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基质隔离六并苯的紫外/可见光谱:相互作用的电子态和天文物理背景。

UV/visible spectroscopy of matrix-isolated hexa-peri-hexabenzocoronene: Interacting electronic states and astrophysical context.

机构信息

Laboratory Astrophysics Group of the Max Planck Institute for Astronomy at the Friedrich Schiller University Jena, Institute of Solid State Physics, Helmholtzweg 3, D-07743 Jena, Germany.

出版信息

J Chem Phys. 2009 Nov 28;131(20):204311. doi: 10.1063/1.3266939.

Abstract

Absorption spectra of hexa-peri-hexabenzocoronene isolated in rare-gas matrices are reported for the wavelength range between 200 and 500 nm. Measurements were carried out in neon and in argon at 5.8 and 12.0 K, respectively. Calculations based on semiempirical models and on density-functional theory were performed to assign the observed features. The electronically excited states involved in Clar's alpha- and p-bands are identified as S(1)(B(2u)) and S(2)(B(1u)), respectively. Although the upper state associated with the beta-band is found to be a (1)E(1u) state, it remains undetermined whether it is S(3) or S(4). Structures in the beta-band are interpreted as resulting from the interaction between the (1)E(1u) state and the e(2g) vibrational manifold of S(2)(B(1u)). The new measurements are used to narrow down the wavelength ranges where the bands of hexa-peri-hexabenzocoronene should be found in the gas phase. A previous estimate of the interstellar abundance of this polycyclic aromatic hydrocarbon is discussed.

摘要

在 200 到 500nm 的波长范围内,报道了六并苯在稀有气体基质中孤立时的吸收光谱。分别在氖气和氩气中于 5.8 和 12.0K 下进行了测量。基于半经验模型和密度泛函理论的计算用于分配观察到的特征。涉及 Clar 的 alpha 和 p-带的电子激发态分别被识别为 S(1)(B(2u))和 S(2)(B(1u))。尽管与 beta 带相关的上态被发现是一个 (1)E(1u)态,但它仍然不确定它是 S(3)还是 S(4)。beta 带中的结构被解释为源自 (1)E(1u)态与 S(2)(B(1u))的 e(2g)振动级联之间的相互作用。新的测量结果用于缩小六并苯在气相中应该出现的波段的波长范围。讨论了先前对这种多环芳烃的星际丰度的估计。

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