3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione
In the title molecule, C11H12N4S2, the dihedral angle between the triazole and benzene rings is 21.31 (5). A weak intramolecular C—H S hydrogen bond generates an S(6) ring motif. In the crystal, pairs of N—H S hydrogen bonds form inversion dimers. In addition, – interactions are observed betwe...
Saved in:
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2013
|
| Subjects: | |
| Online Access: | http://umpir.ump.edu.my/id/eprint/5447/1/acta_2.pdf http://umpir.ump.edu.my/id/eprint/5447/ http://dx.doi.org/10.1107/S1600536813009690 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Institution: | Universiti Malaysia Pahang |
| Language: | English |
| id |
my.ump.umpir.5447 |
|---|---|
| record_format |
eprints |
| spelling |
my.ump.umpir.54472018-05-17T07:19:28Z http://umpir.ump.edu.my/id/eprint/5447/ 3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione Hegde, Gurumurthy Sarojini, B. K. Manjula, P. S. Kour, Dalbir Gupta, Vivek K. Kant, Rajni QC Physics In the title molecule, C11H12N4S2, the dihedral angle between the triazole and benzene rings is 21.31 (5). A weak intramolecular C—H S hydrogen bond generates an S(6) ring motif. In the crystal, pairs of N—H S hydrogen bonds form inversion dimers. In addition, – interactions are observed between the benzene rings, with a centroid–centroid separation of 3.7599 (11) A°. International Union of Crystallography 2013-04-13 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/5447/1/acta_2.pdf Hegde, Gurumurthy and Sarojini, B. K. and Manjula, P. S. and Kour, Dalbir and Gupta, Vivek K. and Kant, Rajni (2013) 3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione. Acta Crystallographica Section E: Structure Reports Online, 69 (5). pp. 718-719. ISSN 1600-5368 http://dx.doi.org/10.1107/S1600536813009690 DOI: 10.1107/S1600536813009690 |
| institution |
Universiti Malaysia Pahang |
| building |
UMP Library |
| collection |
Institutional Repository |
| continent |
Asia |
| country |
Malaysia |
| content_provider |
Universiti Malaysia Pahang |
| content_source |
UMP Institutional Repository |
| url_provider |
http://umpir.ump.edu.my/ |
| language |
English |
| topic |
QC Physics |
| spellingShingle |
QC Physics Hegde, Gurumurthy Sarojini, B. K. Manjula, P. S. Kour, Dalbir Gupta, Vivek K. Kant, Rajni 3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| description |
In the title molecule, C11H12N4S2, the dihedral angle between
the triazole and benzene rings is 21.31 (5). A weak intramolecular C—H S hydrogen bond generates an S(6) ring
motif. In the crystal, pairs of N—H S hydrogen bonds form
inversion dimers. In addition, – interactions are observed
between the benzene rings, with a centroid–centroid separation
of 3.7599 (11) A°. |
| format |
Article |
| author |
Hegde, Gurumurthy Sarojini, B. K. Manjula, P. S. Kour, Dalbir Gupta, Vivek K. Kant, Rajni |
| author_facet |
Hegde, Gurumurthy Sarojini, B. K. Manjula, P. S. Kour, Dalbir Gupta, Vivek K. Kant, Rajni |
| author_sort |
Hegde, Gurumurthy |
| title |
3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| title_short |
3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| title_full |
3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| title_fullStr |
3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| title_full_unstemmed |
3-Methyl-4-{(E)-[4-(methylsulfanyl)-benzylidene]amino}-1H-1, 2,4-triazole-5(4H)-thione |
| title_sort |
3-methyl-4-{(e)-[4-(methylsulfanyl)-benzylidene]amino}-1h-1, 2,4-triazole-5(4h)-thione |
| publisher |
International Union of Crystallography |
| publishDate |
2013 |
| url |
http://umpir.ump.edu.my/id/eprint/5447/1/acta_2.pdf http://umpir.ump.edu.my/id/eprint/5447/ http://dx.doi.org/10.1107/S1600536813009690 |
| _version_ |
1643665197552893952 |