Abstract
A series of cationic Au(i)-BIAN/MIAN complexes, namely [(PPh3)Au(L)]OTf, where L = dpp-bian (1), dpp-mian (2), 2-Me-Ph-bian (3) and 4-Me-Ph-bian (4), has been prepared. All complexes were characterized by analytical and spectroscopic methods and their crystal structures were determined by X-ray diffraction analysis. In all structures, an asymmetric mode of coordination of the di- or monoimine ligand (one shortened Au-N bond and the second elongated Au-N(O) bond) was found, which is a consequence of the so-called antichelate effect. The analysis of the bonding in the coordination environment of gold(i) and the coordination geometry in cations 1-4 was carried out using DFT calculations. The cyclic voltammograms of 1-4 in dichloromethane featured a series of ligand-centered redox processes in the cathodic region. Preliminary bioactivity tests for complexes 1-4 and respective imine ligands have been performed. © 2023 The Royal Society of Chemistry.
| Original language | English |
|---|---|
| Pages (from-to) | 18251-18259 |
| Journal | New Journal of Chemistry |
| Volume | 47 |
| Issue number | 39 |
| Online published | 22 Sept 2023 |
| DOIs | |
| Publication status | Published - 21 Oct 2023 |
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