Semiconductor device manufacturing: process – Having organic semiconductive component
Reexamination Certificate
2011-08-30
2011-08-30
Parker, Ken A (Department: 2815)
Semiconductor device manufacturing: process
Having organic semiconductive component
C257S040000
Reexamination Certificate
active
08008116
ABSTRACT:
A composition comprising a plurality of molecules. Each of the molecules has a core comprising at least one aromatic ring and at least three pendant arms chemically bonded to the core. The pendant arms comprise a phenylene-terminated thiophene oligomer.
REFERENCES:
patent: 5331029 (1994-07-01), Sato et al.
patent: 2005/0089777 (2005-04-01), Ang et al.
patent: 2005/0274954 (2005-12-01), Tanaka et al.
patent: 2006/0009614 (2006-01-01), Yamahara et al.
patent: 2006/0102890 (2006-05-01), Yamahara et al.
patent: 2006/0122364 (2006-06-01), Obara et al.
patent: 2007/0092752 (2007-04-01), Maliakal et al.
patent: 2004009680 (2004-01-01), None
Facchetti, Antonio, et al.,; “Synthesis and Characterization of Diperfluorooctyl-Substituted Phenylene-Thiophene Oligomers as n-type Semiconductors, Molecular Structure”; Chemistry of Materials 16 (2004); pp. 4715-4727.
Donat, B. Pepin, et al.; “Increased field effect mobility from linear to branched thiophene-based polymers”, Synthetic Metals 146 (2004), pp. 225-231.
Ponomarenko, Sergei A., et al.; “1, 4-bis(5-decy1-2,2′-bithien-5-yl)benzene as new stable organic semiconductor for high performance thin film transistors”; Synthetic Metals 149 (2005); pp. 231-235.
Ohishi, Hitoshi, et al.; Amorphous Molecular Materials with High Carrier Mobillities: Thiophene- and Selenophene-Containing Tris(oligoarylenyl)amines; Chemistry Letters, vol. 33, No. 10 (2004); pp. 1266.
Kinoshita, Motoi, et al.; “1,3-Bis[5-(dimesitylboryl)thiopen-s-yl]benzene and 1,3,5-Tris[5-(dimesityl-boryl) thiophen-2-yl]benzene as a Novel Family of Electron-Transporting Hole Blockers for Organic Electroluminescent devices”; Chemistry Letters 2001; pp. 614.
Mushrush, Melissa, et al.; Easily Processable Phenylene-Thiophene-Based Organic Filed-Effect Transistors and Solution-Fabricated Nonvolatile Transistor Memory Elements; J. Am. Chem. Soc. 2003, 125, pp. 9414-9423.
Ando, Shinji, et al.; “High Performance n-Type Organic Field-Effect transistors Based on π-Electronic Systems with Trifluoromethylphenyl Groups”; J. Am. Chem. Society 2005, 127; 5336-5337.
Anthony, John E, et al.; “Functionalized Pentacene: Improved Electronic Properties from Control of Solid-State Order”; J. Am. Chem. Society 2001, 123; pp. 9482-9483.
Pei, Jian, et al.; “Star-Shaped Polycyclic Aromatics Based on Oligothiophene-Functionalized Truxene: Synthesis, Properties, and Facile Emissive Wavelength Tuning”; J. Am. Chem. Soc. 2003, 125; pp. 9944-9945.
Laquindanum, Joyce G., et al.; “Synthesis, Morphology and Field-Effect Mobility of Anthradithiophenes”; J. Am. Chem. Soc. 1998, 120; pp. 664-672.
Ponomarenko, Sergei A.; “Star-Shaped Oligothiophenes for Solution-Processible Organic Field-Effect Transistors”; Adv. Funct. Mater. 2003, 13, No. 8, Aug.; pp. 591-596.
Sun, Yanming; “Oligothiophene-Functionalized Truxene: Star-Shaped Compounds for organic Field-Effect Transistors”; Adv. Funct. Mater, 2005, 15, No. 5, May; pp. 818-822.
Maliakal Ashok J.
Tang Ming L.
Alcatel Lucent
Hitt Gaines PC
Ho Anthony
Parker Ken A
LandOfFree
Branched phenylene-terminated thiophene oligomers does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Branched phenylene-terminated thiophene oligomers, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Branched phenylene-terminated thiophene oligomers will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-2772849