Herein, we report the preparation of chiral, one-dimensional coordination polymers based on trinuclear paddlewheel helices [M 3 (dpa) 4 ] 2+ (M = Co(II) and Ni(II); dpa = the anion of 2,2 -dipyridylamine). Enantiomeric resolution of a racemic mixture of [M 3 (dpa) 4 ] 2+ complexes was achieved by chiral recognition of the respective enantiomer by [∆-As 2 (tartrate) 2 ] 2− or [Λ-As 2 (tartrate) 2 ] 2− in N,N-dimethylformamide (DMF), affording crystalline coordination polymers formed from [(∆-Co 3 (dpa) 4 )(Λ-As 2 (tartrate) 2 )]·3DMF (∆-1), [(Λ-Co 3 (dpa) 4 )(∆-As 2 (tartrate) 2 )]·3DMF (Λ-1), [(∆-Ni 3 (dpa) 4 )(Λ-As 2 (tartrate) 2 )]·(4 − n)DMF·nEt 2 O (∆-2) or [(Λ-Ni 3 (dpa) 4 )(∆-As 2 (tartrate) 2 )]·(4 − n)DMF·nEt 2 O (Λ-2) repeating units. UV-visible circular dichroism spectra of the complexes in DMF solutions demonstrate the efficient isolation of optically active species. The helicoidal [M 3 (dpa) 4 ] 2+ units that were obtained display high stability towards racemization as shown by the absence of an evolution of the dichroic signals after several days at room temperature and only a small decrease of the signal after 3 h at 80 • C.