posted on 2006-04-17, 00:00authored byGuochuan Yin, Maria Buchalova, Andrew M. Danby, Chris M. Perkins, David Kitko, John D. Carter, William M. Scheper, Daryle H. Busch
Olefin epoxidations are a class of reactions appropriate for the investigation of oxygenation processes in general.
Here, we report the catalytic epoxidation of various olefins with a novel, cross-bridged cyclam manganese complex,
Mn(Me<sub>2</sub>EBC)Cl<sub>2</sub> (Me<sub>2</sub>EBC is 4,11-dimethyl-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane), using hydrogen peroxide
as the terminal oxidant, in acetone/water (ratio 4:1) as the solvent medium. Catalytic epoxidation studies with this
system have disclosed reactions that proceed by a nonradical pathway other than the expected oxygen-rebound
mechanism that is characteristic of high-valent, late-transition-metal catalysts. Direct treatment of olefins with freshly
synthesized [Mn<sup>IV</sup>(Me<sub>2</sub>EBC)(OH)<sub>2</sub>](PF<sub>6</sub>)<sub>2</sub> (p<i>K</i><sub>a</sub> = 6.86) in either neutral or basic solution confirms earlier observations
that neither the oxo−Mn<sup>IV</sup> nor oxo−Mn<sup>V</sup> species is responsible for olefin epoxidization in this case. Catalytic epoxidation
experiments using the <sup>18</sup>O labels in an acetone/water (H<sub>2</sub><sup>18</sup>O) solvent demonstrate that no <sup>18</sup>O from water (H<sub>2</sub><sup>18</sup>O)
is incorporated into epoxide products even though oxygen exchange was observed between the Mn<sup>IV</sup> species and
H<sub>2</sub><sup>18</sup>O, which leads to the conclusion that oxygen transfer does not proceed by the well-known oxygen-rebound
mechanism. Experiments using labeled dioxygen, <sup>18</sup>O<sub>2</sub>, and hydrogen peroxide, H<sub>2</sub><sup>18</sup>O<sub>2</sub>, confirm that an oxygen
atom is transferred directly from the H<sub>2</sub><sup>18</sup>O<sub>2</sub> oxidant to the olefin substrate in the predominant pathway. The hydrogen
peroxide adduct of this high-oxidation-state manganese complex, Mn<sup>IV</sup>(Me<sub>2</sub>EBC)(O)(OOH)<sup>+</sup>, was detected by mass
spectra in aqueous solutions prepared from Mn<sup>II</sup>(Me<sub>2</sub>EBC)Cl<sub>2</sub> and excess hydrogen peroxide. A Lewis acid pathway,
in which oxygen is transferred to the olefin from that adduct, Mn<sup>IV</sup>(Me<sub>2</sub>EBC)(O)(OOH)<sup>+</sup>, is proposed for epoxidation
reactions mediated by this novel, non-heme manganese complex. A minor radical pathway is also apparent in
these systems.