13C NMR spectra of 9-methylcarbazoles and electron conductivity of the carbazole ring

Podrobná bibliografie
Parent link:Chemistry of Heterocyclic Compounds
Vol. 20, iss. 2.— 1984.— [P. 165-170]
Další autoři: Filimonov V. D. Viktor Dmitrievich, Filippova T. A., Lopatinskii V. P., Sukhoroslova M. M.
Shrnutí:Title screen
The effect of substituents in the ring of 9-methylcarbazoles on the 13C NMR chemical shifts was determined. Correlation relationships between the inductive and resonance constants of the substituents and the chemical shifts were found. The transmission properties of the carbazole ring with respect to the electronic effects of substituents in the 3 position were evaluated on the basis of the results obtained. Nonadditivity of the effects of the substituents on the NMR chemical shifts within the limits of one phenyl ring of carbazole relative to monosubstituted benzenes was observed.
Режим доступа: по договору с организацией-держателем ресурса
Vydáno: 1984
Témata:
On-line přístup:http://dx.doi.org/10.1007/BF00506286
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=654461
Popis
Shrnutí:Title screen
The effect of substituents in the ring of 9-methylcarbazoles on the 13C NMR chemical shifts was determined. Correlation relationships between the inductive and resonance constants of the substituents and the chemical shifts were found. The transmission properties of the carbazole ring with respect to the electronic effects of substituents in the 3 position were evaluated on the basis of the results obtained. Nonadditivity of the effects of the substituents on the NMR chemical shifts within the limits of one phenyl ring of carbazole relative to monosubstituted benzenes was observed.
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.1007/BF00506286