A modular synthetic approach to conjugated pentacene Di-, Tri-, and tetramers
Lehnherr D, Murray AH, Mcdonald R, Tykwinski R (2010)
Publication Type: Journal article, Original article
Publication year: 2010
Journal
Original Authors: Lehnherr D., Murray A.H., McDonald R., Tykwinski R.R.
Publisher: Wiley-VCH Verlag
Book Volume: 49
Pages Range: 6190-6194
Journal Issue: 35
Abstract
Mind the band gap: π-conjugated pentacene di-, tri-, and tetramers can be synthesized by using a versatile building block in Hay homocoupling as well as Cadiot-Chodkiewicz cross-coupling reactions. This modular approach allows the evaluation of solubility, stability, and the HOMO-LUMO gap as a function of compound length. Long-range three-dimensional π overlap occurs in the iBu3Si-substituted pentacene dimer (see figure; n=2). © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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APA:
Lehnherr, D., Murray, A.H., Mcdonald, R., & Tykwinski, R. (2010). A modular synthetic approach to conjugated pentacene Di-, Tri-, and tetramers. Angewandte Chemie International Edition, 49(35), 6190-6194. https://doi.org/10.1002/anie.201000555
MLA:
Lehnherr, Dan, et al. "A modular synthetic approach to conjugated pentacene Di-, Tri-, and tetramers." Angewandte Chemie International Edition 49.35 (2010): 6190-6194.
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