# Mechanisms of Chiral Induction to Foldamer Backbones

**Authors:** Govinda Prasad Devkota, Roshan Lama, C. Scott Hartley

PMC · DOI: 10.1002/chem.202502433 · Chemistry (Weinheim an Der Bergstrasse, Germany) · 2025-10-08

## TL;DR

This review explains how adding chiral groups to foldamer backbones can control their twist direction, enabling the design of chiral nanostructures.

## Contribution

The paper provides a mechanistic understanding of how point chirality influences the twist sense of achiral foldamers.

## Key findings

- Short-range interactions position chiral groups relative to their attachment point on the foldamer.
- Long-range interactions between chiral groups and distant parts of the backbone determine the overall twist sense.
- The combination of these interactions allows for rational design and prediction of helicity in foldamers.

## Abstract

Foldamers, oligomers that adopt well‐defined conformations, represent an efficient strategy toward nanoscale structural complexity. While most foldamers fold into helices, many abiotic foldamers are built from achiral repeat units and therefore do not have a preferred twist sense. Their handedness can, however, be controlled by attaching groups with chirality centers to the foldamer backbone. This process allows chiral information from readily available compounds to be amplified into larger‐scale structural asymmetry and translated into functional behavior. This review describes mechanisms whereby the point chirality of chiral “controller” groups directs foldamer twist sense. We highlight examples of aromatic oligoamides, oligohydrazides, oligoindoles, oligo(ortho‐phenylenes), oligooxymethylenes, and oligo(aminoisobutyric acids), examining cases where the controller groups are attached at either the helices’ termini or sides. Our emphasis is on applying intuitive concepts from conformational analysis and, where appropriate, computational modeling of small substructures. In each case, we consider first short‐range interactions that orient the controller group relative to its direct point of attachment to the foldamer, and then its long‐range interactions with more‐distant parts of the oligomer. Together, these interactions allow the twist sense to be predicted (or at least rationalized). Understanding these mechanisms should facilitate the design of systems with dynamic control over helicity.

Helical foldamers are often built from achiral components and thus have no inherent bias to their twist sense. This review describes mechanisms for controlling their handedness using appended stereocenters. It examines how point chirality directs the twist sense through a combination of short‐range interactions to the directly attached repeat unit and long‐range interactions with groups farther along the backbone.

## Full-text entities

- **Chemicals:** oligo(aminoisobutyric acids (-)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12587027/full.md

## References

92 references — full list in the complete paper: https://tomesphere.com/paper/PMC12587027/full.md

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Source: https://tomesphere.com/paper/PMC12587027