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气相香芹酮对映体的角分辨C 1s光电子能谱中的圆二色性。

Circular dichroism in the angle-resolved C 1s photoemission spectra of gas-phase carvone enantiomers.

作者信息

Harding Chris J, Mikajlo Elisabeth, Powis Ivan, Barth Silko, Joshi Sanjeev, Ulrich Volker, Hergenhahn Uwe

机构信息

School of Chemistry, University of Nottingham, Nottingham NG7 2RD, United Kingdom.

出版信息

J Chem Phys. 2005 Dec 15;123(23):234310. doi: 10.1063/1.2136150.

Abstract

The inner-shell C 1s photoionization of randomly oriented molecules of the chiral compound carvone has been investigated using circularly polarized synchrotron radiation up to 30 eV above threshold. Binding energies of the C=O and CH2= carbon 1s orbitals were determined to be 292.8+/-0.2 and 289.8+/-0.2 eV, respectively. The remaining C-H C 1s levels substantially overlap under an intense central peak centered at 290.5+/-0.2 eV. The angle-resolved photoemission from the carbonyl carbon C=O core orbital in pure carvone enantiomers shows a pronounced circular dichroism of approximately 6% at the magic angle of 54.7 degrees to the light beam propagation direction. This corresponds to an expected 0 degrees -180 degrees forward-backward electron emission asymmetry of approximately 10%. On changing between the R and S enantiomers of carvone the sense or sign of the asymmetry and associated dichroism effectively reverses. The observed circular dichroism, and its energy dependence, is well accounted for by calculations performed in the pure electric dipole approximation.

摘要

利用圆偏振同步辐射对阈值以上高达30 eV的手性化合物香芹酮随机取向分子的内壳层C 1s光电离进行了研究。C=O和CH2=碳1s轨道的结合能分别确定为292.8±0.2和289.8±0.2 eV。其余C-H C 1s能级在以290.5±0.2 eV为中心的强中心峰下基本重叠。纯香芹酮对映体中羰基碳C=O核心轨道的角分辨光发射在与光束传播方向成54.7度的魔角处显示出约6%的明显圆二色性。这对应于预期的约10%的0度-180度前后向电子发射不对称性。在香芹酮的R和S对映体之间变化时,不对称性和相关二色性的方向或符号有效地反转。通过在纯电偶极近似下进行的计算,很好地解释了观察到的圆二色性及其能量依赖性。

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