Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation, East China University of Technology, Nanchang, 330013, People's Republic of China.
J Am Soc Mass Spectrom. 2017 Oct;28(10):2246-2254. doi: 10.1007/s13361-017-1736-6. Epub 2017 Jul 5.
Intramolecular halogen atom coordinated H transfer reaction in the gas phase dissociation of protonated dichlorvos derivatives has been explored by electrospray ionization tandem mass spectrometry. Upon collisional activation, protonated dichlorvos underwent dissociation reaction via cleavage of the P-O bond to give reactive ion-neutral complex (INC) intermediate, [dimethoxylphosphinoylium + dichloroacetaldehyde]. Besides direct dissociation of the complex, intramolecular chlorine atom coordinated H transfer reaction within the complex takes place, leading to the formation of protonated dimethyl chlorophosphate. To investigate the fragmentation mechanism, deuterium-labeled experiments and several other halogen-substituted (Br and F) analogs of dichlorvos were prepared and evaluated, which display a similar intramolecular halogen transfer. Density functional theory (DFT)-based calculations were performed and the computational results also support the mechanism. Graphical Abstract ᅟ.
通过电喷雾串联质谱研究了质子化敌敌畏衍生物气相解离过程中分子内卤素原子配位的 H 转移反应。在碰撞激活下,质子化敌敌畏通过 P-O 键的断裂发生解离反应,生成反应性离子-中性配合物(INC)中间体[二甲氧基膦鎓+二氯乙醛]。除了复合物的直接解离外,复合物内的分子内氯原子配位 H 转移反应也会发生,导致质子化二甲基磷酸酯的形成。为了研究碎裂机制,制备并评估了氘标记实验和几种其他卤素取代(溴和氟)的敌敌畏类似物,它们表现出类似的分子内卤素转移。进行了基于密度泛函理论(DFT)的计算,计算结果也支持该机制。