دورية أكاديمية

Helically Chiral π‐Expanded Azocines Through Regioselective Beckmann Rearrangement and Their Charged States.

التفاصيل البيبلوغرافية
العنوان: Helically Chiral π‐Expanded Azocines Through Regioselective Beckmann Rearrangement and Their Charged States.
المؤلفون: Borstelmann, Jan, Schneider, Lars, Rominger, Frank, Deschler, Felix, Kivala, Milan
المصدر: Angewandte Chemie; Jul2024, Vol. 136 Issue 29, p1-11, 11p
مصطلحات موضوعية: BECKMANN rearrangement, AZOCINES, HIGH performance liquid chromatography, RADICAL cations, RADICAL anions, CLAISEN rearrangement, DIPYRRINS
مستخلص: We report a synthetic approach to π‐expanded [6]helicenes incorporating tropone and azocine units in combination with a 5‐membered ring, which exhibit intriguing structural, electronic, and chiroptical properties. The regioselective Beckmann rearrangement allows the isolation of helical scaffolds containing 8‐membered lactam, azocine, and amine units. As shown by X‐ray crystallographic analysis, the incorporation of tropone or azocine units leads to highly distorted [6]helicene moieties, with distinct packing motifs in the solid state. The compounds exhibit promising optoelectronic properties with considerable photoluminescence quantum yields and tunable emission wavelengths depending on the relative position of the nitrogen center within the polycyclic framework. Separation of the enantiomers by chiral high‐performance liquid chromatography (HPLC) allowed characterization of their chiroptical properties by circular dichroism (CD) and circularly polarized luminescence (CPL) spectroscopy. The azocine compounds feature manifold redox chemistry, allowing for the characterization of the corresponding radical anions and cations as well as the dications and dianions, with near‐infrared (NIR) absorption bands extending beyond 3000 nm. Detailed theoretical studies provided insights into the aromaticity evolution upon reduction and oxidation, suggesting that the steric strain prevents the azocine unit from undergoing aromatization, while the indene moiety dominates the observed redox chemistry. [ABSTRACT FROM AUTHOR]
Copyright of Angewandte Chemie is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:00448249
DOI:10.1002/ange.202405570