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spelling todo:paper_0022152X_v41_n2_p161_Bonesi2023-10-03T14:27:48Z A study of Substituent Effect on 1H and 13C nmr Spectra of N- and C-Substituted Carbazoles Bonesi, S.M. Ponce, M.A. Erra-Balsells, R. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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
Bonesi, S.M.
Ponce, M.A.
Erra-Balsells, R.
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.
format JOUR
author Bonesi, S.M.
Ponce, M.A.
Erra-Balsells, R.
author_facet Bonesi, S.M.
Ponce, M.A.
Erra-Balsells, R.
author_sort Bonesi, S.M.
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
url http://hdl.handle.net/20.500.12110/paper_0022152X_v41_n2_p161_Bonesi
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AT poncema studyofsubstituenteffecton1hand13cnmrspectraofnandcsubstitutedcarbazoles
AT errabalsellsr studyofsubstituenteffecton1hand13cnmrspectraofnandcsubstitutedcarbazoles
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