Abstract

Molecular orientation within organic solids limits the range of applicable surface reactions, with reactive functionalities often recessed and inaccessible to adsorbates. To induce reactivity in heretofore inert orientations of acenes, a defect-mediated mechanism is utilized to functionalize thin-film phase pentacene. This mechanism was demonstrated via correlation of reaction data to defect density, determined via polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) and atomic force microscopy (AFM). By controllably varying the amount of grain boundaries in the acene films, the reaction can be varied from near zero to coverage exceeding a monolayer. The extensive coverage suggests that the reaction propagates from the defects throughout the grains, a prediction borne out via direct observation of reaction progression along the surface from a single dislocation (via scanning electron microscopy). The results support a mechanism whereby the reaction is initialized at the defect si...

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