Evidence map›Paper›PMID 42106328›Full record

ArticleNature communications2026

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

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

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Kiichi YasuzawaDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
Kouhei SutouDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
Katsuto OnishiDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
Shunsuke OhtaniDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.
Kenichi KatoDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan.ORCID http://orcid.org/0000-0001-5348-5521
Hiroshi YamazakiSchool of Materials and Chemical Technology, Tokyo Institute of Technology, Yokohama, Japan.ORCID http://orcid.org/0000-0002-1773-0398
Junko N KondoChemical Resources Laboratory, Tokyo Institute of Technology, Yokohama, Japan.
Shigehisa AkineGraduate School of Natural Science and Technology, Kanazawa University, Kanazawa, Japan.ORCID http://orcid.org/0000-0003-0447-5057
Tomoki OgoshiDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, Japan. ogoshi.tomoki.3s@kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-4464-0347

Funding

Iketani Science and Technology Foundation 0361068-AMEXT | Japan Society for the Promotion of Science (JSPS) JP24K21247MEXT | Japan Society for the Promotion of Science (JSPS) JP24KJ1487MEXT | Japan Society for the Promotion of Science (JSPS) JP25H00896MEXT | JST | Core Research for Evolutional Science and Technology (CREST) JPMJCR24S6
6 · The paper itself

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.

Identifiers

PMID42106328
PMCPMC13376218

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.