异氰酸酯
超分子化学
试剂
聚氨酯
溶解
高分子化学
胺气处理
溶剂
化学
材料科学
共价键
反应性(心理学)
有机化学
化学工程
分子
氢键
超分子组装
化学改性
作者
Kiichi Yasuzawa,Kouhei Sutou,Katsuto Onishi,Shunsuke Ohtani,Kenichi Kato,Hiroshi Yamazaki,Junko N. Kondo,Shigehisa Akine,Tomoki Ogoshi
标识
DOI:10.1038/s41467-026-72696-y
摘要
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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