Computational Support for Phillips Catalyst Initiation via Cr–C Bond Homolysis in a Chromacyclopentane Site

Using density functional theory, we examine a possible homolysis initiation mechanism for the Phillips catalyst, starting from Cr II sites exposed to ethylene. Spin-crossing in an abundant quintet bis (ethylene) Cr II site leads to cycloaddition to form a chromacyclopentane site. One Cr–C bond then homolyzes to generate a tethered n -butyl radical: [Cr(CH 2 ) 3 CH 2 • ]. If the radical attaches to a nearby inorganic Cr site, it yields two alkylCr III sites capable of Cossee–Arlman polymerization. The overall computed barrier for this initiation process is 132 kJ/mol, which is comparable to the 120 kJ/mol value that we estimated from reported initiation times in industrial reactors. Poisson statistics suggest that this mechanism could activate ∼35% of Cr sites on a commercial catalyst with a loading of 0.4 Cr/nm 2 . Pairwise Cr grafting, amplification by complementary initiation reactions, or the creation of dangling bonds that form as the silica support fractures, might explain the apparent increase in per-site activity at lower Cr loadings.