The first representatives of linear phosphocyclophanes were prepared starting from hydroquinone or 4,4'-dihydroxybiphenyl and phosphorous triamides. The reaction course is influenced by the structures of the aromatic diol and alkyl substituents in the phosphamide moiety. The phosphorus atom readily enters redox reactions and complexation. The complexing power of the aromatic fragments of the synthesized molecules is lower than that of classical p-cyclophanes.
The first representatives of linear phosphocyclophanes were prepared starting from hydroquinone or 4,4'-dihydroxybiphenyl and phosphorous triamides. The reaction course is influenced by the structures of the aromatic diol and alkyl substituents in the phosphamide moiety. The phosphorus atom readily enters redox reactions and complexation. The complexing power of the aromatic fragments of the synthesized molecules is lower than that of classical p-cyclophanes.
Dismutation of arylene phosphorodiamidites: Specific features and aspects of preparative use
作者:E. N. Rasadkina、P. V. Slitikov、E. E. Nifant’ev
DOI:10.1134/s1070363206020046
日期:2006.2
The dismutation ofarylene phosphorodiamidites derived from the simplest phenols and naphthols and of their dibasic analogs was studied. The main regular trends of this process and the limits of its synthetic applicability were determined.