2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile
In the title compound, C6H4N4S3, the 1,3,4-thiadiazole ring is essentially planar, with an r.m.s. deviation of 0.001 Å. The two N—C—S—C torsion angles in the molecule are −23.41 (15) and 0.62 (14)°. One acetonitr...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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International Union of Crystallography
2013-12-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536813032194 |
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author | Mustafa R. Albayati Ahmed M. M. El-Saghier Shaaban K. Mohamed Mehmet Akkurt Joel T. Mague |
author_facet | Mustafa R. Albayati Ahmed M. M. El-Saghier Shaaban K. Mohamed Mehmet Akkurt Joel T. Mague |
author_sort | Mustafa R. Albayati |
collection | DOAJ |
description | In the title compound, C6H4N4S3, the 1,3,4-thiadiazole ring is essentially planar, with an r.m.s. deviation of 0.001 Å. The two N—C—S—C torsion angles in the molecule are −23.41 (15) and 0.62 (14)°. One acetonitrile group is above the plane of the 1,3,4-thiadiazole ring and the other is below it, indicating syn and anti orientations. In the crystal, C—H...N hydrogen bonds link the molecules into ribbons along [010]. |
first_indexed | 2024-12-10T19:32:34Z |
format | Article |
id | doaj.art-4415235461584c0781c1fe8e28c9e6f6 |
institution | Directory Open Access Journal |
issn | 1600-5368 |
language | English |
last_indexed | 2024-12-10T19:32:34Z |
publishDate | 2013-12-01 |
publisher | International Union of Crystallography |
record_format | Article |
series | Acta Crystallographica Section E |
spelling | doaj.art-4415235461584c0781c1fe8e28c9e6f62022-12-22T01:36:12ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682013-12-016912o1855o185510.1107/S16005368130321942,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrileMustafa R. AlbayatiAhmed M. M. El-SaghierShaaban K. MohamedMehmet AkkurtJoel T. MagueIn the title compound, C6H4N4S3, the 1,3,4-thiadiazole ring is essentially planar, with an r.m.s. deviation of 0.001 Å. The two N—C—S—C torsion angles in the molecule are −23.41 (15) and 0.62 (14)°. One acetonitrile group is above the plane of the 1,3,4-thiadiazole ring and the other is below it, indicating syn and anti orientations. In the crystal, C—H...N hydrogen bonds link the molecules into ribbons along [010].http://scripts.iucr.org/cgi-bin/paper?S1600536813032194 |
spellingShingle | Mustafa R. Albayati Ahmed M. M. El-Saghier Shaaban K. Mohamed Mehmet Akkurt Joel T. Mague 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile Acta Crystallographica Section E |
title | 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile |
title_full | 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile |
title_fullStr | 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile |
title_full_unstemmed | 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile |
title_short | 2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile |
title_sort | 2 2 8242 1 3 4 thiadiazole 2 5 diyl bis sulfanediyl diacetonitrile |
url | http://scripts.iucr.org/cgi-bin/paper?S1600536813032194 |
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