Department of Chemistry, Federal University of Santa Catarina, Florianópolis-SC, Brazil.
J Am Chem Soc. 2012 Jan 11;134(1):138-41. doi: 10.1021/ja209570y. Epub 2011 Dec 9.
The reaction mechanism of the GPx-like oxidation of PhSH with H(2)O(2) catalyzed by selenoxides proceeds via formation of the hydroxy perhydroxy selenane, which is a stronger oxidizing agent than selenoxide. A hydroxy perhydroxy selenane intermediate was observed by electrospray ionization mass spectrometry and (77)Se NMR spectroscopy in reactions of selenoxide 8 with H(2)O(2).The initial velocity of oxidation of PhSH by H(2)O(2) with selenoxide 8 is 4 orders of magnitude higher than that of 8 without peroxide. Selenoxide 8 is not reduced to selenide 6 by PhSH in the presence of H(2)O(2). While electronic substituent effects have minimal impact on the catalytic performance of selenoxides, chelating groups increase the rate of catalysis.
硒氧化物催化 PhSH 与 H(2)O(2)的 GPx 样氧化的反应机制是通过形成羟过氧全氢硒烷进行的,后者是比硒氧化物更强的氧化剂。通过电喷雾电离质谱和(77)Se NMR 光谱观察到在硒氧化物 8 与 H(2)O(2)的反应中存在羟过氧全氢硒烷中间体。硒氧化物 8 与 H(2)O(2)氧化 PhSH 的初始速度比没有过氧化物的 8 高 4 个数量级。在 H(2)O(2)存在下,硒氧化物 8 不会被 PhSH 还原为硒化物 6。虽然电子取代基效应对硒氧化物的催化性能影响不大,但螯合基团会提高催化速率。