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Synthesis, crystal structure and solution studies of gold(III) complexes with 1,1-dimethylbiguanide
Two novel gold(III) complexes with biologically active 1,1-dimethylbiguanide have been synthesized and structurally characterized. The reactivity of the neutral complex in solution has been studied. [Display omitted] •Metal complexes with 1,1-dimethylbiguanide are important for biomedical applicatio...
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Published in: | Inorganica Chimica Acta 2023-07, Vol.552, p.121496, Article 121496 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Two novel gold(III) complexes with biologically active 1,1-dimethylbiguanide have been synthesized and structurally characterized. The reactivity of the neutral complex in solution has been studied.
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•Metal complexes with 1,1-dimethylbiguanide are important for biomedical applications.•Synthesis and crystal structures of two novel gold(III) complexes with 1,1-dimethylbiguanide are reported.•The substitution of Cl– by OH – and the redox interaction with glutathione and cysteine in aqueous solution have been studied for [Au(dmbg)Cl2].
New gold(III) complexes of the composition [Au(dmbgH)Cl2][AuCl4] · H2O and [Au(dmbg)Cl2], where dmbgH is 1,1-dimethylbiguanide and dmbg is deprotonated 1,1-dimethylbiguanide, were synthesized. The resulting compounds were characterized by elemental analysis, IR spectroscopy, 1H NMR spectroscopy, X-ray single crystal and X-ray powder diffraction analyses. In both compounds, 1,1-dimethylbiguanide, regardless of its charge (0 or −1), is bidentately coordinated to gold(III) through the nitrogen atoms of the imino groups. The processes occurring in solutions for the neutral [Au(dmbg)Cl2] complex were studied: the equilibrium of substitution of Cl– by OH– and the redox interaction with glutathione and cysteine in an aqueous solution at t = 25 °C and I = 0.2 M (NaCl). |
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ISSN: | 0020-1693 1873-3255 |
DOI: | 10.1016/j.ica.2023.121496 |