Abstract
Complexes [AgL(NO3)CH3CN](1) and [AgLNO3] (2) were formed on reacting AgNO3 with L in acetonitrile for 12 h (at room temperature) and 24 h (at 90 °C), respectively, where L is a (S,N,S) pincer ligand, 4,5-bis(phenylthiomethyl)acridine, synthesized by the reaction of in situ generated PhS(-) with 4,5-bis(bromomethyl)acridine under N2 atmosphere. (1)H and (13)C{(1)H} NMR and the mass spectra of L and its two Ag-complexes were characterized. The structures of complexes 1 and 2 were established with single crystal X-ray crystallography. The Ag-S bond distances of complexes 1 and 2 are 2.5682 (11)/2.5017 (11) Å and 2.4894 (15)/2.4834 (15) Å, respectively. The ligand L in complex 2 is coordinated with the metal in a pincer mode and the complex has a pseudo-pyramidal geometry of donor atoms around the Ag. In 1, the metal is encapsulated by a ten-membered chelate ring. The two Ag(I) complexes were explored for the coupling of aldehyde, alkyne and amine (A(3) reaction) and were found to be efficient as a 2.0 mol% loading of 1 and 0.5 mol% of 2 for good conversion. Complex 2 is a rare example of a catalyst that can efficiently activate A(3) coupling at a 0.5 mol% loading of Ag.
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