Indeno[1,2-b]fluorenes: Fully conjugated antiaromatic analogues of acenes

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Abstract

What IF? Fully conjugated, formally antiaromatic indeno[1,2-b]fluorenes (IFs; see structure) were synthesized from the corresponding diones by the SnCl2-promoted reduction often used to generate acenes. Their optoelectronic properties suggest that indenofluorenes might serve as alternatives to the more traditionally utilized acenes such as pentacene for materials applications. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Chase, D. T., Rose, B. D., McClintock, S. P., Zakharov, L. N., & Haley, M. M. (2011). Indeno[1,2-b]fluorenes: Fully conjugated antiaromatic analogues of acenes. Angewandte Chemie - International Edition, 50(5), 1127–1130. https://doi.org/10.1002/anie.201006312

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