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Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene

The title compound, C(14)H(14)N(2)S(2), was obtained by transmetallation of 2,2′-bis­(tri­methyl­stann­yl)azo­benzene with methyl lithium, and subsequent quenching with dimethyl di­sulfide. The asymmetric unit comprises two half-mol­ecules, the other halves being completed by inversion symmetry at t...

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Detalles Bibliográficos
Autores principales: Hoffmann, Jonas, Kuczmera, Thomas J., Lork, Enno, Staubitz, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829741/
https://www.ncbi.nlm.nih.gov/pubmed/31709113
http://dx.doi.org/10.1107/S2056989019014592
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author Hoffmann, Jonas
Kuczmera, Thomas J.
Lork, Enno
Staubitz, Anne
author_facet Hoffmann, Jonas
Kuczmera, Thomas J.
Lork, Enno
Staubitz, Anne
author_sort Hoffmann, Jonas
collection PubMed
description The title compound, C(14)H(14)N(2)S(2), was obtained by transmetallation of 2,2′-bis­(tri­methyl­stann­yl)azo­benzene with methyl lithium, and subsequent quenching with dimethyl di­sulfide. The asymmetric unit comprises two half-mol­ecules, the other halves being completed by inversion symmetry at the midpoint of the azo group. The two mol­ecules show only slight differences with respect to N=N, S—N and aromatic C=C bonds or angles. Hirshfeld surface analysis reveals that except for one weak H⋯S inter­action, inter­molecular inter­actions are dominated by van der Waals forces only.
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spelling pubmed-68297412019-11-08 Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene Hoffmann, Jonas Kuczmera, Thomas J. Lork, Enno Staubitz, Anne Acta Crystallogr E Crystallogr Commun Research Communications The title compound, C(14)H(14)N(2)S(2), was obtained by transmetallation of 2,2′-bis­(tri­methyl­stann­yl)azo­benzene with methyl lithium, and subsequent quenching with dimethyl di­sulfide. The asymmetric unit comprises two half-mol­ecules, the other halves being completed by inversion symmetry at the midpoint of the azo group. The two mol­ecules show only slight differences with respect to N=N, S—N and aromatic C=C bonds or angles. Hirshfeld surface analysis reveals that except for one weak H⋯S inter­action, inter­molecular inter­actions are dominated by van der Waals forces only. International Union of Crystallography 2019-10-31 /pmc/articles/PMC6829741/ /pubmed/31709113 http://dx.doi.org/10.1107/S2056989019014592 Text en © Hoffmann et al. 2019 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Communications
Hoffmann, Jonas
Kuczmera, Thomas J.
Lork, Enno
Staubitz, Anne
Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title_full Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title_fullStr Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title_full_unstemmed Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title_short Synthesis and crystal structure of (E)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
title_sort synthesis and crystal structure of (e)-1,2-bis­[2-(methyl­sulfan­yl)phen­yl]diazene
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829741/
https://www.ncbi.nlm.nih.gov/pubmed/31709113
http://dx.doi.org/10.1107/S2056989019014592
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