Meurer Eduardo C, Sparrapan Regina, Eberlin Marcos N
Institute of Chemistry, State University of Campinas-UNICAMP, 13083-970 Campinas, SP Brazil.
J Mass Spectrom. 2003 Oct;38(10):1075-80. doi: 10.1002/jms.523.
The intrinsic reactivity of eight gaseous, mass-selected 2-azabutadienyl cations toward polar [4(+) + 2] cycloaddition with ethyl vinyl ether has been investigated by pentaquadrupole mass spectrometric experiments. Cycloaddition occurs readily for all the ions and, with the only exception of those from the N-acyl 2-azabutadienyl cations (N-acyliminium ions), the cycloadducts are found to dissociate readily upon collision activation (CID) both by retro-Diels-Alder reaction and by a characteristic loss of an ethanol (46u) neutral molecule. Ethanol loss from the intact polar [4(+) + 2] cycloadduct functions therefore as a structurally diagnostic test: 72 u neutral gain followed by 46 u neutral loss, i.e., as a combined ion-molecule reaction plus CID 'signature' for N-H, N-alkyl and N-aryl 2-azabutadienyl cations. The two N-acyliminium ions tested are exceptional as they form intact cycloadducts with ethyl vinyl ether which dissociate exclusively by the retro-Diels-Alder pathway.
通过五极杆质谱实验研究了八种气态、经质量选择的2-氮杂丁二烯阳离子与乙烯基乙醚发生极性[4(+) + 2]环加成反应的固有反应活性。所有离子都很容易发生环加成反应,除了那些来自N-酰基2-氮杂丁二烯阳离子(N-酰基亚胺离子)的离子外,发现环加成产物在碰撞活化(CID)时很容易通过逆狄尔斯-阿尔德反应和通过特征性地失去一个乙醇(46u)中性分子而解离。因此,完整的极性[4(+) + 2]环加成产物中乙醇的损失起到了结构诊断测试的作用:72 u中性分子增加后接着46 u中性分子损失,即作为N-H、N-烷基和N-芳基2-氮杂丁二烯阳离子的一种组合离子-分子反应加CID“特征”。所测试的两种N-酰基亚胺离子是例外,因为它们与乙烯基乙醚形成完整的环加成产物,这些产物仅通过逆狄尔斯-阿尔德途径解离。