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Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring

Novel carbazole-based [6]helicenes fused with an azine ring (pyridine, pyrazine or quinoxaline) have been prepared through a five-step synthetic sequence in good overall yields. Commercially available 2,3-dihaloazines were used as starting materials. To discern the effect of merging an azine moiety...

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Autores principales: Tonkoglazova, Daria I, Gulevskaya, Anna V, Chistyakov, Konstantin A, Askalepova, Olga I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801798/
https://www.ncbi.nlm.nih.gov/pubmed/33488827
http://dx.doi.org/10.3762/bjoc.17.2
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author Tonkoglazova, Daria I
Gulevskaya, Anna V
Chistyakov, Konstantin A
Askalepova, Olga I
author_facet Tonkoglazova, Daria I
Gulevskaya, Anna V
Chistyakov, Konstantin A
Askalepova, Olga I
author_sort Tonkoglazova, Daria I
collection PubMed
description Novel carbazole-based [6]helicenes fused with an azine ring (pyridine, pyrazine or quinoxaline) have been prepared through a five-step synthetic sequence in good overall yields. Commercially available 2,3-dihaloazines were used as starting materials. To discern the effect of merging an azine moiety within a helical skeleton, the X-ray structures, UV–vis absorption and fluorescence spectra of the helicenes were investigated and compared to that of the parent carbazole-based [6]helicene (7H-phenanthro[3,4-c]carbazole).
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spelling pubmed-78017982021-01-22 Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring Tonkoglazova, Daria I Gulevskaya, Anna V Chistyakov, Konstantin A Askalepova, Olga I Beilstein J Org Chem Full Research Paper Novel carbazole-based [6]helicenes fused with an azine ring (pyridine, pyrazine or quinoxaline) have been prepared through a five-step synthetic sequence in good overall yields. Commercially available 2,3-dihaloazines were used as starting materials. To discern the effect of merging an azine moiety within a helical skeleton, the X-ray structures, UV–vis absorption and fluorescence spectra of the helicenes were investigated and compared to that of the parent carbazole-based [6]helicene (7H-phenanthro[3,4-c]carbazole). Beilstein-Institut 2021-01-04 /pmc/articles/PMC7801798/ /pubmed/33488827 http://dx.doi.org/10.3762/bjoc.17.2 Text en Copyright © 2021, Tonkoglazova et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms)
spellingShingle Full Research Paper
Tonkoglazova, Daria I
Gulevskaya, Anna V
Chistyakov, Konstantin A
Askalepova, Olga I
Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title_full Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title_fullStr Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title_full_unstemmed Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title_short Synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
title_sort synthesis, crystal structures and properties of carbazole-based [6]helicenes fused with an azine ring
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801798/
https://www.ncbi.nlm.nih.gov/pubmed/33488827
http://dx.doi.org/10.3762/bjoc.17.2
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