Abstract
Herein we report the synthesis and characterization of a series of 6,12-diarylindeno[1,2-b]fluorenes (IFs). Functionalization with electron donor and acceptor groups influences the ability of the IF scaffold to undergo two-electron oxidation and reduction to yield the corresponding 18- and 22-π-electron species, respectively. A single crystal of the pentafluorophenyl-substituted IF can serve as an active layer in an organic field-effect transistor (OFET). The important finding is that the single-crystal OFET yields an ambipolar device that is able to transport holes and electrons. © 2012 American Chemical Society.
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CITATION STYLE
Chase, D. T., Fix, A. G., Kang, S. J., Rose, B. D., Weber, C. D., Zhong, Y., … Haley, M. M. (2012). 6,12-Diarylindeno[1,2- b ]fluorenes: Syntheses, photophysics, and ambipolar OFETs. Journal of the American Chemical Society, 134(25), 10349–10352. https://doi.org/10.1021/ja303402p
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