Abstract

The discrete multinuclear AgI -NHC complexes [Agn (1)n )](X)n ; (n=3 or 4, X=BF4 , PF6 ), synthesized from a bis-NHC ligand 1 and AgI ions via multiligand self-assembly, were observed to be in equilibrium between two forms (tri- and tetranuclear) in solution on the NMR timescale, which is unprecedented in CNHC -donor based chemistry. The existence of both the species was confirmed by various studies such as NMR (1 H, VT, 2D-DOSY) and ESI-MS analysis along with concentration studies. Importantly, replacing AgI with other coinage metals (AuI and CuI ) was found to alter the phenomenon entirely: a slow exchange from the tetra- to trinuclear species was noticed for the AuI complexes (4 a, b), whereas no such process was detected in case of the CuI complexes (5 a, b).

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