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自组装圆柱形胶囊内苯客体的动力学:固态²H NMR与分子动力学模拟联合研究

Dynamics of benzene guest inside a self-assembled cylindrical capsule: a combined solid-state 2H NMR and molecular dynamics simulation study.

作者信息

Albunia Alexandra R, Gaeta Carmine, Neri Placido, Grassi Alfonso, Milano Giuseppe

机构信息

Dipartimento di Chimica, Università di Salerno, Via Ponte don Melillo, I-84084 Fisciano, Salerno, Italy.

出版信息

J Phys Chem B. 2006 Oct 5;110(39):19207-14. doi: 10.1021/jp0617423.

Abstract

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.

摘要

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。

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