Preparation and Characterization of the
Fullerene Diols 1,2-C<sub>60</sub>(OH)<sub>2</sub>,
1,2-C<sub>70</sub>(OH)<sub>2</sub>, and 5,6-C<sub>70</sub>(OH)<sub>2</sub>
The simple fullerene diols C60(OH)2 and C70(OH)2 were prepared by addition of RuO4 followed by acid hydrolysis. The 1,2-C60(OH)2 isomer was
formed from C60, and two isomers (1,2 and 5,6) of C70(OH)2 were formed in the RuO4 hydroxylation of C70. These compounds are much more
soluble in THF and dioxane than the parent fullerenes. More highly hydroxylated materials are formed as well