Kato Kenichi, Hiroi Tatsuki, Okada Seina, Ohtani Shunsuke, Ogoshi Tomoki
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, 615-8510, Japan.
WPI Nano Life Science Institute, Kanazawa University, Kakuma-machi, Kanazawa, 920-1192, Japan.
Beilstein J Org Chem. 2025 Jun 18;21:1183-1191. doi: 10.3762/bjoc.21.95. eCollection 2025.
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.
三维(3D)积木的开发是将刚性π共轭平面的紧密分子组装转变为具有分子尺寸空腔的有机功能材料的关键。为了增加可用3D积木的多样性,我们在此报告萘并稠合的[3.3.3]-和[4.3.3]螺旋烷的亲电甲酰化反应,这是通过萘单元之间的空间电子通信实现的首次选择性单点功能化。螺旋烷骨架同时具有明确的3D结构和适度的柔韧性。因此,单甲酰化产物是用于软材料的良好前体,这些软材料具有分子尺寸的空腔并且需要不对称的积木。作为概念验证,通过还原为相应的醇,然后进行酸介导的缩合反应,制备了亚甲基交替共聚物。线性共聚物表现出良好的溶解性和二氧化碳吸附性。