Abstract
Cationic Au-(I) complexes of indoles embedding Buchwald phosphine ligands are described. A study combining NMR and X-ray crystallography is described in order to understand the nature of the coordination of the cationic Au atom to the C2-C3 double bond of indoles. Our studies reveal an intermediate coordination between η(2) and η(1), demonstrated by a strong sp(3) character of the C3 atom and a significant slippage toward the C3 atom of the indole rings.