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首页> 外文期刊>Chemical Physics: A Journal Devoted to Experimental and Theoretical Research Involving Problems of Both a Chemical and Physical Nature >Photodissociation spectroscopy of (benzene-toluene)~+. Charge delocalization in the hetero-dimer ion
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Photodissociation spectroscopy of (benzene-toluene)~+. Charge delocalization in the hetero-dimer ion

机译:(苯-甲苯)〜+的光解离光谱异二聚体离子中的电荷离域

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摘要

The electronic spectrum of the benzene-toluene hetero-dimer ion is measured in the 380-1400 nm region. The spectrum shows intense bands around 1175 and 670 nm and a weaker band around 920 nm, which correspond to charge resonance (CR) bands of homo-dimer ions. The observation indicates that the positive charge stays on the benzene part in some probability, although the ionization potential of benzene is 0.4162 eV higher than that of toluene. A local excitation (LE) band is observed around 420 nm, where a π ← π transition is locally excited in the charged benzene or toluene molecule. On the basis of the positions of the CR-like bands, as well as the intensity of the LE band relative to that of homo-dimer ions, the probability of finding the charge on the benzene molecule is analyzed to be approximately 36%.
机译:苯-甲苯异二聚体离子的电子光谱在380-1400 nm范围内测量。光谱显示在1175和670 nm附近有很强的能带,而在920 nm附近有较弱的能带,它们对应于同二聚体离子的电荷共振(CR)带。观察结果表明,尽管苯的电离电势比甲苯的电离电势高0.4162 eV,但仍有一定的电荷留在苯部分。在420 nm附近观察到局部激发(LE)带,其中在带电的苯或甲苯分子中局部激发π←π跃迁。根据CR样带的位置以及LE带相对于同二聚体离子的强度,分析发现在苯分子上发现电荷的可能性约为36%。

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