Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate

The title compound, C16H16N2S2, was obtained from the condensation reaction of benzyl dithiocarbazate and 2-methylbenzaldehyde. The asymmetric unit contains two independent molecules. In both molecules, the methylphenyl ring and the dithiocarbazate fragment are located on opposite sides of the C=N b...

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Main Authors: Shang Shan, Zhao Wang, Yan-Lan Huang, Han-Qi Guo, Deng-Feng Li
Format: Article
Language:English
Published: International Union of Crystallography 2011-09-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536811033113
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spelling doaj-fb355c9958494b75ab138c0e702756122020-11-25T01:13:22ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-09-01679o2497o249710.1107/S1600536811033113Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazateShang ShanZhao WangYan-Lan HuangHan-Qi GuoDeng-Feng LiThe title compound, C16H16N2S2, was obtained from the condensation reaction of benzyl dithiocarbazate and 2-methylbenzaldehyde. The asymmetric unit contains two independent molecules. In both molecules, the methylphenyl ring and the dithiocarbazate fragment are located on opposite sides of the C=N bond, showing an E conformation. In each molecule, the dithiocarbazate fragment is approximately planar, the r.m.s deviations being 0.018 and 0.025 Å. The mean plane of dithiocarbazate group is oriented at dihedral angles of 7.9 (3) and 68.24 (12)°, respectively, to the methylphenyl and phenyl rings in one molecule, while the corresponding angles in the other molecule are 10.9 (3) and 69.76 (16)°. Intermolecular N—H...S hydrogen bonding occurs in the crystal structure to generate inversion dimers for both molecules.http://scripts.iucr.org/cgi-bin/paper?S1600536811033113
collection DOAJ
language English
format Article
sources DOAJ
author Shang Shan
Zhao Wang
Yan-Lan Huang
Han-Qi Guo
Deng-Feng Li
spellingShingle Shang Shan
Zhao Wang
Yan-Lan Huang
Han-Qi Guo
Deng-Feng Li
Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
Acta Crystallographica Section E
author_facet Shang Shan
Zhao Wang
Yan-Lan Huang
Han-Qi Guo
Deng-Feng Li
author_sort Shang Shan
title Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
title_short Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
title_full Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
title_fullStr Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
title_full_unstemmed Benzyl (E)-3-(2-methylbenzylidene)dithiocarbazate
title_sort benzyl (e)-3-(2-methylbenzylidene)dithiocarbazate
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2011-09-01
description The title compound, C16H16N2S2, was obtained from the condensation reaction of benzyl dithiocarbazate and 2-methylbenzaldehyde. The asymmetric unit contains two independent molecules. In both molecules, the methylphenyl ring and the dithiocarbazate fragment are located on opposite sides of the C=N bond, showing an E conformation. In each molecule, the dithiocarbazate fragment is approximately planar, the r.m.s deviations being 0.018 and 0.025 Å. The mean plane of dithiocarbazate group is oriented at dihedral angles of 7.9 (3) and 68.24 (12)°, respectively, to the methylphenyl and phenyl rings in one molecule, while the corresponding angles in the other molecule are 10.9 (3) and 69.76 (16)°. Intermolecular N—H...S hydrogen bonding occurs in the crystal structure to generate inversion dimers for both molecules.
url http://scripts.iucr.org/cgi-bin/paper?S1600536811033113
work_keys_str_mv AT shangshan benzyle32methylbenzylidenedithiocarbazate
AT zhaowang benzyle32methylbenzylidenedithiocarbazate
AT yanlanhuang benzyle32methylbenzylidenedithiocarbazate
AT hanqiguo benzyle32methylbenzylidenedithiocarbazate
AT dengfengli benzyle32methylbenzylidenedithiocarbazate
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