Pregled bibliografske jedinice broj: 7442
Intrinsic Deuterium Induced Isotope Effects in C-13 NMR Spectra of Protonated Benzylideneaniline and Azobenzene Isotopomers
Intrinsic Deuterium Induced Isotope Effects in C-13 NMR Spectra of Protonated Benzylideneaniline and Azobenzene Isotopomers // Book of Abstracts (http://ocwww.chemie.uni-linz.ac.at/posters.html) / Mueller, Nobert (ur.).
Linz: Johannes Kepler University Linz, 1997. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Intrinsic Deuterium Induced Isotope Effects in C-13 NMR Spectra of Protonated Benzylideneaniline and Azobenzene Isotopomers
Autori
Smrečki, Vilko ; Vikić-Topić, Dražen ; Novak, Predrag ; Meić, Zlatko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts (http://ocwww.chemie.uni-linz.ac.at/posters.html)
/ Mueller, Nobert - Linz : Johannes Kepler University Linz, 1997
Skup
International Symposion on Advances in NMR
Mjesto i datum
Linz, Austrija, 18.02.1997. - 19.02.1997
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Sažetak
Differently deuterium labelled trans-N-benzylideneaniline (1) and trans-azobenzene (2) isotopomers were prepared, protonated and studied by C-13 NMR spectroscopy. A number of deuterium isotope effects (DIE) on C-13 chemical shifts have been observed for protonated and unprotonated species.
The protonation was performed by CF_3COOH and spectra measured in C_6D_6 solution. The changes of magnitude, sign and extent of isotope effects in unprotonated and protonated trans-N-benzylideneaniline and trans-azobenzene isotopomers are quite different, what together with only four observed bands in C-13 NMR spectra of protonated trans-azobenzene indicate the fast proton exchange in that molecule (not possible in trans-N-benzylideneaniline). The importance of steric effects and lone-pair interactions in transmission of isotope effects is also discussed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija