Aulin Yaroslav V, Liu Mengdi, Piotrowiak Piotr
Department of Chemistry , Rutgers University-Newark , 73 Warren Street , Newark , New Jersey 07102 , United States.
J Phys Chem Lett. 2019 May 16;10(10):2434-2438. doi: 10.1021/acs.jpclett.9b00406. Epub 2019 May 1.
Vibrational cooling of azulene encapsulated in a hemicarcerand molecular container was studied by pump-probe spectroscopy. Within 1.5 ps of excitation of azulene to the S state, rapid internal conversion through a conical intersection leads to the formation of a vibrationally hot (∼1080 K) ground state, the subsequent cooling of which can be monitored by tracking the evolution of the red-shifted hot band at the edge of the ground-state absorption. It was found that the cooling of the hot S state of azulene in the host-guest complex (hemicarceplex) is 2-4 times faster than that in common organic solvents. Such large acceleration points to a high density of matching vibrational modes and efficient mechanical coupling between the guest and the host. The experimental observations were fully corroborated by the results of molecular dynamics simulations.
通过泵浦-探测光谱研究了封装在半笼形分子容器中的薁的振动冷却。在将薁激发到S态的1.5皮秒内,通过锥形交叉点的快速内转换导致形成振动热的(约1080K)基态,其随后的冷却可以通过跟踪基态吸收边缘处红移热带的演化来监测。发现主客体复合物(半笼合物)中薁的热S态的冷却速度比普通有机溶剂中快2至4倍。如此大的加速表明匹配振动模式的高密度以及客体与主体之间有效的机械耦合。分子动力学模拟结果充分证实了实验观察结果。