# Engineering Free Volume within Frontal Ring‐Opening Metathesis Polymerization via Pendant Plasticization

**Authors:** Kevin A. Stewart, Francesca J. Lombardi, Sky D. Cao, Claire M. Massouh, Jacob J. Lessard

PMC · DOI: 10.1002/adma.202519676 · Advanced Materials (Deerfield Beach, Fla.) · 2025-12-23

## TL;DR

Researchers developed a new method to create tunable, soft materials using a polymerization technique by adjusting side-chain lengths.

## Contribution

A side-chain plasticization strategy is introduced to expand the properties of FROMP materials into elastomeric regimes.

## Key findings

- Incorporating n-alkyl pendants tunes free volume, reducing Tg and moduli while enabling elastomers with over 800% elongation.
- Free-volume analysis confirms pendant length and distribution as key factors in network porosity and mobility.
- High-alkyl-content formulations show nonlinear front propagation and strain-induced whitening for structural programming.

## Abstract

Frontal ring‐opening metathesis polymerization (FROMP) enables rapid, energy‐efficient access to high‐performance thermosets and thermoplastics, but the range of accessible properties remains constrained by the rigidity of norbornene‐type backbones. Here we introduce a side‐chain plasticization strategy for FROMP, wherein norbornene esters bearing n‐alkyl groups of varying length (n = 8, 12, 16) are copolymerized with dicyclopentadiene (DCPD) or hydrogenated DCPD (DCPD‐H2). Systematic incorporation of these pendants tunes free volume, resulting in predictable reductions in glass transition temperature (T
g), decreased moduli, and a transition from rigid thermosets to elastomers exceeding 800% elongation at break. Free‐volume analysis via dynamic mechanical analysis and solvent swelling ratios confirms pendant length and distribution as key parameters governing network porosity and mobility. Moreover, high‐alkyl‐content formulations exhibit nonlinear front propagation (spin modes) and strain‐induced whitening—features that highlight opportunities for spatial patterning and cooperative molecular alignment under load. Collectively, these results establish side‐chain engineering as a versatile design principle for expanding FROMP into elastomeric regimes, providing a scalable pathway to soft, tunable, and structurally programmable materials.

Norbornene‐based copolymers with tunable n‐alkyl pendant length provide control over matrix free volume, enabling elastomeric materials via frontal ring‐opening metathesis polymerization (FROMP).

## Linked entities

- **Chemicals:** dicyclopentadiene (PubChem CID 6492)

## Full-text entities

- **Chemicals:** DCPD-H2 (-), DCPD (MESH:C004689), norbornene (MESH:C046060)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12910533/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12910533/full.md

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Source: https://tomesphere.com/paper/PMC12910533