Jacob K, Vogt W, Knedel M, Scháfer W
Biomed Mass Spectrom. 1976 Apr;3(2):64-70. doi: 10.1002/bms.1200030205.
The mass spectra of the dimethylphosphinic, dimethylthiophosphinic and dimethylphosphinous ester derivatives of several monohydroxy steroids are reported. The fragmentations of the derivatized steroids largely depend on the nature of the phosphorus-containing ester group. Phenolic ester derivatives exhibit the base peak at the molecular ion, whereas the spectra of the secondary phosphinic esters are dominated by very intense protonated phosphinic acid ions [Me2P(XH)(OH)]+ at m/e 95 (X =O) or at m/e 111 (x = s). The present results also indicate the low ionization potential for the phosphinic ester group. Due to their good gas chromatographic properties, these steroid derivatives appear to be particularly suitable for gas chromatographic mass spectrometric analysis of biochemical materials.
报道了几种单羟基甾体的二甲基次膦酸酯、二甲基硫代次膦酸酯和二甲基亚膦酸酯衍生物的质谱。衍生化甾体的裂解很大程度上取决于含磷酯基的性质。酚酯衍生物的分子离子处出现基峰,而仲次膦酸酯的质谱则以m/e 95(X = O)或m/e 111(X = S)处非常强的质子化次膦酸离子[Me2P(XH)(OH)]+为主。目前的结果还表明次膦酸酯基的电离电位较低。由于它们具有良好的气相色谱性质,这些甾体衍生物似乎特别适合于生化材料的气相色谱 - 质谱分析。