21961-74-0Relevant academic research and scientific papers
A CONVENIENT SYNTHESIS OF GERMACYCLOBUTANES
Seetz, Johannes W. F. L.,Heisteeg, Bartholomeus J.J. van de,Schat, Gerrit,Akkerman, Otto D.,Bickelhaupt, Friedrich
, p. 319 - 322 (1984)
The reaction of the di-Grignard reagents BrMgCH2CR2CH2MgBr (2a: R = H; 2b: R = Me) with dichlorodimethylgermane gave 1,1-dimethylgermacyclobutane (1a) and its 3,3-dimethyl derivative 1b, respectively, in more than 95percent yield.
Kinetics and mechanism of the thermal decomposition of 1,1-dimethylgermetane
Namavari, Mohammed,Conlin, Robert T.
, p. 3307 - 3312 (2008/10/08)
The gas-phase unimolecular decomposition of 1,1-dimethylgermetane has been investigated over the temperature range 683.9-751.2 K at pressures of ca. 15 Torr. Four products, cyclopropane, propene, ethene, and 1,1,2,2-tetramethylgermacyclopentane, are formed. Arrhenius parameters for the primary decomposition channels to (1) 1,1-dimethylgermene and ethene and (2) dimethylgermylene, cyclopropane, and propene are reported: (1) log k1/s-1 = 14.7 ± 0.4 - 63.1 ± 1.2 kcal mol-1/RT ln 10; (2) log k2/s-1 = 14.1 ± 0.3 - 60.7 ± 0.8 kcal mol-1/RT ln 10. (Matrix Presented) The surprisingly high activation energy for the 2 + 2 cycloreversion is interpreted in terms of a strong Ge-C bond dissociation enthalpy and/or reduced ring strain in the germetane.
