The photoreduction of graphite oxide (GO) films and solutions by UV light was studied. The electrical resistance of a GO film decreases upon irradiation by more than an order of magnitude. The threshold of photoreduction was determined to be 3.2 eV. The photoreduction is accompanied by an increase in absorption in the visible spectral region, and the CO, CO₂, O₂, and H₂O molecules were found in the gas phase above the irradiated GO film.

The paper presents data on the synthesis, IR, electronic, X-ray photoelectron, and ESR spectroscopies of fullerene C₆₀ molecular complexes with various types of donor compounds, namely, substituted tetrathiafulvalenes, aromatic hydrocarbons, diazodithiafulvalene, tetra-phenyldipyranylidene, tetrasulfur tetranitride, saturated amines, some metallocenes, and Co(II) and Mn(II) tetraphenylporphyrins. Crystal structures of some of these complexes are discussed. The degree of charge transfer in the complexes is evaluated from the shift of the F_1u(4) C₆₀ mode in the IR spectra. The factors responsible for the appearance of the symmetry-forbidden C₆₀ vibrations and the splitting of the absorption bands of C₆₀ in the complexes are considered. The electronic absorption spectra of some complexes show the decrease of the intensity of electron transitions of C₆₀ at 420–530 nm and the appearance of new absorption bands attributed to charge transfer from the donor to C₆₀. The dependences of the energy of charge transfer in the C₆₀ complexes on ionisation and redox potentials of substituted tetra-thiafulvalenes are derived. Peculiarities of donor–acceptor interaction of donor molecules with the spherical C₆₀ are considered.