WO2002072654A2 - Polymers and oligomers, their synthesis, and electronic devices incorporating same - Google Patents

Polymers and oligomers, their synthesis, and electronic devices incorporating same Download PDF

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Publication number
WO2002072654A2
WO2002072654A2 PCT/US2002/007420 US0207420W WO02072654A2 WO 2002072654 A2 WO2002072654 A2 WO 2002072654A2 US 0207420 W US0207420 W US 0207420W WO 02072654 A2 WO02072654 A2 WO 02072654A2
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Prior art keywords
groups
group
substituents
hydrogen
independently selected
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PCT/US2002/007420
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English (en)
French (fr)
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WO2002072654A3 (en
Inventor
Arthur Epstein
Daike Wang
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Ohio State University
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Ohio State University
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Priority to CA002441745A priority Critical patent/CA2441745A1/en
Priority to DE60238546T priority patent/DE60238546D1/de
Priority to KR1020037011754A priority patent/KR100886051B1/ko
Priority to JP2002571559A priority patent/JP4274797B2/ja
Priority to AT02721356T priority patent/ATE490990T1/de
Priority to AU2002252292A priority patent/AU2002252292A1/en
Priority to EP02721356A priority patent/EP1434813B1/en
Publication of WO2002072654A2 publication Critical patent/WO2002072654A2/en
Anticipated expiration legal-status Critical
Publication of WO2002072654A3 publication Critical patent/WO2002072654A3/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/40—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
    • C07C15/56—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic condensed
    • C07C15/58—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals polycyclic condensed containing two rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/53—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides

Definitions

  • the invention relates to polymers and oligomers, methods of their synthesis, and electronic devices comprising them.
  • the present invention is directed to polymeric compositions useful in producing electronic devices. It is an object of the present invention to produce stable compositions capable of functioning in a wide variety of electronic devices. Novel features and advantages of the present invention, in addition to those mentioned above, will become apparent to those skilled in the art from a reading of the following description or from practice of the invention.
  • the present invention includes compositions of matter including polymers, oligomer and their constituent monomeric units.
  • the present invention also includes methods of making the compositions and devices made therefrom.
  • the present invention includes a composition of matter comprising a polymer of the general structure:
  • R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently be either ortho, meta or para with respect to the pyridyl nitrogen; wherein bonds C and D may be either ortho, meta or para with respect one another; and wherein bonds E and F may be either ortho, meta or para with respect one another; wherein Y may be a moiety selected from the group consisting of -(CH 2 ) x -,-(CH 2 ) x O-, - O(CH 2 ) x - and
  • the R2 substituent is preferably a methoxy group with most preferably at least two R2 substituents being methoxy groups.
  • the R3 substituent is preferably a methoxy group with most preferably at least two R3 substituents being methoxy groups.
  • vinyl linkages A and B attach at positions ortho to the pyridyl nitrogen. It is also preferred that bonds C and D be para with respect one another, and that E and F be para with respect one another.
  • x be an integer in the range of 1 to 6 inclusive.
  • the present invention includes a composition of matter comprising a polymer of the general structure:
  • R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently be either ortho, meta or para with respect to the pyridyl nitrogen; wherein bonds C and D may be either ortho , meta or para with respect one another; wherein bonds E and F may be either ortho , meta or para with respect one another; wherein bonds G and H may be either ortho , meta or para with respect one another
  • R1 , R2, R3 and R4 substituents preferably are methoxy groups with most preferably at least two of the R1 , R2, R3 and R4 substituents being methoxy groups.
  • vinyl linkages A and B attach at positions ortho to the pyridyl nitrogen. It is also preferred that bonds C and D be para with respect one another, and that E and F be para with respect one another.
  • x be an integer in the range of 1 to 6 inclusive.
  • the present invention includes a composition of matter comprising an oligomer of the general structure:
  • R3/R2 C A R1 B D R4/R5 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may be either ortho, meta or para from one another; wherein bond C may be either ortho, meta or para with respect to the respective quinoyl nitrogen as indicated by the dotted lines; and wherein bond D may be either ortho, meta or para with respect to the respective quinoyl nitrogen as
  • the vinyl linkages A and B attach at positions para to one another.
  • composition of matter comprising an oligomer of the general structure:
  • R2 A R1 B D R3 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently be either ortho, meta or para from one another; wherein bond C may be either ortho or para with respect to the respective pyridyl nitrogen as indicated by the dotted lines; and wherein bond D may be either ortho or para with respect to the respective pyridyl nitrogen as indicated by the dotted lines.
  • the R1 , R2 and R3 substituents preferably are methoxy groups with most preferably at least two of the R1 , R2 and R3 substituents being methoxy groups.
  • the vinyl linkages A and B attach at positions para to one another.
  • the present invention also includes a composition of matter comprising an oligomer of the general structure:
  • R3/R2 A R1 B D R4/R5 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently.be either ortho, meta or para from one another. Bonds C and D may attach at any position onto rings R2/R3 and R4/R5, respectively, although it iis preferred that they attach as shown above.
  • the R1 substituent preferably is a methoxy group with most preferably at least two of the R1 substituents being methoxy groups.
  • the present invention also includes a composition of matter comprising an oligomer of the general structure:
  • R2 C A R1 B D R3 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; and wherein bonds A and B may independently be either ortho, meta or para from the pyridyl nitrogen.
  • the R1 , R2 and R3 substituents preferably are methoxy groups with most preferably at least two of the R1 , R2 and R3 substituents being methoxy groups. Three of the R2 and R3 substituents may also preferably be methoxy groups.
  • composition of matter comprising a polymer of the general structure:
  • R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups;
  • the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may be either ortho or para with respect one another; wherein bonds C and D may be either ortho or para with respect one another; wherein bonds E and F may be either ortho or para with respect one another; wherein Y may be a moiety selected from the group consisting of -(CH 2 ) x -,-(CH 2 ) x O-, - O(CH 2 ) x - and -O(CH
  • the R1 , R2 and R3 substituents preferably are methoxy groups with most preferably at least two of the R1 , R2 and R3 substituents being methoxy groups.
  • the present invention includes a number of block co-polymer compositions derived from the oligomers described above.
  • the present invention also includes a composition of matter comprising a block co-polymer of the general structure:
  • the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups
  • the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups
  • the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups
  • the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups
  • the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups
  • bonds A and B may independently be either ortho, meta or para from one another
  • bond C may be either ortho
  • block co-polymers may have geometries and substituents as do the oligomers from which they are derived, as described above.
  • 3 & 4 (Y. R & Z)
  • the present invention also includes a composition of matter comprising a block co- polymer of the general structure:
  • R6 Z R3/R2 C A R1 B D R4/R5 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R6 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently be either ortho, meta or para from one another; wherein bond C may be either ortho, meta or para with respect to the respective
  • block co-polymers may have geometries and substituents, as do the oligomers from which they are derived, as described above.
  • the present invention also includes a composition of matter comprising a block co- polymer of the general structure:
  • R2 C A R1 B D R3 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may independently be either ortho, meta or para from one another; wherein bond C may be either ortho, meta or para with respect to the respective pyridyl nitrogen; wherein bond D may be either ortho, meta or para with respect to the respective pyridyl nitrogen; wherein Y may be a moiety attached at any point on ring R2, and may be selected from the group consisting of -(CH 2 ) x -,-(CH 2 ) x O-, -O(CH 2 ) x - and -O(CH 2 )
  • block co-polymers may have geometries and substituents, as do the oligomers from which they are derived, as described above.
  • the present invention also includes a composition of matter comprising a block co-polymer of the general structure:
  • Block Co-polymers may have geometries and substituents as do the oligomers from which they are derived, as described above.
  • Block Co-polvmer of Oligomers 9 & 10 (Y only)
  • the present invention also includes a composition of matter comprising a block co- polymer of the general structure:
  • R3/R2 A R1 B D R4/R5 wherein the R1 substituents are independently selected from the group consisting of hydrogen, - alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may be either ortho, meta or para from one another; wherein Y may be a moiety attached at any point on rings R2 or R3, and may be selected from the group consisting of -(CH 2 ) x -,-(CH 2 ) x O-
  • the present invention also includes a composition of matter comprising a block co- polymer of the general structure:
  • R6 R3/R2 C A R1 B D R4/R5 wherein the R1 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R2 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R3 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R4 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R5 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; the R6 substituents are independently selected from the group consisting of hydrogen, alkyl groups, alkoxy groups, and aryl groups; wherein bonds A and B may be either ortho, meta or para from one another; wherein Y may be a moiety attached at any point on ring R6,
  • compositions of the present invention may be used to fabricate a wide variety of electronic devices, such as those that may be made in accordance with known production procedures. These devices include polymeric light emitting devices, including mono- and multi-color devices, color-variable devices, infrared-emitting devices; so-called SCALE devices, including two-color and multi-color SCALE deveices. Other devices in which compositions of the present invention may be used include photovoltaic devices and polymer-based transistors. Examples of these devices that are disclosed in U.S. patents Nos.
  • compositions of the present invention may be ambipolar such that they may be used in layered polymeric devices, and may form part of as electron- or hole- transmissive materials and/or light emitting layers, in accordance with known arrangements.
  • the compositions may also be used as components of blends in the devices described above. DETAIL DESCRIPTION OF PREFERRED EMBODIMENT S)
  • DETAIL DESCRIPTION OF PREFERRED EMBODIMENT S represent illustrative examples of the invention, and include the best mode.
  • the preferred embodiments herein described are not intended to be exhaustive or to limit the invention to the precise variations disclosed. They are chosen and described to explain the compositions and methods of the invention, and the application of the compositions, so that others skilled in the art may practice the invention.
  • This Example shows the synthetic scheme through which a polymer in accordance with one embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which a polymer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 5 Oligomer 3: 30 mg This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 6 Oligomer 4: 100 mg This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 10 - Oligomer 8 30 mg This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 11 - Oligomer 9 320 mg This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 12 - Oligomer 10 400 mg This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • Example 13 - Polymer 6 This Example shows the synthetic scheme through which a polymer in accordance with another embodiment of the present invention may be produced.
  • Example 14 - Polymer 7 60 mg This Example shows the synthetic scheme through which a polymer in accordance with another embodiment of the present invention may be produced.
  • Example 15 - Polymer 8 70 mg This Example shows the synthetic scheme through which a polymer in accordance with another embodiment of the present invention may be produced.
  • Example 16 - Polymer 9 110 mg This Example shows the synthetic scheme through which a polymer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.
  • This Example shows the synthetic scheme through which an oligomer in accordance with another embodiment of the present invention may be produced.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polyethers (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Quinoline Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Polymerisation Methods In General (AREA)
PCT/US2002/007420 2001-03-13 2002-03-12 Polymers and oligomers, their synthesis, and electronic devices incorporating same Ceased WO2002072654A2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002441745A CA2441745A1 (en) 2001-03-13 2002-03-12 Polymers and oligomers, their synthesis, and electronic devices incorporating same
DE60238546T DE60238546D1 (de) 2001-03-13 2002-03-12 Polymere, ihre synthese und ihre enthaltende elektronische bauteile
KR1020037011754A KR100886051B1 (ko) 2001-03-13 2002-03-12 중합체 및 소중합체, 이들의 합성 방법, 및 이들을 혼입하는 전자 장치
JP2002571559A JP4274797B2 (ja) 2001-03-13 2002-03-12 ポリマーおよびオリゴマー、それらの合成、ならびにこれらを組み込んだ電子デバイス
AT02721356T ATE490990T1 (de) 2001-03-13 2002-03-12 Polymere, ihre synthese und ihre enthaltende elektronische bauteile
AU2002252292A AU2002252292A1 (en) 2001-03-13 2002-03-12 Polymers and oligomers, their synthesis, and electronic devices incorporating same
EP02721356A EP1434813B1 (en) 2001-03-13 2002-03-12 Polymers , their synthesis, and electronic devices incorporating same

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US27544301P 2001-03-13 2001-03-13
US60/275,443 2001-03-13
US27576201P 2001-03-14 2001-03-14
US60/275,762 2001-03-14
US10/084,866 US6777532B2 (en) 2001-03-13 2002-02-28 Polymers and oligomers, their synthesis, and electronic devices incorporating same
US10/084,866 2002-02-28

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KR (3) KR100883474B1 (enExample)
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