Comparative Study of Ni(II) Complexes with Dithiocarbazate- and Thiosemicarbazone-Based Ligands: Synthesis, Crystal Structures, and Anticancer Activity

The present work reports a comparative study of thiosemicarbazone (H<sub>2</sub>L<sup>1</sup>) and dithiocarbazate (H<sub>2</sub>L<sup>2</sup>) ligands and their Ni(II) complexes; [Ni(L<sup>1</sup>)(PPh<sub>3</sub>)] (<b>1</b>); [Ni(L<sup>1</sup>)(Py)] (<b>2</b>); [Ni(L<sup>2</sup>)(PPh<sub>3</sub>)] (<b>3</b>); and [Ni(L<sup>2</sup>)(Py)] (<b>4</b>). All compounds were characterized by spectroscopy analysis; and the complexes were also characterized by single-crystal X-ray diffraction. The crystal structures of the complexes revealed a distorted square planar geometry with the Ni(II) atoms coordinated to a double-deprotonated and tridentate ligand molecule by the <i>ONS</i> donor system. The coordination sphere is completed by the incorporation of pyridine or triphenylphosphine coligands at the metal center. Biological assays were conducted against the cell lines breast cancer (MCF-7); cisplatin-resistant ovarian cancer (A2780cis); lung cancer (A549); and nontumoral lung (MRC-5). The results show that cytotoxicity was significantly enhanced upon complexation for complexes (<b>2</b>) and (<b>4</b>); whereas it was suppressed for complexes (<b>1</b>) and (<b>3</b>) against the A2780cis and A549 cell lines. Notably; complex (<b>2</b>) exhibited superior cytotoxicity compared to cisplatin against both MCF-7 and A2780cis.

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Journal
Molecules
Published
2025-08-28
DOI
https://doi.org/10.3390/molecules30173516
Citations
1
Primary Topic
Metal complexes synthesis and properties
Type
article
Field-Weighted Citation Impact
1.05

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article

Comparative Study of Ni(II) Complexes with Dithiocarbazate- and Thiosemicarbazone-Based Ligands: Synthesis, Crystal Structures, and Anticancer Activity

Marta Viana, Gabriel S. Pessoa, Claudia C. Gatto, Katia M. Oliveira
1 citations
Molecules
Metal complexes synthesis and properties
1.05
article

Comparative Study of Ni(II) Complexes with Dithiocarbazate- and Thiosemicarbazone-Based Ligands: Synthesis, Crystal Structures, and Anticancer Activity

Marta Viana, Gabriel S. Pessoa, Claudia C. Gatto, Katia M. Oliveira
article en
1 citations

Abstract

The present work reports a comparative study of thiosemicarbazone (H<sub>2</sub>L<sup>1</sup>) and dithiocarbazate (H<sub>2</sub>L<sup>2</sup>) ligands and their Ni(II) complexes; [Ni(L<sup>1</sup>)(PPh<sub>3</sub>)] (<b>1</b>); [Ni(L<sup>1</sup>)(Py)] (<b>2</b>); [Ni(L<sup>2</sup>)(PPh<sub>3</sub>)] (<b>3</b>); and [Ni(L<sup>2</sup>)(Py)] (<b>4</b>). All compounds were characterized by spectroscopy analysis; and the complexes were also characterized by single-crystal X-ray diffraction. The crystal structures of the complexes revealed a distorted square planar geometry with the Ni(II) atoms coordinated to a double-deprotonated and tridentate ligand molecule by the <i>ONS</i> donor system. The coordination sphere is completed by the incorporation of pyridine or triphenylphosphine coligands at the metal center. Biological assays were conducted against the cell lines breast cancer (MCF-7); cisplatin-resistant ovarian cancer (A2780cis); lung cancer (A549); and nontumoral lung (MRC-5). The results show that cytotoxicity was significantly enhanced upon complexation for complexes (<b>2</b>) and (<b>4</b>); whereas it was suppressed for complexes (<b>1</b>) and (<b>3</b>) against the A2780cis and A549 cell lines. Notably; complex (<b>2</b>) exhibited superior cytotoxicity compared to cisplatin against both MCF-7 and A2780cis.

MoleculesVol. 30(17)
Universidade de Brasília (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Apoio à Pesquisa do Distrito Federal
Openalex Percentile: Top 18%
Metal complexes synthesis and properties
1.05
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Comparative Study of Ni(II) Complexes with Dithiocarbazate- and Thiosemicarbazone-Based Ligands: Synthesis, Crystal Structures, and Anticancer Activity — Marta Viana, Gabriel S. Pessoa, et al. · Molecules (2025) | TGRS Research Map | TGRS