A new series of bioactive Mo(V)2O2S2-based thiosemicarbazone complexes: Solution and DFT studies, and antifungal and antioxidant activities

Autor/a

Cebotari, Diana

Buils, Jordi

Garbuz, Olga

Balan, Greta

Marrot, Jérôme

Guérineau, Vincent

Touboul, David

Haouas, Mohamed

Segado-Centelles, Mireia

Bo, Carles

Gulea, Aurelian

Floquet, Sébastien

Data de publicació

2023-05-18



Resum

This paper deals with the synthesis, characterization, and studies of biological properties of a series of 5 coordination compounds based on binuclear core [MoV2O2S2]2+ with thiosemicarbazones ligands bearing different substituents on the R1 position of the ligand. The complexes are first studied using MALDI-TOF mass spectrometry and NMR spectroscopy to determine their structures in solution in relation to single-crystal X-Ray diffraction data. In a second part, the antifungal and antioxidative activities are explored and the high potential of these coordination compounds compared to the uncoordinated ligands is demonstrated for these properties. Finally, DFT calculation provides important support to the solution studies by identifying the most stable isomers in each [Mo2O2S2]2+/Ligand system, while the determination of HUMO and LUMO levels is performed to explain the antioxidative properties of these systems

Tipus de document

Article
Versió acceptada

Llengua

Anglès

Matèries CDU

00 - Ciència i coneixement. Investigació. Cultura. Humanitats

Paraules clau

Química

Pàgines

42 p.

Publicat per

Elsevier

Número de l'acord de la subvenció

This work is supported by the “ADI 2019” project funded by the IDEX Paris-Saclay, ANR-11-IDEX-0003-02, “Joint research projects AUF-MECR 2020-2021” funding program, and National Agency for Research and Development (ANCD) of the Republic of Moldova (Project No 20.80009.5007.10 and Project No 20.80009.7007.12)

This study results from an International collaboration supported by IRN-CNRS 2019-2023

Documents

J Inorg Biochem 2023 112256_A new series of bioactive.pdf

1.624Mb

 

Drets

CC-BY

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