4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate

The title compound, C16H12FN3OS, a fluorinated dithiocarbazate imine derivative, was synthesized by the one-pot, multi-component condensation reaction of hydrazine hydrate, carbon disulfide, 4-fluorobenzyl chloride and isatin. The compound demonstrates near-planarity across much of the molecule in t...

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Published in:IUCrData
Main Author: Manan M.A.F.A.; Cordes D.B.; McKay A.P.
Format: Article
Language:English
Published: International Union of Crystallography 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85189660845&doi=10.1107%2fS2414314624002359&partnerID=40&md5=a4062051964fdb0a6a4466a0b129b329
id 2-s2.0-85189660845
spelling 2-s2.0-85189660845
Manan M.A.F.A.; Cordes D.B.; McKay A.P.
4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
2024
IUCrData
9
Pt 3
10.1107/S2414314624002359
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85189660845&doi=10.1107%2fS2414314624002359&partnerID=40&md5=a4062051964fdb0a6a4466a0b129b329
The title compound, C16H12FN3OS, a fluorinated dithiocarbazate imine derivative, was synthesized by the one-pot, multi-component condensation reaction of hydrazine hydrate, carbon disulfide, 4-fluorobenzyl chloride and isatin. The compound demonstrates near-planarity across much of the molecule in the solid state and a Z configuration for the azomethine C N bond. The Z form is further stabilized by the presence of an intramolecular N—H. . .O hydrogen bond. In the extended structure, molecules are linked into dimers by N—H. . .O hydrogen bonds and further connected into chains along either [210] or [100] by weak C—H. . .S and C—H. . .F hydrogen bonds, which further link into corrugated sheets and in combination form the overall three-dimensional network. © 2024 International Union of Crystallography. All rights reserved.
International Union of Crystallography
24143146
English
Article
All Open Access; Gold Open Access
author Manan M.A.F.A.; Cordes D.B.; McKay A.P.
spellingShingle Manan M.A.F.A.; Cordes D.B.; McKay A.P.
4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
author_facet Manan M.A.F.A.; Cordes D.B.; McKay A.P.
author_sort Manan M.A.F.A.; Cordes D.B.; McKay A.P.
title 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
title_short 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
title_full 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
title_fullStr 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
title_full_unstemmed 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
title_sort 4-Fluorobenzyl (Z)-2-(2-oxoindolin-3-ylidene) hydrazine-1-carbodithioate
publishDate 2024
container_title IUCrData
container_volume 9
container_issue Pt 3
doi_str_mv 10.1107/S2414314624002359
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85189660845&doi=10.1107%2fS2414314624002359&partnerID=40&md5=a4062051964fdb0a6a4466a0b129b329
description The title compound, C16H12FN3OS, a fluorinated dithiocarbazate imine derivative, was synthesized by the one-pot, multi-component condensation reaction of hydrazine hydrate, carbon disulfide, 4-fluorobenzyl chloride and isatin. The compound demonstrates near-planarity across much of the molecule in the solid state and a Z configuration for the azomethine C N bond. The Z form is further stabilized by the presence of an intramolecular N—H. . .O hydrogen bond. In the extended structure, molecules are linked into dimers by N—H. . .O hydrogen bonds and further connected into chains along either [210] or [100] by weak C—H. . .S and C—H. . .F hydrogen bonds, which further link into corrugated sheets and in combination form the overall three-dimensional network. © 2024 International Union of Crystallography. All rights reserved.
publisher International Union of Crystallography
issn 24143146
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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