16090-53-2Relevant articles and documents
Ring contraction of 1,2-digermacyclohexa-3,5-dienes initiated by electron transfer reactions with TCNE
Mochida, Kunio,Shimizu, Hiromi,Nanjo, Masato
, p. 1226 - 1227 (2007/10/03)
The thermal reaction of 1,2-digermacyclohexa-3,5-dienes with tetracyanoethylene (TCNE) gave 1-germacyclopenta-2,4-diene as a germylene extrusion compound through a charge-transfer complex. The 1-germacyclopenta-2,4-diene was trapped with TCNE to give 5,5,6,6-tetracyano-7-germanor-bornene.
Thermolyse, pyrolyse et photolyse d'heterocycles germanies et soufres a 4 et 5 chainons: especes intermediaires a germanium doublement lie
Barrau, J.,Rima, G.,El-Amine, M.,Satge, J.
, p. 39 - 50 (2007/10/02)
The thermolysis, pyrolysis and photolysis of thiagermetane , dithiagermolane and thiagermetane dioxide have been studied.Thiagermetane and dithiagermolane decompose leading to various new germylated heterocycles: , and probably proceed by two competitive mechanisms which involve the transient species germaethene , germathione , thiagermirane and thiadigermetane .Pyrolysis of thiagermetane dioxide also involves germaethene and probably a new doubly-bonded germanium species, the germasulfene (by mass spectroscopy), which finally gives germoxanes (Me2GeO)n (n = 3,4).