作者:Genevieve Pfister-Guillouzo、Francoise Gracian、Anna Senio、Francois Bourdon、Yannick Vallee、Jean Louis Ripoll
DOI:10.1021/ja00054a046
日期:1993.1
Thioformyl cyanide, HCSCN, was generated, under flash vacuum thermolysis conditions, by retro-ene and retro-Diels-Alder cleavages of allylcyanomethyl sulfide and 3-cyano-2-thiabicyclo[2.2.1]hept-5-ene, respectively, and unambiguously characterized in the gas phase by photoelectron spectroscopy. Its unimolecular decomposition into carbon monosulfidic and hydrogen cyanide was found to be strongly disfavored
在快速真空热解条件下,分别通过烯丙基氰基甲基硫醚和 3-氰基-2-硫双环[2.2.1]庚-5-烯的逆烯和逆狄尔斯-阿尔德裂解生成硫甲酰氰,HCSCN,以及通过光电子能谱在气相中明确表征。强烈反对将其单分子分解为一硫化碳和氰化氢