Carbon–sulfur bond formation by reductive elimination of gold(iii) thiolates. Issue 18 (10th April 2018)

• Record Type: Journal Article
• Authors: Currie, Lucy; Rocchigiani, Luca; Hughes, David L.; Bochmann, Manfred
• Is Part Of: Dalton transactions. Volume 47:Issue 18(2018)
• Page Start: 6333
• Page End: 6343
• Publication Date: 2018-04-10
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c8dt00906f
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Thiols were found to cleave Au–C bonds in (C^N^C)gold(iii ) pincer complexes and to induce C–S reductive elimination reactions, to give aryl thioethers. Abstract : Whereas the reaction of the gold(iii ) pincer complex (C^N^C)AuCl with 1-adamantyl thiol (AdSH) in the presence of base affords (C^N^C)AuSAd, the same reaction in the absence of base leads to formation of aryl thioethers as the products of reductive elimination of the Au–C and Au–S ligands (C^N^C = dianion of 2-6-diphenylpyridine or 2-6-diphenylpyrazine). Although high chemical stability is usually taken as a characteristic of pincer complexes, results show that thiols are capable of cleaving one of the pincer Au–C bonds. This reaction is not simply a function of S–H acidity, since no cleavage takes place with other more acidic X–H compounds, such as carbazole, amides, phenols and malonates. The reductive C–S elimination follows a second-order rate law, −d[1a ]/d t = k [1a ][AdSH]. Reductive elimination is enabled by displacement of the N-donor by thiol; this provides the conformational flexibility necessary for C–S bond formation to occur. Alternatively, reductive C–S bond formation can be induced by reaction of pre-formed thiolates (C^N^C)AuSR with a strong Brønsted acid, followed by addition of SMe2 as base. On the other hand, treatment of (C^N^C)AuR (R = Me, aryl, alkynyl) with thiols under similar conditions leads to selective C–C rather than C–S bond formation. The reaction of (C^N^C)AuSAd with H + in the absence of a donor ligand affords the thiolato-bridged complex [{(C^N–CH)Au(μ-SAd)}2 ] 2+ which was crystallographically characterised.