首页> 外文期刊>Bulletin of the Korean Chemical Society >Rearrangement of Benzyl-type Radical in Corona Discharge of 2,6-Dichlorotoluene
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Rearrangement of Benzyl-type Radical in Corona Discharge of 2,6-Dichlorotoluene

机译:2,6-二氯甲苯电晕放电中苄基自由基的重排

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Using a pinhole-type glass nozzle equipped for a corona-excited supersonic expansion (CESE), precursor 2,6-dichlorotoluene seeded in a large amount of inert carrier gas helium was discharged to produce jet-cooled but electronically excited benzyl-type radicals. The visible vibronic emission spectrum was recorded with a long-path monochromator to observe vibronic bands in the D1 ℃ D0 electronic transition of benzyl-type radicals. The spectral analysis revealed the generation of not only the 2,6-dichlorobenzyl radical as a typical product, but also the o-chlorobenzyl radical as an unexpected species, which indicates the possible molecular rearrangement in eliminating a chlorine atom from the benzene ring. A possible mechanism is proposed for the formation of the o-chlorobenzyl radical from the precurs or in the gas phase.
机译:使用配备有用于电晕激发的超音速膨胀(CESE)的针孔型玻璃喷嘴,可以将晶种在大量惰性载气氦气中的前体2,6-二氯甲苯排出,以产生射流冷却但受电子激发的苄基型自由基。用长距离单色仪记录可见的电子发射光谱,观察苄基型自由基在D 1 ℃D 0 电子跃迁中的振动带。光谱分析表明不仅生成了2,6-二氯苄基自由基,而且还生成了 o -氯苄基自由基,这是一个意外的现象,这表明消除氯原子时可能发生分子重排苯环上的原子。提出了由前体或在气相中形成 o -氯苄基的可能机理。

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