Characterization of manganese(V)-oxo polyoxometalate intermediates and their properties in oxygen-transfer reactions

A manganese(III)-substituted polyoxometalate, [alpha(2)-P2MnIII(L)W17O61](7-)(P2W17MnIII), was studied as an oxidation catalyst using iodopentafluorobenzene bis(tifluoroacetate) (F5PhI(TFAc)(2)) as a monooxygen donor. Pink P2W17MnIII turns green upon addition of F5PhI(TFAc)(2). The F-19 NMR spectrum of F5PhI(TFAc) 2 with excess P2W17MnIII at -50 degrees C showed the formation of an intermediate attributed to P2W17MnIII-(FPhI)-Ph-5(TFAc) 2 that disappeared upon warming. The P-31 NMR spectra of P2W17MnIII with excess F5PhI(TFAc) 2 at -50 and -20 degrees C showed a pair of narrow peaks attributed to a diamagnetic, singlet manganese(V)oxo species, P2W17MnV=O. An additional broad peak at -10.6 ppm was attributed to both the P2W17MnIII- F5PhI(TFAc)(2) complex and a paramagnetic, triplet manganese(V)-oxo species. The electronic structure and reactivity of P2W17MnV=O were modeled by DFT calculations using the analogous Keggin compound, [PMnV=(OWO39)-O-11](4-). Calculations with a pure functional, UBLYP, showed singlet and triplet ground states of similar energy. Further calculations using both the UBLYP and UB3LYP functionals for epoxidation and hydroxylation of propene showed lowest lying triplet transition states for both transformations, while singlet and quintet transition states were of higher energy. The calculations especially after corrections for the solvent effect indicate that [PMnV=OW11O39](4-) should be highly reactive, even more reactive than analogous MnVdO porphyrin species. Kinetic measurements of the reaction of P2W17MnV=O with 1-octene indicated, however, that P2W17MnV=O was less reactive than a MnVdO porphyrin. The experimental enthalpy of activation confirmed that the energy barrier for epoxidation is low, but the highly negative entropy of activation leads to a high free energy of activation. This result originates in our view from the strong solvation of the highly charged polyoxometalate by the polar solvent used and adventitious water. The higher negative charge of the polyoxometalate in the transition versus ground state leads to electrostriction of the solvent molecules and to a loss of degrees of freedom, resulting in a highly negative entropy of activation and slower reactions.