9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride

The whole mol­ecule of the title compound, C(26)H(16)N(2)S(4), is generated by twofold rotational symmetry. The carbazole skeleton is nearly planar [maximum deviation = 0.054 (5) Å]. In the crystal, aromatic π–π stacking is observed between parallel carbazole ring systems of adjacent mol­ecules, the...

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Autores principales: Uludağ, Nesimi, Ateş, Murat, Çaylak Delibaş, Nagihan, Çelik, Ömer, Hökelek, Tuncer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648295/
https://www.ncbi.nlm.nih.gov/pubmed/23723915
http://dx.doi.org/10.1107/S1600536813010349
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author Uludağ, Nesimi
Ateş, Murat
Çaylak Delibaş, Nagihan
Çelik, Ömer
Hökelek, Tuncer
author_facet Uludağ, Nesimi
Ateş, Murat
Çaylak Delibaş, Nagihan
Çelik, Ömer
Hökelek, Tuncer
author_sort Uludağ, Nesimi
collection PubMed
description The whole mol­ecule of the title compound, C(26)H(16)N(2)S(4), is generated by twofold rotational symmetry. The carbazole skeleton is nearly planar [maximum deviation = 0.054 (5) Å]. In the crystal, aromatic π–π stacking is observed between parallel carbazole ring systems of adjacent mol­ecules, the shortest centroid–centroid distances between pyrrole and benzene rings being 3.948 (3) and 3.751 (3) Å.
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spelling pubmed-36482952013-05-30 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride Uludağ, Nesimi Ateş, Murat Çaylak Delibaş, Nagihan Çelik, Ömer Hökelek, Tuncer Acta Crystallogr Sect E Struct Rep Online Organic Papers The whole mol­ecule of the title compound, C(26)H(16)N(2)S(4), is generated by twofold rotational symmetry. The carbazole skeleton is nearly planar [maximum deviation = 0.054 (5) Å]. In the crystal, aromatic π–π stacking is observed between parallel carbazole ring systems of adjacent mol­ecules, the shortest centroid–centroid distances between pyrrole and benzene rings being 3.948 (3) and 3.751 (3) Å. International Union of Crystallography 2013-04-20 /pmc/articles/PMC3648295/ /pubmed/23723915 http://dx.doi.org/10.1107/S1600536813010349 Text en © Uludağ 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
Uludağ, Nesimi
Ateş, Murat
Çaylak Delibaş, Nagihan
Çelik, Ömer
Hökelek, Tuncer
9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title_full 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title_fullStr 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title_full_unstemmed 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title_short 9H-Carbazole-9-carbo­thioic di­thio­peroxy­anhydride
title_sort 9h-carbazole-9-carbo­thioic di­thio­peroxy­anhydride
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648295/
https://www.ncbi.nlm.nih.gov/pubmed/23723915
http://dx.doi.org/10.1107/S1600536813010349
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AT caylakdelibasnagihan 9hcarbazole9carbothioicdithioperoxyanhydride
AT celikomer 9hcarbazole9carbothioicdithioperoxyanhydride
AT hokelektuncer 9hcarbazole9carbothioicdithioperoxyanhydride

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