Cyclotrigermenyl radical

Notably, the bicyclic radical 41 is localized, in sharp contrast to the allylic-type delocalization of cyclotrigermenyl radical 39 and cyclotetrasilenyl radical 40. The obvions reason for snch a distinction is the absence of the neighboring to the Ge-radical center tt-bond necessary for the effective throngh-bond delocalization of the unpaired electron in the radical 41, whereas the through-space radical-C=C bond interaction is not sufficiently strong to indnce the effective delocalization of the unpaired electron. 

Germylene 185 can be reduced with substoichiometric amounts of KCg to give the cyclotrigermenyl radical 186, which has been structurally characterized (Equation (329)), while reaction of 185 with an excess (2 equiv.) of KC8 produces 187 which is the germanium analog of the allyl anion (Equation (330)).400 The structure of 187 has been obtained as well. 

In the cyclotrigermenyl radical 96 the average Ge = Ge distance is 2.35(7) A.81 In valence bond terms the ring is expected to involve a double bond between two Ge with the unpaired electron located on the third Ge atom. Thus, the three following forms 96a, 96b, and 96c can be written. 

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