We investigated the polymorphic stability and reversibility of thin films of a series of naphthalene diimides (NTCDIs) with varying alkyl substitutions. Each derivative adopts its β-phase upon thermal evaporation; post-deposition processing via solvent-vapor annealing converts the β-phase to the α-phase in two of the four derivatives. NTCDIs adopt layered structures driven by strong intralayer π-π interactions and weaker interlayer van der Waals interactions.  The presence of interlayer short contacts effectively locks the structure in place, preventing any molecular reorganization. The absence of such short interlayer contacts is instead correlated with reversible access of both polymorphs; judicious selection of post-deposition processing conditions tunes the polymorph accessed. This finding is generalizable across a wide range of molecular semiconductors that adopt layered structures, including derivatives of benzothiophene and functionalized acenes. Beyond organic electronics, this finding has implications on pharmaceutics and the food industry as polymorphic stability governs bioavailability and solubility.<br/>

Understanding polymorphic accessibility and stability in molecular semiconductor thin films

253rd National Meeting (2017)

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