NEAR-INFRARED FOURIER-TRANSFORM RAMAN-SPECTRA OF PROTONATED AND DEUTERATED TRANS-AZOBENZENE ISOTOPOMERS

Citation
V. Smrecki et al., NEAR-INFRARED FOURIER-TRANSFORM RAMAN-SPECTRA OF PROTONATED AND DEUTERATED TRANS-AZOBENZENE ISOTOPOMERS, Journal of molecular structure, 408, 1997, pp. 405-408
Citations number
14
Categorie Soggetti
Chemistry Physical
ISSN journal
00222860
Volume
408
Year of publication
1997
Pages
405 - 408
Database
ISI
SICI code
0022-2860(1997)408:<405:NFROPA>2.0.ZU;2-V
Abstract
Near-infrared Fourier transform (NIR FT) Raman spectra of five irans-a zobenzene isotopomers and their protonated and deuterated forms were r ecorded. Trifluoroacetic acid was found to be a good protonation agent for measuring Raman spectra of protonated azobenzene. An assignment o f the most relevant vibrational modes (N=N stretching and N-H/N-H-2 in -plane bending) of the protonated and deuterated species is proposed. The N=N stretching band in irans-azobenzene isotopomers decreases by a bout 40 cm(-1) upon protonation, while it varies within +/- 10 cm(-1) upon deuteration with respect to the unprotonated (undeuterated) form. A comparison is made with the protonated form of the isoelectronic tr ans-N-benzylideneaniline. (C) 1997 Elsevier Science B.V.