Jašík Juraj, Navrátil Rafael, Němec Ivan, Roithová Jana
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.
J Phys Chem A. 2015 Dec 24;119(51):12648-55. doi: 10.1021/acs.jpca.5b08462. Epub 2015 Dec 7.
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.
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。