6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole

The title compound, C(30)H(36)N(2)O(2), was prepared in a twofold Cadogan cyclization. The mol­ecule is located about a center of inversion. The indolocarbazole skeleton is essentially planar [maximum deviation = 0.028 (2) Å], the C—N bond lengths are nearly identical and the C—C bond lengths of the...

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Autores principales: Wrobel, Norma, Witulski, Bernhard, Schollmeyer, Dieter, Detert, Heiner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588340/
https://www.ncbi.nlm.nih.gov/pubmed/23476379
http://dx.doi.org/10.1107/S1600536812050611
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author Wrobel, Norma
Witulski, Bernhard
Schollmeyer, Dieter
Detert, Heiner
author_facet Wrobel, Norma
Witulski, Bernhard
Schollmeyer, Dieter
Detert, Heiner
author_sort Wrobel, Norma
collection PubMed
description The title compound, C(30)H(36)N(2)O(2), was prepared in a twofold Cadogan cyclization. The mol­ecule is located about a center of inversion. The indolocarbazole skeleton is essentially planar [maximum deviation = 0.028 (2) Å], the C—N bond lengths are nearly identical and the C—C bond lengths of the pyrrole unit are significantly longer than those of the benzene subunits.
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spelling pubmed-35883402013-03-08 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole Wrobel, Norma Witulski, Bernhard Schollmeyer, Dieter Detert, Heiner Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(30)H(36)N(2)O(2), was prepared in a twofold Cadogan cyclization. The mol­ecule is located about a center of inversion. The indolocarbazole skeleton is essentially planar [maximum deviation = 0.028 (2) Å], the C—N bond lengths are nearly identical and the C—C bond lengths of the pyrrole unit are significantly longer than those of the benzene subunits. International Union of Crystallography 2012-12-19 /pmc/articles/PMC3588340/ /pubmed/23476379 http://dx.doi.org/10.1107/S1600536812050611 Text en © Wrobel et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Wrobel, Norma
Witulski, Bernhard
Schollmeyer, Dieter
Detert, Heiner
6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title_full 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title_fullStr 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title_full_unstemmed 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title_short 6,12-Bis(hex­yloxy)-5H,11H-indolo[3,2-b]carbazole
title_sort 6,12-bis(hex­yloxy)-5h,11h-indolo[3,2-b]carbazole
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588340/
https://www.ncbi.nlm.nih.gov/pubmed/23476379
http://dx.doi.org/10.1107/S1600536812050611
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AT detertheiner 612bishexyloxy5h11hindolo32bcarbazole

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