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首页> 外文期刊>The Journal of Chemical Physics >Photolysis wavelength dependence of the translational anisotropy and the angular momentum polarization of O-2(a(1)Delta(g)) formed from the UV photodissociation of O-3 - art. no. 244321
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Photolysis wavelength dependence of the translational anisotropy and the angular momentum polarization of O-2(a(1)Delta(g)) formed from the UV photodissociation of O-3 - art. no. 244321

机译:平移各向异性的光解波长依赖性和O-3的紫外光解离形成的O-2(a(1)Delta(g))的角动量极化。没有。 244321

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The translational anisotropy and angular momentum polarization of the O-2(a (1)Delta(g),v=0;J=15-27) molecular photofragment produced from the UV photodissociation of O-3 in the range from 270 to 300 nm have been determined using resonance-enhanced multiphoton ionization in conjunction with time-of-flight mass spectrometry. At the shortest photolysis wavelengths used, the fragments exhibit the anisotropic vector correlations expected from a prompt dissociation via the B-1(2)<-(1)A(1) transition. Deviations from this behavior are observed at longer photolysis wavelengths with, in particular, the angular momentum orientation showing a significant reduction in magnitude. This indicates that the dissociation can no longer be described by a purely impulsive model and a change in geometry of the dissociating molecule is implied. This observation is substantiated by the variation of the translational anisotropy with photolysis wavelength. We also observe that the bipolar moments describing the angular momentum polarization of the odd J states probed are consistently lower in magnitude than those of the even J states and that this variation is observed for all photolysis wavelengths. (c) 2005 American Institute of Physics.
机译:由O-3的紫外线光解产生的O-2(a(1)Delta(g),v = 0; J = 15-27)分子光碎片的平移各向异性和角动量极化在270至300之间使用共振增强的多光子电离技术结合飞行时间质谱仪已经确定了50 nm。在使用的最短光解波长下,片段显示出各向异性的矢量相关性,该矢量相关性是通过B-1(2)<-(1)A(1)跃迁迅速解离所期望的。在较长的光解波长处观察到与该行为的偏差,尤其是角动量方向显示出幅度的显着减小。这表明离解​​不再能够通过纯粹的脉冲模型来描述,并且暗示了离解分子的几何形状的变化。该平移各向异性随光解波长的变化而得到证实。我们还观察到,描述所探测的奇J态的角动量极化的双极矩的大小始终低于偶J态,并且在所有光解波长下都观察到了这种变化。 (c)2005年美国物理研究所。

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