π-Bonding of Group 11 Metals to a Tantalum Alkylidyne Alkyl Complex Promotes Unusual Tautomerism to Bis-alkylidene and CO2 to Ketenyl Transformation.

Abstract

A salt metathesis synthetic strategy is used to access rare tantalum/coinage metal (Cu, Ag, Au) heterobimetallic complexes. Specifically, complex [Li(THF)2][Ta(CtBu)(CH2tBu)3], 1, reacts with (IPr)MCl (M = Cu, Ag, Au, IPr = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene) to afford the alkylidyne-bridged species [Ta(CH2tBu)3(μ-CtBu)M(IPr)] 2-M. Interestingly, π-bonding of group 11 metals to the Ta─C moiety promotes a rare alkylidyne alkyl to bis-alkylidene tautomerism, in which compounds 2-M are in equilibrium with [Ta(CHtBu)(CH2tBu)2(μ-CHtBu)M(IPr)] 3-M. This equilibrium was studied in detail using NMR spectroscopy and computational studies. This reveals that the equilibrium position is strongly dependent on the nature of the coinage metal going down the group 11 triad, thus offering a new valuable avenue for controlling this phenomenon. Furthermore, we show that these uncommon bimetallic couples could open attractive opportunities for synergistic reactivity. We notably report an uncommon deoxygenative carbyne transfer to CO2 resulting in rare examples of coinage metal ketenyl species, (tBuCCO)M(IPr), 4-M (M = Cu, Ag, Au). In the case of the Ta/Li analogue 1, the bis(alkylidene) tautomer is not detected, and the reaction with CO2 does not cleanly yield ketenyl species, which highlights the pivotal role played by the coinage metal partner in controlling these unconventional reactions.