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Unique Method for Facile Postsynthetic Modification of Nonisocyanate Polyurethanes

Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s...

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Bibliographic Details
Published in:Macromolecules 2024-03, Vol.57 (5), p.2385-2393
Main Authors: Zubkevich, Sergei V., Makarov, Maksim, Dieden, Reiner, Puchot, Laura, Berthé, Vincent, Westermann, Stephan, Shaplov, Alexander S., Schmidt, Daniel F.
Format: Article
Language:English
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Summary:Nonisocyanate polyurethanes (NIPUs) are broadly investigated as a potential replacement for conventional polyurethanes (PUs) to eliminate the use of toxic isocyanates and reduce occupational hazards. One of the most popular approaches to NIPU synthesis is the polyaddition of cyclic bis­(carbonate)­s and diamines to form poly­(hydroxyurethane)­s (PHUs). However, such PHUs are highly hydrophilic due to the presence of two hydroxyl groups per repeat unit, and the resulting moisture absorption significantly degrades their thermomechanical performance and physical stability upon exposure to humidity, thus limiting their utility. Here, we introduce a simple and scalable approach for the modification of PHUs to increase hydrophobicity and adjust their properties. The proposed reaction between aldehydes and appropriately spaced hydroxyl groups in the polymer backbone resulted in high degrees of modification (up to 84%) and up to 3-fold reductions in water uptake at 85% RH. Furthermore, the use of aromatic aldehydes in particular enabled the retention of mechanical properties over a wide range of humidity levels, resulting in performance comparable to conventional PUs. Finally, we note that this approach is not limited to reducing moisture sensitivity alone and provides ample opportunities for imparting a broad range of novel properties to PHUs through an appropriate selection of functional aldehydes.
ISSN:0024-9297
1520-5835
DOI:10.1021/acs.macromol.3c02232