Oxygen rebound mechanism for hydrocarbon hydroxylation by high-valent
metal complexes is critically analyzed and is shown to be contradictor
y in certain aspects. The synchronous insertion of O atom mechanism is
found to be significantly less contradictory (at least for the most i
nteresting cases of strong C-H bonds, for example in methane) if it is
supplemented by the stage of formation of the five-coordinate carbon
intermediate complex of a hydrocarbon molecule via oxygen atom of an a
ctive center.