Nam Yeonsig, Chergui Majed, Young Linda, Rouxel Jérémy R
Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
Elettra-Sincrotrone Trieste, SS 14 - km 163.5, 34149 Basovizza, Trieste, Italy.
J Phys Chem Lett. 2025 May 15;16(19):4652-4661. doi: 10.1021/acs.jpclett.5c00389. Epub 2025 May 5.
Recent advancements in X-ray light sources enable element-sensitive nonlinear spectroscopies for probing molecular chirality. We simulate X-ray absorption spectroscopy, X-ray circular dichroism (XCD), and nonlinear optical/X-ray SFG and DFG (OX SFG/DFG) signals for two prototypical chiral molecules, fenchone and cysteine. Our multireference simulations reproduce experimental data and reveal how novel X-ray spectroscopies exploit the site- and element-sensitivity of X-rays to uncover molecular asymmetry. The XCD spectra show strong asymmetries at chiral centers, while distant atoms contribute weaker signals. The OX SFG/DFG signals, under fixed resonant optical excitation, strongly depend on the core and valence excitations. This allows us to introduce two-dimensional (2D) chirality-sensitive valence-core spectroscopy, which provides insight into the overlap between valence orbitals and local molecular asymmetry. Finally, our estimates using realistic laser and X-ray pulse parameters demonstrate that such nonlinear experiments are feasible at XFELs, offering a promising tool for investigating chiral molecules.
X射线光源的最新进展使得能够进行元素敏感的非线性光谱学研究,以探测分子手性。我们模拟了两种典型手性分子葑酮和半胱氨酸的X射线吸收光谱、X射线圆二色性(XCD)以及非线性光学/X射线和频与差频(OX SFG/DFG)信号。我们的多参考模拟重现了实验数据,并揭示了新型X射线光谱学如何利用X射线的位点和元素敏感性来揭示分子不对称性。XCD光谱在手性中心显示出强烈的不对称性,而远处的原子贡献较弱的信号。在固定的共振光激发下,OX SFG/DFG信号强烈依赖于芯能级和价电子激发。这使我们能够引入二维(2D)手性敏感价-芯光谱学,从而深入了解价轨道与局部分子不对称性之间的重叠。最后,我们使用实际的激光和X射线脉冲参数进行的估计表明,此类非线性实验在X射线自由电子激光(XFEL)上是可行的,为研究手性分子提供了一种有前景的工具。