Vibrational spectra of cyclopentadienyltrimethylplatinum(IV)

1971 ◽  
Vol 24 (5) ◽  
pp. 911 ◽  
Author(s):  
JR Hall ◽  
BE Smith
Keyword(s):  
Solid State ◽  
Spectral Data ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Local Symmetry ◽  
Stretching Vibrations ◽  
Polarized Raman

The Raman spectra of cyclopentadienyltrimethylplatinum(IV) in the solid state and solution have been recorded and interpreted in conjunction with the corresponding infrared spectra over the range 4000-30 cm-1. Assignments have been made on the basis of local symmetry. Polarized Raman lines at 561 and 263 cm-1 have been assigned to symmetric Pt-CH3 stretching and Pt-cp stretching vibrations respectively. The spectral data are consistent with a pentahapto π-bonded cp ring.

The vibrational spectra of 4-pyridone, and its 2,3,5,6-tetradeutero, N-deutero, N-methyl, N-cyano, and 3,5-dihalogeno derivatives. Mixing between C=C and C=O stretching vibrations

1969 ◽  
Vol 22 (12) ◽  
pp. 2581 ◽  
Author(s):  
BD Batts ◽  
E Spinner
Keyword(s):  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Parent Compound ◽  
The Other ◽  
Medium Effects ◽  
Oxide Structure ◽  
Stretching Vibrations ◽  
Electron Withdrawing Substituents

The infrared spectra of the above compounds, and the Raman spectra of the parent compound and its 2,3,5,6-D4, 1-D, and 1-Me derivatives have been determined. The effects of electron-withdrawing substituents, N- methylation, and deuteration on the two intense infrared bands in the 1480-1650 cm-1 region are not compatible with one being a C=O and the other a C=C stretching band. These two vibrations must be extensively mixed; occasionally very pronounced medium effects, which are not straightforward, are observed for one or both of these bands. The spectra are not in accord with a mostly zwitterionic (N-protonated pyrid-4-oxide) structure (II) of 4-pyridone. Band assignments are made for the parent compound.

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.

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.

THE VIBRATIONAL SPECTRA OF THE FORMATE, ACETATE, AND OXALATE IONS

1956 ◽  
Vol 34 (2) ◽  
pp. 170-178 ◽  
Author(s):  
K. Ito ◽  
H. J. Bernstein
Keyword(s):  
Aqueous Solution ◽  
Raman Spectra ◽  
Infrared Spectra ◽  
Vibrational Spectra ◽  
Vibrational Assignments ◽  
Oxalate Ions ◽  
Oxalate Ion ◽  
Depolarization Ratios

The infrared spectra of the formate, acetate, and oxalate ions have been obtained for both the solid and aqueous solution. The Raman spectra of these ions with depolarization ratios have been obtained in aqueous solution. Vibrational assignments have been made which differ slightly for the acetate ion and more markedly for the oxalate ion from earlier work. The depolarization ratios confirm Fonteyne’s assignment for the formate ion.

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.

Darstellung und Schwingungsspektren von Alkyl-und Rhodanohydrohexaboraten / Preparation and Vibrational Spectra of Alkyl and Rhodano Hydrohexaborates

1988 ◽  
Vol 43 (10) ◽  
pp. 1327-1331 ◽  
Author(s):  
A Heinrich ◽  
W Preetz
Keyword(s):  
Frequency Shift ◽  
Raman Spectra ◽  
Organic Solvents ◽  
Vibrational Spectra ◽  
High Frequency ◽  
Acidity Constants ◽  
High Frequency Shift ◽  
Basic Solutions ◽  
Stretching Vibrations ◽  
Ir And Raman

Treatment of B6H62- with iodoalkanes and (SCN)2 in organic solvents affords the monosubstituted protonated hexaborates RB6H6-, R = CH3, C2H5< C3H7, C4H9, C8H17 and SCN, respectively. The acidity constants of these weak Brönsted acids range for the alkylated species from 8.8 to 9.6, and for R = SCN the pka value is ~5. From basic solutions the salts Cs2RB6H5 can be precipitated, which show band patterns in the IR and Raman spectra typical for monosubstituted hydrohexaborates. The protonated compounds RB6H6- are distinguished from the corresponding Brönsted bases RB6H52- by a high frequency shift of the BH stretching vibrations in the order of 100 cm-1. For Cs2(SCN)B6H5, S coordination of SCN- is supposed because of the high frequency of νCN: 2144 cm-1.

The influence of hydrogen bonding on the character of N—H and C=O stretching modes in 2-thiopyrrole-1,2-dicarboximide

1984 ◽  
Vol 62 (9) ◽  
pp. 1845-1849 ◽  
Author(s):  
Shanker Ram
Keyword(s):  
Hydrogen Bonding ◽  
Transition Temperature ◽  
Solid State ◽  
Hydrogen Bonds ◽  
Spectral Data ◽  
Infrared Spectra ◽  
Cyclic Dimer ◽  
Dilute Solutions ◽  
Two Phases ◽  
Thermodynamical Functions

The infrared spectra (200–4000 cm−1) of 2-thiopyrrole-1,2-dicarboximide (TPH) in solid and solution forms have been measured as a function of temperature, and a direct correlation has been obtained between the two phases and the type and extent of hydrogen bonding. It is suggested that TPH exists as cyclic dimer in the solid state (below 310 K) and in dilute solutions by the formation of two equivalent hydrogen bonds. At the transition temperature, ~310 K, the cyclic dimer undergoes to the open-cyclic dimer and persists in this structure till 410 K. In addition, the thermodynamical functions ΔH0, and ΔS0 have been estimated using the spectral data in solution.

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.

Die Schwingungsspektren der Silylanionen (SiH3)nSiH⊖3-n und (SiD3)nSiD⊖3-n / Vibrational Spectra of the Silyl Anions (SiH3)nSiH⊖3-n and (SiD3)nSiD⊖3-n

1974 ◽  
Vol 29 (9-10) ◽  
pp. 647-653 ◽  
Author(s):  
Hans Bürger ◽  
Reint Eujen
Keyword(s):  
Raman Spectra ◽  
Vibrational Spectra ◽  
Negative Charge ◽  
Lone Pair ◽  
Normal Coordinate Analysis ◽  
Ir And Raman Spectra ◽  
Normal Coordinate ◽  
Normal Vibrations ◽  
Stretching Vibrations ◽  
Ir And Raman

The IR and Raman spectra of SiH3⊖, SiH3SiH2⊖, (SiH3)2SiH⊖, (SiH3)3Si⊖ and their deuterated derivatives have been recorded in HMPT and HMPT-d18 solutions. Most normal vibrations have been identified. The SiH and SiSi stretching vibrations are considerably lower than for analogous silanes and silylphosphines, ∼ 2050 and 1850-1900 cm-1 being characteristic for SiH3 and SiH⊖n groups respectively. The assignments are proved by a normal coordinate analysis, and force constants have been calculated. The negative charge is mainly localized on the trivalent Si atom and the lone pair acts repulsively rather than strengthening the SiSi bond through (p→d)π effects.

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