Graduate School of Engineering, Muroran Institute of Technology, 27-1 Mizumoto-cho, Muroran, Hokkaido, 050-8585, Japan.
Chemphyschem. 2019 Oct 2;20(19):2531-2538. doi: 10.1002/cphc.201900681. Epub 2019 Sep 2.
We report absorption, fluorescence, and Raman spectroscopy of 7,7,8,8-tetracyanoquinodimethane (TCNQ) in a variety of solvents. The fluorescence quantum yields (QYs) of linear alkane solutions are similar to one another, but QY is shown to acutely decrease in other solvents with increasing polarities. The slope of the solvatochromic plot of absorption maxima is inverted from negative to positive with an increase in solvent polarity. A significant change in the frequency of carbon-carbon double bond stretching modes is not observed in Raman spectra of TCNQ in different solvents. The molar absorption coefficient is determined to calculate the oscillator strength of the absorption band. The radiative decay rate constant calculated from the oscillator strength is approximately ten times larger than that elucidated from the fluorescence lifetime and QY. These spectroscopic parameters reveal that the relaxation occurs from a Franck-Condon excited state to a distinct fluorescence emissive state with a smaller transition dipole moment.
我们报告了 7,7,8,8-四氰基对醌二甲烷(TCNQ)在多种溶剂中的吸收、荧光和拉曼光谱。线性烷烃溶液的荧光量子产率(QY)彼此相似,但QY 在其他极性增加的溶剂中急剧下降。随着溶剂极性的增加,吸收最大值的溶剂变色图的斜率从负变为正。在不同溶剂中,TCNQ 的拉曼光谱中没有观察到碳-碳双键伸缩模式频率的显著变化。通过摩尔吸光系数确定吸收带的振子强度。从振子强度计算的辐射衰减速率常数比从荧光寿命和 QY 得出的速率常数大约大十倍。这些光谱参数表明,弛豫是从 Franck-Condon 激发态到具有较小跃迁偶极矩的独特荧光发射态发生的。