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Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate

The title compound, C(17)H(18)N(2)O(2)S(2), synthesized via a condensation reaction between S-benzyl di­thio­carbazate and 3,4-di­meth­oxy­benzaldehyde, crystallized with two independent mol­ecules (A and B) in the asymmetric unit. Both mol­ecules have an L-shape but differ in the orientation of the...

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Autores principales: Tan, Yew-Fung, Break, Mohammed Khaled bin, Tahir, M. Ibrahim M., Khoo, Teng-Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384544/
https://www.ncbi.nlm.nih.gov/pubmed/25878829
http://dx.doi.org/10.1107/S205698901500095X
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author Tan, Yew-Fung
Break, Mohammed Khaled bin
Tahir, M. Ibrahim M.
Khoo, Teng-Jin
author_facet Tan, Yew-Fung
Break, Mohammed Khaled bin
Tahir, M. Ibrahim M.
Khoo, Teng-Jin
author_sort Tan, Yew-Fung
collection PubMed
description The title compound, C(17)H(18)N(2)O(2)S(2), synthesized via a condensation reaction between S-benzyl di­thio­carbazate and 3,4-di­meth­oxy­benzaldehyde, crystallized with two independent mol­ecules (A and B) in the asymmetric unit. Both mol­ecules have an L-shape but differ in the orientation of the benzyl ring with respect to the 3,4-di­meth­oxy­benzyl­idine ring, this dihedral angle is 65.59 (8)° in mol­ecule A and 73.10 (8)° in mol­ecule B. In the crystal, the A and B mol­ecules are linked via pairs of N—H⋯S hydrogen bonds, forming dimers with an R (2) (2)(8) ring motif. The dimers are linked via pairs of C—H⋯O hydrogen bonds, giving inversion dimers of dimers. These units are linked by C—H⋯π inter­actions, forming ribbons propagating in the [100] direction.
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spelling pubmed-43845442015-04-15 Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate Tan, Yew-Fung Break, Mohammed Khaled bin Tahir, M. Ibrahim M. Khoo, Teng-Jin Acta Crystallogr E Crystallogr Commun Research Communications The title compound, C(17)H(18)N(2)O(2)S(2), synthesized via a condensation reaction between S-benzyl di­thio­carbazate and 3,4-di­meth­oxy­benzaldehyde, crystallized with two independent mol­ecules (A and B) in the asymmetric unit. Both mol­ecules have an L-shape but differ in the orientation of the benzyl ring with respect to the 3,4-di­meth­oxy­benzyl­idine ring, this dihedral angle is 65.59 (8)° in mol­ecule A and 73.10 (8)° in mol­ecule B. In the crystal, the A and B mol­ecules are linked via pairs of N—H⋯S hydrogen bonds, forming dimers with an R (2) (2)(8) ring motif. The dimers are linked via pairs of C—H⋯O hydrogen bonds, giving inversion dimers of dimers. These units are linked by C—H⋯π inter­actions, forming ribbons propagating in the [100] direction. International Union of Crystallography 2015-01-31 /pmc/articles/PMC4384544/ /pubmed/25878829 http://dx.doi.org/10.1107/S205698901500095X Text en © Tan et al. 2015 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Research Communications
Tan, Yew-Fung
Break, Mohammed Khaled bin
Tahir, M. Ibrahim M.
Khoo, Teng-Jin
Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title_full Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title_fullStr Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title_full_unstemmed Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title_short Crystal structure of benzyl (E)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
title_sort crystal structure of benzyl (e)-2-(3,4-di­meth­oxy­benzyl­idene)hydrazine-1-carbodi­thio­ate
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384544/
https://www.ncbi.nlm.nih.gov/pubmed/25878829
http://dx.doi.org/10.1107/S205698901500095X
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