Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 790-784, South Korea.
J Phys Chem A. 2013 Feb 21;117(7):1400-5. doi: 10.1021/jp311884b. Epub 2013 Feb 7.
Proton transfer is one of the most important elementary reactions in chemistry and biology. The role of proton in the course of proton transfer, whether it is active or passive, has been the subject of intense investigations. Here we demonstrate the active role of proton in the excited state intramolecular proton transfer (ESIPT) of 10-hydroxybenzo[h]quinoline (HBQ). The ESIPT of HBQ proceeds in 12 ± 6 fs, and the rate is slowed down to 25 ± 5 fs for DBQ where the reactive hydrogen is replaced by deuterium. The results are consistent with the ballistic proton wave packet transfer within the experimental uncertainty. This ultrafast proton transfer leads to the coherent excitation of the vibrational modes of the product state. In contrast, ESIPT of 2-(2'-hydroxyphenyl)benzothiazole (HBT) is much slower at 62 fs and shows no isotope dependence implying complete passive role of the proton.
质子转移是化学和生物学中最重要的基本反应之一。质子在质子转移过程中的作用,无论是主动的还是被动的,一直是人们研究的热点。在这里,我们证明了质子在 10-羟基苯并[h]喹啉(HBQ)的激发态分子内质子转移(ESIPT)中的主动作用。HBQ 的 ESIPT 在 12±6fs 内进行,而对于反应性氢被氘取代的 DBQ,速率减慢至 25±5fs。结果与实验不确定度内的弹道质子波包转移一致。这种超快的质子转移导致产物态的振动模式的相干激发。相比之下,2-(2'-羟基苯基)苯并噻唑(HBT)的 ESIPT 要慢得多,为 62fs,且没有同位素依赖性,这意味着质子完全处于被动状态。