Dithiophene-Fused Tetra­cyano­naphtho­quino­dimethanes (DT-TNAPs): Synthesis and Characterization of π‑Extended Quinoidal Compounds for n‑Channel Organic Semiconductor

Abstract

Dithiophene-fused tetra­cyano­naphtho­quino­dimethanes (DTTNAPs) were synthesized and evaluated as n-channel organic semiconductors. DTTNAPs, regardless of isomeric structures and substituents, have low-lying LUMO energy levels (∼4.6 eV below the vacuum level), suitable for stable n-channel field-effect transistors (FETs) under ambient conditions. In fact, α-DTTNAP derivatives afforded solution-processed FETs showing an electron mobility of 10<sup>–3</sup> cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup>, indicating that DTTNAPs are a potential molecular framework for n-channel organic semiconductors

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