کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1323987 | 977316 | 2006 | 4 صفحه PDF | دانلود رایگان |

First-order rate constants of Brook-type isomerization of acylpolysilanes (Me3Si)3SiCOR (R = iso-Pr, tert-Bu, Ad, 2,6-xylyl, and Mes) leading to silenes (Me3Si)2SiC(OSiMe3)R at various temperatures were determined. Their Eyring plots gave kinetic parameters of ΔH‡ = 26.6–29.4 kcal mol−1 and ΔS‡ = −11.5 to −14.6 cal mol−1 K−1. The isomerization was accelerated by introducing an electron-donating alkyl substituent on the carbonyl carbon. These results are in accordance with a concerted mechanism involving a four-centered transition state.
First-order rate constants of Brook-type isomerization of acylpolysilanes to silenes at various temperatures were determined. Their Eyring plots gave kinetic parameters of ΔH‡ = 26.6–29.4 kcal mol−1 and ΔS‡ = −11.5 to −14.6 cal mol−1 K−1, in good agreement with a mechanism involving a four-centered transition state.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 691, Issue 4, 1 February 2006, Pages 541–544