Preparation, Electronic and Liquid Crystalline Properties of Electron-Accepting Azaacene Derivatives
journal contributionposted on 19.10.2018 by Takashi Takeda, Tomohiro Ikemoto, Shunsuke Yamamoto, Wakana Matsuda, Shu Seki, Masaya Mitsuishi, Tomoyuki Akutagawa
Any type of content formally published in an academic journal, usually following a peer-review process.
A series of electron-accepting azaacene-type materials 1–4 with different kinds and degrees of intermolecular interactions were synthesized. Simple modification of the terminal substituents significantly modulated the photophysical and electrochemical properties. The degree of weak intermolecular interaction determined the emergence of a liquid crystalline (LC) phase for each compound. Dipole–dipole interaction, π–π interaction, and van der Waals interaction all contributed to stabilize the LC phase of 1 and 2. The introduction of strong hydrogen bonding interaction enabled the formation of a highly ordered LC phase in 4. Charge-transport properties of 1, 2, and 4 were also investigated.