Related Experiment Video
Updated: Jul 16, 2026

Preparation of SNS Cobalt(II) Pincer Model Complexes of Liver Alcohol Dehydrogenase
Published on: March 19, 2020
Perthionitrite-Induced Persulfidation in Binuclear Cobalt(II) Complexes§
Anuj Baran Chakraborty1, Rajib Hazra1, Amit Majumdar1
1School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A & 2B Raja S. C. Mullick Road, Kolkata700032, West Bengal, India.
This study shows that perthionitrite (SSNO⁻) can mediate the persulfidation of thiol groups, mimicking biological processes. This finding reveals a new role for SSNO⁻ in sulfur signaling pathways.
Area of Science:
- Bioinorganic Chemistry
- Sulfur Chemistry
- Biochemistry
Background:
- Persulfidation of thiols is a critical physiological process involving sulfur redox reactions.
- The exact mechanisms and mediating species in biological persulfidation remain incompletely understood.
Purpose of the Study:
- To investigate the role of dicobalt(II)-nitrito complexes in mediating persulfidation reactions.
- To explore the potential of perthionitrite (SSNO⁻) as a key species in thiol persulfidation.
Main Methods:
- Synthesis and characterization of dicobalt(II)-nitrito complexes and their reaction products.
- Utilized structural and spectroscopic methods for product and intermediate identification.
- Employed control experiments to validate reaction pathways.
Main Results:
- Two dicobalt(II)-nitrito complexes reacted with thiocarboxylic acids to yield persulfidated complexes in high yields.
- Identified perthionitrite (SSNO⁻) as a key intermediate generated in situ.
- Demonstrated that SSNO⁻ effectively persulfidates coordinated thiocarboxylates.
Conclusions:
- Perthionitrite (SSNO⁻) is shown to be an effective mediator for the persulfidation of sulfhydryl groups.
- This study provides the first evidence for SSNO⁻ mediating persulfidation, suggesting a potential biological role.
- Highlights a novel S/N-crosstalk mechanism relevant to physiological sulfur modifications.
Related Concept Videos
Formation of Complex Ions
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Preparation and Reactions of Sulfides
Precipitation and Co-precipitation
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
Valence Bond Theory

