Trujillo Cristina, Mó Otilia, Yáñez Manuel, Salpin Jean-Yves, Tortajada Jeanine
Departamento de Química, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
Chemphyschem. 2007 Jun 25;8(9):1330-7. doi: 10.1002/cphc.200700113.
The gas-phase reactions between Ca(2+) and thiourea are investigated by means of electrospray ionization/mass spectrometry experiments. The MS/MS spectra of Ca(thiourea) complexes show the appearance of new doubly charged species formed by the loss of NH(3) and HNCS. Other intense peaks at m/z 43, 56, 60, 73, 76 and 98 are also observed, and assigned to monocations produced in different coulomb-explosion processes. The structures and bonding characteristics of the different stationary points of the Ca(thiourea) potential energy surface (PES) were theoretically studied by DFT calculations carried out at B3LYP/cc-pWCVTZ level. The analysis of the topology of this PES permits to propose different mechanisms for the loss of ammonia and HNCS, and to identify, the m/z 43, 56, 60, 73, 76 and 98 peaks as H(2)NCNH(+), CaNH(2) (+), H(2)NCS(+), CaSH(+), thiourea(+) and CaNCS(+) ions respectively. There are significant dissimilarities between the reactivity of urea and thiourea, which are related to the lower ionization energy of the latter, and to the fact that thioenols are intrinsically more stable than enols with respect to the corresponding keto forms.
通过电喷雾电离/质谱实验研究了Ca(2+)与硫脲之间的气相反应。Ca(硫脲)配合物的串联质谱表明,出现了因失去NH(3)和HNCS而形成的新的双电荷物种。在m/z 43、56、60、73、76和98处还观察到其他强峰,并将其归属于不同库仑爆炸过程中产生的单电荷离子。通过在B3LYP/cc-pWCVTZ水平上进行的密度泛函理论计算,从理论上研究了Ca(硫脲)势能面(PES)不同驻点的结构和键合特征。对该PES拓扑结构的分析有助于提出氨和HNCS损失的不同机制,并确定m/z 43、56、60、73、76和98峰分别为H(2)NCNH(+)、CaNH(2) (+)、H(2)NCS(+)、CaSH(+)、硫脲(+)和CaNCS(+)离子。尿素和硫脲的反应活性存在显著差异,这与硫脲较低的电离能有关,也与硫代烯醇相对于相应酮式结构而言本质上比烯醇更稳定这一事实有关。