Abstract
The binuclear Co(II) complexes of calix[4]arene substituted 2-vanillin (R1) and 2-hydroxy naphthaldimine (R2), Schiff bases (Co2L1 and Co2L2) have been synthesized, characterized and employed as models to mimic monooxygenase in the catalytical oxidation of olefins. The kinetic mathematical model (oxygen rebound mechanism) for olefin cleavage catalyzed by the complexes has been proposed. The results show that, compared to the calix[4]arene-free analogous, the mono and multinuclear complexes of calix[4]arene Schiff bases as catalyst exhibit high activity in the olefin catalytic oxidation.
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