A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles

1H and 13C nmr spectra of several N- and C-substituted carbazoles (Series 1, 2, 3 and 4) were measured. Correlations between chemical shifts and substituent constants show that these parameters describe properly the substituent effect on the nmr phenomena. Atomic charge densities for carbazoles of S...

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Publicado: 2004
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v41_n2_p161_Bonesi
http://hdl.handle.net/20.500.12110/paper_0022152X_v41_n2_p161_Bonesi
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spelling paper:paper_0022152X_v41_n2_p161_Bonesi2023-06-08T14:46:49Z A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles 1 aminocarbazole 1 benzoylcarbazole 1 bromocarbazole 1 chlorocarbazole 1 iodocarbazole 1 nitrocarbazole 2 hydroxycarbazole 3 (2 oxopropyl)carbazole 3 (n,n dimethylamino) n ethylcarbazole 3 acetamido n ethylcarbazole 3 acetyl 2 hydroxycarbazole 3 amino n ethylcarbazole 3 benzenesulfonyl 2 hydroxycarbazole 3 benzoyl 2 hydroxycarbazole 3 benzoylcarbazole 3 bromo 2 hydroxycarbazole 3 bromocarbazole 3 chloro 2 hydroxycarbazole 3 chlorocarbazole 3 iodocarbazole 3 nitrocarbazole carbazole derivative n acetylcarbazole n benzoylcarbazole n benzylcarbazole n methylcarbazole n phenylcarbazole unclassified drug acetylation article carbon nuclear magnetic resonance chemical structure photolysis proton nuclear magnetic resonance synthesis 1H and 13C nmr spectra of several N- and C-substituted carbazoles (Series 1, 2, 3 and 4) were measured. Correlations between chemical shifts and substituent constants show that these parameters describe properly the substituent effect on the nmr phenomena. Atomic charge densities for carbazoles of Series 1, 2, 3 and 4 were calculated by using the semi empirical PM3 method. These values also show a linear correlation with the 13C chemical shifts. The synthesis of several carbazole derivatives 1a - 1g, 2a - 2g, 3a - 3j and 4a - 4g have been carried out according to literature procedures. The carbazoles 3i, 3j and 4c have been synthesized and fully characterized for the first time. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v41_n2_p161_Bonesi http://hdl.handle.net/20.500.12110/paper_0022152X_v41_n2_p161_Bonesi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 1 aminocarbazole
1 benzoylcarbazole
1 bromocarbazole
1 chlorocarbazole
1 iodocarbazole
1 nitrocarbazole
2 hydroxycarbazole
3 (2 oxopropyl)carbazole
3 (n,n dimethylamino) n ethylcarbazole
3 acetamido n ethylcarbazole
3 acetyl 2 hydroxycarbazole
3 amino n ethylcarbazole
3 benzenesulfonyl 2 hydroxycarbazole
3 benzoyl 2 hydroxycarbazole
3 benzoylcarbazole
3 bromo 2 hydroxycarbazole
3 bromocarbazole
3 chloro 2 hydroxycarbazole
3 chlorocarbazole
3 iodocarbazole
3 nitrocarbazole
carbazole derivative
n acetylcarbazole
n benzoylcarbazole
n benzylcarbazole
n methylcarbazole
n phenylcarbazole
unclassified drug
acetylation
article
carbon nuclear magnetic resonance
chemical structure
photolysis
proton nuclear magnetic resonance
synthesis
spellingShingle 1 aminocarbazole
1 benzoylcarbazole
1 bromocarbazole
1 chlorocarbazole
1 iodocarbazole
1 nitrocarbazole
2 hydroxycarbazole
3 (2 oxopropyl)carbazole
3 (n,n dimethylamino) n ethylcarbazole
3 acetamido n ethylcarbazole
3 acetyl 2 hydroxycarbazole
3 amino n ethylcarbazole
3 benzenesulfonyl 2 hydroxycarbazole
3 benzoyl 2 hydroxycarbazole
3 benzoylcarbazole
3 bromo 2 hydroxycarbazole
3 bromocarbazole
3 chloro 2 hydroxycarbazole
3 chlorocarbazole
3 iodocarbazole
3 nitrocarbazole
carbazole derivative
n acetylcarbazole
n benzoylcarbazole
n benzylcarbazole
n methylcarbazole
n phenylcarbazole
unclassified drug
acetylation
article
carbon nuclear magnetic resonance
chemical structure
photolysis
proton nuclear magnetic resonance
synthesis
A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
topic_facet 1 aminocarbazole
1 benzoylcarbazole
1 bromocarbazole
1 chlorocarbazole
1 iodocarbazole
1 nitrocarbazole
2 hydroxycarbazole
3 (2 oxopropyl)carbazole
3 (n,n dimethylamino) n ethylcarbazole
3 acetamido n ethylcarbazole
3 acetyl 2 hydroxycarbazole
3 amino n ethylcarbazole
3 benzenesulfonyl 2 hydroxycarbazole
3 benzoyl 2 hydroxycarbazole
3 benzoylcarbazole
3 bromo 2 hydroxycarbazole
3 bromocarbazole
3 chloro 2 hydroxycarbazole
3 chlorocarbazole
3 iodocarbazole
3 nitrocarbazole
carbazole derivative
n acetylcarbazole
n benzoylcarbazole
n benzylcarbazole
n methylcarbazole
n phenylcarbazole
unclassified drug
acetylation
article
carbon nuclear magnetic resonance
chemical structure
photolysis
proton nuclear magnetic resonance
synthesis
description 1H and 13C nmr spectra of several N- and C-substituted carbazoles (Series 1, 2, 3 and 4) were measured. Correlations between chemical shifts and substituent constants show that these parameters describe properly the substituent effect on the nmr phenomena. Atomic charge densities for carbazoles of Series 1, 2, 3 and 4 were calculated by using the semi empirical PM3 method. These values also show a linear correlation with the 13C chemical shifts. The synthesis of several carbazole derivatives 1a - 1g, 2a - 2g, 3a - 3j and 4a - 4g have been carried out according to literature procedures. The carbazoles 3i, 3j and 4c have been synthesized and fully characterized for the first time.
title A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
title_short A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
title_full A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
title_fullStr A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
title_full_unstemmed A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles
title_sort study of substituent effect on 1h and 13c nmr spectra of n- and c-substituted carbazoles
publishDate 2004
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v41_n2_p161_Bonesi
http://hdl.handle.net/20.500.12110/paper_0022152X_v41_n2_p161_Bonesi
_version_ 1768546054130630656