Tunable electron acceptors based on cyclopenta[hi]aceanthrylenes

TETRAHEDRON LETTERS

卷:56

Article

Plunkett, Kyle N.¹ 

[1] So Illinois Univ, Dept Chem & Biochem, Carbondale, IL 62901 USA

关键词: Cyclopenta-fused;    Polycyclic aromatic hydrocarbons;    Electron acceptors;    Organic electronics;   

DOI  :  10.1016/j.tetlet.2015.11.022

来源: Elsevier

【 摘 要 】

A series of substituted cyclopenta[hi]aceanthrylene derivatives with electron donating (NH2, OCH3), neutral (H), and electron withdrawing (COOH, CF3, CN, NO2) substituents were prepared. A room-temperature Sonogashira cross-coupling reaction between 2,7-dibromocyclopenta[hi]aceanthrylene and an appropriately functionalized phenylene ethynylene precursor was utilized to access the materials that were characterized by Nuclear Magnetic Resonance Spectroscopy (NMR), cyclic voltammetry (CV), and UV Vis spectroscopy. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) were systematically varied when proceeding from electron donating to electron withdrawing substituents. The optical band gap was significantly altered for the most electron donating species, while little change was observed between different electron withdrawing substituents. This study demonstrates the ability to control the frontier orbital energies of this class of cyclopenta-fused polycyclic aromatic hydrocarbon materials through selective substitution. (C) 2015 Elsevier Ltd. All rights reserved.

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