The Raman parameters (frequency, intensity and depolarization ratio) of the VI-I band of charge transfer complexes of iodine with several pyridine derivatives have been studied in dichloromethane solution at 296 OK. Complex formation brings about an enhancement of the intensity and depolarization de
Vibrational spectra of the charge transfer complexes between organic sulfides and iodine
β Scribed by T. Tveter; P. Klaeboe; C.J. Nielsen
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 798 KB
- Volume
- 40
- Category
- Article
- ISSN
- 1386-1425
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β¦ Synopsis
1.r. spectra of the charge transfer complexes between nine organic sulfides (as well as diethvlselenide) with iodine were recorded between 1SOOand 400 cm-' in CS, and Ccl, solutions and in the region 60&50&1-' in C61-l~2 and C6Hs solutions. Raman spectra of the complexes were recorded below 600 cm-'. For each system, i.r. and Raman bands in the 2OG160 cm-' were assigned to the I-I stretching mode of the complex. Additional i.r. bands below 160cm-', absent in Raman, were ascribed to intermolecular S..I stretching vibrations. The integral intensities of these bands were determined and correlated with the thermodynamic functions. Some Raman active fundamentals of 1,4dithiane became i.r. active in the iodine complex in accordance with a break down of the Czi symmetry. A force constant calculation was carried out for the dimethylsulfideiodine complex and simplified calculations of the three point mass models were made for all the systems.
π SIMILAR VOLUMES
The far infrared spectra of some complexes of pyridines with iodine and bromine have been studied in benzene solution. The infrared intensity of the halogen stretching vibration band has been determined for several complexes with different substituted pyridines. A calculation of transition moments a
The enthalpies of formation for charge transfer complexes of the type [R&1.1,] (R = CH3, C2F5, n-C3H,, n-&H,) have been measured by calorimetry. The data are analysed using Mulliken's resonance structure theory, to produce the different energy contributions to the formation ofand the charge transfer