Please use this identifier to cite or link to this item: http://hdl.handle.net/10311/1032
Title: Bis(pyrazolyl) palladium(II), platinum(II) and gold(III) complexes: Syntheses, molecular structures and substitution reactions with L-cysteine
Authors: Keter, F.K.
Ojwach, S.O.
Oyetunji, O.A.
Guzei, I.A.
Darkwa, J.
Keywords: Bis(pyrazolyl)acetic acid compounds
Cytotoxicity
Pseudo first-order
Substitution
L-cysteine
Issue Date: 2009
Publisher: Elsevier Science Ltd, www.elsevier.com/locate/ica
Citation: Keter, F.K. et al. (2009) Bis(pyrazolyl) palladium(II), platinum(II) and gold(III) complexes: Syntheses, molecular structures and substitution reactions with L-cysteine, Inorganica Chimica Acta, Vol. 362, No. 8, pp. 2595–2602
Abstract: A series of pyrazolyl palladium(II), platinum(II) and gold(III) complexes, [PdCl2(3,5-R2bpza)] {R = H (1), R = Me (2), bpza = bis-pyrazolyl acetic acid}, [PtCl2(3,5-R2bpza)] {R = H (3a), R = Me (4)}, [AuCl2(3,5- R2bpza)]Cl {R = H (5a), R = Me (6a)} and [PdCl2(3,5-R2bpzate)] {R = Me (7)} have been synthesised and structurally characterised. Single crystal X-ray crystallography showed that the pyrazolyl ligands exhibit N^N-coordination with the metals. Anticancer activities of six complexes 1–6a were investigated against CHO cells and were found to have low activities. Substitution reactions of selected complexes 1, 2, 3a and 5a with L-cysteine show that the low anticancer activities compounds and that the rate of substitution with sulfur-containing compounds is not the cause of the low anticancer activities.
URI: http://hdl.handle.net/10311/1032
ISSN: 0020-1693
Appears in Collections:Research articles (Dept of Chemistry)

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