Ji Na, Shen Yuen-Ron
Department of Physics, University of California at Berkeley, and Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
J Am Chem Soc. 2005 Sep 21;127(37):12933-42. doi: 10.1021/ja052715d.
A theoretical formulation for optically active sum frequency generation (OA-SFG) from isotropic chiral solutions was proposed for molecules with a chiral side chain and an intrinsically achiral chromophore. Adapting an electron correlation model first proposed by Höhn and Weigang for linear optical activity, we presented a dynamic coupling model for OA-SFG near the electronic resonance of the achiral chromophore. As a demonstration, we used this model to explain the observed OA-SFG spectra of a series of amino acids near the electronic resonance of the intrinsically achiral carboxyl group. Our model shows that the nonlinear chiroptical response comes about by the through-space correlative electronic interactions between the chiral side chain and the achiral chromophore, and its magnitude is determined by the position and orientation of the bonds that make up the chiral side chain. Using the bond polarizability values in the literature and the conformations of amino acids obtained from calculation, we were able to reproduce the relative OA-SFG strength from a series of amino acids.
针对具有手性侧链和本质上非手性发色团的分子,提出了一种从各向同性手性溶液中产生旋光和频产生(OA-SFG)的理论公式。我们采用了由霍恩和魏刚首次提出的用于线性光学活性的电子相关模型,提出了一种在手性发色团电子共振附近的OA-SFG动态耦合模型。作为一个示例,我们使用该模型来解释一系列氨基酸在本质上非手性羧基电子共振附近观察到的OA-SFG光谱。我们的模型表明,非线性手性光学响应是由手性侧链和非手性发色团之间的空间相关电子相互作用产生的,其大小由构成手性侧链的键的位置和取向决定。利用文献中的键极化率值和计算得到的氨基酸构象,我们能够重现一系列氨基酸的相对OA-SFG强度。