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In the photochemical bis-germylation of C-60 with 1,1,2,2-tetrakis(2,6 diet
hylphenyl)-1,2-digermirane (1), a cycloadduct (2) is obtained in high yield
for the first time. Spectroscopic analysis and theoretical investigation c
onfirm that 2 (which has C-1 symmetry) results from 1,4-cycloaddition. Cont
rol experiments and laser flash photolysis experiments suggest that an exci
plex intermediate is responsible for the formation of 2. The redox properti
es of 2 were examined by differential pulse voltammetry.