Radical Cations of Branched Alkanes in Solutions: Time-Resolved Magnetic Field Effect and Quantum Chemical Studies

被引:12
|
作者
Potashov, Pavel A. [1 ]
Borovkov, Vsevolod T. [1 ,2 ]
Shchegoleva, Lyudmila N. [3 ]
Gritsan, Nina P. [1 ,2 ]
Bagryansky, Victor A. [1 ,2 ]
Molin, Yuriy N. [1 ]
机构
[1] Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
[3] Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2012年 / 116卷 / 12期
关键词
SPIN-RESONANCE SPECTRA; PARAMAGNETIC RELAXATION; ION PAIRS; LIQUID; CYCLOHEXANE;
D O I
10.1021/jp2113208
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
Radical cations of heptane and octane isomers, as well as several longer branched alkanes, were detected in irradiated n-hexane solutions at room temperature by the method of time-resolved magnetic field effect (TR MFE). To identify radical cations, the hyperfine coupling constants as determined by simulation of the TR MFE curves were compared to the constants calculated using the density functional theory (DFT) approach. The g-values of the observed radical cations were close to that of the 2,2,3,3-tetramethylbutane radical cation studied earlier by optically detected electron spin resonance (ESR) and TR MFE techniques. No evidence of the decay of the radical cations of branched alkanes to produce olefin radical cations was found, which was further supported by the observation of positive charge transfer from the observed radical cations to cycloalkane molecules. The lifetimes of the radical cations of the branched alkanes were found to be longer than tens of nanoseconds.
引用
收藏
页码:3110 / 3117
页数:8
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