Correlation of mobility and molecular packing in organic transistors based on cycloalkyl naphthalene diimides

Abstract

A series of cycloalkyl-substituted naphthalene tetracarboxylic diimides (Cyn-NTCDIs, n = 3–8) are prepared and the transistor properties and molecular packings are systematically investigated. Cy5–Cy8-NTCDIs have similar brickwork structures, where two molecules are located on the top of a molecule with large displacement along the molecular short axis. The intermolecular overlap is maximized when the small slipping along the molecular long axis makes the molecules nearly perpendicular to the substrate. Consequently, the mobility decreases exactly in the same order as the interlayer d-spacings.