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邻苯二酚气相热解生成的自由基:1.邻-苯醌半醌自由基和同-邻苯二酚自由基。

Radicals from the gas-phase pyrolysis of catechol: 1. o-Semiquinone and ipso-catechol radicals.

机构信息

Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, USA.

出版信息

J Phys Chem A. 2010 Feb 18;114(6):2306-12. doi: 10.1021/jp908243q.

Abstract

The formation of environmentally persistent free radicals (EPFRs) from the gas-phase pyrolysis of catechol (CT) was studied over a temperature range of 400-750 degrees C using the technique of low-temperature matrix isolation electron paramagnetic resonance (LTMI-EPR) spectroscopy. A split singlet EPR spectrum with a g value of 2.0052 was observed. To aid in the interpretation of this spectrum, a detailed analysis of the potential energy surface of CT decomposition pathways was performed employing CBS-QB3 multilevel and DFT individual methods. The energetically favored channels were the formation of ipso- and alpha-CT isomers of CT as well as o-semiquinone (o-SQ) radicals from ipso- and alpha-CT. ipso-CT as well as open ipso-CT radicals were apparently unstable intermediates that could not be accumulated in sufficiently high concentrations to be detected by EPR. The calculated EPR spectrum of o-SQ radical is consistent with the formation of an oxygen-centered radical with a high g value observed experimentally. The hyperfine splitting of the observed spectrum can be attributed to the formation of hydrogen bonds in radical dimers. The lack of experimental observation of o-benzoquinone, an anticipated pyrolysis product, has been explained based on theoretical calculations.

摘要

采用低温基质隔离电子顺磁共振(LTMI-EPR)光谱技术,研究了邻苯二酚(CT)在气相热解过程中形成环境持久性自由基(EPFRs)的情况,温度范围为 400-750°C。观察到具有 g 值为 2.0052 的分裂单线 EPR 谱。为了帮助解释该谱图,使用 CBS-QB3 多级和 DFT 个别方法对 CT 分解途径的势能面进行了详细分析。有利的通道是 CT 的 ipso-和 alpha-CT 异构体以及 o-半醌(o-SQ)自由基的形成,以及来自 ipso-和 alpha-CT 的 o-SQ 自由基。ipso-CT 以及开放的 ipso-CT 自由基显然是不稳定的中间体,不能以足够高的浓度积累,无法通过 EPR 检测到。所观察到的 o-SQ 自由基的计算 EPR 谱与实验中观察到的具有高 g 值的氧中心自由基的形成一致。观察到的谱的超精细分裂可归因于自由基二聚体中氢键的形成。根据理论计算,解释了预期的热解产物邻苯醌未被实验观察到的原因。

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