作者:M.Teodor Căproiu、Nicolae Negoiţă、Alexandru T. Balaban
DOI:10.1016/s0040-4020(01)90899-3
日期:1983.1
The synthesis of 3,5-di-t-butylphenyl-polynitrophenylamines is reported, with 2,6-dinitro- and 2,4,6-trinitrophenyl groups. Oxidation converts these amines into capto-dative diarylaminyls which are stable in solution at room temperature. Their ESR spectra are described; simulation yields hyperfine coupling constants with lower values for the acceptor than for the donor group. This is the first time
据报道,具有2,6-二硝基-和2,4,6-三硝基苯基的3,5-二叔丁基苯基-多硝基苯胺的合成。氧化将这些胺转化为在室温下在溶液中稳定的巯基二芳基芳基。描述了它们的ESR光谱。模拟产生的超精细耦合常数的受体值低于供体基团。这是具有多硝基苯基基团的戊基酯的EST光谱第一次可以令人满意地模拟。