Crosslinkable or chain extendable polyarylpolyamines and films t

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From ketone or ketene reactant

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

528 38, 528348, 528422, C08G 1200, C08G 6926, C08G 7300

Patent

active

059291940

ABSTRACT:
The invention relates to poly(tertiary di- or polyarylamines) which have more than one aryl moiety which is further substituted with a moiety capable of chain extension or crosslinking. In another aspect, the invention relates to poly(tertiary di- or polyarylamines) which have more than one aryl moiety which is further substituted with a moiety capable of chain extension or crosslinking which are partially or completely crosslinked or chain extended. The invention further relates to films prepared from such chain extended or crosslinked poly(tertiary di- or polyarylamines). The invention further relates to electrophotographic devices and electroluminescent devices, such as polymeric light-emitting diodes, containing such films.

REFERENCES:
patent: 3995299 (1976-11-01), Partridge
patent: 4356429 (1982-10-01), Tang
patent: 4525256 (1985-06-01), Martin
patent: 4528366 (1985-07-01), Woo et al.
patent: 4539507 (1985-09-01), VanSlyke et al.
patent: 4720432 (1988-01-01), VanSlyke et al.
patent: 4769292 (1988-09-01), Tang et al.
patent: 4885211 (1989-12-01), Tang et al.
patent: 4952667 (1990-08-01), Shikatani et al.
patent: 5047687 (1991-09-01), VanSlyke
patent: 5059862 (1991-10-01), VanSlyke et al.
patent: 5061569 (1991-10-01), VanSlyke et al.
patent: 5247190 (1993-09-01), Friend et al.
patent: 5256945 (1993-10-01), Imai et al.
patent: 5352554 (1994-10-01), Mishima et al.
patent: 5352834 (1994-10-01), Morishita et al.
patent: 5356743 (1994-10-01), Yanus et al.
patent: 5639914 (1997-06-01), Tomiyama et al.
J. Chem. Soc. (C), 1970, pp. 488-492, I.G.C. Coutts et al, "Organs-boron Compounds, Part IIIk, Aliphatic & Aromatic Diboronic Acids".
Bulletin of the Chemical Society of Japan, vol. 51(7), pp. 2091-2097, Iakakaz, Yamamoto et al., A novel type of Polycondensation utilizing Transition metal catalyzed C-C Coupling I. Preparation of Thermostable Poly-phenyleno Type Polymers.
ACS, 1991, Thomas I. Wallow et al., pp. 7411-7412, "In Aqua Synthesis of Water-Soluble Poly(phenylene) Derivatives".
Letters to Nature, pp. 539-541, J.A. Burroughes et al., "Light-emitting Diodes based on Conjugated Polymers".
Synthetic Communications, 11(7), pp. 513-519, (1981), N. Miyaura et al., "The Palladium -Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the presence of Bases".
Prog. Polym. Sci. vol. 17, pp. 1153-1205, 1992, Takakazu Yamamoto "Electronically Conducting & Thermally Stable The-Conjugated Polyl arylenes prepared by Organometallic Processes".
Bull. Chem. Soc. Jpn., 63, pp. 80-87, 1990, Masahitio Igota et al., "Homo coupling of arylhalides Using Nickel(II) Complex and Zinc in the Presence of EtyNI. An Efficient Method for the Synthesis of Bipyridines", Jul. 18, 1989.
ACS Symposium Series 367, "Cross-linked Polymers, Chemistry, Properties & Applications " Carduner et al, pp. 380--394m Carbon-13 NMR Investigation of Oligomerization of Bismaleimidophenyl Methane w/Diallyl Bisplanol A, 1988.
PCS, Polymer Preprints, vol. 34, No. 1, 1993, pp. 413-414, "Perfluorocyclo-butane aromatic ether polymers," Davis A. Babb et al.
ACS, Polymers Preprints, vol. 53, No. 1, 1992 M.T. Bishop et al "AB-BCB-Maleimide Resins for High Temperature Composites".
Amerian Institute of Physics, 1990, pp. 799-801, "Blue light-emitting organic electro lumiescent devices", Chihaya Adachi et al.
J. Phys. Chem., 1984, 88, pp. 4714-4717, D.M. Pai et al, "Trap-controlled Hopping Transport".
Advanced Materials, 1993, Wataru Ishikawa et al, Novel Amor-phous Molecular Materials: The Starburst Molecular 1,3,5-TriszN-(4-diphenyl-aminophenyl)phenylamino 1 benzene, pp. 559-561, vol. 5, No. 718.
Advanced Materials, 1994, vol. 6, No. 9, Y Kumabara et al, "Thermally stable Multi layered Organic Electroluminescent Devices Using Novel Starburst Molecules, 4,4', 4"-Tri (N-carbazolul)triphenyl-amino (TCTA) and 4,4',4", -Tris (3-methylphenyl phenyl-amino) triplenylamino (M-MTDATA), as Hole-Transport Materials".
Synthetic Materials, 40 (1991) pp. 231-238, M. Ishkikawa et al, Synthesis & properties of electroncially conducting polytriphenyl-aminos.
Appl. Phys. Lett. 51(12), pp. 913-915, "Organic electroluminescent diodes", C.N. Tang et al, Sep. 21, 1987.
Appl. Phys. Lett. 61(A), pp. 761-763, "Organic electroluminescent devices based on molecularly coped polymers" J. Kido et al, Aug. 17, 1992.
Encyclopedia of Polymer Science & Engineering, vol. 11, pp. 186-196, "Photopolymerization" H.F. Mark et al, 1988.
"Reactive Oligomers", Frank W. Harris et al, "High Temperature Polymers from Thermally Curable Oligomers", pp. 1-16, Chapter 1, Chapter 8, pp. 91-103, Apr. 8-13, 1984.
J. Org. Chem., 1986, 51, pp. 2627-2637, Ismael Colon et al, "Coupling of Aryl Chlorides by Hidel and Reducing Metals."
Journal of Polymer Science: Part A, Polymer-Chemistry, vol. 28, pp. 367-383, I. Colon et al, "High Molecular Weight Aromatic Polymers by Nickel Coupling of Aryl Polychlorides", 1990.
Kawamura et al., Chemical Abstracts, vol. 125, Abstract 234547 (1996).
Li et al., Chemcial Abstracts, vol. 127, Abstract 101179 (1997).
Mihara et al., Chemical Abstracts, vol. 123, Abstract 183676 (1995).
Muto et al., Chemical Abstracts, vol. 111, Abstract 184162 (1989).
Shimada et al., Chemical Abstracts, vol. 115, Abstract 194199 (1991).
Tamano et al., Chemical Abstracts, vol. 127, Abstract 115061 (1997).
Tamoto et al., Chemical Abstracts, vol. 123, Abstract 183055 (1995).
Tamoto et al., Chemical Abstracts, vol. 123, Abstract 285572 (1995).
Tomiyama et al., Chemical Abstracts, vol. 123, Abstract 183664 )1005).
Umeda et al., Chemical Abstracts, vol. 123, Abstract 22137 (1995).
Adachi, Chihaya 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. Letter, vol. 57, No. 6, pp. 531-533 (Aug. 6, 1990).
Baker, Nelson T. III, et al., "Electrophillic Substitution Reactions of Triphenylamine", Journal of Organic Chemistry, vol. 30, pp. 3714-3718 (Nov. 1965).
Davis, M. J. et al., "The UV-Curing Behaviour of Some Photoinitiators and Photoactivators", J. Oil Col. Chem. Assoc., vol. 61, pp. 256-263 (1978).
Gautier, Sylvie et al., "Phase-Transfer Catalysis in the Ullmann Synthesis of Substituted Triphenylamines", Synthesis, pp. 383-385 (Apr. 1987).
Guram, Aril S. et al., "A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines", Angew. Chem. Int. Ed. Engl., vol. 34, No. 12, pp. 1348-1350 (1995).
Kohler, E.P. et al., "An Apparatus for Determining Both the Quality of Gas Evolved and the Amount of Reagent Consumed in Reactions with Methyl Magnesium Iodide", Journal of the American Chemical Society, vol. 49, pp. 3181-3188 (Dec. 1927).
Walter, Robert I., "Triarylaminium Salt Free Radicals", Journal of the American Chemical Society, vol. 77, pp. 5999-6002 (Nov. 20, 1995).
Chemical Abstract 91-069941/10 (1991).
Chemical Abstract 91-069927/10 (1991).
Chemical Abstract 93-365193/46 (1993).
Derwent 97-359265/199733 (JP 915137 A).

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

Crosslinkable or chain extendable polyarylpolyamines and films t does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Crosslinkable or chain extendable polyarylpolyamines and films t, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Crosslinkable or chain extendable polyarylpolyamines and films t will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-879730

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