Gold(<scp>i</scp>) and gold(<scp>iii</scp>) complexes of triazolyl-functionalised NHCs

Novel triazolyl-functionalised imidazolium salts and their corresponding Au<sup>I</sup>/Au<sup>III</sup> complexes were synthesised and characterised by spectroscopic techniques and X-ray diffraction studies. The reaction of (mono and bis carbene) Au<sup>I</sup> complexes with thionyl chloride gave Au<sup>III</sup> complexes. These Au<sup>III</sup> complexes are reduced to Au<sup>I</sup> complexes by DMSO dissolution, and react with silver nitrate to afford chelating complexes, where the triazolyl N atoms bind to gold. The triazolyl-functionalised Au<sup>I</sup> complexes showed potency against ovarian cancer cells (OVCAR-8 cells, IC<sub>50</sub> < 15 μM).

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra02655e
Citations
4
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
3.74

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article

Gold(i) and gold(iii) complexes of triazolyl-functionalised NHCs

Hani Al‐Salami, Stephen A. Moggach, Karrar Al‐Ameed, Murray V. Baker et al.
4 citations
RSC Advances
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
3.74
article

Gold(i) and gold(iii) complexes of triazolyl-functionalised NHCs

Hani Al‐Salami, Stephen A. Moggach, Karrar Al‐Ameed, Murray V. Baker, Vito Ferro, Hawraa S. Al‐Buthabhak, Alexandre N. Sobolev, Yu Yu
article en
4 citations

Abstract

Novel triazolyl-functionalised imidazolium salts and their corresponding Au<sup>I</sup>/Au<sup>III</sup> complexes were synthesised and characterised by spectroscopic techniques and X-ray diffraction studies. The reaction of (mono and bis carbene) Au<sup>I</sup> complexes with thionyl chloride gave Au<sup>III</sup> complexes. These Au<sup>III</sup> complexes are reduced to Au<sup>I</sup> complexes by DMSO dissolution, and react with silver nitrate to afford chelating complexes, where the triazolyl N atoms bind to gold. The triazolyl-functionalised Au<sup>I</sup> complexes showed potency against ovarian cancer cells (OVCAR-8 cells, IC<sub>50</sub> < 15 μM).

RSC AdvancesVol. 15(23)
The University of Queensland (AU), The University of Western Australia (AU), Curtin University (AU), University of Kerbala (IQ), University of Warith Al-Anbiyaa, University of Kufa (IQ)
European Commission, University of Queensland, Curtin University of Technology, University of Western Australia, Higher Committee for Education Development in Iraq, Medical Research Council, Australian Research Council, National Health and Medical Research Council, Horizon 2020
Openalex Percentile: Top 7%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
3.74
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