Pure and Applied Chemistry

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• Bedis Hanène, Kouki Fayçal, Bouchriha Habib: Effect of the oligothiophene chain length on the performance of organic photovoltaic cells. Appl. Phys. A 2013, 110, 163. <http://dx.doi.org/10.1007/s00339-012-7046-8>
• Irfan Ahmad, Ijaz Fatima, Al-Sehemi Abdullah G., Asiri Abdullah M.: Quantum chemical approach toward rational designing of highly efficient oxadiazole based oligomers used in organic field effect transistors. J Comput Electron 2012, 11, 374. <http://dx.doi.org/10.1007/s10825-012-0417-8>
• Chen Jian, Shu Jie, Schobloch Simone, Kroeger Anja, Graf Robert, Muñoz-Espí Rafael, Landfester Katharina, Ziener Ulrich: A New Design Strategy for the Synthesis of Unsubstituted Polythiophene with Defined High Molecular Weight. Macromolecules 2012, 45, 5108. <http://dx.doi.org/10.1021/ma301074p>
• Sears W.M., MacKinnon C.D., Kraft T.M.: The effect of chain length on the dielectric and optical properties of oligothiophenes. Synthetic Metal 2011, 161, 1566. <http://dx.doi.org/10.1016/j.synthmet.2011.05.020>
• Huang J., Dawidczyk T. J., Jung B. J., Sun J., Mason A. F., Katz H. E.: Response diversity and dual response mechanism of organic field-effect transistors with dinitrotoluene vapor. J Mater Chem 2010, 20, 2644. <http://dx.doi.org/10.1039/b916037j>
• Cosseddu Piero, Vogel Jörn-Oliver, Fraboni Beatrice, Rabe Jurgen P., Koch Norbert, Bonfiglio Annalisa: Continuous Tuning of Organic Transistor Operation from Enhancement to Depletion Mode. Adv Mater 2009, 21, 344. <http://dx.doi.org/10.1002/adma.200800373>
• Malav�����Osuna Reyes, Ruiz���Delgado M.���Carmen, Hern��ndez V��ctor, L��pez���Navarrete Juan���T., Vercelli Barbara, Zotti Gianni, Novoa Juan���J., Suzuki Yoshitake, Yamaguchi Shigehiro, Henssler John���T.: Oxidation of End-Capped Pentathienoacenes and Characterization of Their Radical Cations. Chem Eur J 2009, 15, 12346. <http://dx.doi.org/10.1002/chem.200900246>
• Sears W.A., Sears W.M., MacKinnon C.D.: The effect of end group substitution on the electrical conductivity of mesoporous terthiophene. Synthetic Metal 2008, 158, 50. <http://dx.doi.org/10.1016/j.synthmet.2007.12.002>
• Sanji Takanobu, Kato Nobu, Tanaka Masato: Chirality Control in Oligothiophene through Chiral Wrapping. Org Lett 2006, 8, 235. <http://dx.doi.org/10.1021/ol052494g>
• Okujima Tetsuo, Kikuchi Makoto, Yamada Hiroko, Uno Hidemitsu, Ono Noboru: A new synthesis of tetra(quinoxalino)tetraazaporphyrin by the retro Diels-Alder reaction of a soluble precursor. J. Porphyrins Phthalocyanines 2006, 10, 1197. <http://dx.doi.org/10.1142/S1088424606000569>
• Singh Th. Birendra, Sariciftci Niyazi Serdar: PROGRESS IN PLASTIC ELECTRONICS DEVICES. Annu Rev Mater Res 2006, 36, 199. <http://dx.doi.org/10.1146/annurev.matsci.36.022805.094757>
• Moret Massimo, Campione Marcello, Borghesi Alessandro, Miozzo Luciano, Sassella Adele, Trabattoni Silvia, Lotz Bernard, Thierry Annette: Structural characterisation of single crystals and thin films of α,ω-dihexylquaterthiophene. J Mater Chem 2005, 15, 2444. <http://dx.doi.org/10.1039/b504233j>
• Barbarella G, Favaretto L, Sotgiu G, Zambianchi M, Antolini Luciano, Marseglia Elisabeth A, Tedesco Emilio, Gigli Giuseppe, Cingolani Roberto: New light-emitting functionalized oligothiophenes. Synthetic Metal 2000, 115, 47. <http://dx.doi.org/10.1016/S0379-6779(00)00299-X>
• Hu Wenping, Liu Yunqi, Xu Yu, Liu Shenggao, Zhou Shuqin, Zhu Daoben: The application of Langmuir–Blodgett films of a new asymmetrically substituted phthalocyanine, amino-tri-tert-butyl-phthalocyanine, in diodes and in all organic field-effect-transistors. Synthetic Metal 1999, 104, 19. <http://dx.doi.org/10.1016/S0379-6779(99)00036-3>