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有机混合价化合物中的电子耦合:光电子能谱的贡献。

Electronic couplings in organic mixed-valence compounds: the contribution of photoelectron spectroscopy.

作者信息

Coropceanu Veaceslav, Gruhn Nadine E, Barlow Stephen, Lambert Christoph, Durivage Jason C, Bill Tonja G, Nöll Gilbert, Marder Seth R, Brédas Jean-Luc

机构信息

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, USA.

出版信息

J Am Chem Soc. 2004 Mar 10;126(9):2727-31. doi: 10.1021/ja039263u.

Abstract

We show that the electronic coupling in strongly coupled organic mixed-valence systems can be effectively probed by means of gas-phase ultraviolet photoelectron spectroscopy (UPS). Taking six diamines as examples, the UPS estimates for the electronic couplings H(ab) are compared with the corresponding values determined from the intervalence charge-transfer absorption bands and from electronic structure calculations. Similar trends are observed for the H(ab) values estimated from UPS and optical spectra; this provides support for the applicability of Hush theory to strongly coupled organic mixed-valence systems. The UPS electronic couplings are found to be somewhat smaller than those from optical spectroscopy, which is attributed to the role of vibronic coupling to symmetrical modes; when corrected for this vibronic coupling, the UPS H(ab) estimates confirm that triarylamine-based mixed-valence systems are close to the class-II/class-III borderline.

摘要

我们表明,强耦合有机混合价体系中的电子耦合可以通过气相紫外光电子能谱(UPS)有效地探测。以六种二胺为例,将UPS对电子耦合H(ab)的估计值与由价间电荷转移吸收带和电子结构计算确定的相应值进行比较。从UPS和光谱估计得到的H(ab)值观察到相似的趋势;这为赫什理论在强耦合有机混合价体系中的适用性提供了支持。发现UPS电子耦合比光谱学得到的耦合稍小,这归因于振动耦合对对称模式的作用;当校正这种振动耦合时,UPS对H(ab)的估计证实基于三芳基胺的混合价体系接近II类/III类边界。

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