4,5-Diferrocenyl-1,2-di­thiole-3-thione

The structure of 4,5-diferrocenyl-1,2-di­thiole-3-thione, [Fe(2)(C(5)H(5))(2)(C(13)H(8)S(3))] or C(23)H(18)Fe(2)S(3), at 130 K has monoclinic (P2(1)/c) symmetry. The molecule has two ferrocenyl units attached to a 1,2-di­thiole-3-thione moiety. It is of inter­est with respect to the question if the...

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Detalles Bibliográficos
Autores principales: Sánchez-García, Jessica J., Flores-Alamo, Marcos, Nuñez-Gordillo, Amairany, Klimova, Elena I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638058/
https://www.ncbi.nlm.nih.gov/pubmed/36405852
http://dx.doi.org/10.1107/S2414314622010112
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author Sánchez-García, Jessica J.
Flores-Alamo, Marcos
Nuñez-Gordillo, Amairany
Klimova, Elena I.
author_facet Sánchez-García, Jessica J.
Flores-Alamo, Marcos
Nuñez-Gordillo, Amairany
Klimova, Elena I.
author_sort Sánchez-García, Jessica J.
collection PubMed
description The structure of 4,5-diferrocenyl-1,2-di­thiole-3-thione, [Fe(2)(C(5)H(5))(2)(C(13)H(8)S(3))] or C(23)H(18)Fe(2)S(3), at 130 K has monoclinic (P2(1)/c) symmetry. The molecule has two ferrocenyl units attached to a 1,2-di­thiole-3-thione moiety. It is of inter­est with respect to the question if the introduction of ferrocenyl substituents into biologically active mol­ecules offers the potential to obtain more efficacious therapeutic drugs. The crystal structure displays inter­molecular contacts of the C—H⋯S and S—π(C—C) types. [Image: see text]
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spelling pubmed-96380582022-11-18 4,5-Diferrocenyl-1,2-di­thiole-3-thione Sánchez-García, Jessica J. Flores-Alamo, Marcos Nuñez-Gordillo, Amairany Klimova, Elena I. IUCrdata Data Reports The structure of 4,5-diferrocenyl-1,2-di­thiole-3-thione, [Fe(2)(C(5)H(5))(2)(C(13)H(8)S(3))] or C(23)H(18)Fe(2)S(3), at 130 K has monoclinic (P2(1)/c) symmetry. The molecule has two ferrocenyl units attached to a 1,2-di­thiole-3-thione moiety. It is of inter­est with respect to the question if the introduction of ferrocenyl substituents into biologically active mol­ecules offers the potential to obtain more efficacious therapeutic drugs. The crystal structure displays inter­molecular contacts of the C—H⋯S and S—π(C—C) types. [Image: see text] International Union of Crystallography 2022-10-25 /pmc/articles/PMC9638058/ /pubmed/36405852 http://dx.doi.org/10.1107/S2414314622010112 Text en © Sánchez-García et al. 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Sánchez-García, Jessica J.
Flores-Alamo, Marcos
Nuñez-Gordillo, Amairany
Klimova, Elena I.
4,5-Diferrocenyl-1,2-di­thiole-3-thione
title 4,5-Diferrocenyl-1,2-di­thiole-3-thione
title_full 4,5-Diferrocenyl-1,2-di­thiole-3-thione
title_fullStr 4,5-Diferrocenyl-1,2-di­thiole-3-thione
title_full_unstemmed 4,5-Diferrocenyl-1,2-di­thiole-3-thione
title_short 4,5-Diferrocenyl-1,2-di­thiole-3-thione
title_sort 4,5-diferrocenyl-1,2-di­thiole-3-thione
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638058/
https://www.ncbi.nlm.nih.gov/pubmed/36405852
http://dx.doi.org/10.1107/S2414314622010112
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