oxidation of organosilanes to silanols with H2O2 under neutral reaction conditions has been accomplished. A variety of organosilanes with alkyl, aryl, alknyl, and heterocyclic substituents were tolerated, as well as sterically hindered organosilanes. The oxidation appears to proceed by a concerted process involving a manganese hydroperoxide species. Featuring mild reaction conditions, fast oxidation,
在中性反应条件下,用H 2 O 2进行的第一次锰催化的有机硅烷氧化为硅烷醇。可以耐受具有烷基,芳基,炔基和杂环取代基的多种有机硅烷,以及受阻位有机硅烷。氧化似乎是通过涉及氢过氧化锰物质的协同过程进行的。该方案具有温和的反应条件,快速的氧化作用,并且没有废副产物,可实现硅烷醇和硅烷二醇的低成本,生态友好的合成。
Dejak,B. et al., Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques, 1969, vol. 17, p. 7 - 12