POLYHYDROGENATION OF [60]-FULLERENES AND [70]-FULLERENES

Reduction with Zn-conc. HCl in either benzene or toluene solution, res ults in rapid and quantitative conversion of [60]- and [70]-fullerenes into mainly C60H36 and C70H36/38. Significant amounts of more highly hydrogenated derivatives are also formed. Mass spectra under EI condit ions can be obtained free of peaks due to either less-hydrogenated spe cies or the parent fullerenes, provided they are obtained immediately, since both compounds undergo rapid light-catalysed degradation in the presence of oxygen, to give the parent fullerenes, oxygen-containing derivatives (fullerenols) and lower hydrides; C60H18 is the main produ ct from C60H36. Formation of reduced fullerenes up to C60D44 and C70D4 8 on reaction of[60]- and [70]-fullerenes with Zn-conc. DCI, is attrib uted to the higher stability of C-D compared with C-H bonds, which pro vides greater compensation for the loss of resonance energy and the gr eater steric compression that accompanies reduction beyond the 36 H le vel. Laser-desorption time-of-flight mass spectrometry indicates that the absence of the corresponding higher hydrides (as opposed to deuter ides) is not due to decomposition during EI mass spectrometry. The hyd rides do not undergo hydrogen exchange with D2O either alone or in the presence of either sodium hydrogen carbonate or sodium hydroxide. C60 H36 has considerable thermal stability but that for C70H36/38 is lower . HPLC chromatograms, as well as IR, UV-VIS, H-1 NMR, and mass spectra have been obtained for both compounds. Each appears to be highly resi stant to further reduction by hydrogen-catalyst, but shows a surprisin g tendency to form trimethylene adducts, by an unknown mechanism.