Laboratoire Physique et Chimie Théoriques UMR 7019, CNRS - Université de Lorraine, BP239, Boulevard des Aiguillettes, 54 506 Vandoeuvre-lès-Nancy-Cedex, France.
Phys Chem Chem Phys. 2019 Feb 27;21(9):4810-4821. doi: 10.1039/c8cp07452f.
We study at the DFT level the ionization and the fragmentation of uracil in the presence of zero, one and two water molecules, to unravel the effect of microhydration on the reactivity of this nucleobase. We show that the microhydration lowers the adiabatic and vertical ionization potentials by 0.41 eV and 0.22 eV, respectively. Furthermore, microhydration increases the activation energies of the different dissociation channels up to 0.5 eV and restricts the formation of some fragments, in particular those corresponding to the C5-C6 fragmentation pathway. For the first time, our theoretical study shows new transition states and minima not found for the gas phase, hence indicating a change in the fragmentation mechanisms, as well as a stabilizing effect of microhydration, confirming previous experimental studies.
我们在 DFT 水平上研究了零、一和两个水分子存在下尿嘧啶的电离和断裂,以揭示微水合对这种碱基反应性的影响。我们表明,微水合分别将绝热和垂直电离势降低了 0.41 eV 和 0.22 eV。此外,微水合将不同解离通道的活化能提高了 0.5 eV,并限制了一些碎片的形成,特别是那些对应于 C5-C6 断裂途径的碎片。我们的理论研究首次表明,在气相中没有发现新的过渡态和最小值,因此表明了断裂机制的变化,以及微水合的稳定作用,证实了先前的实验研究。