σ‑Donor/Acceptor-Confused Ligands: The Case of a Chlorostibine

• Published in: Inorganic chemistry Vol. 52; no. 12; pp. 7145 - 7151
• Main Authors: Ke, Iou-Sheng, Gabbaï, François P.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 17.06.2013
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/ic400736b

In search for new examples of σ-acceptor ligands, we have investigated the tridentate ligands (o-(iPr2P)C6H4)2SbPh) (LPh) and (o-(iPr2P)C6H4)2SbCl) (LCl) which react with (tht)AuCl (tht = tetrahydrothiophene) to afford LPhAuCl (1) and LClAuCl (2), respectively. As suggested by the structure of these complexes, which confirm complexation of the SbP2 ligands to the gold chloride fragment, and in agreement with the results of the density functional theory (DFT) and natural bond orbital (NBO) calculations, the gold and antimony atom of 1 and 2 are involved in a Au→Sb donor–acceptor interaction. The magnitude of this interaction is higher in complex 2 which possesses a chlorinated and thus more Lewis acidic antimony center. We have also compared the strength of the Au→Sb interaction present in 2 with the Au→Bi interaction observed in the newly prepared bismuth analogue [(o-(iPr2P)C6H4)2BiCl]AuCl (3). This comparison reveals that 2 possesses a stronger Au→Pn bond (Pn = pnictogen), an observation reconciled by invoking the greater Lewis acidity of antimony(III) halides. Finally, complexes 1 and 2 undergo a clean antimony-centered oxidation when treated with ortho-chloranyl. These oxidation reactions afford complexes [(o-(iPr2P)C6H4)2(o-C6Cl4O2)SbPh]AuCl (5) and [(o-(iPr2P)C6H4)2(o-C6Cl4O2)SbCl]AuCl (6). Structural and computational studies of 5 show that the Au→Sb bond becomes shorter and more covalent upon oxidation of the antimony atom. Although the structure of 6 has not been experimentally determined, spectroscopic and computational results show a similar effect in this complex. Complex 5 and 6 constitute rare examples of metalated six coordinate antimony compounds.