“…Maier et al [33] found that silene was stable only under argon matrix isolation at 10 K and it dimerized to 1,3-disilacyclobutane upon thawing of the matrix at 35 K. In a study of thermal decomposition of 1,1-dimethyl-1-silacyclobutane [34], although kinetic evidence supports the existence of an unstable intermediate, 1,1-dimethyl-1-silene, the only products detected are ethene and 1,1,3,3-tetramethyl-1,3-disilacyclobutane. 1,1-Dimethylsilene, an analog of silene, was found to undergo similar dimerization reactions to yield 1,1,3,3-tetramethyl-1,3-disilacyclobutane: (16) Our study of the hot wire decomposition of silacyclobutane [35] also showed that silene (H 2 Si CH 2 ) was produced, supported by the observation of its dimer signal, 1,3-disilacyclobutane. For the pyrolysis of TMS, 1,1,3,3-tetramethyl-1,3-disilacyclobutane (m/z = 144) [24,29] were previously observed as a product from the analysis by gas chromatography (GC) or GC-MS.…”