Dissecting transmetalation reactions at the molecular level: C-B versus F-B bond activation in phenyltrifluoroborate silver complexes.

The gas-phase unimolecular reactions of the silver(i) complex [Ag(PhBF3)2]-, formed via electrospray ionisation mass spectrometry of solutions containing the phenyltrifluoroborate salt and AgNO3, are examined. Upon collision induced dissociation (CID) three major reaction channels were observed for [Ag(PhBF3)2]-: Ph- group transfer via a transmetalation reaction to yield [PhAg(PhBF3)]-; F- transfer to produce [FAg(PhBF3)]-; and release of PhBF3-. The anionic silver product complexes of these reactions, [LAg(PhBF3)]- (where L = Ph and F), were then mass-selected and subjected to a further stage of CID. [PhAg(PhBF3)]- undergoes a Ph- group transfer via transmetalation to yield [Ph2Ag]- with loss of BF3. [FAg(PhBF3)]- solely fragments via loss of BF4-, a reaction that involves Ph- group transfer from B to Ag in conjunction with F- transfer from Ag to B. Density functional theory (DFT) calculations on the various competing pathways reveal that: (i) the overall endothermicities govern the experimentally observed product ion abundances; (ii) the Ph- group and F- transfer reactions proceed via late transition states; and (iii) formation of BF4- from [FAg(PhBF3)]- is a multistep reaction in which Ph- group transfer from B to Ag proceeds first to produce a [FAgPh(BF3)]- complex in which the BF3 moiety is initially weakly bound to the ipso-carbon of the phenyl group and then migrates across the linear [FAgPh]- moiety from C to Ag to F yielding [PhAg(BF4)]-, which can then dissociate via loss of PhAg.