110209-73-9Relevant academic research and scientific papers
Diels-Alder reactions of 1,1-dimethyl-2,3,4,5-tetraphenyl-1-silacyclopentadiene, 1,1-dimethyl-2,5-diphenyl-1-silacyclopentadiene and 1,1-dimethyl-3,4-diphenyl-1-silacyclopentadiene with maleic anhydride; kinetic measurements
Henry, George K.,Shinimoto, Ronald,Zhou, Qingshan,Weber, William P.
, p. 3 - 8 (1988)
Diels-Alder reactions of 1,1-dimethyl-2,3,4,5-tetraphenyl-1-silacyclopentadiene, 1,1-dimethyl-2,5-diphenyl-1-silacyclopentadiene and 1,1-dimethyl-3,4-diphenyl-2-silacyclopentadiene with maleic anhydride have been carried out.The rates of these second order reactions have been measured by 1H FT NMR over a range of temperatures.Arrhenius plots of these data yield the activation parameters for these reactions.The synthesis of 1,1-dimethyl-3,4-diphenyl-1-silacyclopentadiene is reported.
DIE CHEMIE DER SCHWEREN CARBEN-ANALOGEN R2M, M=Si, Ge, Sn. XI. REAKTIONEN VON THERMISCH ERZEUGTEM DIMETHYLSILYLEN MIT C-C-MEHRFACHBINDUNGEN
Appler, Hubertus,Neumann, Wilhelm P.
, p. 261 - 272 (2007/10/02)
Phenylated alkynes from 1,4-disila-cyclohexadienes (VIII-X) with thermally generated Me2Si (200 deg C).Bulky substituents (CMe3, SiMe3) prevent the addition.The strained cycloalkyne 3,3,6,6-tetramethyl-1-thia-cycloheptyne-4 (XI), however, yields the known silirene XII (2,2,6,6,8,8-hexamethyl-8-sila-4-thia-bicycloΔ1.7>octane); its transformation to the 1,4-disila-cyclohexadiene is prevented by steric effects.Thermally stable 1,3-dienes give, depending on their substitution pattern, 1-silacyclopentenes-2 or -3.A mechanism is proposed giving the observed products via an initial 1,2-addition.
