Kinetic and mechanistic studies of vanadium-based, extended catalytic lifetime catechol dioxygenases.

Recently we showed that V-containing polyoxometalates such as (n-Bu4N)7SiW9V3O40 or (n-Bu4N)9P2W15V3O62, as well as eight other V-containing precatalysts tested, evolve to high-activity, long catalytic lifetime (> or = 30,000-100,000 total turnovers) 3,5-di-tert-butylcatechol (DTBC) dioxygenases in which Pierpont's complex [VO(DBSQ)(DTBC)]2 is apparently a common catalyst resting state [Yin, C.-X.; Finke, R. G. J. Am. Chem. Soc. 2005, 107, 9003-9013]. In a separate paper, autoxidation of DTBC to the corresponding benzoquinone and H2O2 was shown to be a key to the catalyst evolution process: the H2O2, DTBC, and O2 plus virtually any V-based precatalyst tested form [VO(DBSQ)(DTBC)]2 under the catalytic conditions, that catalyst formation process being autocatalytic in H2O2. The resulting novel concept is that of an autoxidation-product-initiated dioxygenase [Yin, C.-X.; Sasaki, Y.; Finke, R. G. Inorg Chem. 2005, in press]. Herein the following questions about this record catalytic lifetime 3,5-di-tert-butylcatechol dioxygenase catalyst are explored: (i) What is the rate law for 3,5-di-tert-butylcatechol dioxygenation when one begins with Pierpont's [VO(DBSQ)(DTBC)]2? (ii) Does it support the hypothesis that this complex is a catalyst resting state or, perhaps, even the true catalyst? (iii) Can a mechanism be written from that information and from the knowledge in the dioxygenase literature? The results answer each of these questions and provide considerable mechanistic insight into the most catalytically active and long-lived DTBC dioxygenase catalyst presently known.