2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide
All non-H atoms of the title compound, C(6)H(7)N(3)OS, which exists in the thione form, lie in a common plane (r.m.s. of non-H atoms = 0.08 angstrom). The amino group of the -NH-NH(2) substituent forms an intramolecular hydrogen bond to the S atom. The terminal -NH(2) group is pyramidally coordinate...
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International Union of Crystallography
2010
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my.um.eprints.80872019-01-31T01:29:35Z http://eprints.um.edu.my/8087/ 2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide Ariffin, Azhar Ng, S.W. Mansor, S. Yehye, W.A. QD Chemistry All non-H atoms of the title compound, C(6)H(7)N(3)OS, which exists in the thione form, lie in a common plane (r.m.s. of non-H atoms = 0.08 angstrom). The amino group of the -NH-NH(2) substituent forms an intramolecular hydrogen bond to the S atom. The terminal -NH(2) group is pyramidally coordinated; it forms a weak N-H center dot center dot center dot O and a weak N-H center dot center dot center dot S hydrogen bond. Furthermore, the N atom is an acceptor for a C-H center dot center dot center dot N contact. The amino group of the ring is a hydrogen-bond donor to the carbonyl O atom of an adjacent molecule, this interaction giving rise to a linear chain motif running along the b axis. International Union of Crystallography 2010 Article PeerReviewed application/pdf en http://eprints.um.edu.my/8087/1/Mansor-2010-2-Sulfanylidene-1%2C2-.pdf Ariffin, Azhar and Ng, S.W. and Mansor, S. and Yehye, W.A. (2010) 2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide. Acta Crystallographica Section E: Structure Reports Online, 66 (10). O2516-U64. ISSN 1600-5368 http://journals.iucr.org/e/issues/2010/10/00/bt5335/bt5335.pdf 10.1107/s160053681003521x |
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QD Chemistry Ariffin, Azhar Ng, S.W. Mansor, S. Yehye, W.A. 2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
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All non-H atoms of the title compound, C(6)H(7)N(3)OS, which exists in the thione form, lie in a common plane (r.m.s. of non-H atoms = 0.08 angstrom). The amino group of the -NH-NH(2) substituent forms an intramolecular hydrogen bond to the S atom. The terminal -NH(2) group is pyramidally coordinated; it forms a weak N-H center dot center dot center dot O and a weak N-H center dot center dot center dot S hydrogen bond. Furthermore, the N atom is an acceptor for a C-H center dot center dot center dot N contact. The amino group of the ring is a hydrogen-bond donor to the carbonyl O atom of an adjacent molecule, this interaction giving rise to a linear chain motif running along the b axis. |
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Article |
author |
Ariffin, Azhar Ng, S.W. Mansor, S. Yehye, W.A. |
author_facet |
Ariffin, Azhar Ng, S.W. Mansor, S. Yehye, W.A. |
author_sort |
Ariffin, Azhar |
title |
2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
title_short |
2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
title_full |
2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
title_fullStr |
2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
title_full_unstemmed |
2-Sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
title_sort |
2-sulfanylidene-1,2-dihydropyridine-3-carbohydrazide |
publisher |
International Union of Crystallography |
publishDate |
2010 |
url |
http://eprints.um.edu.my/8087/1/Mansor-2010-2-Sulfanylidene-1%2C2-.pdf http://eprints.um.edu.my/8087/ http://journals.iucr.org/e/issues/2010/10/00/bt5335/bt5335.pdf |
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