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- W1566592818 endingPage "428" @default.
- W1566592818 startingPage "407" @default.
- W1566592818 abstract "Polycyclic aromatic hydrocarbons (PAHs) are regarded as promising organic semiconducting materials for organic field-effect transistors (OFETs), organic light-emitting diodes (OLEDs), and organic solar cells. The oligoacenes from benzene to anthracene can be extracted from crude oil, coal, and coal tar, while those larger than anthracene can be obtained only by multistep synthesis. The Diels-Alder reaction ([4+2] cycloaddition) provides one of the most powerful methods for the construction of PAHs because it affords one-step formation of the six-membered ring framework, the basic unit of these derivatives. This chapter highlights the synthesis of substituted oligoacenes including anthracene, tetracene, and pentacene cores by Diels-Alder reactions using arynes and quinones as dienophile components and furans, thiophene-1,1-dioxides, and o-quinodimethane as diene components. The synthetic methodology is accompanied by discussions on molecular and packing structures as well as solid-state optical properties." @default.
- W1566592818 created "2016-06-24" @default.
- W1566592818 creator A5060103385 @default.
- W1566592818 date "2014-01-10" @default.
- W1566592818 modified "2023-10-14" @default.
- W1566592818 title "Synthesis of Substituted Oligoacenes via Diels–Alder Reactions and Substituent Effects on Molecular Structure, Packing Arrangement, and Solid‐State Optical Properties" @default.
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