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Interactions between simple radicals and water
被引:24
作者:
Crespo-Otero, Rachel
[1
,2
]
Sanchez-Garcia, Elsa
[1
]
Suardiaz, Reynier
[2
]
Montero, Luis A.
[2
]
Sander, Wolfram
[1
]
机构:
[1] Ruhr Univ Bochum, Lehrstuhl Organ Chem 2, D-44780 Bochum, Germany
[2] Univ La Habana, Fac Quim, Lab Quim Computac & Teor, Havana 10400, Cuba
关键词:
Hydrogen bonds;
Radicals;
Water;
Weak interactions;
Natural bond orbital;
D O I:
10.1016/j.chemphys.2008.08.012
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The interactions of the simple radicals CH3, NH2, OR and F with water have been studied by DFT (UB3LYP/6-311++G(2d,2p)) and ab initio (RHF-UCCSD(T)/6-311++G(2d,2p)) methods. In this order the number of lone pairs (from zero to three), the electronegativity, and the strength of the X-H bonds increase (X = C, N, and O). The various minima of the radical-water complexes were located using the multiple minima hypersurface (MMH) approach which had previously been proven to be useful for closed-shell molecules, The role of the unpaired electron in hydrogen bonding was investigated using the natural bond orbital (NBO) analysis. A considerable contribution of the unpaired electron to the complex stabilization was only found for the methyl radical and the fluorine atom, whereas in the aminyl and the hydroxyl radical the role of the Unpaired electron is negligible. (C) 2008 Elsevier B.V. All rights reserved.
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页码:193 / 201
页数:9
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