共轭体系
化学
Boosting(机器学习)
戒指(化学)
融合
组合化学
纳米技术
有机化学
人工智能
聚合物
计算机科学
材料科学
语言学
哲学
作者
Teng Wang,Dongyue An,Jiangyu Zhu,Xiaozhi Zhang,Jiaxi Zhang,Yuanhe Gu,Xuefeng Lu,Yunqi Liu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-05-31
卷期号:26 (23): 5010-5015
被引量:2
标识
DOI:10.1021/acs.orglett.4c01675
摘要
Two fully fused acceptor–donor–acceptor (A–D–A) architecture conjugated derivatives (NPF and NCF) comprising an electron-withdrawing naphthalimide (NMI) and two different electron-donating cores, phenanthrene and carbazole, respectively, were conveniently synthesized by bismuth(III)-catalyzed selective cyclization of vinyl ethers. Compared with their corresponding single bond-linked A–D–A molecules NPS and NCS, both having a moderately twisted aromatic configuration, the ring fusion strategy leads to fully coplanar conjugated skeletons and greatly changes the electronic structures, photophysical properties, self-assembling behaviors, and molecular packing motifs. In particular, the naphthalimide/carbazole derivative NCF exhibits intriguing 2D brickwork packing and significantly enhanced self-assembling properties.
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