| Autor: |
Firme CL; Universidade Federal do Rio Grande do Norte, Instituto de Química, Av. Salgado Filho, s/n, Lagoa Nova, Natal/RN, CEP 59072-970, Brazil. caiofirme@quimica.ufrn.br, Garden SJ, de Lucas NC, Nicodem DE, Correa RJ |
| Jazyk: |
angličtina |
| Zdroj: |
The journal of physical chemistry. A [J Phys Chem A] 2013 Jan 17; Vol. 117 (2), pp. 439-50. Date of Electronic Publication: 2013 Jan 07. |
| DOI: |
10.1021/jp307505e |
| Abstrakt: |
The density functional theory (DFT) and quantum theory of atoms in molecules (QTAIM) have been used to study the lowest lying spin states of the photochemical hydrogen abstraction reaction by formaldehyde, acetaldehyde, and acetone in the presence of different hydrogen donors: propane, 2-propanol, and methylamine. Calculations of all the critical points on the PES of these reactions were performed at uB3LYP/6-311++G(d,p). Methylamine is the best hydrogen donor, in thermodynamic and kinetic terms, followed by 2-propanol and finally propane. Secondary C-H hydrogen abstraction in 2-propanol and C-H abstraction in methylamine is thermodynamically and kinetically favored with respect to hydrogen abstraction from the OH and NH functional groups. Charge transfer takes place before the transition state when methylamine is the hydrogen donor, and for other hydrogen donors, charge transfer begins only in the transition state. The extent of the charge transfer in the transition states corresponds to about 50% of the total change in electron density of the oxygen atom of the T(1) carbonyl compounds during the course of the hydrogen abstraction reactions. The effect of solvent was investigated using the continuum solvation model for the reaction of triplet acetaldehyde in acetonitrile, which resulted in a barrierless transition state for hydrogen abstraction from methylamine. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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