Emissive, high charge transport polymers

Electricity: conductors and insulators – Conduits – cables or conductors – Insulated

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C252S299400, C252S582000, C257SE21259, C349S001000, C428S011000, C525S063000

Reexamination Certificate

active

07041910

ABSTRACT:
The present invention generally relates to stable emissive aggregates of polymers. The aggregates are composed of various polymer molecules arranged in such a way as to allow extended electronic couplings between nearby polymer molecules, enhancing exciton transport, while minimizing the effects of quenching due to interchain interactions. For example, the polymer molecules may be arranged in a non-aligned, electronically-communicative manner (for example, at an oblique angle), stabilized by various methods such as chemical linkages or physical interactions. Within the aggregate, electronic interactions along the polymer molecule may extend to nearby polymer molecules, which may be observed as a shift in the absorption spectra relative to a random dispersion. Light emitted from the aggregate may be polarized in some cases, for example, linearly or circularly, which may be caused by chiral arrangements of polymers within the aggregate (the polymers themselves may or may not be chiral). These aggregates may find widespread use, for example, in enantiomeric detectors, electrochemical devices, photodetectors, organic diodes, sensors, light sources, or photovoltaic devices.

REFERENCES:
patent: 4356429 (1982-10-01), Tang
patent: 4687732 (1987-08-01), Ward et al.
patent: 4927768 (1990-05-01), Coughlin et al.
patent: 4946890 (1990-08-01), Meador
patent: 4992302 (1991-02-01), Lindmayer
patent: 5155149 (1992-10-01), Atwater et al.
patent: 5194393 (1993-03-01), Hugl et al.
patent: 5236808 (1993-08-01), Smothers
patent: 5244813 (1993-09-01), Walt et al.
patent: 5254633 (1993-10-01), Han et al.
patent: 5364797 (1994-11-01), Olson et al.
patent: 5414069 (1995-05-01), Cumming et al.
patent: 5451683 (1995-09-01), Barrett et al.
patent: 5511547 (1996-04-01), Markle et al.
patent: 5512490 (1996-04-01), Walt et al.
patent: 5532129 (1996-07-01), Heller
patent: 5540999 (1996-07-01), Yamamoto et al.
patent: 5546889 (1996-08-01), Wakita et al.
patent: 5554747 (1996-09-01), Sharma et al.
patent: 5556524 (1996-09-01), Albers
patent: 5563056 (1996-10-01), Swan et al.
patent: 5565322 (1996-10-01), Heller
patent: 5580527 (1996-12-01), Bell et al.
patent: 5585646 (1996-12-01), Kossovsky et al.
patent: 5591787 (1997-01-01), Schlennert et al.
patent: 5597890 (1997-01-01), Jenekhe
patent: 5607864 (1997-03-01), Ricchiero et al.
patent: 5679773 (1997-10-01), Holmes
patent: 5700696 (1997-12-01), Chandross et al.
patent: 5705348 (1998-01-01), Meade et al.
patent: 5709994 (1998-01-01), Pease et al.
patent: 5710197 (1998-01-01), Fischer et al.
patent: 5723218 (1998-03-01), Haugland et al.
patent: 5869562 (1999-02-01), Lindquist et al.
patent: 6020426 (2000-02-01), Yamaguchi et al.
patent: 6259277 (2001-07-01), Tour et al.
patent: 6589731 (2003-07-01), Chen et al.
patent: 6713298 (2004-03-01), McDevitt et al.
patent: 2002/0040805 (2002-04-01), Swager
patent: 2002/0150697 (2002-10-01), Swager et al.
patent: 2003/0134959 (2003-07-01), Hancock et al.
patent: 2003/0178607 (2003-09-01), Swager et al.
patent: 2004/0043251 (2004-03-01), Epstein et al.
patent: 2004/0121337 (2004-06-01), Deans et al.
patent: 2004/0235184 (2004-11-01), Swager
patent: 19744792 (1999-04-01), None
patent: 19806037 (1999-08-01), None
patent: 0442123 (1991-08-01), None
patent: 0933655 (1999-08-01), None
patent: 1011154 (2000-06-01), None
patent: 06-322078 (1999-11-01), None
patent: WO 89/00593 (1989-01-01), None
patent: WO 95/16681 (1995-06-01), None
patent: WO 99/57222 (1999-11-01), None
patent: WO 01/57140 (2001-08-01), None
patent: WO 02/16463 (2002-02-01), None
patent: WO 03/048226 (2003-06-01), None
patent: WO 04/007634 (2004-01-01), None
patent: WO 04/057014 (2004-07-01), None
Zahn, S., et al., Three-Dimensional Electronic Delocalization in Chiral Conjugated Polymers,Agnew. Chem. Int. Ed., 2002, 41, No. 22, p. 4225-4230, WILEY-VCH Verlag Gmbh & Co., KGaA, Weinheim.
Brabec, C., et al. “Plastic Solar Cells″,”Adv. Funct. Mater, 11(1), (2001), pp. 15-26.
Chen, L., et al., “Highly sensitive biological and chemical sensors based on reversible fluorescence quenching in a conjugated polymer,”PNAS, 96(22), (1999), pp.: 12287-12292.
Chen, L., et al., “Tuning the Properties of Conjugated Polyelectrolytes through Surfactant Complexation,”Journal of the American Chemical Society, 122, pp. 9302-9303.
Cotts, P.M., et al., “Equilibrium Flexibility of a Rigid Linear Conjugated Polymer,”Macromolecules, 29 (1996), pp. 7323-7328.
Deans, R., et al., “A Poly(p-phenyleneethynylene) with a Highly Emissive Aggregated Phase″,”Journal of the American Chemical Society, 122 (2000), pp. 8565-8566.
Fiesel, R., et al., “Aggregation-induced CD effects in chiral poly(2,5-dialkoxy-1,4-phenylene)s,”Acta Polym., 49, (1998), pp. 445-449.
Fiesel, R., et al., “A chiral poly(para-phenyleneethynylene) (PPE) derivative,”Macromol. Rapid Commun., 19, (1998), pp. 427-431.
Fiesel, R., et al., “On the Solid State Aggregation of Chiral Substituted Poly(para-phenylene)s (PPPs),”Synthetic Metals, 102, (1999), pp. 1457-1458.
Fu, D., et al., “Alternating Poly(PyridylVinyenePhenylene Vinylene)s: Synthesis and Solid State Organizations,”Tetrahedron, 53(45), (1997), pp.: 15487-15494.
Gaylord, B.S., et al., “DNA detection using water-soluble conjugated polymers and peptide nucleic acid probes,”PNAS, 99 (17), (2002), pp. 10954-10957.
Gaylord, B., et al., “Water-Soluble Conjugated Oligomers: Effect of Chain Length and Aggregation on Photoluminescence-Quenching Efficiencies,”J. Am. Soc., 123, (2001), pp.: 6417-6418.
Goldfinger, M. et al., “Fused Polycyclic Aromatics via Electrophile-Induced Cyclization Reactions: Application to the Synthesis of Graphite Ribbons”,Journal of the American Chemical Society, 116, (1994), pp. 7895-7896.
Halkyard, C.E., “Evidence of Aggregate Formation of 2,5-Dialkylpoly (p-phenyleneethynylenes) in Solution and Thin Films,”Macromolecules, 31(25), (1998), pp.: 8655-8659.
Harrison, B.S., et al., “Amplified Fluorescence Quenching in a Poly(p-phenylene)-Based Cationic Polyelectrolyte,”J. Am. Chem. Soc., 122, (2000), pp.: 8561-8562.
Heeger, P.S., et al., “Making sense of polymer-based biosensors,”PNAS, 96(22), (1999), pp.: 12219-12221.
Höger S., et al., “Synthesis, Aggregation, and Adsorption Phenomena of Shape-Persistent Macrocycles with Extraannular Polyalkuly Substituents,”Journal of the American Chemical Society, 123(24), (2001), pp. 5651-5659.
Jones, R.M., et al., “Superquenching and Its Applications in J-Aggregated Cyanine Polymers,”Langmuir, 17, (2001), pp. 2568-2571.
Kim, J., et al., “Nanoscale Fibrils and Grids: Aggregated Structures from Rigid-Rod Conjugated Polymers,”Macromolecules, 32(5), (1999), pp.: 1500-1507.
Kim, J., et al., “Ion-Specific Aggregation in Conjugated Polymers: Highly Sensitive and Selective Fluorescent Ion Chemosensors,”Agnew Chem. Int. Ed., 39(21), (2000), pp. 3868-3872.
Kim, J., et al., “Control of conformational and interpolymer effects in conjugated polymers,”Nature, 411, (2001), pp. 1030-1034.
Kim, J., et al., “Directing Energy Transfer within Conjugated Polymer Thin Films,”Journal of the American Chemical Society, 123(46), (2001), pp. 11488-11489.
Kim, J., et al., “Structural Control in Thin Layers of Poly)P-phenyleneethynylene)s: Photophysical Studies of Langmuir and Langmuir-Blodgett Films,”Journal of the American Chemical Society, 124 (26), (2002), p. 7710.
Kim, Y., et al., “Ultrafast Energy-Transfer Dynamics between Block Copolymer and π-Conjugated Polymer Chains in Blended Polymeric Systems,”Chemistry of Materials, 13(8), 266.
Köhler, B., et al., “Novel Chiral Macrocycles Containing Two Electronically Interacting Arylene Chromophores,”Chem. Eur. J., 7(14), (2001), pp. 3000-3004.
Kraft, A., et al., “Electroluminescent Conjugated Polymers—Seeing Polymers in a N

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

Emissive, high charge transport polymers does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Emissive, high charge transport polymers, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Emissive, high charge transport polymers will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3560419

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