# Urethane Macromonomers: Key Components for the Development of Light-Cured High-Impact Denture Bases

**Authors:** Benjamin Grob, Pascal Fässler, Iris Lamparth, Sadini Omeragic, Kai Rist, Loïc Vidal, Jacques Lalevée, Yohann Catel

PMC · DOI: 10.3390/polym17131761 · Polymers · 2025-06-26

## TL;DR

Researchers developed light-cured denture base materials with high impact resistance using urethane macromonomers and a toughening agent, suitable for 3D printing.

## Contribution

The study introduces a new class of urethane macromonomers and a formulation strategy that meets high-impact denture standards for 3D printing.

## Key findings

- BCP1 significantly increases fracture toughness in low crosslink density networks.
- UM1 and UM2 macromonomers achieved ISO20795-1:2013 high-impact standards with optimized BCP1 content.
- Structure of urethane macromonomers critically affects the balance of mechanical properties.

## Abstract

The development of high-impact denture base formulations that are suitable for digital light processing (DLP) 3D printing is demanding. Indeed, a combination of high flexural strength/modulus and high fracture toughness is required. In this contribution, eight urethane macromonomers (UMs1-8) were synthesized in a one-pot, two-step procedure. Several rigid diols were first reacted with two equivalents of trimethylhexamethylene diisocyanate. The resulting diisocyanates were subsequently end-capped with a free-radically polymerizable monomer bearing a hydroxy group. UMs1-8 were combined with the monofunctional monomer (octahydro-4,7-methano-1H-indenyl)methyl acrylate and a poly(ε-caprolactone)-polydimethylsiloxane-poly(ε-caprolactone) (PCL-PDMS-PCL) triblock copolymer (BCP1) as a toughening agent. The double-bond conversion, glass transition temperature (Tg), and mechanical properties (flexural strength/modulus, fracture toughness) of corresponding light-cured materials were measured (cured in a mold using a light-curing unit). The results showed that the incorporation of BCP1 was highly efficient at significantly increasing the fracture toughness, as long as the obtained networks exhibited a low crosslink density. The structure of the urethane macromonomer (nature of the rigid group in the spacer; nature and number of polymerizable groups) was demonstrated to be crucial to reach the desired properties (balance between flexural strength/modulus and fracture toughness). Amongst the evaluated macromonomers, UM1 and UM2 were particularly promising. By correctly adjusting the BCP1 content, light-cured formulations based on those two urethane dimethacrylates were able to fulfill ISO20795-1:2013 standard requirements regarding high-impact materials. These formulations are therefore suitable for the development of 3D printable high-impact denture bases.

## Linked entities

- **Chemicals:** trimethylhexamethylene diisocyanate (PubChem CID 3033881), (octahydro-4,7-methano-1H-indenyl)methyl acrylate (PubChem CID 22051805)

## Full-text entities

- **Chemicals:** urethane dimethacrylates (MESH:C029824), polydimethylsiloxane (MESH:C013830), diols (MESH:D011276), poly(epsilon-caprolactone) (MESH:C016240), BCP1 (-), Urethane (MESH:D014520)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12252331/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12252331/full.md

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Source: https://tomesphere.com/paper/PMC12252331