JP5307349B2 - 官能化ヘテロアセン類およびそれから作製された電子デバイス - Google Patents
官能化ヘテロアセン類およびそれから作製された電子デバイス Download PDFInfo
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- JP5307349B2 JP5307349B2 JP2007098064A JP2007098064A JP5307349B2 JP 5307349 B2 JP5307349 B2 JP 5307349B2 JP 2007098064 A JP2007098064 A JP 2007098064A JP 2007098064 A JP2007098064 A JP 2007098064A JP 5307349 B2 JP5307349 B2 JP 5307349B2
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- aryl
- alkyl
- anthryl
- thin film
- halogen
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- 239000004065 semiconductor Substances 0.000 claims abstract description 37
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 34
- 125000003118 aryl group Chemical group 0.000 claims abstract description 29
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 23
- 239000001257 hydrogen Substances 0.000 claims abstract description 23
- 239000010409 thin film Substances 0.000 claims abstract description 23
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 22
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 21
- 150000002367 halogens Chemical class 0.000 claims abstract description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 18
- 239000001301 oxygen Substances 0.000 claims abstract description 18
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 14
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims abstract description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052711 selenium Inorganic materials 0.000 claims abstract description 10
- 239000011669 selenium Substances 0.000 claims abstract description 10
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 10
- 239000011593 sulfur Substances 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 9
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- -1 pentylphenyl Chemical group 0.000 claims description 205
- 239000000758 substrate Substances 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- 125000003944 tolyl group Chemical group 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 6
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 claims description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 5
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- DAMUWSYTQPWFIY-UHFFFAOYSA-N anthra[2,3-b:6,7-b inverted exclamation marka]dithiophene Chemical compound C1=C2C=C(C=C3C(C=CS3)=C3)C3=CC2=CC2=C1C=CS2 DAMUWSYTQPWFIY-UHFFFAOYSA-N 0.000 claims description 3
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims description 3
- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 claims description 3
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 claims description 3
- 125000005008 perfluoropentyl group Chemical group FC(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 claims description 3
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 244000131360 Morinda citrifolia Species 0.000 claims 1
- 125000005549 heteroarylene group Chemical group 0.000 claims 1
- 235000017524 noni Nutrition 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 abstract description 26
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 25
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 23
- 239000010410 layer Substances 0.000 description 52
- 229920000642 polymer Polymers 0.000 description 14
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 229910052710 silicon Inorganic materials 0.000 description 10
- 239000010703 silicon Substances 0.000 description 10
- 238000007639 printing Methods 0.000 description 8
- 239000010408 film Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920001940 conductive polymer Polymers 0.000 description 6
- 239000000976 ink Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000004528 spin coating Methods 0.000 description 6
- 0 *c([s]c1cc2c(c3c4cc5[s]c(*)cc5c3)C#Cc3ccc(*)cc3)cc1cc2c4C#Cc1ccc(*)cc1 Chemical compound *c([s]c1cc2c(c3c4cc5[s]c(*)cc5c3)C#Cc3ccc(*)cc3)cc1cc2c4C#Cc1ccc(*)cc1 0.000 description 5
- 239000004642 Polyimide Substances 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- 239000002985 plastic film Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 229920001721 polyimide Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- JESXATFQYMPTNL-UHFFFAOYSA-N 2-ethenylphenol Chemical compound OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 230000005669 field effect Effects 0.000 description 4
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 4
- 229910052737 gold Inorganic materials 0.000 description 4
- 239000010931 gold Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000004377 microelectronic Methods 0.000 description 4
- 229920000620 organic polymer Polymers 0.000 description 4
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000004417 polycarbonate Substances 0.000 description 4
- 229920000515 polycarbonate Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000007650 screen-printing Methods 0.000 description 3
- 229910052814 silicon oxide Inorganic materials 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- 238000010129 solution processing Methods 0.000 description 3
- 125000001544 thienyl group Chemical group 0.000 description 3
- 125000004665 trialkylsilyl group Chemical group 0.000 description 3
- 238000001771 vacuum deposition Methods 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000002800 charge carrier Substances 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- ILLHQJIJCRNRCJ-UHFFFAOYSA-N dec-1-yne Chemical compound CCCCCCCCC#C ILLHQJIJCRNRCJ-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 229910052809 inorganic oxide Inorganic materials 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229920000301 poly(3-hexylthiophene-2,5-diyl) polymer Polymers 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005596 polymer binder Polymers 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- 125000005106 triarylsilyl group Chemical group 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- LJIOTBMDLVHTBO-CUYJMHBOSA-N (2s)-2-amino-n-[(1r,2r)-1-cyano-2-[4-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]phenyl]cyclopropyl]butanamide Chemical compound CC[C@H](N)C(=O)N[C@]1(C#N)C[C@@H]1C1=CC=C(C=2C=CC(=CC=2)S(=O)(=O)N2CCN(C)CC2)C=C1 LJIOTBMDLVHTBO-CUYJMHBOSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- IPBLYQKBIBINLQ-UHFFFAOYSA-N 2-thiophen-2-yl-3-undecylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCCCCCCCC IPBLYQKBIBINLQ-UHFFFAOYSA-N 0.000 description 1
- DDDCJSKXYUPZQU-UHFFFAOYSA-N 3-butyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCC DDDCJSKXYUPZQU-UHFFFAOYSA-N 0.000 description 1
- AXQXKWOXIMDIPN-UHFFFAOYSA-N 3-decyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCCCCCCC AXQXKWOXIMDIPN-UHFFFAOYSA-N 0.000 description 1
- NEAKJQNYAACPQW-UHFFFAOYSA-N 3-ethyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CC NEAKJQNYAACPQW-UHFFFAOYSA-N 0.000 description 1
- VBAZHEXHWLJSHW-UHFFFAOYSA-N 3-heptyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCCCC VBAZHEXHWLJSHW-UHFFFAOYSA-N 0.000 description 1
- PRGHPYJUUWHUQC-UHFFFAOYSA-N 3-hexyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCCC PRGHPYJUUWHUQC-UHFFFAOYSA-N 0.000 description 1
- XXUFLJSHACAZMA-UHFFFAOYSA-N 3-methyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1C XXUFLJSHACAZMA-UHFFFAOYSA-N 0.000 description 1
- NNMGVYWVCGFIDY-UHFFFAOYSA-N 3-nonyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCCCCCC NNMGVYWVCGFIDY-UHFFFAOYSA-N 0.000 description 1
- PDCPJZGJXCYLFS-UHFFFAOYSA-N 3-pentyl-2-thiophen-2-ylthiophene Chemical group C1=CSC(C=2SC=CC=2)=C1CCCCC PDCPJZGJXCYLFS-UHFFFAOYSA-N 0.000 description 1
- APGNXGIUUTWIRE-UHFFFAOYSA-N 4-Pentylphenylacetylene Chemical compound CCCCCC1=CC=C(C#C)C=C1 APGNXGIUUTWIRE-UHFFFAOYSA-N 0.000 description 1
- LKOPHKFLISFEHT-UHFFFAOYSA-N 6,16-dithiapentacyclo[11.7.0.03,11.05,9.015,19]icosa-1(13),3(11),4,7,9,14,17,19-octaene-2,12-dione Chemical compound C1=C2C(=O)C3=CC=4C=CSC=4C=C3C(=O)C2=CC2=C1SC=C2 LKOPHKFLISFEHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 229910021523 barium zirconate Inorganic materials 0.000 description 1
- DQBAOWPVHRWLJC-UHFFFAOYSA-N barium(2+);dioxido(oxo)zirconium Chemical compound [Ba+2].[O-][Zr]([O-])=O DQBAOWPVHRWLJC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 125000005266 diarylamine group Chemical group 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229920002457 flexible plastic Polymers 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- BDVZHDCXCXJPSO-UHFFFAOYSA-N indium(3+) oxygen(2-) titanium(4+) Chemical compound [O-2].[Ti+4].[In+3] BDVZHDCXCXJPSO-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000006384 methylpyridyl group Chemical group 0.000 description 1
- GVOISEJVFFIGQE-YCZSINBZSA-N n-[(1r,2s,5r)-5-[methyl(propan-2-yl)amino]-2-[(3s)-2-oxo-3-[[6-(trifluoromethyl)quinazolin-4-yl]amino]pyrrolidin-1-yl]cyclohexyl]acetamide Chemical compound CC(=O)N[C@@H]1C[C@H](N(C)C(C)C)CC[C@@H]1N1C(=O)[C@@H](NC=2C3=CC(=CC=C3N=CN=2)C(F)(F)F)CC1 GVOISEJVFFIGQE-YCZSINBZSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 229960002796 polystyrene sulfonate Drugs 0.000 description 1
- 239000011970 polystyrene sulfonate Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 150000003577 thiophenes Chemical class 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/484—Insulated gate field-effect transistors [IGFETs] characterised by the channel regions
-
- 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
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Thin Film Transistor (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Description
この電子デバイスおよびその特定の成分は、米国標準技術局(NIST)により付与された米国政府共同契約番号70NANBOH3033によって補助されたものである。米国政府は、以下に示すデバイスおよび特定の半導体成分に関連する特定の権利を有する。
(I)
(式中、Rはアルキル、アルコキシ、アリール、ヘテロアリールまたは適切な炭化水素を表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレン、またはNR’(R’は水素、アルキルまたはアリールである)を表し、nおよびmは反復単位の数を表す。)
(I)
(式中、Rは炭化水素を表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレン、またはNR’(R’は水素、アルキルまたはアリールである)を表し、mおよびnは環の数を表す。)
(I)
(式中、Rは適切な炭化水素様アルキル、アリールまたはヘテロアリールを表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレンまたはNR’(R’は水素、アルキルまたはアリールである)を表し、mおよびnはそれぞれ、例えば零(0)〜約3などの環の数を表し、より具体的には、xおよびyは例えば0〜約12であってよく、より具体的には、各xおよびyは約3〜約7である。)
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
(18)
(19)
(20)
(21)
(22)
(23)
(24)
(25)
(26)
(27)
(28)
(I)
(式中、Rはアルキル、アリールまたはヘテロアリールを表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレンまたはNR’(R’は水素、アルキルまたはアリールである)を表し、nおよびmは反復単位の数を表す。)
(I)
(式中、Rは炭化水素を表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレン、またはNR’(R’は水素、アルキルまたはアリールである)を表し、mおよびnは環の数を表す。)
(式中、R5はメチル、エチル、プロピル、ブチル、ペンチル、ヘキシル、ヘプチル、オクチル、ノニル、デシル、ウンデシル、ドデシル、トリデシル、テトラデシル、ペンタデシル、ヘキサデシル、ヘプタデシルまたはオクタデシル;トリフルオロメチル、フルオロエチル、ペルフルオロプロピル、ペルフルオロブチル、ペルフルオロペンチル、ペルフルオロヘキシル、ペルフルオロヘプチル、ペルフルオロオクチル、ペルフルオロノニル、ペルフルオロデシル、ペルフルオロウンデシルまたはペルフルオロドデシル;フェニル、メチルフェニル(トリル)、エチルフェニル、プロピルフェニル、ブチルフェニル、ペンチルフェニル、ヘキシルフェニル、ヘプチルフェニル、オクチルフェニル、ノニルフェニル、デシルフェニル、ウンデシルフェニル、ドデシルフェニル、トリデシルフェニル、テトラデシルフェニル、ペンタデシルフェニル、ヘキサデシルフェニル、ヘプタデシルフェニル、オクタデシルフェニル、トリフルオロメチルフェニル、フルオロエチルフェニル、ペルフルオロプロピルフェニル、ペルフルオロブチルフェニル、ペルフルオロペンチルフェニル、ペルフルオロヘキシルフェニル、ペルフルオロヘプチルフェニル、ペルフルオロオクチルフェニル、ペルフルオロノニルフェニル、ペルフルオロデシルフェニル、ペルフルオロウンデシルフェニルまたはペルフルオロドデシルフェニルであり、XはF、Cl、Br、CNまたはNO2である。)
(I)
(式中、Rはアルキル、アリールまたはヘテロアリールを表し、各R1およびR2は独立に、水素(H)、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、R3およびR4は独立に、適切な炭化水素、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレンまたはNR’(R’は水素、アルキルまたはアリールである)を表し、nおよびmは反復単位の数を表す)
(式中、RおよびR’は水素、アルキル、不飽和アルキル、アリール、アルキル置換アリール、不飽和アルキル置換アリールまたはその混合物であり、nは3以上、例えば約3〜約2,000の環の数を表し、より具体的にはn=5であり、R’=Hであり、R=ドジシン(dodycyne)である)
Claims (7)
- 式(I)の成分を含む半導体材料を含むことを特徴とする電子デバイス。
(I)
(式中、Rは6〜30個の炭素原子を有するアルキル、アルコキシ、6〜48個の炭素原子を有するアリール、7〜37個の炭素原子を有するヘテロアリールを表し、各R1およびR2は独立に、水素(H)、アルキル、アリール、ヘテロ原子含有基、シアノ、ニトロ、またはハロゲンであり、R3およびR4は独立に、アルキル、アリール、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレン、またはNR’(R’は水素、アルキルまたはアリールである)を表し、nおよびmは反復単位の数を表す。) - 請求項1に記載の電子デバイスであって、
R1およびR2の少なくとも1つは水素であるか、
R1およびR2の少なくとも1つはアルキルであるか、
R1およびR2の少なくとも1つはアリールであるか、
R1およびR2の少なくとも1つはハロゲンであるか、
R1およびR2の少なくとも1つはシアノまたはニトロであるか、
R3およびR4の少なくとも1つはアルキルであるか、あるいは、
R3およびR4の少なくとも1つはアリールであることを特徴とする電子デバイス。 - 請求項1に記載の電子デバイスであって、
mは0〜3の数であるか、
mは2であるか、
mは1であるか、
nは0〜3の数であるか、
xは0〜12の数であるか、あるいは、
yは0〜12の数であることを特徴とする電子デバイス。 - 基板と、ゲート電極と、ゲート誘電体層と、ソース電極と、ドレイン電極と、次式の成分を含む、前記ソース及び/又はドレイン電極および前記ゲート誘電体層と接触している半導体層とを含むことを特徴とする薄膜トランジスタ。
(I)
(式中、Rは6〜30個の炭素原子を有するアルキル、アルコキシ、6〜48個の炭素原子を有するアリール、7〜37個の炭素原子を有するヘテロアリールを表し、各R1およびR2は独立に、水素(H)、アルキル、アリール、ヘテロ原子含有基、シアノ、ニトロ、またはハロゲンであり、R3およびR4は独立に、アルキル、アリール、ヘテロ原子含有基またはハロゲンであり、xおよびyは基の数を表し、Zはイオウ、酸素、セレン、またはNR’(R’は水素、アルキルまたはアリールである)を表し、mおよびnは環の数を表す。) - 請求項4に記載の薄膜トランジスタであって、
アリールが、フェニル、トリル、ブチルフェニル、ペンチルフェニル、ヘキシルフェニル、ヘプチルフェニル、オクチルフェニル、ノニルフェニル、デシルフェニル、ウンデシルフェニル、ドデシルフェニル、トリデシルフェニル、テトラデシルフェニル、ペンタデシルフェニル、ヘキサデシルフェニル、ヘプタデシルフェニル、オクタデシルフェニル、ナフチル、メチルナフチル、エチルナフチル、プロピルナフチル、ブチルナフチル、ペンチルナフチル、ヘキシルナフチル、ヘプチルナフチル、オクチルナフチル、ノニルナフチル、デシルナフチル、ウンデシルナフチル、ドデシルナフチル、アントリル、メチルアントリル、エチルアントリル、プロピルアントリル、ブチルアントリル、ペンチルアントリル、オクチルアントリル、ノニルアントリル、デシルアントリル、ウンデシルアントリルまたはドデシルアントリルであることを特徴とする薄膜トランジスタ。 - 請求項4に記載の薄膜トランジスタであって、
前記半導体層が以下の式及び/又は構造、
(1)
(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
(18)
(19)
(20)
(21)
(22)
(23)
(24)
(25)
(26)
(27)
(28)
(式中、R5はメチル、エチル、プロピル、ブチル、ペンチル、ヘキシル、ヘプチル、オクチル、ノニル、デシル、ウンデシル、ドデシル、トリデシル、テトラデシル、ペンタデシル、ヘキサデシル、ヘプタデシルまたはオクタデシル;トリフルオロメチル、フルオロエチル、ペルフルオロプロピル、ペルフルオロブチル、ペルフルオロペンチル、ペルフルオロヘキシル、ペルフルオロヘプチル、ペルフルオロオクチル、ペルフルオロノニル、ペルフルオロデシル、ペルフルオロウンデシルまたはペルフルオロドデシル;フェニル、メチルフェニル(トリル)、エチルフェニル、プロピルフェニル、ブチルフェニル、ペンチルフェニル、ヘキシルフェニル、ヘプチルフェニル、オクチルフェニル、ノニルフェニル、デシルフェニル、ウンデシルフェニル、ドデシルフェニル、トリデシルフェニル、テトラデシルフェニル、ペンタデシルフェニル、ヘキサデシルフェニル、ヘプタデシルフェニル、オクタデシルフェニル、トリフルオロメチルフェニル、フルオロエチルフェニル、ペルフルオロプロピルフェニル、ペルフルオロブチルフェニル、ペルフルオロペンチルフェニル、ペルフルオロヘキシルフェニル、ペルフルオロヘプチルフェニル、ペルフルオロオクチルフェニル、ペルフルオロノニルフェニル、ペルフルオロデシルフェニル、ペルフルオロウンデシルフェニルまたはペルフルオロドデシルフェニルであり、XはF、Cl、Br、CNまたはNO2である)
の官能化ヘテロアセンであることを特徴とする薄膜トランジスタ。 - 請求項4に記載の薄膜トランジスタであって、
前記半導体層が、5,11−デシニルアントラ[2,3−b:6,7−b’]ジチオフェン及び/又は5,11−デシニルアントラ[2,3−b:7,6−b’]ジチオフェン(1a)ならびに5,11−ビス(4−フェニルエチニル)アントラ[2,3−b:6,7−b’]ジチオフェン及び/又は5,11−ビス(4−フェニルエチニル)アントラ[2,3−b:7,6−b’]ジチオフェン(8a)、またはそのトランス異性体とシス異性体の混合物であることを特徴とする薄膜トランジスタ。
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US20080142793A1 (en) * | 2006-11-10 | 2008-06-19 | Tang Ming L | Organic Semiconductors |
WO2008107089A1 (en) * | 2007-03-07 | 2008-09-12 | University Of Kentucky Research Foundation | Silylethynylated heteroacenes and electronic devices made therewith |
US8212239B2 (en) | 2007-12-13 | 2012-07-03 | E I Du Pont De Nemours And Company | Electroactive materials |
US8115200B2 (en) | 2007-12-13 | 2012-02-14 | E.I. Du Pont De Nemours And Company | Electroactive materials |
US8216753B2 (en) * | 2007-12-13 | 2012-07-10 | E I Du Pont De Nemours And Company | Electroactive materials |
US8461291B2 (en) * | 2007-12-17 | 2013-06-11 | E I Du Pont De Nemours And Company | Organic electroactive materials and an organic electronic device having an electroactive layer utilizing the same material |
US8067764B2 (en) * | 2007-12-17 | 2011-11-29 | E. I. Du Pont De Nemours And Company | Electroactive materials |
RU2012139316A (ru) | 2010-02-15 | 2014-03-27 | Мерк Патент Гмбх | Полупроводниковые полимеры |
US8425808B2 (en) | 2010-04-27 | 2013-04-23 | Xerox Corporation | Semiconducting composition |
US9306172B2 (en) | 2010-08-13 | 2016-04-05 | Merck Patent Gmbh | Anthra[2,3-b:7,6-b']dithiophene derivatives and their use as organic semiconductors |
GB201203159D0 (en) * | 2012-02-23 | 2012-04-11 | Smartkem Ltd | Organic semiconductor compositions |
JP6094831B2 (ja) * | 2012-04-17 | 2017-03-15 | ソニー株式会社 | 有機半導体層、電子デバイス、及び、電子デバイスの製造方法 |
CN103554138B (zh) * | 2013-10-31 | 2016-02-17 | 兰州大学 | 一种具有有机场效应晶体管性质的材料及其制备方法 |
JP6314807B2 (ja) * | 2014-12-08 | 2018-04-25 | 株式会社デンソー | 有機半導体装置およびその製造方法 |
US20210403320A1 (en) | 2018-10-31 | 2021-12-30 | Hamamatsu Photonics K.K. | Method for manufacturing semiconductor substrate, method for manufacturing damascene wiring structure, semiconductor substrate, and damascene wiring structure |
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