# Easy ROMP of Quinine Derivatives Toward Novel Chiral Polymers That Discriminate Mandelic Acid Enantiomers

## TL;DR

This paper introduces a new method to create chiral polymers using quinine derivatives that can distinguish between enantiomers of mandelic acid.

## Contribution

The study presents a general and practical approach for ROMP polymerization of cinchona alkaloid derivatives to create chiral polymers with enantioselective properties.

## Key findings

- The polymers were synthesized with controlled length and solubility using Cu(I)-catalyzed click chemistry and ROMP.
- The resulting polymers showed excellent thermal stability and a preference for the (R)-stereoisomer of mandelic acid.
- The method allows for regular decoration of the polymer chain with quinine moieties, which is not achievable with typical immobilization methods.

## Abstract

A novel and general approach to the practical ROMP polymerization of cinchona alkaloid derivatives providing novel hybrid materials having quinine attached on a poly(norbornene-5,6-dicarboxyimide) matrix is presented. The concept involves an easy modification of quinine (in general, any cinchona alkaloid) toward clickable 9-azide that reacts with N-propargyl-cis-5-norbornene-exo-2,3-dicarboxylic imide in Cu(I)-catalyzed Huisgen cycloaddition (click chemistry). The resulting monomers undergo a controllable ROMP reaction that leads to novel polymers of a desired length and solubility. This sequence allows for the facile preparation of a regularly decorated polymeric material having one quinine moiety per single mer of the polymer chain inaccessible using typical immobilization methods. A poly(norbornene-5,6-dicarboxyimide) type of polymeric matrix was selected due to the high reactivity of the exo-norbornene motif in Ru(II)-catalyzed ROMP and its chemical and thermal stability as well as convenient, scalable access from inexpensive cis-5-norbornene-exo-2,3-dicarboxylic anhydride (‘one-pot’ Diels–Alder reaction of dicyclopentadiene and maleic anhydride). An appropriate combination of a Grubbs catalyst, Ru(II) (G1, G2), and ROMP conditions allowed for the efficient synthesis of well-defined soluble polymers with mass parameters in the range Mn = 2.24 × 104 – 2.26 × 104 g/mol and Mw = 2.90 × 104–3.05 × 104 g/mol with good polydispersity, ĐM = 1.32–1.35, and excellent thermal stability (up to 309°C Td10). Spectroscopic studies (NMR and electronic circular dichroism (ECD)) of these products revealed a linear structure with the slight advantage of a trans-configuration of an olefinic double bond. The resulting short-chain polymer discriminates mandelic acid enantiomers with a preference for the (R)-stereoisomer in spectrofluorimetric assays. This concept seems to be rather general with respect to other molecules dedicated to incorporation into the poly(norbornene-5,6-dicarboxyimide) chain.