Hydride Transfer to Gold: Yes or No? Exploring the Unexpected Versatility of Au⋅⋅⋅H-M Bonding in Heterobimetallic Dihydrides.

The potential for coordination and H-transfer from Cp MH (M=Zr, W) to gold(I) and gold(III) complexes was explored in a combined experimental and computational study. [(L)Au] cations react with Cp WH giving [(L)Au(κ -H WCp )] (L=IPr (1), cyclic (alkyl)(amino)carbene (2), PPh (3) and Dalphos-Me (4) [IPr=1,3-bis(diisopropylphenyl)imidazolylidene; Dalphos-Me=di(1-adamantyl)-2-(dimethylamino)phenyl-phosphine], while [Au(DMAP) ] (DMAP=p-dimethylaminopyridine) affords the C -symmetric [Au(κ-H WCp ) ] (5). The Dalphos complex 4 can be protonated to give the bicationic adduct 4 H, showing Au ⋅⋅⋅H -N hydrogen bonding. The gold(III) Lewis acid [(C^N-CH)Au(C F )(OEt )] binds Cp WH to give an Au-H-W σ-complex. By contrast, the pincer species [(C^N^C)Au] adds Cp WH by a purely dative W→Au bond, without Au⋅⋅⋅H interaction. The biphenylyl-based chelate [(C^C)Au] forms [(C^C)Au(μ-H) WCp ] , with two 2-electron-3-centre W-H⋅⋅⋅Au interactions and practically no Au-W donor acceptor contribution. In all these complexes, strong but polarized W-H bonds are maintained, without H-transfer to gold. On the other hand, the reactions of Cp ZrH with gold complexes led in all cases to rapid H-transfer and formation of gold hydrides. Relativistic DFT calculations were used to rationalize the striking reactivity and bonding differences in these heterobimetallic hydride complexes along with an analysis of their characteristic NMR parameters and UV/Vis absorption properties.