Novel soluble pentacene and anthradithiophene derivatives for organic thin-film transistors
摘要:
Four new solution-processable pentacene- (PEN) and anthradithiophene- (ADT) based organic semiconductors bearing two phenylethynyl (PE-) or triethylsilylphenylethynyl (TESPE-) substituents have been synthesized, characterized, and incorporated in thin-film transistors (TFTs). The molecular structures of these four materials have been determined by single-crystal X-ray diffraction. Thin films of all four compounds have been fabricated via drop-casting and exhibited p-channel OTFT transport with hole mobilities as high as similar to 0.01 cm(2)/V s. Compared to PEN derivatives, ADT-based compounds exhibited superior device performance and photooxidative stability in ambient. The film morphologies and microstructures of these compounds have been characterized by optical microscopy and X-ray diffraction to rationalize device performance trends. (C) 2010 Elsevier B.V. All rights reserved.
Novel soluble pentacene and anthradithiophene derivatives for organic thin-film transistors
摘要:
Four new solution-processable pentacene- (PEN) and anthradithiophene- (ADT) based organic semiconductors bearing two phenylethynyl (PE-) or triethylsilylphenylethynyl (TESPE-) substituents have been synthesized, characterized, and incorporated in thin-film transistors (TFTs). The molecular structures of these four materials have been determined by single-crystal X-ray diffraction. Thin films of all four compounds have been fabricated via drop-casting and exhibited p-channel OTFT transport with hole mobilities as high as similar to 0.01 cm(2)/V s. Compared to PEN derivatives, ADT-based compounds exhibited superior device performance and photooxidative stability in ambient. The film morphologies and microstructures of these compounds have been characterized by optical microscopy and X-ray diffraction to rationalize device performance trends. (C) 2010 Elsevier B.V. All rights reserved.
The protection of terminal ethynyl groups in Grignard syntheses
作者:C. Eaborn、A. R. Thompson、D. R. M. Walton
DOI:10.1039/j39670001364
日期:——
The trimethylsilyl group can be used to protect a terminalethynylgroup in Grignardsyntheses. For example, a Grignard reagent can be made in tetrahydrofuran from the easily prepared compound (p-bromophenylethynyl)-trimethylsilane, and carbonation gives the acid (p-carboxyphenylethynyl)trimethylsilane, which on treatment with dilute alkali gives p-ethynylbenzoic acid in 55% overall yield. The corresponding