期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 61, 期 18, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202201494
关键词
Azulene; Helicenes; Non-Benzenoid Aromatics; Polycyclic Aromatic Hydrocarbons
资金
- National Natural Science Foundation of China [21790362, 22075310]
- Strategic Priority Research Program of Chinese Academy of Sciences [XDB12010100]
- Science and Technology Commission of Shanghai Municipality [19XD1424700]
This study successfully synthesized azulene-embedded [n]helicenes and discovered their unique physicochemical properties, such as low-lying energy state, small energy gap, and strong optical response. These [n]helicenes are of great significance for constructing a non-benzenoid helicene library and understanding the structure-property relationships.
Azulene is a non-benzenoid aromatic building block with unique chemical structure and physicochemical properties. By using the bottom-up synthetic strategy, we synthesized three azulene-embedded [n]helicenes ([n]AzHs, n=5, 6 and 7), in which one terminal azulene subunit was fused with n-2 benzene rings. P- and M-enantiomers were observed in the packing diagrams of [5]-, and [6]AzHs. However, P- and M-[7]AzHs could be isolated by recrystallization of the racemic mixture. These [n]AzHs were endowed with new properties through the azulene moiety such as low-lying first electric state (S-1), small optical energy gap and anti-Kasha emission. [6]-, and [7]AzHs exhibit strong chiroptical responses with high absorption dissymmetry factor (g(abs)) maxima of about 0.02, which is among the highest |g(abs)| values of helicenes in the visible range. These azulene-embedded [n]helicenes contribute to the non-benzenoid helicene library and allow the structure-property relationships to be better understood.
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