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Enantiospecificity in NMR enabled by chirality-induced spin selectivity

  • T. Georgiou,
  • J. L. Palma,
  • V. Mujica,
  • S. Varela,
  • M. Galante,
  • V. J. Santamaría-García,
  • L. Mboning,
  • R. N. Schwartz,
  • G. Cuniberti,
  • L.-S. Bouchard

摘要

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.