A series of new naphthalene diimide (NDI) semiconducting derivatives with different N-phenyl bicyclic side groups were rationally designed and synthesized in this study. The solubility of the orthogonal-shaped NDI derivatives with 5-tetralinyl and 4-indanyl side groups was found to be up to two orders of magnitude higher than that of the linear-shaped NDI derivatives with 6-tetralinyl and 5-indanyl side groups. The orthogonal-shaped NDI derivative with a 5-tetralinyl side group exhibited excellent solution processability due to its high solubility (e.g., 4 g/100 g dichlorobenzene), high thermal stability (e.g., lowest phase transition temperature of 380 °C), and high vertical carrier mobility (e.g., space-current-limited-current electron mobility of 7 × 10−5 cm2/V·s). Therefore, the introduction of N-phenyl bicyclic side groups on organic semiconductors was confirmed to be a highly promising design strategy for achieving the desired physical properties.
These authors (J. B. Lee and B. M. Oh) contributed equally to this work. This work has been supported by the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning, and the Ministry of Education, Korea (No. 2021R1A5A6002853 , 2019K1A3A1A14057973 , and 2019R1A6A1A11051471 ). X-ray structural analysis was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Korea ( 2019R1I1A2A01058066 ).