The final outcome of cycloaddition of isocyanuratoalkyl azides to C-60 depends on the temperature. the thermal stability of azides, the substituents in the isocyanurate ring, and the number of methylene groups in the alkyl radical. The thermal transformations of the monoadducts obtained were studied.
N-Isocyanurato-substituted aziridino[1,2][60]fullerenes were synthesized for the first time as the main products by the reaction of isocyanurato-substituted azides with C-60. The thermal stability and the electrochemical behavior of the compounds synthesized were studied.
Synthesis and electrochemical properties of individual isomers of isocyanurate-substituted bis-organodiazadihomofullerenes
作者:I. P. Romanova、G. G. Yusupova、O. A. Larionova、A. A. Balandina、Sh. K. Latypov、D. G. Yakhvarov、V. V. Zverev、O. G. Sinyashin
DOI:10.1007/s11172-006-0315-y
日期:2006.4
The reactions of fullerene C60 with isocyanurate-substituted azides afforded individual regioisomers of bis-adducts. The structures of the regioisomers depend on the structure of the organic fragment in azide and are determined primarily by the bulkiness of this fragment.