Here
we report magneto-chiral dichroism (MChD) detected through
visible and near-infrared light absorption of a chiral dysprosium(III)
coordination polymer. The two enantiomers of [DyIII(H6(py)2)(hfac)3]
n
[H6(py)2 = 2,15-bis(4-pyridyl)ethynylcarbo[6]helicene; hfac– = 1,1,1,5,5,5-hexafluoroacetylacetonate], where the chirality is
provided by a functionalized helicene ligand, were structurally, spectroscopically,
and magnetically investigated. Magnetic measurements reveal a slow
relaxation of the magnetization, with differences between enantiopure
and racemic systems rationalized on the basis of theoretical calculations.
When the enantiopure complexes are irradiated with unpolarized light
in a magnetic field, they exhibit multiple MChD signals associated
with the f–f electronic transitions of DyIII, thus
providing the coexistence of MChD-active absorptions and single-molecule-magnet
(SMM) behavior. These findings clearly show the potential that rationally
designed chiral SMMs have in enabling the optical readout of magnetic
memory through MChD.