Selective monoformylation of naphthalene-fused propellanes for methylene-alternating copolymers
Development of three-dimensional (3D) building blocks is a key to change tight molecular assemblies of rigid π-conjugated planes into organic functional materials endowed with molecular-size cavities. To increase the diversity of available 3D building blocks, we herein report electrophilic formylation of naphthalene-fused [3.3.3]- and [4.3.3]propellanes as the first selective single-point functionalization by virtue of through-space electronic communications between the naphthalene units. The propellane skeletons have well-defined 3D structures and moderate flexibility at the same time. Therefore, the monoformyl products are good precursors for soft materials which show molecular-size cavities and require desymmetrized building blocks. As a proof of concept, methylene-alternating copolymers were prepared by reduction to corresponding alcohols followed by acid-mediated condensation. The linear copolymers show good solubility and carbon dioxide adsorption.
Authors
- Shunsuke Ohtani (ORCID: https://orcid.org/0000-0002-8669-1089)
- Tomoki Ogoshi (ORCID: https://orcid.org/0000-0002-4464-0347)
- Tatsuki Hiroi
- Kenichi Kato (ORCID: https://orcid.org/0000-0001-5348-5521)
- Seina Okada
Institutions
- Kanazawa University (JP)
- Kyoto University (JP)
- Life Science Institute (JP)
- Kyoto Katsura Hospital (JP)
Publication Details
- Journal
- Beilstein Journal of Organic Chemistry
- Published
- 2025-06-18
- DOI
- https://doi.org/10.3762/bjoc.21.95
- Citations
- 1
- Primary Topic
- Covalent Organic Framework Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.52
Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Tokuyama Science Foundation
- Yazaki Memorial Foundation for Science and Technology
- Japan Society for the Promotion of Science