C-H versus C-O Addition: A DFT Study of the Catalytic Cleavage of the β-O-4 Ether Linkage in Lignin by Iridium and Cobalt Pincer Complexes

Abstract

The potential energy surfaces of the reactions involved in the catalytic cleavage of 2-phenoxy-1-phenylethanol, a model of the β-O-4 linkage in lignin, by (iprPCP)-Ir, (iprPCOP)-Ir, (iprPCP)-Co and (iprPCOP)-Co complexes have been studied using the M06/6-311G**/LANL2TZ level of theory. Both iridium and cobalt are found to be active towards the cleavage of the β-O-4 linkage, with rate constants of 44.7 s−1 and 5.1 × 106 s−1, respectively. The iridium catalysts prefer the ‘initial C-H addition’ pathway, showing a kinetic preference of 16.8 kcal mol−1 over the ‘direct C-O insertion’ pathway, while the cobalt catalysts prefer the ‘direct C-O insertion’ route which is kinetically favored by 15.7 kcal mol−1 over the ‘initial C-H addition’ pathway. A two-state reactivity occurs along the preferred pathway for the cobalt-catalyzed reaction.