Your browser doesn't support javascript.
loading
Synthesis, characterization, solution chemistry and anticancer activity of [NiCl2(Ph2P-N(R)-PPh2)] (R = 2-CH2Py, CH2Ph and p-tol) complexes.
Albuquerque, Carla C V; Teixeira, Thallita M; Dos Santos, Rafael S; Abreu, Davi C; Silveira-Lacerda, Elisângela de P; Back, Davi F; da Silva, Juliana P; de Araujo, Márcio P.
Affiliation
  • Albuquerque CCV; Department of Chemistry, Federal University of Santa Catarina, 88040-900 Florianópolis, SC, Brazil.
  • Teixeira TM; Department of Genetics, Institute of Biological Sciences, Federal University of Goiás, 74001-970 Goiânia, GO, Brazil.
  • Dos Santos RS; Department of Chemistry, Federal University of Paraná, Polytechnique Center, 81531-980 Curitiba, PR, Brazil.
  • Abreu DC; Department of Genetics, Institute of Biological Sciences, Federal University of Goiás, 74001-970 Goiânia, GO, Brazil.
  • Silveira-Lacerda EP; Department of Genetics, Institute of Biological Sciences, Federal University of Goiás, 74001-970 Goiânia, GO, Brazil.
  • Back DF; Department of Chemistry, Federal University of Santa Maria, 97105-900 Santa Maria, RS, Brazil.
  • da Silva JP; Department of Chemistry, Federal University of Santa Catarina, 88040-900 Florianópolis, SC, Brazil.
  • de Araujo MP; Department of Chemistry, Federal University of Santa Catarina, 88040-900 Florianópolis, SC, Brazil; Department of Chemistry, Federal University of Paraná, Polytechnique Center, 81531-980 Curitiba, PR, Brazil. Electronic address: mparaujo@ufpr.br.
J Inorg Biochem ; 240: 112119, 2023 03.
Article in En | MEDLINE | ID: mdl-36639323
In this work three Ni2+ complexes with general formula [NiCl2(Ph2P-N(R)-PPh2)], R = 2-CH2Py (Py = pyridine) - 1, CH2Ph (Ph = phenyl) - 2 and p-tol (p-tol = p-tolyl) - 3, were synthesized and characterized. These complexes were obtained in high yield by the reaction of NiCl2.6H2O and the corresponding diphenylphosphinoamine ligand (Ph2P-N(R)-PPh2) in CH2Cl2/MeOH (1:1) solution, at room temperature (∼25 °C), and characterized by 1H and 31P {1H} NMR, vibrational spectroscopy in the infrared region, electronic spectroscopy in the UV-Vis regions, elemental analysis (%C, %H, %N) and single-crystal X-ray diffraction. The solution chemistry was studied in CDCl3/dmso-d6 (dimethylsulfoxide) or neat dmso-d6 using complex 2 as a model. The complexes were evaluated as cytotoxic agents against two cancer cells lines, A549 (lung cancer cells), B16F10 (melanoma cells) and the health cells HaCaT (human epithelial keratinocytes).
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dimethyl Sulfoxide Limits: Humans Language: En Journal: J Inorg Biochem Year: 2023 Document type: Article Affiliation country: Brazil Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dimethyl Sulfoxide Limits: Humans Language: En Journal: J Inorg Biochem Year: 2023 Document type: Article Affiliation country: Brazil Country of publication: United States