Chiral separation by a terminal chirality triggered P-helical quinoline oligoamide foldamer
文摘

A quinoline oligoamide-grafted silica was synthesized as an HPLC stationary phase.

The oligoamide adopted a helical chiral secondary structure on the silica surface.

This new stationary phase showed enantioselectivity toward chiral aromatic compounds.

Extremely high selectivity was observed toward same handedness of quinoline oligomers.

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