分子内力
氢键
激发态
光激发
质子
基态
光化学
势能
化学
计算化学
化学物理
原子物理学
分子
立体化学
物理
量子力学
有机化学
作者
Changjiao Shang,Yunjian Cao,Chaofan Sun,Huifang Zhao
摘要
state, and the corresponding energy barrier is gradually enlarged with increasing solvent polarity. To further expound the weakened IHB-induced ESIPT mechanism, the scanned PESs connecting the transition state (TS) structures and the initial forms indicate that the ESIPT process is infeasible without the appropriate structural torsion. Our work not only unveils the extraordinary ESIPT process of L, but also complements the results obtained from previous experiments.
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