CA2439060A1 - Emissive multichromophoric systems - Google Patents

Emissive multichromophoric systems Download PDF

Info

Publication number
CA2439060A1
CA2439060A1 CA002439060A CA2439060A CA2439060A1 CA 2439060 A1 CA2439060 A1 CA 2439060A1 CA 002439060 A CA002439060 A CA 002439060A CA 2439060 A CA2439060 A CA 2439060A CA 2439060 A1 CA2439060 A1 CA 2439060A1
Authority
CA
Canada
Prior art keywords
diode
compound
light
layer
source
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
CA002439060A
Other languages
English (en)
French (fr)
Inventor
Michael J. Therien
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
University of Pennsylvania Penn
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2439060A1 publication Critical patent/CA2439060A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/30—Coordination compounds
    • H10K85/361—Polynuclear complexes, i.e. complexes comprising two or more metal centers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1416—Condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1408—Carbocyclic compounds
    • C09K2211/1425—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1441—Heterocyclic
    • C09K2211/1466—Heterocyclic containing nitrogen as the only heteroatom
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/18—Metal complexes
    • C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/18—Metal complexes
    • C09K2211/188—Metal complexes of other metals not provided for in one of the previous groups
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
    • H10K71/10—Deposition of organic active material
    • H10K71/18—Deposition of organic active material using non-liquid printing techniques, e.g. thermal transfer printing from a donor sheet
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/10—Organic polymers or oligomers
    • H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/30—Coordination compounds
    • H10K85/381—Metal complexes comprising a group IIB metal element, e.g. comprising cadmium, mercury or zinc
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Inorganic Chemistry (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Led Devices (AREA)
  • Light Receiving Elements (AREA)
  • Luminescent Compositions (AREA)
CA002439060A 2001-02-26 2002-02-26 Emissive multichromophoric systems Abandoned CA2439060A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US27152001P 2001-02-26 2001-02-26
US60/271,520 2001-02-26
US30650401P 2001-07-19 2001-07-19
US60/306,504 2001-07-19
PCT/US2002/005584 WO2002104072A2 (en) 2001-02-26 2002-02-26 Emissive multichromophoric systems

Publications (1)

Publication Number Publication Date
CA2439060A1 true CA2439060A1 (en) 2002-12-27

Family

ID=26954969

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002439060A Abandoned CA2439060A1 (en) 2001-02-26 2002-02-26 Emissive multichromophoric systems

Country Status (5)

Country Link
EP (1) EP1363916A4 (de)
JP (2) JP2005503453A (de)
AU (1) AU2002327166A1 (de)
CA (1) CA2439060A1 (de)
WO (1) WO2002104072A2 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7682603B2 (en) * 2003-07-25 2010-03-23 The Trustees Of The University Of Pennsylvania Polymersomes incorporating highly emissive probes
US7378520B2 (en) * 2004-07-08 2008-05-27 North Carolina State University Synthesis of porphyrins designed for attachment to electroactive surfaces via one or more carbon tethers
DE102004044717B8 (de) * 2004-09-10 2010-12-16 BAM Bundesanstalt für Materialforschung und -prüfung Verfahren und Kit zur Kalibrierung eines Photolumineszenzmesssystems
US10510914B2 (en) * 2013-03-21 2019-12-17 Board Of Trustees Of Michigan State University Transparent energy-harvesting devices

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07113031B2 (ja) * 1989-12-15 1995-12-06 財団法人生産開発科学研究所 ポルフィリン多量体及びその製造法
US5599924A (en) * 1992-08-14 1997-02-04 Trustees Of The University Of Pennsylvania Electron-deficient porphyrins and processes and intermediates for preparing same
US5371199B1 (en) * 1992-08-14 1995-12-26 Univ Pennsylvania Substituted porphyrins porphyrin-containing polymers and synthetic methods therefor
CA2201576A1 (en) * 1996-04-17 1997-10-17 James Edward Dickinson, Jr. Rare earth doped oxyhalide laser glass
JP3150948B2 (ja) * 1998-09-21 2001-03-26 科学技術振興事業団 メソ位直結型ポルフィリンポリマーとその製造方法
TW528789B (en) * 2000-12-22 2003-04-21 Koninkl Philips Electronics Nv Electroluminescent device comprising an electroluminescent material of at least two metal chelates

Also Published As

Publication number Publication date
JP2005503453A (ja) 2005-02-03
AU2002327166A1 (en) 2003-01-02
WO2002104072A3 (en) 2003-06-05
EP1363916A2 (de) 2003-11-26
EP1363916A4 (de) 2006-06-28
JP2007221168A (ja) 2007-08-30
WO2002104072A2 (en) 2002-12-27

Similar Documents

Publication Publication Date Title
Liu et al. Near-infrared-absorbing B–N lewis pair-functionalized anthracenes: electronic structure tuning, conformational isomerism, and applications in photothermal cancer therapy
Bessette et al. Design, synthesis and photophysical studies of dipyrromethene-based materials: insights into their applications in organic photovoltaic devices
Chapran et al. An ambipolar BODIPY derivative for a white exciplex OLED and cholesteric liquid crystal laser toward multifunctional devices
Wong et al. Recent Progress on the Photonic Properties of Conjugated Organometallic Polymers Built Upon the trans‐Bis (para‐ethynylbenzene) bis (phosphine) platinum (ii) Chromophore and Related Derivatives
You et al. Photofunctional triplet excited states of cyclometalated Ir (III) complexes: beyond electroluminescence
Sommer et al. Photophysical properties of near-infrared phosphorescent π-extended platinum porphyrins
Finikova et al. Synthesis of symmetrical tetraaryltetranaphtho [2, 3] porphyrins
Shimizu et al. HOMO–LUMO energy-gap tuning of π-conjugated zwitterions composed of electron-donating anion and electron-accepting cation
Li et al. Rational design and characterization of heteroleptic phosphorescent complexes for highly efficient deep-red organic light-emitting devices
Razi et al. Ping-Pong energy transfer in a boron dipyrromethane containing Pt (II)–Schiff base complex: synthesis, photophysical studies, and anti-Stokes shift increase in triplet–triplet annihilation upconversion
Guo et al. New bichromophoric triplet photosensitizer designs and their application in triplet–triplet annihilation upconversion
Jung et al. A new BODIPY material for pure color and long lifetime red hyperfluorescence organic light-emitting diode
Fukui et al. Embedding heteroatoms: an effective approach to create porphyrin-based functional materials
Zhao et al. Impact of the linker on the electronic and luminescent properties of diboryl compounds: molecules with two BMes2 groups and the peculiar behavior of 1, 6-(BMes2) 2pyrene
Tasior et al. Energy-and Electron-Transfer Processes in Corrole− Perylenebisimide− Triphenylamine Array
Zeng et al. A p‐Quinodimethane‐Bridged Porphyrin Dimer
Zawadzka et al. Nonlinear absorption properties of 5, 10-A 2 B 2 porphyrins—correlation of molecular structure with the nonlinear responses
Du et al. Singlet and triplet energy transfers in tetra-(meso-truxene) zinc (II)-and tetra-(meso-tritruxene) zinc (II) porphyrin and porphyrin-free base dendrimers
Nguyen et al. Pushing pentacene-based fluorescence to the near-infrared region by platination
Sharma et al. Panchromatic Light Capture and Efficient Excitation Transfer Leading to Near‐IR Emission of BODIPY Oligomers
El-Khouly et al. Annulation of tetrathiafulvalene to the bay region of perylenediimide: fast electron-transfer processes in polar and nonpolar solvents
Jin et al. Exploring Structure–Property Relations of B, S-Doped Polycyclic Aromatic Hydrocarbons through the Trinity of Synthesis, Spectroscopy, and Theory
Özcan et al. Synthesis, photophysical, DFT and photodiode properties of subphthalocyanine–BODIPY dyads
Baser-Kirazli et al. Tuning the donor− π–acceptor character of arylborane–arylamine macrocycles
Yarnell et al. Positional effects from Σ-bonded platinum (II) on intersystem crossing rates in perylenediimide complexes: synthesis, structures, and photophysical properties

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued

Effective date: 20150213