Charge-transporting material containing diazapentacene...

Stock material or miscellaneous articles – Composite – Of inorganic material

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C428S917000, C313S504000, C313S506000, C257S040000

Reexamination Certificate

active

06902832

ABSTRACT:
A charge transporting material, a light emitting material and an organic electroluminescent device having high efficiency using a specified diazapentacene derivative represented by the following general formula (1):(in the general formula (1), R1to R10each represents independently a hydrogen atom, a halogen atom, an alkyl group of 1 to 6 carbon atoms, an alkoxy group, a substituted or not-substituted amino group, an aryl group or a heterocyclic group, in which the substituted or not-substituted aryl group or heterocyclic group, when they are adjacent with each other, may be of a structure condensed to each other, X1and X2each represents independently an oxygen atom or a sulfur atom, and Y1and Y2each represents independently a substituted or not-substituted alkyl group of 1 to 6 carbon atoms, an aryl group or a heterocyclic group).

REFERENCES:
patent: 4047948 (1977-09-01), Horgan
patent: 4536457 (1985-08-01), Tam
patent: 4539507 (1985-09-01), VanSlyke et al.
patent: 4665233 (1987-05-01), Podder et al.
patent: 4769292 (1988-09-01), Tang et al.
patent: 5047687 (1991-09-01), VanSlyke
patent: 5061569 (1991-10-01), VanSlyke et al.
patent: 5256945 (1993-10-01), Imai et al.
patent: 5487953 (1996-01-01), Shirota et al.
patent: 5554450 (1996-09-01), Shi et al.
patent: 5840217 (1998-11-01), Lupo et al.
patent: 25 34 713 (1977-02-01), None
patent: 57-144558 (1982-09-01), None
patent: 61-62038 (1986-03-01), None
patent: 61-112164 (1986-05-01), None
patent: 61-124949 (1986-06-01), None
patent: 61-134354 (1986-06-01), None
patent: 61-134355 (1986-06-01), None
patent: 63-264692 (1988-11-01), None
patent: 4-212286 (1992-08-01), None
patent: 4-308688 (1992-10-01), None
patent: 4-363891 (1992-12-01), None
patent: 5-234681 (1993-09-01), None
patent: 5-239455 (1993-09-01), None
patent: 6-1972 (1994-01-01), None
patent: 6-32307 (1994-04-01), None
patent: 6-267658 (1994-09-01), None
patent: 6-312979 (1994-11-01), None
patent: 7-90256 (1995-04-01), None
patent: 7-97355 (1995-04-01), None
patent: 7-126226 (1995-05-01), None
patent: 7-126615 (1995-05-01), None
patent: 7-138560 (1995-05-01), None
patent: 7-278637 (1995-10-01), None
patent: 7-331238 (1995-12-01), None
patent: 8-48656 (1996-02-01), None
patent: 8-87122 (1996-04-01), None
patent: 8-100172 (1996-04-01), None
patent: 8-259940 (1996-10-01), None
T. Okamoto et al., “Synthesis and properties of benzooxazinophenooxazine and the related compounds”, Synthetic Metals 120, pp. 933-934 (Mar. 15, 2001).
C.W. Tang et al., “Electroluminescence of doped organic thin films”, J. Appl. Phys., vol. 65, No. 9, pp. 3610-3616, May 1, 1989.
Chihaya Adachi et al., “Electroluminescence in Organic Films with Three-Layer Structure”, Japanese Journal of Applied Physics, vol. 27, No. 2, pp. L269-L271, Feb. 1988.
Chihaya Adachi et al., “Confinement of charge carriers and molecular excitons within 5-nm-thick emitter layer in organic electroluminescent devices with a double heterostructure”, Appl. Phys. Lett., vol. 57, No. 6, pp. 531-533, Aug. 6, 1990.
Yoshiyuki Kuwabara et al., “Thermally Stable Multilayered Organic Electroluminescent Devices Using Novel Starburst Molecules, 4,4′,4″-Tris(N-carbazolyl)triphenylamine (TCTA) and 4,4′4″-Tri(3-methylphenylphenyl-amino)triphenylamine (m-MTDATA), as Hole-Transport Materials”, Advanced Materials, vol. 6, No. 9, pp. 677-679, 1994, no month.
Hiromitsu Tanaka et al., “Novel hole-transporting materials based on triphenylamine for organic electroluminescent devices”, Chem. Commun., pp. 2175-2176, 1996, no month.
Ioan A. Silberg et al., “Free Radicals of Phenothiazine and Related Compounds. VI-Free Radicals and Charge Transfer Complexes of Some Oligophenothiazines”, Heterocyclic Communications, vol. 2, pp. 117-124, 1996.
“Organic Electroluminescent Devices Using Distyryl Compound”, Chemical Society of Japan, 72nd National Meeting, Lecture, vol. 2, 2PB098, p. 1392, 1997.
Yasuhiro Yamaguchi et al., “Application of Unsymmetrical Diphenoquinone Derivatives of Xerography (l) Molecular Design of a Novel Class of Polymer—dispersible Electron—transport—active Compounds”, Journal of the Society of Electrophotography of Japan, vol. 30, No. 3, pp. 266-273, Jul. 1991.
Chihaya Adachi et al., “Organic Electroluminescent Device with a Three-Layer Structure”, Japanese Journal of Applied Physics, vol. 27, No. 4, pp. L713-L715, Apr. 1988.
Chihaya Adachi et al., “Organic electroluminescent device having a hole conductor as an emitting layer”, Appl. Phys. Lett., vol. 55, No. 15, pp. 1489-1491, Oct. 9, 1989.
Junji Kido et al., “1,2,4-Triazole Derivative as an Electron Transport Layer in Organic Electroluminescent Devices”, Jpn. J. Appl. Phys., vol. 32, pp. L917-L920, Jul. 1993.
J. Kido et al., “Organic electroluminescent devices using 1,3,4-thiadiazole derivatives”, Polymer Preprints Japan, vol. 43, No. 3, Pla007, p. 978, 1994, no month.
T. Izumizawa et al., “Study on Electroluminescent Behaviors of Metal (III)-quinolinolates”, IEICE Technical Report, vol. 92, No. 311, pp. 43-48, Nov. 1992.
Takakazu Yamamoto et al., Polymer Light-Emitting Diodes with Single- and Double-Layer Structures Using Poly(2,3-diphenylquinoxaline-5,8-diyl), Jpn. J. Appl. Phys., vol. 33, pp. L250-L253, Feb. 1994.
H. Nakada et al., “Blue Organic Electroluminescent Devices Using Phenanthroline Derivatives as an Electron Transport Layer”, Polymer Preprints, Japan, vol. 43, No. 7, pp. 2450-2451, 1994, no month.
“Optical Function Material”, Functional Polymer Material Series, edited by Society of Polymer Science, Japan, Kyoritsu Shiuppan Co., Ltd., pp. 236-241, 1991, no month.
The Society of Applied Physics and Related Societies, vol. 40, No. 3, p. 1146, Mar. 1993.
Jingping Zhang et al., “The Ground State Spin Multiplicity of Schlenk-type Biradicals and the Influence of additional Linkage to Ladder Type Structures”, Chemical Physics, vol. 206, No. 3, pp. 339 to 351, Jun., 1996.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Charge-transporting material containing diazapentacene... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Charge-transporting material containing diazapentacene..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Charge-transporting material containing diazapentacene... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3510148

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.