Organic semiconductor material, organic semiconductor...

Active solid-state devices (e.g. – transistors – solid-state diode – Organic semiconductor material

Reexamination Certificate

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C257SE51029, C549S083000

Reexamination Certificate

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07408188

ABSTRACT:
An organic semiconductor material characterized by having a structure represented by chemical formula 1, the planarity of a main chain A1-X-A2 being disintegrated by steric hindrance between B1 and X and steric hindrance between B2 and X, the organic semiconductor material having a number average molecular weight of about 2,000 to about 200,000:wherein A1, A2, B1, B2 and X each have a skeleton structure comprising L 6 π electron rings, M 8 π electron rings, N 10 π electron rings, O 12 π electron rings, P 14 π electron rings, Q 16 π electron rings, R 18 π electron rings, S 20 π electron rings, T 22 π electron rings, U 24 π electron rings, and V 26 π electron rings, wherein L, M, N, O, P, Q, R, S, T, U, and V are each an integer of 0 (zero) to 6 and L+M+N+O+P+Q+R+S+T+U+V=1 to 6; and B1 and B2 have an alkyl group.

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patent: 2006/0128969 (2006-06-01), Li et al.
patent: 2003-221434 (2003-08-01), None
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Xia, C., et al, “A First Synthesis of Thiophene Dendrimers”, Organic Letters, 2002, vol. 4 No. 12, 2067-2070.
Engelmann, G., et al., “Doped Polymers by Oxidative Polymerization 4. Oxidative Coupling of Methylated Oligothiophenes by FeCl3-6H20 as a Model Raction for the Oxidative Polymerization of Thiophene Derivatives”, Macromolecules 1996, 29, 3370-3375.□□
de Oliveira, M.A., et al., “Structure an Electronic Prooperties of Alkylthiophenes Coupled by Head-to-Tail and Head-to-Head Regioselectivity”, J. Braz.Chem.Soc., vol. 15, No. 6 832-838, 2004.□□

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