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In this work, a facile and versatile strategy for the synthesis of contorted polycyclic aromatic hydrocarbons (PAHs) starting from the functionalized pentacene was established. A series of novel PAHs 1–4 and their derivatives were synthesized through a simple two‐step synthesis procedure involving an intramolecular reductive Friedel–Crafts cyclization of four newly synthesized pentacene aldehydes 5–8 as a key step. All the molecules were confirmed by single‐crystal X‐ray diffraction and their photophysical and electrochemical properties were studied in detail. Interestingly, the most striking feature of 1–4 is their highly contorted carbon structures and the accompanying helical chirality. In particular, the optical resolution of 2 was successfully achieved by chiral‐phase HPLC, and the enantiomers were characterized by circular dichroism and circularly polarized luminescence spectroscopy. Despite the highly nonplanar conformations, these contorted PAHs exhibited emissive properties with moderate‐to‐good fluorescence quantum yields, implying the potential utility of this series PAHs as high‐quality organic laser dyes. By using a self‐assembly method with the help of epoxy resin, a bottle microlaser based on 3 a was successfully illustrated with a lasing wavelength of 567.8 nm at a threshold of 0.3 mJ/cm2. We believe that this work will shed light on the chemical versatility of pentacene and its derivatives in the construction of novel functionalized PAHs. [ABSTRACT FROM AUTHOR]