey-Bradley Force Constants of the Trifluoromethyltrifluoroborate(1-) Anion

1973 ◽  
Vol 27 (3) ◽  
pp. 209-213 ◽  
Author(s):  
John F. Jackovitz ◽  
Charles E. Falletta ◽  
James C. Carter
Keyword(s):  
Potential Energy ◽  
Vibrational Spectrum ◽  
Energy Distribution ◽  
Force Field ◽  
Raman Spectra ◽  
Normal Modes ◽  
Force Constants ◽  
Potential Energy Distribution ◽  
Infrared And Raman Spectra ◽  
Normal Coordinate

Infrared and Raman spectra for (K+) (CF3BF3−) have been obtained from 4000 to 50 cm−1. Spectral assignments were made on the basis of C3v symmetry using both 10B and 11B compounds. In addition, a normal coordinate analysis was performed to obtain the potential energy distribution of the normal modes. A Urey-Bradley type force field was used, and force constants obtained for the CF3 and BF3 groupings were compared to those in C2F6 and BF4−.

Low frequency infrared and Raman spectra of the N,N,N′,N′-tetramethyl-ethylenediamine adducts of the Group IIb dihalides

1970 ◽  
Vol 48 (1) ◽  
pp. 181-184 ◽  
Author(s):  
M. H. Abraham ◽  
F. W. Parrett
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Low Frequency ◽  
Infrared And Raman Spectra ◽  
Cadmium Complexes ◽  
Mercury Complexes ◽  
Vibrational Bands

A study of the low frequency vibrational spectra of the complexes MX2.TMED (where M = Zn, Cd, Hg; X = Cl, Br, I; TMED = N,N,N′,N′-tetramethylethylenediamine suggests that in the solid state the zinc and mercury complexes are 4-coordinated but the cadmium complexes are all based on octahedral halogen bridged structures. Assignments of the vibrational bands are discussed.

INFRARED AND RAMAN SPECTRA OF 1-CHLOROPROPYNE AND 1-CHLOROPROPYNE-d3

1955 ◽  
Vol 33 (7) ◽  
pp. 1226-1249 ◽  
Author(s):  
D. W. Davidson ◽  
H. J. Bernstein
Keyword(s):  
Raman Spectra ◽  
Isotope Effects ◽  
Infrared And Raman Spectra ◽  
Coriolis Coupling ◽  
Coupling Coefficients ◽  
Normal Coordinate ◽  
Vapor State ◽  
Complete Assignment ◽  
Stretching Vibration ◽  
Normal Coordinate Calculation

The infrared spectra of 1-chloropropyne and 1-chloropropyne-d3 have been investigated in the vapor state, in solution, and, in part, in the liquid over the spectral region 3 to 35 μ. Intensities of the infrared bands have been measured from the spectra of the solutions. The Raman spectra of the compounds in the liquid state, together with standard intensities and depolarization ratios of the Raman bands, were obtained. A complete assignment, based on a normal-coordinate calculation of the fundamentals, has been made. Coriolis coupling coefficients of three of the perpendicular-type fundamentals of CH3≡CCl were determined and those of the other two shown to be near unity. Two coupling coefficients for CD3C≡CCl were obtained. The potential function and isotope effects on Raman intensity and Raman displacement of the CCl stretching vibration are discussed.

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