In the current contribution, the synthesis and characterization of new diaminomaleonitrile-based salen cobalt complexes L1Co and L2Co (L1-H = 2,3-bis[[(2,4-dihydroxy-phenyl)(methylene)]amino]-2-butenedinitrile, L2-H = 2,3-bis[[(2-hydroxy-4-(diethylamino)phenyl)(methylene)]amino]-2-butenedinitrile) are reported. Structural analysis and electronic properties of the complexes were assessed, providing a basis for their application as H2S sensors. Spectroscopic investigations revealed an enhancement in the fluorescence intensities upon H2S addition. A reversible fluorescence response was observed when the systems were shifted from H2S-rich to oxygenated environments, demonstrating their reusability and adaptability. To further establish the mechanism of interaction of the HS- with the cobalt complexes, electrochemical analysis was conducted, providing evidence of HS- coordination to the cobalt centers. Moreover, biological assessment of the sensors was performed in HepG2 cells, revealing their low cytotoxicity and efficient cell permeability. Fluorescence imaging experiments provided evidence of intracellular detection of exogenous H2S. The reversibility of the sensing mechanism was confirmed in living cells: subsequent addition of HS- and oxygen-saturated buffer to the cells tunes their fluorescence accordingly, in a cyclable manner, as in the experiments performed in vitro. This study provides evidence that cobalt-based DAMN complexes work as robust, reversible, and selective detection systems for H2S, demonstrating their suitability for applications in both biological and environmental contexts.

Diaminomaleonitrile (DAMN)-Based Salen-Type Cobalt Complexes as Cyclable Sensors for H2S/HS–: Biological Applications

Trerotola, Alessio;Vykhovanets, Viktoriia;Caruso, Tonino;Guarnieri, Daniela;Lamberti, Marina;Milione, Stefano;Strianese, Maria
2025

Abstract

In the current contribution, the synthesis and characterization of new diaminomaleonitrile-based salen cobalt complexes L1Co and L2Co (L1-H = 2,3-bis[[(2,4-dihydroxy-phenyl)(methylene)]amino]-2-butenedinitrile, L2-H = 2,3-bis[[(2-hydroxy-4-(diethylamino)phenyl)(methylene)]amino]-2-butenedinitrile) are reported. Structural analysis and electronic properties of the complexes were assessed, providing a basis for their application as H2S sensors. Spectroscopic investigations revealed an enhancement in the fluorescence intensities upon H2S addition. A reversible fluorescence response was observed when the systems were shifted from H2S-rich to oxygenated environments, demonstrating their reusability and adaptability. To further establish the mechanism of interaction of the HS- with the cobalt complexes, electrochemical analysis was conducted, providing evidence of HS- coordination to the cobalt centers. Moreover, biological assessment of the sensors was performed in HepG2 cells, revealing their low cytotoxicity and efficient cell permeability. Fluorescence imaging experiments provided evidence of intracellular detection of exogenous H2S. The reversibility of the sensing mechanism was confirmed in living cells: subsequent addition of HS- and oxygen-saturated buffer to the cells tunes their fluorescence accordingly, in a cyclable manner, as in the experiments performed in vitro. This study provides evidence that cobalt-based DAMN complexes work as robust, reversible, and selective detection systems for H2S, demonstrating their suitability for applications in both biological and environmental contexts.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/4912237
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