Related Experiment Video
Updated: Aug 20, 2025

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
4,5-Diferrocenyl-1,2-di-thiole-3-thione
Jessica J Sánchez-García1, Marcos Flores-Alamo1, Amairany Nuñez-Gordillo1
1Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Ciudad de México, 04510, Mexico.
The crystal structure of diferrocenyl dithiole thione was determined at 130 K. This compound
Area of Science:
- Organometallic Chemistry
- Crystallography
- Materials Science
Background:
- Ferrocene derivatives are explored for potential therapeutic applications.
- The 1,2-di-thiole-3-thione moiety is a structural component in various compounds.
- Understanding molecular structure is crucial for drug development.
Purpose of the Study:
- To determine the crystal structure of 4,5-diferrocenyl-1,2-di-thiole-3-thione.
- To investigate the potential of ferrocenyl substituents in biologically active molecules.
- To analyze intermolecular interactions in the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction at 130 K.
- Structural analysis of the monoclinic crystal system (P21/c).
- Identification of intermolecular contacts (C-H⋯S and S-π(C-C)).
Main Results:
- The compound 4,5-diferrocenyl-1,2-di-thiole-3-thione (C23H18Fe2S3) was synthesized and structurally characterized.
- The molecule exhibits monoclinic symmetry (P21/c) at 130 K.
- Key intermolecular interactions, including C-H⋯S and S-π(C-C) contacts, were identified.
Conclusions:
- The crystal structure provides a foundation for understanding the properties of this ferrocene derivative.
- The study contributes to the exploration of ferrocene-containing compounds for potential pharmaceutical uses.
- Further research is warranted to evaluate the biological activity and therapeutic efficacy of such molecules.
More Related Videos
Related Concept Videos
Preparation and Reactions of Thiols
Preparation and Reactions of Sulfides
Structure and Nomenclature of Thiols and Sulfides
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
Diazonium Group Substitution: –OH and –H

![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)