TWI408154B - 萘-醯亞胺半導體聚合物 - Google Patents
萘-醯亞胺半導體聚合物 Download PDFInfo
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- TWI408154B TWI408154B TW098103780A TW98103780A TWI408154B TW I408154 B TWI408154 B TW I408154B TW 098103780 A TW098103780 A TW 098103780A TW 98103780 A TW98103780 A TW 98103780A TW I408154 B TWI408154 B TW I408154B
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- Prior art keywords
- alkyl
- group
- haloalkyl
- aryl
- alkenyl
- Prior art date
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 97
- 125000000217 alkyl group Chemical group 0.000 claims description 204
- 125000003118 aryl group Chemical group 0.000 claims description 85
- 125000001188 haloalkyl group Chemical group 0.000 claims description 56
- 125000003342 alkenyl group Chemical group 0.000 claims description 54
- -1 naphthyl imine Chemical class 0.000 claims description 41
- 229910052757 nitrogen Inorganic materials 0.000 claims description 36
- 229910052736 halogen Inorganic materials 0.000 claims description 35
- 125000001424 substituent group Chemical group 0.000 claims description 32
- 125000003545 alkoxy group Chemical group 0.000 claims description 31
- 125000000304 alkynyl group Chemical group 0.000 claims description 25
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 24
- 125000005843 halogen group Chemical group 0.000 claims description 23
- 229910052799 carbon Inorganic materials 0.000 claims description 22
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 22
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
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- 230000005669 field effect Effects 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000002950 monocyclic group Chemical group 0.000 claims description 12
- 125000006708 (C5-C14) heteroaryl group Chemical group 0.000 claims description 11
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- 125000003106 haloaryl group Chemical group 0.000 claims description 8
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- 125000006649 (C2-C20) alkynyl group Chemical group 0.000 claims description 5
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 4
- 125000006707 (C3-C12) heterocycloalkyl group Chemical group 0.000 claims description 4
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims description 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
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- HCTBXWTVGRRILT-UHFFFAOYSA-N trimethyl-(1-methylpyrrol-2-yl)stannane Chemical compound CN1C=CC=C1[Sn](C)(C)C HCTBXWTVGRRILT-UHFFFAOYSA-N 0.000 description 1
- RLOXGRVPXAGABQ-UHFFFAOYSA-N trimethyl-(2,3,5,6-tetrafluoro-4-trimethylstannylphenyl)stannane Chemical compound C[Sn](C)(C)C1=C(F)C(F)=C([Sn](C)(C)C)C(F)=C1F RLOXGRVPXAGABQ-UHFFFAOYSA-N 0.000 description 1
- KKRPPVXJVZKJON-UHFFFAOYSA-N trimethyl-(5-trimethylstannylthiophen-2-yl)stannane Chemical compound C[Sn](C)(C)C1=CC=C([Sn](C)(C)C)S1 KKRPPVXJVZKJON-UHFFFAOYSA-N 0.000 description 1
- PJTUHSIPKNCCLE-UHFFFAOYSA-N trimethyl-(6-trimethylstannylnaphthalen-2-yl)stannane Chemical compound C1=C([Sn](C)(C)C)C=CC2=CC([Sn](C)(C)C)=CC=C21 PJTUHSIPKNCCLE-UHFFFAOYSA-N 0.000 description 1
- KGCTTXKCIXIGRZ-UHFFFAOYSA-N trimethyl-[2-(5-trimethylstannyl-1,3-thiazol-2-yl)-1,3-thiazol-5-yl]stannane Chemical compound S1C([Sn](C)(C)C)=CN=C1C1=NC=C([Sn](C)(C)C)S1 KGCTTXKCIXIGRZ-UHFFFAOYSA-N 0.000 description 1
- VSRBKQFNFZQRBM-UHFFFAOYSA-N tuaminoheptane Chemical compound CCCCCC(C)N VSRBKQFNFZQRBM-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
- C08G61/10—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aromatic carbon atoms, e.g. polyphenylenes
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- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
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- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
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- C09B69/102—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds containing an anthracene dye containing a perylene dye
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- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
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- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/124—Intrinsically conductive polymers
- H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
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- 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
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- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
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- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/464—Lateral top-gate IGFETs comprising only a single gate
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- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/466—Lateral bottom-gate IGFETs comprising only a single gate
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- 2009-02-05 EP EP09707663.2A patent/EP2240529B1/en active Active
- 2009-02-05 TW TW098103780A patent/TWI408154B/zh active
- 2009-02-05 TW TW098103783A patent/TW200951160A/zh unknown
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- 2009-02-05 US US12/812,531 patent/US8796672B2/en active Active
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- 2009-02-05 EP EP20090708280 patent/EP2240530B1/en active Active
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- 2009-02-05 CN CN2009801042916A patent/CN101939351A/zh active Pending
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