Redox behavior of nitro substituents of cage complexes

作者: Peter A. Lay , Alan M. Sargeson

DOI: 10.1021/IC00340A011

关键词:

摘要: The redox behavior of nitro groups bonded in the apical positions sar (sar=3,6,10,13,16,19-hexaazabicyclo[6.6.6]icosane) cage complexes is very diverse. Nitroso, hydroxylamine, amine, and radical anions result as primary products from such reductions, depending on type reductant, pH, solvent, amount reductant supplied. ultimate reduction with Zn/HCl contain amine substituents, whereas reductions Sn 2+ /HCl or S 2 O 4 2− , electrochemical at a Hg-pool electrode, yield hydroxylamine-substituted

参考文章(0)