Synthesis of New Iron-Containing Carbon Cages by Reaction of C60 Fullerene with Ferrocene

Reaction of C₆₀ fullerene with ferrocene in the presence of aluminum chloride and aluminum in an inert atmosphere gave ferrocenyl-substituted fullerene 2C₆₀ ·1.5(C₅H₅)₂Fe ·3H₂O. The product is a thermally stable iron-containing carbon cage in which the intersphere cavity is formed by three C₆₀ polyhedra and is closed by cyclopentadienyl ligands via formation of four carbon-carbon bonds.     

Spectral studies of bridged bisindenylmetallocenes and products of their reactions with polymethylalumoxane in toluene and dichloromethane in the visible region

Quantitative characteristics of changes in the energy of charge transfer from -bonded ligands to metal are presented for the series of structurally similar ansa-metallocene complexes of IVB Group elements. The changes are caused by the solvation effect, replacement of -bonded chlorine ligands by methyl groups and of bridging ethylene groups by dimethylsilylene moieties, introduction of the methyl substituent into position 2 and phenyl substituent into position 4 of the indenyl system, variation of the transition metal in metallocene, and formation of complexes with polymethylalumoxane (MAO) at different Al_MAO/Zr ratios. These effects are found to be additive.     

Crystal structure of the oxime of 2-acetylpyridine

Institute of Chemical Physics, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 3, pp. 113–115, May–June, 1991.     

Thermal rearrangement of 2,5-diaryl-3,3,4,4-tetracyanopyrrolidines

It was shown that briefly boiling solutions of 2,5-diaryl-3,3,4,4-tetracyanopyrrolidines in DMF caused rearrangement into 5-aryl-2-(N-arylidenamino)-3,4-dicyanopyrroles, which are methylated with diazomethane both at the NH bond and at the carbon atom of the azomethine fragment.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 42–46, January, 1995.