Activation of dihydrogen and coordination of molecular H2 on transition metals

Fifty years ago, when this journal was founded, organometallic chemists could not have imagined that common small molecules such as dinitrogen and especially dihydrogen could function as ligands. Dihydrogen has long been vital in catalytic processes such as hydrogenation and conversions of organic compounds and is now being considered as a future energy storage medium. Dihydrogen is only useful chemically when the two strongly bound H atoms are split apart in a controlled fashion. Although metal hydrides were first well established in 1955, the structure and mechanism by which H-2 binds to and undergoes cleavage on transition metals was not ascertained until even more recently in the history of inorganometallic chemistry, about 20 years after this journal was first published. The activation of dihydrogen is a fascinating saga that has slowly unfolded over the past 80+ years, as will be chronicled in this Perspective. There is a marvelous analogy between the metal-olefin pi bonding model first brought to light by Dewar, Chatt, and Duncanson 60 years ago and the bonding model for side-on sigma-bond coordination discovered by us 30 years ago. There are two separate pathways for H-H (and X-H s-bond activation in general) that directly depend on the electronics of the metal sigma-ligand bonding. Metal d to sigma* X-H backdonation is the key to stabilizing s-bond coordination and also is crucial to its homolytic cleavage (oxidation addition). For electrophilic complexes, particularly cationic systems with minimal backdonation, heterolytic cleavage of H-2 is common and is a key reaction in industrial and biological catalysis. (C) 2013 Elsevier B. V. All rights reserved.