Department of Chemistry, University of Hong Kong, Hong Kong 999077, China.
Guangdong-Hong Kong-Macao Joint Laboratory of Optoelectronic and Magnetic Functional Materials, Hong Kong 999077, China.
Int J Mol Sci. 2021 Oct 14;22(20):11103. doi: 10.3390/ijms222011103.
Excited state intramolecular proton transfer (ESIPT) in 3-hydroxyflavone (3HF) has been known for its dependence on excitation wavelength. Such a behavior violates Kasha's rule, which states that the emission and photochemistry of a compound would only take place from its lowest excited state. The photochemistry of 3HF was studied using femtosecond transient absorption spectroscopy at a shorter wavelength excitation (266 nm), and these new experimental findings were interpreted with the aid of computational studies. These new results were compared with those from previous studies that were obtained with a longer wavelength excitation and show that there exists a pathway of proton transfer that bypasses the normal first excited state from the higher excited state to the tautomer from first excited state. The experimental data correlate with the electron density difference calculations such that the proton transfer process is faster on the longer excitation wavelength than compared to the shorter excitation wavelength.
激发态分子内质子转移(ESIPT)在 3-羟基黄酮(3HF)中是众所周知的,其依赖于激发波长。这种行为违反了 Kasha 的规则,该规则指出化合物的发射和光化学反应仅会在其最低激发态发生。使用飞秒瞬态吸收光谱技术在较短波长激发(266nm)下研究了 3HF 的光化学,这些新的实验发现借助于计算研究进行了解释。将这些新结果与之前使用较长波长激发获得的研究结果进行了比较,结果表明存在一种质子转移途径,可以从较高激发态绕过正常的第一激发态,直接到达第一激发态的互变异构体。实验数据与电子密度差计算相关联,表明质子转移过程在较长的激发波长下比在较短的激发波长下更快。