Laboratoire Interuniversitaire des Systèmes Atmosphériques (LISA) CNRS UMR 7583, Université Paris-Est Créteil, Université de Paris, Institut Pierre Simon Laplace, 61 avenue du Général de Gaulle, 94010, Créteil, France.
Chemphyschem. 2020 Aug 4;21(15):1682-1687. doi: 10.1002/cphc.202000419. Epub 2020 Jul 13.
Large amplitude motion of methyl groups in isolated molecules is a fundamental phenomenon in molecular physics. The methyl torsional barrier is sensitive to the steric and electronic environment in the surrounding of the methyl group, making the methyl group a detector of the molecular structure. To probe this effect, the microwave spectrum of 2,6-dimethylfluorobenzene, one of the six isomers of dimethylfluorobenzene, was measured using two pulsed molecular jet Fourier transform microwave spectrometers operating in the frequency range from 2 to 40 GHz. Due to internal rotations of two equivalent methyl groups with relatively low torsional barriers, all rotational transitions split into quartets with separations of up to several hundreds of MHz. The splittings were analyzed and modeled to deduce a torsional barrier of 236.7922 (21) cm . The results are compared to those obtained from quantum chemical calculations and with other fluorine substituted toluene derivatives of the current literature where the methyl group is adjacent to a fluorine atom.
孤立分子中甲基的大振幅运动是分子物理中的一个基本现象。甲基的扭转势垒对甲基周围的空间和电子环境敏感,使甲基成为分子结构的探测器。为了探究这种效应,我们使用两台工作在 2 到 40GHz 频率范围内的脉冲分子射流傅里叶变换微波光谱仪,测量了二甲基氟苯的 6 个异构体之一的 2,6-二甲基氟苯的微波光谱。由于两个等效甲基的内部旋转具有相对较低的扭转势垒,所有的转动跃迁都分裂成四分体,分裂间隔高达数百兆赫。我们对这些分裂进行了分析和建模,推导出了 236.7922(21)cm-1 的扭转势垒。结果与量子化学计算以及当前文献中与氟原子相邻的其他氟取代甲苯衍生物的结果进行了比较。