Rhee Hanju, Ha Jeong-Hyon, Jeon Seung-Joon, Cho Minhaeng
Department of Chemistry and Center for Multidimensional Spectroscopy, Korea University, Seoul 136-701, Republic of Korea.
J Chem Phys. 2008 Sep 7;129(9):094507. doi: 10.1063/1.2968130.
Optical activities such as circular dichroism (CD) and optical rotatory dispersion (ORD) are manifested by almost all natural products. However, the CD is an extremely weak effect so that time-resolved CD spectroscopy has been found to be experimentally difficult and even impossible for vibrational CD with current technology. Here, we show that the weak-signal and nonzero background problems can be overcome by heterodyned spectral interferometric detection of the phase and amplitude of optical activity free-induction-decay (OA FID) field. A detailed theoretical description and a cross-polarization scheme for selectively measuring the OA FID are presented and discussed. It is shown that the parallel and perpendicular electric fields when the solution sample contains chiral molecules are coupled to each other. Therefore, simultaneous spectral interferometric measurements of the parallel and perpendicular FID fields can provide the complex susceptibility, which is associated with the circular dichroism and optical rotatory dispersion as its imaginary and real parts, respectively. On the basis of the theoretical results, to examine its experimental possibility, we present numerical simulations for a model system. We anticipate the method discussed here to be a valuable tool for detecting electronic or vibrational optical activity in femtosecond time scale.
几乎所有天然产物都表现出诸如圆二色性(CD)和旋光色散(ORD)等光学活性。然而,CD效应极其微弱,以至于利用当前技术,时间分辨CD光谱法在实验上已被证明很难,甚至对于振动CD来说是不可能的。在此,我们表明,通过对光学活性自由感应衰减(OA FID)场的相位和幅度进行外差光谱干涉检测,可以克服弱信号和非零背景问题。本文给出并讨论了用于选择性测量OA FID的详细理论描述和交叉极化方案。结果表明,当溶液样品包含手性分子时,平行和垂直电场会相互耦合。因此,对平行和垂直FID场进行同步光谱干涉测量可以提供复磁化率,其虚部和实部分别与圆二色性和旋光色散相关。基于理论结果,为检验其实验可行性,我们给出了一个模型系统的数值模拟。我们预期本文所讨论的方法将成为在飞秒时间尺度上检测电子或振动光学活性的有价值工具。