Physikalische und Theoretische Chemie, Institut für Chemie und Biochemie, Freie Universität Berlin, Takustr. 3, 14195 Berlin, Germany.
Phys Chem Chem Phys. 2012 Jul 14;14(26):9397-402. doi: 10.1039/c2cp23451c. Epub 2012 Feb 6.
The gas-to-solid shift of benzene is reported in the C 1s-core level regime, where the C 1s → π*-transition is investigated between 284.0 eV and 286.5 eV. Simultaneous experiments on the gas phase and condensed species are used to determine the gas-to-solid shift within an accuracy of ±5 meV. Specifically, it is observed that the vibrationally resolved C 1s → π*-transition in solid benzene is red-shifted by 55 ± 5 meV relative to the transition of the isolated molecule. Contrary to previously reported experimental data and estimates this gas-to-solid shift is somewhat smaller than the gas-to-cluster shift. It is significantly smaller than that determined in previous work on gaseous and condensed benzene. These results are discussed in terms of structural properties of molecular clusters and solid benzene by involving ab initio calculations as well as processes leading to spectral shifts of core-excited variable size matter. Finally, changes in the shape of the C 1s → π*-band upon the formation of solid benzene and benzene clusters are discussed.
苯的气-固转变在 C 1s 芯能级范围内被报道,其中 C 1s → π*-跃迁在 284.0 eV 和 286.5 eV 之间进行研究。同时对气相和凝聚相进行实验,以在 ±5 meV 的精度内确定气-固转变。具体而言,观察到在固体苯中,振动分辨的 C 1s → π*-跃迁相对于孤立分子的跃迁红移了 55 ± 5 meV。与先前报道的实验数据和估计相反,这种气-固转变略小于气-团簇转变。它明显小于先前关于气态和凝聚态苯的工作中确定的值。通过涉及从头算计算以及导致芯激发不同大小物质的光谱位移的过程,根据分子团簇和固体苯的结构性质讨论了这些结果。最后,讨论了在形成固体苯和苯团簇时 C 1s → π*-带形状的变化。