Synthesis, structures, and properties of new thiophosphorylated fullerenopyrrolidines. First example of the Pishchimuka reaction in fullerene derivatives
作者:G. M. Fazleeva、V. P. Gubskaya、F. G. Sibgatullina、V. V. Yanilkin、N. V. Nastapova、Sh. K. Latypov、A. A. Balandina、I. E. Ismaev、V. V. Zverev、Yu. Ya. Efremov、I. A. Nuretdinov
DOI:10.1007/s11172-006-0284-1
日期:2006.3
The reactions of fullerene C60 with thiophosphorylated mono-or dialdehydes and N-methylglycine in toluene afforded new thiophosphorylated fullerenopyrrolidines, including those containing the free aldehyde group. The purity and compositions of the reaction products were confirmed by MALDI-TOF mass spectrometry and HPLC. The structures of the reaction products were established by two-dimensional homo-and
Phosphorus cryptands 3–5 are obtained via[2 + 3] cyclocondensations between phosphodiydrazides 1a, b and phosphorus-p,p-dialdehydes 2a, b while another phosphorus cryptand 10 is prepared by treatment of the sodium salt of a phosphodihydrazone 8 with a dihalogenated phosphorus-containing macrocycle 9.
磷隐色体 3-5 是通过磷二酰肼 1a, b 和磷-p,p-二醛 2a, b 之间的[2+3]环缩合作用获得的,而另一种磷隐色体 10 则是通过磷二腙 8 的钠盐与二卤化含磷大环 9 的处理而制备的。