The wavenumbers of C=O stretching vibrations of maleinimides

1985 ◽  
Vol 50 (6) ◽  
pp. 1305-1311 ◽  
Author(s):  
Alexander Perjéssy ◽  
Manfred Augustin ◽  
Manfred Köhler
Keyword(s):  
Experimental Data ◽  
Infrared Spectra ◽  
Linear Correlation ◽  
Vibrational Coupling ◽  
Stretching Vibrations

The infrared spectra in the region of fundamental C=O stretching vibrations in tetrachloromethane and chloroform were measured for 59 maleinimide derivatives. A linear correlation between the wavenumbers of symmetric and antisymmetric C=O stretching vibrations was found for a series of 102 experimental data obtained in both solvents. The slope of the νs(C=O) vs νas(C=O) dependence as well as the degree of the vibrational coupling in imide system were discussed and compared with those for analogical five-membered cyclic 1,3-diketones.

scholarly journals CONTRIBUTION TO THE INFRARED SPECTRA OF ORGANOSULPHUR COMPOUNDS

1964 ◽  
Vol 42 (1) ◽  
pp. 36-42 ◽  
Author(s):  
C. N. R. Rao ◽  
R. Venkataraghavan ◽  
T. R. Kasturi
Keyword(s):  
Infrared Spectra ◽  
Relative Intensity ◽  
Normal Coordinate ◽  
Vibrational Coupling ◽  
Fermi Interaction ◽  
Stretching Vibrations ◽  
Marked Dependence ◽  
Coordinate Treatment

Infrared spectra of various types of organosulphur compounds have been examined and group frequencies arising from G—S, S—S, N—S, O—S, and C=S stretching vibrations have been assigned and discussed. The C—S bands of thioketals and S—S bands of tri- and tetra-sulphides show splittings due to vibrational coupling. The O—S and N—S stretching frequencies are found around 890 and 820 cm−1 respectively, values which are much higher than the C—S stretching frequencies. Potassium alkyl xanthates exhibit the asymmetric and symmetric stretching frequencies of the CS2− ion. The splitting of C—O and C=S stretching bands in dialkyl dixanthogens have been interpreted in terms of the Fermi interaction with the combination tone of C—S and S—S stretching vibrations and with the overtone of S—S stretching vibrations respectively. The relative intensity of the C=S stretching bands in a few derivatives show marked dependence on the electronegativities of the elements directly linked to the thiocarbonyl group. It is found that the earlier assignments of the "[Formula: see text] bands" due to mixed vibrations in thioamide type derivatives have been found to be well justified on the basis of the recent normal coordinate treatment. Another band tentatively designated as the "[Formula: see text] IV band" has been assigned for these derivatives in the region 850–680 cm−1. Examination of the spectra of a number of thioamide type derivatives has shown no evidence for the presence of thiol tautomers. All of them exist as thiones exhibiting characteristic N—H absorption and "[Formula: see text] bands".

Infrared spectra and substituent effects in 2-(3-, and 4-substituted phenylmethylene)-1,3-cycloheptanediones

1983 ◽  
Vol 48 (2) ◽  
pp. 586-595 ◽  
Author(s):  
Alexander Perjéssy ◽  
Pavol Hrnčiar ◽  
Ján Šraga
Keyword(s):  
Substituent Effects ◽  
Phenyl Group ◽  
Wave Number ◽  
Vibrational Coupling ◽  
Wave Numbers ◽  
Stretching Vibration ◽  
Stretching Vibrations ◽  
The Relationship ◽  
Derivatives Of ◽  
Effect Of Structure

The wave numbers of the fundamental C=O and C=C stretching vibrations, as well as that of the first overtone of C=O stretching vibration of 2-(3-, and 4-substituted phenylmethylene)-1,3-cycloheptanediones and 1,3-cycloheptanedione were measured in tetrachloromethane and chloroform. The spectral data were correlated with σ+ constants of substituents attached to phenyl group and with wave number shifts of the C=O stretching vibration of substituted acetophenones. The slope of the linear dependence ν vs ν+ of the C=C stretching vibration of the ethylenic group was found to be more than two times higher than that of the analogous correlation of the C=O stretching vibration. Positive values of anharmonicity for asymmetric C=O stretching vibration can be considered as an evidence of the vibrational coupling in a cyclic 1,3-dicarbonyl system similarly, as with derivatives of 1,3-indanedione. The relationship between the wave numbers of the symmetric and asymmetric C=O stretching vibrations indicates that the effect of structure upon both vibrations is symmetric. The vibrational coupling in 1,3-cycloheptanediones and the application of Seth-Paul-Van-Duyse equation is discussed in relation to analogous results obtained for other cyclic 1,3-dicarbonyl compounds.

Synthesis, spectral and electrochemical study of coordination molecules Cu4OX6L4: 4-cyanopyridine Cu4OBrnCl(6−n)(4-CNpy)4 complexes

2010 ◽  
Vol 64 (3) ◽  
Author(s):  
Gregor Ondrejovič ◽  
Adela Kotočová ◽  
Marian Koman ◽  
Peter Segľa
Keyword(s):  
Cyclic Voltammetry ◽  
Infrared Spectra ◽  
Electronic Spectra ◽  
Pyridine Ring ◽  
Pyridine Complexes ◽  
Half Wave ◽  
Out Of Plane ◽  
Donor Acceptor ◽  
Back Bonding ◽  
Stretching Vibrations

AbstractNew 4-cyanopyridine halide and mixed-halide Cu4OBrnCl(6−n)(4-CNpy)4 complexes (4-CNpy = 4-cyanopyridine, n = 0–6) were synthesised, characterised, and studied by infrared spectra, electronic spectra, and cyclic voltammetry. Infrared spectra revealed donor-acceptor vibrational couplings of the Cu4O, Cu-Cl, and Cu-N stretching vibrations with the in-plane and out-of-plane pyridine ring vibrations. The infrared spectra, electronic spectra, and half-wave potentials correspond to a weak donor and a strong acceptor behaviour of the 4-cyanopyridine ligands and to π-back bonding, Cu(II)→pyridine rings. The results were compared with the related pyridine and 4-substituted pyridine complexes.

scholarly journals Laboratory Spectra of Amorphous and Crystalline Olivine: An Application to Comet Halley IR Spectrum

1991 ◽  
Vol 126 ◽  
pp. 125-128 ◽  
Author(s):  
A. Blanco ◽  
V. Orofino ◽  
E. Bussoletti ◽  
S. Fonti ◽  
L. Colangeli ◽  
...  
Keyword(s):  
Experimental Data ◽  
Infrared Spectra ◽  
Ir Spectrum ◽  
Emission Feature ◽  
Cosmic Dust ◽  
Dust Grains ◽  
Natural Mineral ◽  
The Third ◽  
Different Types ◽  
Comet Halley

AbstractAmong the various silicates proposed as components of cosmic dust grains, olivine is considered one of the most likely materials. In this work we present the infrared spectra of three different types of olivine grains: crystalline, amorphous and synthetic (also amorphous). While the first and second sample derive from the same natural mineral, the third one has been prepared in the laboratory according to the relative cosmic abundances of the elements. The experimental data are used to fit the emission feature observed in the comet Halley spectrum between 8 and 13μm.Satisfactory results are obtained by using synthetic olivine mixed with a small amount (5%) of crystalline grains.

The infrared spectra of theobromine salts

1967 ◽  
Vol 45 (23) ◽  
pp. 2899-2902 ◽  
Author(s):  
Denys Cook ◽  
Zephyr R. Regnier
Keyword(s):  
Hydrogen Bond ◽  
Nitrogen Atom ◽  
Infrared Spectra ◽  
Imidazole Ring ◽  
Free Base ◽  
Absorption Bands ◽  
Out Of Plane ◽  
Stretching Vibrations ◽  
Deformation Modes ◽  
Infrared Absorption Bands

From the infrared spectra of theobromine salts it is concluded that the salts are probably arranged in hydrogen-bonded centrosymmetric pairs involving [Formula: see text] interactions. [Formula: see text] anion− hydrogen bonds are formed by protonation of the free nitrogen atom (N9) in the imidazole ring. Infrared absorption bands arising from the former hydrogen bond constantly appear near 3 000 cm−1, whereas those from the latter shift from 2 580 to 3 300 cm−1, depending on the anion. In-plane NH and N+H deformation modes give bands near 1 485 and 1 160 cm−1, respectively. Out-of-plane NH modes have been located, but precise assignments are not possible.The assignments for some other bands which show deuteration shifts are detailed, and the carbonyl stretching vibrations which increase in frequency on protonation of the free base are identified.

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