摘要
The addition of Lewis or Brönsted acids (LA = Zn(OTf) 2 , B(C 6 F 5 ) 3 , HBAr F , TFA) to the high-valent manganese-oxo complex Mn V (O)(TBP 8 Cz) results in the stabilization of a valence tautomer Mn IV (O-LA)(TBP 8 Cz •+ ). The Zn II and B(C 6 F 5 ) 3 complexes were characterized by manganese K-edge X-ray absorption spectroscopy (XAS). The position of the edge energies and the intensities of the pre-edge (1s to 3d) peaks confirm that the Mn ion is in the +4 oxidation state. Fitting of the extended X-ray absorption fine structure (EXAFS) region reveals 4 N/O ligands at Mn-N ave = 1.89 Å and a fifth N/O ligand at 1.61 Å, corresponding to the terminal oxo ligand. This Mn-O bond length is elongated compared to the Mn V (O) starting material (Mn-O = 1.55 Å). The reactivity of Mn IV (O-LA)(TBP 8 Cz •+ ) toward C-H substrates was examined, and it was found that H • abstraction from C-H bonds occurs in a 1:1 stoichiometry, giving a Mn IV complex and the dehydrogenated organic product. The rates of C-H cleavage are accelerated for the Mn IV (O-LA)(TBP 8 Cz •+ ) valence tautomer as compared to the Mn V (O) valence tautomer when LA = Zn II , B(C 6 F 5 ) 3 , and HBAr F , whereas for LA = TFA, the C-H cleavage rate is slightly slower than when compared to Mn V (O). A large, nonclassical kinetic isotope effect of k H /k D = 25-27 was observed for LA = B(C 6 F 5 ) 3 and HBAr F , indicating that H-atom transfer (HAT) is the rate-limiting step in the C-H cleavage reaction and implicating a potential tunneling mechanism for HAT. The reactivity of Mn IV (O-LA)(TBP 8 Cz •+ ) toward C-H bonds depends on the strength of the Lewis acid. The HAT reactivity is compared with the analogous corrole complex Mn IV (O-H)(tpfc •+ ) recently reported (J. Am. Chem. Soc. 2015, 137, 14481-14487).