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气相中罗丹明离子在3K时的红外和可见光解离光谱

Infrared and Visible Photodissociation Spectra of Rhodamine Ions at 3 K in the Gas Phase.

作者信息

Jašík Juraj, Navrátil Rafael, Němec Ivan, Roithová Jana

机构信息

Department of Organic Chemistry and †Department of Inorganic Chemistry, Faculty of Science, Faculty of Science, Charles University in Prague , Hlavova 2030/8, 12843 Prague 2, Czech Republic.

出版信息

J Phys Chem A. 2015 Dec 24;119(51):12648-55. doi: 10.1021/acs.jpca.5b08462. Epub 2015 Dec 7.

Abstract

Helium-tagging predissociation spectroscopy in the visible spectral range (He@VisPD) is shown for Rhodamine 123, Rhodamine 110, and Rhodamine 110's silver salt (silver carboxylate). It is shown that the spectra reflect single-photon absorption. The helium-tagged ions are in the ground vibrational state, and the He@VisPD spectra feature the Franck-Condon envelopes for the excitation to the first excited singlet state that agree very well with theoretical simulations. The S0 → S1 excitation energies are 2.712 ± 0.006 eV for Rhodamine 123, 2.700 ± 0.006 eV for Rhodamine 110, and 2.751 ± 0.006 eV for the silver salt of Rhodamine 110. The determined energies can be slightly blue-shifted due to the binding energy of helium. The Rhodamine ions were also characterized by helium-tagging infrared photodissociation spectroscopy. The distinctive spectral features of the individual derivatives are described and the spectra are compared to the classical solid-state IR spectra.

摘要

本文展示了罗丹明123、罗丹明110及其银盐(羧酸银)在可见光谱范围内的氦标记预解离光谱(He@VisPD)。结果表明,这些光谱反映了单光子吸收。氦标记离子处于基振动态,He@VisPD光谱具有激发到第一激发单重态的弗兰克-康登包络,与理论模拟结果非常吻合。罗丹明123的S0→S1激发能为2.712±0.006 eV,罗丹明110为2.700±0.006 eV,罗丹明110银盐为2.751±0.006 eV。由于氦的结合能,所测定的能量可能会有轻微的蓝移。罗丹明离子还通过氦标记红外光解离光谱进行了表征。描述了各个衍生物独特的光谱特征,并将光谱与经典的固态红外光谱进行了比较。

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