Georgiou T, Palma J L, Mujica V, Varela S, Galante M, Santamaría-García V J, Mboning L, Schwartz R N, Cuniberti G, Bouchard L-S
Molecular Biology Interdepartmental Program (MBIDP), The Molecular Biology Institute, University of California Los Angeles, 611 Charles E. Young Drive East, Los Angeles, CA, 90095-1570, USA.
Department of Chemistry, Penn State University, 2201 University Drive, Lemont Furnace, PA, 15456, USA.
Nat Commun. 2024 Aug 27;15(1):7367. doi: 10.1038/s41467-024-49966-8.
Spin polarization in chiral molecules is a magnetic molecular response associated with electron transport and enantioselective bond polarization that occurs even in the absence of an external magnetic field. An unexpected finding by Santos and co-workers reported enantiospecific NMR responses in solid-state cross-polarization (CP) experiments, suggesting a possible additional contribution to the indirect nuclear spin-spin coupling in chiral molecules induced by bond polarization in the presence of spin-orbit coupling. Herein we provide a theoretical treatment for this phenomenon, presenting an effective spin-Hamiltonian for helical molecules like DNA and density functional theory (DFT) results on amino acids that confirm the dependence of J-couplings on the choice of enantiomer. The connection between nuclear spin dynamics and chirality could offer insights for molecular sensing and quantum information sciences. These results establish NMR as a potential tool for chiral discrimination without external agents.
手性分子中的自旋极化是一种与电子传输和对映选择性键极化相关的磁分子响应,即使在没有外部磁场的情况下也会发生。Santos及其同事的一项意外发现报道了固态交叉极化(CP)实验中的对映体特异性NMR响应,这表明在存在自旋-轨道耦合的情况下,键极化对手性分子中间接核自旋-自旋耦合可能有额外贡献。在此,我们对这一现象进行了理论处理,给出了像DNA这样的螺旋分子的有效自旋哈密顿量以及氨基酸的密度泛函理论(DFT)结果,证实了J耦合对对映体选择的依赖性。核自旋动力学与手性之间的联系可为分子传感和量子信息科学提供见解。这些结果确立了NMR作为一种无需外部试剂进行手性识别的潜在工具。