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碘-苯配合物作为双分子反应实时控制的候选物。对在固态氪中分离出的1:1配合物性质的光谱研究。

Iodine-benzene complex as a candidate for a real-time control of a bimolecular reaction. Spectroscopic studies of the properties of the 1:1 complex isolated in solid krypton.

作者信息

Kiviniemi Tiina, Hulkko Eero, Kiljunen Toni, Pettersson Mika

机构信息

Nanoscience Center, Department of Chemistry, P.O. Box 35, FI-40014 University of Jyväskylä, Finland.

出版信息

J Phys Chem A. 2009 Jun 4;113(22):6326-33. doi: 10.1021/jp902012u.

Abstract

The properties of the 1:1 iodine-benzene complex isolated in a solid Kr matrix at low temperatures have been studied using UV-vis absorption, FTIR, resonance Raman, and femtosecond coherent anti-Stokes Raman spectroscopy (fs-CARS). The use of all these techniques on similar samples provides a wide view on the spectroscopic properties of the complex and allows comparison and combination of the results from different methods. The results for the complex cover its structure, the changes in the iodine molecule's vibrational frequencies and electronic absorption spectrum upon complexation, and the dynamics of the complexed I(2) molecule on both ground and excited electronic states. In addition, polarization beats between uncomplexed benzene and iodine molecules are detected in the fs-CARS spectra, showing an amplification of an electronically nonresonant CARS signal by the resonant iodine signal. The possibility of controlling the charge-transfer reaction of the I(2)-Bz complex using the excitation of a well-defined ground-state vibrational wavepacket, according to the Tannor-Rice-Kosloff scheme, is discussed on the basis of the experimental findings.

摘要

利用紫外可见吸收光谱、傅里叶变换红外光谱、共振拉曼光谱和飞秒相干反斯托克斯拉曼光谱(fs-CARS),研究了低温下在固态氪基质中分离出的1:1碘 - 苯配合物的性质。对类似样品使用所有这些技术,能全面了解该配合物的光谱性质,并能对不同方法的结果进行比较和综合。该配合物的研究结果涵盖了其结构、配合过程中碘分子振动频率和电子吸收光谱的变化,以及配合态I₂分子在基态和激发态电子态上的动力学。此外,在fs-CARS光谱中检测到未配合的苯和碘分子之间的极化拍频,表明共振碘信号对非共振电子CARS信号有放大作用。基于实验结果,根据Tannor-Rice-Kosloff方案,讨论了利用定义明确的基态振动波包激发来控制I₂ - Bz配合物电荷转移反应的可能性。

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