Reversible Dihydrogen Activation and Catalytic H/D Exchange with Group 10 Heterometallic Complexes**

Abstract

Reaction of a hexagonal planar palladium complex featuring a [PdMg 3 H 3 ] core with H 2 is reversible and leads to the formation of a new [PdMg 2 H 4 ] tetrahydride species alongside an equivalent of a magnesium hydride co-product [MgH]. While the reversibility of this process prevented isolation of [PdMg 2 H 4 ], analogous [PtMg 2 H 4 ] and [PtZn 2 H 4 ] complexes could be isolated and characterised through independent syntheses. Computational analysis (DFT, AIM, NCIPlot) of the bonding in a series of heterometallic tetrahydride compounds (Ni-Pt; Mg and Zn) suggests that these complexes are best described as square planar with marginal metal-metal interactions; the strength of which increases slightly as group 10 is descended and increases from Mg to Zn. DFT calculations support a mechanism for H 2 activation involving a ligand-assisted oxidative addition to Pd. These findings were exploited to develop a catalytic protocol for H/D exchange into magnesium hydride and zinc hydride bonds.

Photochemical H2 activation by an Zn–Fe heterometallic: a mechanistic investigation

“…In the past few years there has been growing interest in using heterometallic complexes for H 2 activation. Transition metal complexes supported by Lewis-acidic B, 1–3 Al, 4 Zn, 5,6 Mg, 7,8 and Sn 9,10 ligands have all been documented to react with H 2 under thermal conditions. Despite the rapid growth of this area, examples of photolytic H 2 splitting using these types of heterometallic complexes are rare.…”