Bis(thiophen-2-yl)-diketopyrrolopyrrole (DPP) dyes bearing various alkyl substituents at the amide positions ( n -butyl, n -pentyl, n -hexyl, n -heptyl, n -octyl, 2-ethylhexyl) and chlorine (Cl), bromine (Br), or cyano (CN) substituents at the thiophene positions have been synthesized and investigated with regard to their molecular and semiconducting properties. Intense absorption, strong fl uorescence, and reversible oxidation and reduction processes are common to all of these dyes. Their characterization as organic semiconductors in vacuumprocessed thin-fi lm transistors reveals p-channel operation with fi eld-effect mobilities ranging from 0.01 to 0.7 cm 2 V −1 s −1 . The highest mobility is found for the DPP dyes bearing the 2-ethylhexyl substituents, which is surprising, considering that as a result of the chiral substituents, this material is a mixture of ( R , R ), ( S , S ), and ( R , S ) stereoisomers. The high carrier mobility in the fi lms of the DPPs bearing stereoisomerically inhomogeneous ethylhexyl groups is rationalized here by single-crystal X-ray diffraction (XRD) analysis in combination with XRD and atomic force microscopy studies on thin fi lms, which reveal the presence of slightly different 2D layer arrangements for the n -alkyl and the 2-ethylhexyl derivatives. For the cyano-substituted DPPs possessing the lowest LUMO levels, ambipolar transport characteristics are observed.leading consistently to the largest carrier mobilities within each individual series of H-, Cl-, Br-, and CN-DPPs, despite their presence as "impure" mixtures of ( R , R ), ( S , S ), and ( R , S ) stereoisomers. [ 6b , 7e,9 ]