Circularly polarised fluorescence and phosphorescence calculations on organic molecules using the approximate coupled-cluster model CC2.

We report the first calculations of rotational strengths for circularly polarised phosphorescence at the coupled cluster level. The rotational strengths for circular dichroism (CD), circularly polarised fluorescence (CPF) and circularly polarised phosphorescence (CPP) were calculated for ß,γ-enones and ketones with conjugated double bonds using the CC2 model. To compute spin-forbidden CPP, spin-orbit coupling with perturbation theory is employed within a response theory framework (SOC-PT-CC2). For closed-shell molecules containing only light elements, a spin-free formalism is used to treat the singlet-triplet transitions. It is verified that the simplification obtained in the spin-free formulation from the Wigner-Eckart theorem for spin-forbidden oscillator strengths is also valid for the rotational strengths. Our implementation utilises the resolution of identity (RI) approximation for two-electron integrals which facilitates applications to larger molecules. In the current study, the rotational strength for spin-forbidden circularly-polarised phosphorescence was calculated for a chiral aromatic system, S-DMBDA, containing 44 atoms.

Vectorial Electron Spin Filtering by an All-Chiral Metal-Molecule Heterostructure.

The discovery of the electrons' chiral induced spin selective transmission (CISS) through chiral molecules has opened the pathway for manipulating spin transport in nonmagnetic structures on the nanoscale. CISS has predominantly been explored in structurally helical molecules on surfaces, where the spin selectivity affects only the spin polarization of the electrons along their direction of propagation. Here, we demonstrate a spin selective electron transmission for the point-chiral molecule 3-methylcyclohexanone (3-MCHO) adsorbed on the chiral Cu(643)R surface. Using spin- and momentum-resolved photoelectron spectroscopy, we detect a spin-dependent electron transmission through a single layer of 3-MCHO molecules that depends on all three components of the electrons' spin. Crucially, exchanging the enantiomers alters the electrons' spin component oriented parallel to the terraces of the Cu(643)R surface. The findings are attributed to the enantiomer-specific adsorption configuration on the surface. This opens the intriguing opportunity to selectively tune CISS by the enantiospecific molecule-surface interaction in all-chiral heterostructures.