Inserting Nitrogen: An Effective Concept To Create Nonplanar and Stimuli-Responsive Perylene Bisimide Analogues

• Published in: Journal of the American Chemical Society Vol. 141; no. 50; pp. 19807 - 19816
• Main Authors: Hayakawa, Sakiho, Kawasaki, Ayumi, Hong, Yongseok, Uraguchi, Daisuke, Ooi, Takashi, Kim, Dongho, Akutagawa, Tomoyuki, Fukui, Norihito, Shinokubo, Hiroshi
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 18.12.2019; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Multidisciplinary; Physical Sciences; Science & Technology; ASSEMBLIES; CARBON NANOTUBE; AROMATIC SADDLES; SYSTEMS; NAPHTHALENE; TRIBENZOTRIQUINACENE; CONFORMATION; CHIRALITY; DERIVATIVES; MOLECULES
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.9b09556

Establishing design principles to create nonplanar π-conjugated molecules is crucial for the development of novel functional materials. Herein, we describe the synthesis and properties of dinaphtho­[1,8-bc:1′,8′-ef]­azepine bisimides (DNABIs). Their molecular design is conceptually based on the insertion of a nitrogen atom into a perylene bisimide core. We have synthesized several DNABI derivatives with a hydrogen atom, a primary alkyl group, or an aryl group on the central nitrogen atom. These DNABIs exhibit nonplanar conformations, flexible structural changes, and ambipolar redox activity. The steric effect around the central nitrogen atom substantially affects the overall structures and results in two different conformations: a nonsymmetric bent conformation and a symmetric twisted conformation, accompanied by a drastic change in electronic properties. Notably, the nonsymmetric DNABI undergoes unique structural changes in response to the application of an external electric field, which is due to molecular motions that are accompanied by an orientational fluctuation of the dipole moment. Furthermore, the addition of a chiral Brønsted base to N-unsubstituted DNABI affords control over the helical chirality via hydrogen-bonding interactions.