Zeise's Salt, K[Pt(C2H4)Cl3], Anhydrous and Monohydrate and the Platinum–Olefin Interaction

1972 ◽  
Vol 50 (10) ◽  
pp. 1596-1600 ◽  
Author(s):  
J. Hubert ◽  
P. C. Kong ◽  
F. D. Rochon ◽  
T. Theophanides
Keyword(s):  
Double Bond ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Ring Structure ◽  
Original Method ◽  
Platinum Atom ◽  
New Method ◽  
Laser Raman ◽  
Laser Raman Spectra

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.

Vibrational spectra of some perfluoro-arsenates and antimonates with nitrogen heterocations

1970 ◽  
Vol 48 (20) ◽  
pp. 3117-3123 ◽  
Author(s):  
A. M. Qureshl ◽  
F. Aubke
Keyword(s):  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Mutual Exclusion ◽  
Laser Raman ◽  
Laser Raman Spectra ◽  
Almost All

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.

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
Keyword(s):  
Organic Chemistry ◽  
Raman Spectroscopy ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Double Bonds ◽  
Laser Raman ◽  
Laser Raman Spectra

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.

Vibrational spectra of η5-cyclopentadienyldicarbonyl(thiocarbonyl)-manganese(I) and η5-cyclopentadienylcarbonyl(dithiocarbonyl)-manganese(I)

1976 ◽  
Vol 54 (1) ◽  
pp. 110-117 ◽  
Author(s):  
G. G. Barna ◽  
I. S. Butler ◽  
K. R. Plowman
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Vapor Phase ◽  
Vibrational Spectra ◽  
State Data ◽  
Laser Raman ◽  
Change Of State ◽  
Laser Raman Spectra ◽  
Local Symmetries ◽  
Phase Solution

The ir and laser Raman spectra of η5-C5H5Mn(CO)2(CS) and η5-C5H5Mn(CO)(CS)2 have been investigated. In the case of the monothiocarbonyl complex, vapor phase, solution, and solid-state measurements were made, while for the dithiocarbonyl, only solid-state data were obtained. The vibrational spectra of both complexes have been assigned satisfactorily in terms of the C5v and Cs local symmetries of the η5-C5H5—Mn and Mn(CO)2(CS) (or Mn(CO)(CS)2) moieties, respectively. The effect of change of state on the spectra of the monothiocarbonyl complex is discussed.

Vibrational spectra of halopentacarbonylmanganese(I) derivatives

1969 ◽  
Vol 47 (22) ◽  
pp. 4117-4128 ◽  
Author(s):  
I. S. Butler ◽  
H. K. Spendjian
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Vibrational Spectra ◽  
Low Frequency ◽  
Laser Raman ◽  
Laser Raman Spectra

The solid-state infrared (i.r.) and laser Raman spectra of the halopentacarbonylmanganese(I) derivatives, Mn(CO)5X (X = Cl, Br,and I), have been recorded in the C—O stretching and the low frequency (700–33 cm−1) regions. The i.r. overtone and combination spectra recorded in the regions 2800–2250 and 1350–700 cm−1 have been used to help in the assignment of some of the low frequency fundamentals. The solid-state i.r. and laser Raman spectra of the dimeric halotetracarbonylmanganese(I) derivatives, [Mn(CO)4X]2 (X = Br and I), have been recorded in the C—O stretching and the low frequency regions for comparative purposes and shown to be consistent with the expected D2h symmetry of the molecules.

Vibrational spectra of substituted toluenes – 4-amino-3-bromotoluene and 5-amino-2-bromotoluene

1984 ◽  
Vol 62 (11) ◽  
pp. 2238-2244 ◽  
Author(s):  
N. Syam Sundar
Keyword(s):  
Raman Spectra ◽  
Infrared Absorption ◽  
Vibrational Spectra ◽  
Vibrational Analysis ◽  
Laser Raman ◽  
Laser Raman Spectra ◽  
Substituted Toluenes

The infrared absorption and laser Raman spectra of 4-amino-3-bromotoluene and 5-amino-2-bromotoluene have been recorded. The vibrational analysis is presented assuming Cs symmetry for the molecules.

Vibrations moléculaires du nitrate de di-μ-hydroxo-bis(diammine) platine (II) [(NH3)2Pt(OH)2Pt(NH3)2] (NO3)2. Partie 1: étude spectroscopique Raman et infrarouge

1982 ◽  
Vol 60 (17) ◽  
pp. 2216-2221 ◽  
Author(s):  
Michel Manfait ◽  
Alain J. P. Alix ◽  
Jacqueline Delaunay-Zeches ◽  
Théophile Theophanides
Keyword(s):  
Solid State ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Nitrate Ion ◽  
Laser Raman ◽  
Square Planar ◽  
Laser Raman Spectra

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.

An interpretation of the low-frequency lines seen in the laser Raman spectra of living cells

1983 ◽  
Vol 96 (3) ◽  
pp. 157-159 ◽  
Author(s):  
Ernesto Rottoli
Keyword(s):  
Raman Spectra ◽  
Low Frequency ◽  
Living Cells ◽  
Laser Raman ◽  
Laser Raman Spectra
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