Albunia Alexandra R, Gaeta Carmine, Neri Placido, Grassi Alfonso, Milano Giuseppe
Dipartimento di Chimica, Università di Salerno, Via Ponte don Melillo, I-84084 Fisciano, Salerno, Italy.
J Phys Chem B. 2006 Oct 5;110(39):19207-14. doi: 10.1021/jp0617423.
The reorientational dynamics of benzene-d(6) molecules hosted into the cavity of a cavitand-based, self-assembled capsule was investigated by Molecular Dynamics (MD) simulations and temperature-dependent solid-state (2)H NMR spectroscopy. MD simulations were preliminarily performed to assess the motional models of the guest molecules inside the capsules. An in-plane fast reorientation of the benzene guest around the C(6) symmetry axis (B1 motion), characterized by correlation times of the order of picoseconds, was predicted with an activation barrier ( approximately 8 kJ/mol) very similar to that found for neat benzene in the liquid state. An out-of-plane reorientation corresponding to a nutation of the C(6) symmetry axis in a cone angle of 39 degrees (B2 motion, 373 K) with an activation barrier ( approximately 39 kJ/mol) definitely larger than that of liquid benzene was also anticipated. In the temperature range 293-373 K correlation times of the order of a nanosecond have been calculated and a transition from fast to slow regime in the (2)H NMR scale has been predicted between 293 and 173 K. (2)H NMR spectroscopic analysis, carried out in the temperature range 173-373 K on the solid capsules containing the perdeuterated guest (two benzene molecules/capsule), confirmed the occurrence of the B1 and B2 motions found in slow exchange in the (2)H NMR time scale. Line shape simulation of the (2)H NMR spectral lines permitted defining a cone angle value of 39 degrees at 373 K and 35 degrees at 173 K for the nutation axis. The T(1) values measured for the (2)H nuclei of the encapsulated aromatic guest gave correlation times and energetic barrier for the in-plane motion B1 in fine agreement with theoretical calculation. The experimental correlation time for B2 as well as the corresponding energetic barrier are in the same range found for B1. A molecular mechanism for the encapsulated guest accounting for the B1 and B2 motions was also provided.
通过分子动力学(MD)模拟和温度依赖的固态(2)H核磁共振光谱,研究了容纳在基于穴状配体的自组装胶囊腔内的苯-d(6)分子的重定向动力学。首先进行MD模拟以评估胶囊内客体分子的运动模型。预测苯客体围绕C(6)对称轴的面内快速重定向(B1运动),其相关时间为皮秒量级,活化能垒(约8 kJ/mol)与液态纯苯的非常相似。还预期了对应于C(6)对称轴在39度锥角内的章动的面外重定向(B2运动,373 K),其活化能垒(约39 kJ/mol)肯定大于液态苯的。在293 - 373 K温度范围内计算出了纳秒量级的相关时间,并预测在293和173 K之间(2)H NMR尺度上会从快速转变为慢速状态。在173 - 373 K温度范围内对含有全氘代客体(两个苯分子/胶囊)的固体胶囊进行的(2)H NMR光谱分析,证实了在(2)H NMR时间尺度上慢速交换中发现的B1和B2运动的发生。(2)H NMR谱线的线形模拟允许确定373 K时章动轴的锥角值为39度,173 K时为35度。对封装的芳香族客体的(2)H核测量的T(1)值给出了面内运动B1的相关时间和能量垒,与理论计算非常吻合。B2的实验相关时间以及相应的能量垒与B1处于相同范围。还提供了一种解释封装客体的B1和B2运动的分子机制。