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Infrared absorption of gaseous CH2BrOO detected with a step-scan Fourier-transform absorption spectrometer

机译:用步进扫描傅里叶变换吸收光谱仪检测到的气态CH2BrOO的红外吸收

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摘要

CH2BrOO radicals were produced upon irradiation, with an excimer laser at 248 nm, of a flowing mixture of CH2Br2 and O-2. A step-scan Fourier-transform spectrometer coupled with a multipass absorption cell was employed to record temporally resolved infrared (IR) absorption spectra of reaction intermediates. Transient absorption with origins at 1276.1, 1088.3, 961.0, and 884.9 cm (1) are assigned to nu(4) (CH2-wagging), nu(6) (O-O stretching), nu(7) (CH2-rocking mixed with C-O stretching), and nu(8) (C-O stretching mixed with CH2-rocking) modes of syn-CH2BrOO, respectively. The assignments were made according to the expected photochemistry and a comparison of observed vibrational wavenumbers, relative IR intensities, and rotational contours with those predicted with the B3LYP/aug-cc-pVTZ method. The rotational contours of nu(7) and nu(8) indicate that hot bands involving the torsional (nu(12)) mode are also present, with transitions 7(0)(1)12(nu)(nu) and 8(0)(1)12(nu)(nu), nu = 1-10. The most intense band (nu(4)) of anti-CH2BrOO near 1277 cm(-1) might have a small contribution to the observed spectra. Our work provides information for directly probing gaseous CH2BrOO with IR spectroscopy, in either the atmosphere or laboratory experiments. (C) 2014 AIP Publishing LLC.
机译:用准分子激光在248nm下照射流动的CH 2 Br 2和O-2的混合物产生CH 2 BrOO自由基。使用步进扫描傅立叶变换光谱仪与多程吸收池耦合,以记录反应中间体的时间分辨红外(IR)吸收光谱。起源于1276.1、1088.3、961.0和884.9 cm(1)的瞬态吸收被分配给nu(4)(CH2摆动),nu(6)(OO拉伸),nu(7)(CH2摇摆与CO混合)拉伸)和nu(8)(CO拉伸与CH2摇摆混合)模式分别为syn-CH2BrOO。根据预期的光化学以及将观察到的振动波数,相对红外强度和旋转轮廓与用B3LYP / aug-cc-pVTZ方法预测的轮廓进行比较,进行分配。 nu(7)和nu(8)的旋转轮廓表明还存在涉及扭转(nu(12))模式的热带,其过渡为7(0)(1)12(nu)(nu)和8( 0)(1)12(nu)(nu),nu = 1-10。 1277 cm(-1)附近的抗CH2BrOO的最强带(nu(4))可能对观察到的光谱影响很小。我们的工作提供了在大气或实验室实验中通过红外光谱直接探测气态CH2BrOO的信息。 (C)2014 AIP Publishing LLC。

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