Stabilities of nanohydrated thymine radical cations: insights from multiphoton ionization experiments and ab initio calculations

被引:10
|
作者
Pandey, Rahul [1 ]
Lalande, Mathieu [2 ]
Ryszka, Michal [1 ]
Limao-Vieira, Paulo [3 ]
Mason, Nigel J. [1 ]
Poully, Jean-Christophe [2 ]
Eden, Samuel [1 ]
机构
[1] Open Univ, Sch Phys Sci, Walton Hall, Milton Keynes MK7 6AA, Bucks, England
[2] Univ Caen Normandie, CIMAP, UMR 6252, CEA CNRS ENSICAEN, Caen, France
[3] Univ Nova Lisboa, Dept Fis, FCT, Lab Colisoes Atom & Mol,CEFITEC, P-2829516 Caparica, Portugal
来源
EUROPEAN PHYSICAL JOURNAL D | 2017年 / 71卷 / 07期
基金
英国工程与自然科学研究理事会;
关键词
NUCLEIC-ACID BASES; PROTON-TRANSFER; DNA-BASE; ADENINE; WATER; DISSOCIATION; SPECTROSCOPY; NUCLEOBASES; POTENTIALS; HYDRATION;
D O I
10.1140/epjd/e2017-70827-1
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Multi-photon ionization experiments have been carried out on thymine-water clusters in the gas phase. Metastable H2O loss from T+( H2O)(n) was observed at n >= 3 only. Ab initio quantum-chemical calculations of a large range of optimized T+( H2O)(n) conformers have been performed up to n = 4, enabling binding energies of water to be derived. These decrease smoothly with n, consistent with the general trend of increasing metastable H2O loss in the experimental data. The lowest-energy conformers of T+( H2O)(3) and T+( H2O)(4) feature intermolecular bonding via charge-dipole interactions, in contrast with the purely hydrogen-bonded neutrals. We found no evidence for a closed hydration shell at n = 4, also contrasting with studies of neutral clusters.
引用
收藏
页数:8
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