Alkane Dehydrogenation by C–H Activation at Iridium(III)

Abstract

Stoichiometric alkane dehydrogenation utilizing an Ir<sup>III</sup> pincer complex, (<sup><i>dm</i></sup>Phebox)­Ir­(OAc)<sub>2</sub>(OH<sub>2</sub>) (<b>1a</b>), has been described. The reaction between <b>1a</b> and octane resulted in quantitative formation of (<sup><i>dm</i></sup>Phebox)­Ir­(OAc)­(H) (<b>3a</b>) and octene. At early reaction times 1-octene is the major product, indicative of terminal C–H activation by <b>1a</b>. In contrast to prior reports of alkane dehydrogenation with Ir, C–H bond activation occurs at Ir<sup>III</sup> and the dehydrogenation is not inhibited by nitrogen, olefin, or water

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