Supramolecular protection of isocyanates from water by encapsulation within hydrophobic crystalline pillar[n]arene macrocycles

The high reactivity of isocyanate groups not only makes them excellent precursors for polyurethanes and polyureas, but it also leads to their degradation through reactions with atmospheric moisture. Conventionally, blocking reagents containing alcohol or amine groups have been used to protect isocyanate groups. However, such covalent protection approaches often require harsh deprotection conditions. Herein, we report a non-covalent supramolecular strategy that provides both high protection efficiency and facile deprotection of isocyanate compounds. In this approach, the isocyanate groups are encapsulated within crystalline pillar[n]arene macrocycles. Owing to the highly hydrophobic nature of the pillar[n]arene crystals, the isocyanate guests are effectively protected from water in the crystalline state: the isocyanate groups are active even after the crystalline complexes are exposed to water vapour or directly immersed in water. Furthermore, although the host-guest complex is stabilized in the crystalline state, simple dissolution in an appropriate reaction solvent simultaneously triggers deprotection, enabling subsequent polyurethane synthesis.

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Publication Details

Journal
Nature Communications
Published
2026-05-09
DOI
https://doi.org/10.1038/s41467-026-72696-y
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
0.00

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article

Supramolecular protection of isocyanates from water by encapsulation within hydrophobic crystalline pillar[n]arene macrocycles

Katsuto Onishi, Hiroshi Yamazaki, Shigehisa Akine, Junko N. Kondo et al.
Nature Communications
Polymer composites and self-healing
article

Supramolecular protection of isocyanates from water by encapsulation within hydrophobic crystalline pillar[n]arene macrocycles

Katsuto Onishi, Hiroshi Yamazaki, Shigehisa Akine, Junko N. Kondo, Kiichi Yasuzawa, Kouhei Sutou, Shunsuke Ohtani, Kenichi Kato, Tomoki Ogoshi
article en

Abstract

The high reactivity of isocyanate groups not only makes them excellent precursors for polyurethanes and polyureas, but it also leads to their degradation through reactions with atmospheric moisture. Conventionally, blocking reagents containing alcohol or amine groups have been used to protect isocyanate groups. However, such covalent protection approaches often require harsh deprotection conditions. Herein, we report a non-covalent supramolecular strategy that provides both high protection efficiency and facile deprotection of isocyanate compounds. In this approach, the isocyanate groups are encapsulated within crystalline pillar[n]arene macrocycles. Owing to the highly hydrophobic nature of the pillar[n]arene crystals, the isocyanate guests are effectively protected from water in the crystalline state: the isocyanate groups are active even after the crystalline complexes are exposed to water vapour or directly immersed in water. Furthermore, although the host-guest complex is stabilized in the crystalline state, simple dissolution in an appropriate reaction solvent simultaneously triggers deprotection, enabling subsequent polyurethane synthesis.

Nature Communications
Kanazawa University (JP), Tokyo Institute of Technology (JP), Kyoto University (JP), Life Science Institute (JP)
Ministry of Education, Culture, Sports, Science and Technology, Iketani Science and Technology Foundation, Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology
Clean water and sanitation
Openalex Percentile: Top 10%
Polymer composites and self-healing
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