Naphtho[2,1-b:6,5-b′]difuran: A Versatile Motif Available for Solution-Processed Single-Crystal Organic Field-Effect Transistors with High Hole Mobility
We here report naphtho[2,1-b:6,5-b′]difuran derivatives as new p-type semiconductors that achieve hole mobilities of up to 3.6 cm2 V–1 s–1 along with high I on/I off ratios in solution-processed single-crystal organic field-effect transistors. These features originate from the dense crystal packing...
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Veröffentlicht in: | Journal of the American Chemical Society 2012-03, Vol.134 (12), p.5448-5451 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We here report naphtho[2,1-b:6,5-b′]difuran derivatives as new p-type semiconductors that achieve hole mobilities of up to 3.6 cm2 V–1 s–1 along with high I on/I off ratios in solution-processed single-crystal organic field-effect transistors. These features originate from the dense crystal packing and the resulting large intermolecular π-orbital overlap as well as from the small reorganization energy, all of which originate from the small radius of an oxygen atom. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja2120635 |