TWI650307B

TWI650307B - 電荷輸送性清漆

電荷輸送性清漆 Download PDF

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Publication number: TWI650307B
Authority: TW; Taiwan
Prior art keywords: charge; bis; transporting; group; carbon atoms
Prior art date: 2014-09-10

Application number

TW104129943A

Other languages

English (en)

Chinese (zh)

Other versions

TW201623216A (zh

Inventor

古賀春香

中家直樹

Original Assignee

日商日產化學工業股份有限公司

Priority date

2014-09-10

Filing date

2015-09-10

Publication date

2019-02-11

2015-09-10 Application filed by 日商日產化學工業股份有限公司 filed Critical 日商日產化學工業股份有限公司

2016-07-01 Publication of TW201623216A publication Critical patent/TW201623216A/zh

2019-02-11 Application granted granted Critical

2019-02-11 Publication of TWI650307B publication Critical patent/TWI650307B/zh

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239000002966 varnish Substances 0.000 title claims abstract description 81
-1 organosilane compound Chemical class 0.000 claims abstract description 123
239000000126 substance Substances 0.000 claims abstract description 46
229910052801 chlorine Inorganic materials 0.000 claims abstract description 27
239000000460 chlorine Substances 0.000 claims abstract description 21
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 20
125000001424 substituent group Chemical group 0.000 claims abstract description 16
239000003960 organic solvent Substances 0.000 claims abstract description 13
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 6
125000004432 carbon atom Chemical group C* 0.000 claims description 73
238000000034 method Methods 0.000 claims description 46
125000000217 alkyl group Chemical group 0.000 claims description 33
239000000758 substrate Substances 0.000 claims description 28
238000005401 electroluminescence Methods 0.000 claims description 25
239000002904 solvent Substances 0.000 claims description 22
229910000077 silane Inorganic materials 0.000 claims description 21
125000003118 aryl group Chemical group 0.000 claims description 18
238000002347 injection Methods 0.000 claims description 17
239000007924 injection Substances 0.000 claims description 17
150000001875 compounds Chemical group 0.000 claims description 10
239000011964 heteropoly acid Substances 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 8
230000005525 hole transport Effects 0.000 claims description 7
239000000463 material Substances 0.000 abstract description 23
239000010409 thin film Substances 0.000 abstract description 20
SWYZNMNIUXTWTF-UHFFFAOYSA-N (4-chlorophenyl)-trimethoxysilane Chemical compound CO[Si](OC)(OC)C1=CC=C(Cl)C=C1 SWYZNMNIUXTWTF-UHFFFAOYSA-N 0.000 abstract description 9
239000010408 film Substances 0.000 description 49
229910052757 nitrogen Inorganic materials 0.000 description 49
229910052741 iridium Inorganic materials 0.000 description 44
GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 42
125000004435 hydrogen atom Chemical group [H]* 0.000 description 30
239000002253 acid Substances 0.000 description 22
125000005843 halogen group Chemical group 0.000 description 19
125000001153 fluoro group Chemical group F* 0.000 description 18
125000003342 alkenyl group Chemical group 0.000 description 17
238000000576 coating method Methods 0.000 description 16
230000000052 comparative effect Effects 0.000 description 16
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
229910052731 fluorine Inorganic materials 0.000 description 14
150000002430 hydrocarbons Chemical group 0.000 description 14
239000007787 solid Substances 0.000 description 14
125000000304 alkynyl group Chemical group 0.000 description 12
229910052799 carbon Inorganic materials 0.000 description 12
239000002019 doping agent Substances 0.000 description 11
IYDGMDWEHDFVQI-UHFFFAOYSA-N phosphoric acid;trioxotungsten Chemical compound O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O IYDGMDWEHDFVQI-UHFFFAOYSA-N 0.000 description 11
ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 10
241000208340 Araliaceae Species 0.000 description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 10
235000003140 Panax quinquefolius Nutrition 0.000 description 10
229910052776 Thorium Inorganic materials 0.000 description 10
235000008434 ginseng Nutrition 0.000 description 10
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
229920000642 polymer Polymers 0.000 description 10
125000004093 cyano group Chemical group *C#N 0.000 description 9
125000001072 heteroaryl group Chemical group 0.000 description 9
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
150000001448 anilines Chemical class 0.000 description 8
229910052751 metal Inorganic materials 0.000 description 8
239000002184 metal Substances 0.000 description 8
229910052782 aluminium Inorganic materials 0.000 description 7
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
125000001309 chloro group Chemical group Cl* 0.000 description 7
238000007789 sealing Methods 0.000 description 7
125000000542 sulfonic acid group Chemical group 0.000 description 7
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
150000007513 acids Chemical class 0.000 description 6
239000011248 coating agent Substances 0.000 description 6
238000010304 firing Methods 0.000 description 6
RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 6
IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 6
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 6
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 5
VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 5
125000003172 aldehyde group Chemical group 0.000 description 5
125000003277 amino group Chemical group 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 5
125000002843 carboxylic acid group Chemical group 0.000 description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 5
238000005259 measurement Methods 0.000 description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 5
DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 description 5
238000004528 spin coating Methods 0.000 description 5
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 5
125000003396 thiol group Chemical group [H]S* 0.000 description 5
238000007740 vapor deposition Methods 0.000 description 5
HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
230000000903 blocking effect Effects 0.000 description 4
XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 4
238000004140 cleaning Methods 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
125000001624 naphthyl group Chemical group 0.000 description 4
229910052760 oxygen Inorganic materials 0.000 description 4
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
239000002861 polymer material Substances 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
239000000243 solution Substances 0.000 description 4
125000005504 styryl group Chemical group 0.000 description 4
229910052716 thallium Inorganic materials 0.000 description 4
BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
UDONPJKEOAWFGI-UHFFFAOYSA-N 1-methyl-3-phenoxybenzene Chemical compound CC1=CC=CC(OC=2C=CC=CC=2)=C1 UDONPJKEOAWFGI-UHFFFAOYSA-N 0.000 description 3
RICKKZXCGCSLIU-UHFFFAOYSA-N 2-[2-[carboxymethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]ethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]acetic acid Chemical compound CC1=NC=C(CO)C(CN(CCN(CC(O)=O)CC=2C(=C(C)N=CC=2CO)O)CC(O)=O)=C1O RICKKZXCGCSLIU-UHFFFAOYSA-N 0.000 description 3
POXIZPBFFUKMEQ-UHFFFAOYSA-N 2-cyanoethenylideneazanide Chemical group [N-]=C=[C+]C#N POXIZPBFFUKMEQ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
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DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000010405 anode material Substances 0.000 description 3
150000004982 aromatic amines Chemical class 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
239000004305 biphenyl Substances 0.000 description 3
UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 3
238000009835 boiling Methods 0.000 description 3
238000000151 deposition Methods 0.000 description 3
230000008021 deposition Effects 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical group C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
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239000012535 impurity Substances 0.000 description 3
AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 3
239000011261 inert gas Substances 0.000 description 3
150000002739 metals Chemical class 0.000 description 3
239000000203 mixture Substances 0.000 description 3
229910052750 molybdenum Inorganic materials 0.000 description 3
239000011733 molybdenum Substances 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
238000004381 surface treatment Methods 0.000 description 3
238000001308 synthesis method Methods 0.000 description 3
ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 3
WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
229910052721 tungsten Inorganic materials 0.000 description 3
239000010937 tungsten Substances 0.000 description 3
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
DCTMXCOHGKSXIZ-UHFFFAOYSA-N (R)-1,3-Octanediol Chemical compound CCCCCC(O)CCO DCTMXCOHGKSXIZ-UHFFFAOYSA-N 0.000 description 2
ONUFSRWQCKNVSL-UHFFFAOYSA-N 1,2,3,4,5-pentafluoro-6-(2,3,4,5,6-pentafluorophenyl)benzene Chemical group FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F ONUFSRWQCKNVSL-UHFFFAOYSA-N 0.000 description 2
HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 2
PKURFTDCIWJBDF-UHFFFAOYSA-N 2-hexylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCCCC)=CC=C21 PKURFTDCIWJBDF-UHFFFAOYSA-N 0.000 description 2
FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 2
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 2
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 2
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VFUDMQLBKNMONU-UHFFFAOYSA-N 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole Chemical group C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 VFUDMQLBKNMONU-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
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NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
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XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
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229910045601 alloy Inorganic materials 0.000 description 2
239000000956 alloy Substances 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
229940092714 benzenesulfonic acid Drugs 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 2
239000010406 cathode material Substances 0.000 description 2
ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 2
HASCQPSFPAKVEK-UHFFFAOYSA-N dimethyl(phenyl)phosphine Chemical compound CP(C)C1=CC=CC=C1 HASCQPSFPAKVEK-UHFFFAOYSA-N 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
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238000007598 dipping method Methods 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
CJMZLCRLBNZJQR-UHFFFAOYSA-N ethyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate Chemical compound CCOC(=O)C1=C(N)SC=C1C1=CC=C(F)C=C1 CJMZLCRLBNZJQR-UHFFFAOYSA-N 0.000 description 2
LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000004744 fabric Substances 0.000 description 2
GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 2
AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 2
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
238000003475 lamination Methods 0.000 description 2
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 2
239000000395 magnesium oxide Substances 0.000 description 2
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 2
229960003540 oxyquinoline Drugs 0.000 description 2
125000005010 perfluoroalkyl group Chemical group 0.000 description 2
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
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AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
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NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
229910052772 Samarium Inorganic materials 0.000 description 1
229910018287 SbF 5 Inorganic materials 0.000 description 1
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DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
CASNTVCBKWKWNV-UHFFFAOYSA-N [2-(2,4-difluorophenyl)phenyl]-trioxido-phenyl-lambda5-phosphane iridium(3+) 2-[5-(trifluoromethyl)-1H-pyrazol-3-yl]pyridine Chemical compound [Ir+3].FC1=C(C=CC(=C1)F)C1=C(C=CC=C1)P([O-])([O-])([O-])C1=CC=CC=C1.FC(C1=NNC(=C1)C1=NC=CC=C1)(F)F.FC(C1=NNC(=C1)C1=NC=CC=C1)(F)F CASNTVCBKWKWNV-UHFFFAOYSA-N 0.000 description 1
GWFGARXUJNKOMY-UHFFFAOYSA-N [3,5-di(carbazol-9-yl)phenyl]-triphenylsilane Chemical compound C1=CC=CC=C1[Si](C=1C=C(C=C(C=1)N1C2=CC=CC=C2C2=CC=CC=C21)N1C2=CC=CC=C2C2=CC=CC=C21)(C=1C=CC=CC=1)C1=CC=CC=C1 GWFGARXUJNKOMY-UHFFFAOYSA-N 0.000 description 1
WIHKEPSYODOQJR-UHFFFAOYSA-N [9-(4-tert-butylphenyl)-6-triphenylsilylcarbazol-3-yl]-triphenylsilane Chemical compound C1=CC(C(C)(C)C)=CC=C1N1C2=CC=C([Si](C=3C=CC=CC=3)(C=3C=CC=CC=3)C=3C=CC=CC=3)C=C2C2=CC([Si](C=3C=CC=CC=3)(C=3C=CC=CC=3)C=3C=CC=CC=3)=CC=C21 WIHKEPSYODOQJR-UHFFFAOYSA-N 0.000 description 1
LKBREHQHCVRNFR-UHFFFAOYSA-K [B+3].[Br-].[Br-].[Br-] Chemical compound [B+3].[Br-].[Br-].[Br-] LKBREHQHCVRNFR-UHFFFAOYSA-K 0.000 description 1
CNZAMPLGEANWCA-UHFFFAOYSA-N [F].[Mg] Chemical compound [F].[Mg] CNZAMPLGEANWCA-UHFFFAOYSA-N 0.000 description 1
PWTLNDQMJGFIJE-UHFFFAOYSA-K [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C(CCCCC)C1=CC=C(C=C1)C1=NC=CC2=CC=CC=C12.C(CCCCC)C1=CC=C(C=C1)C1=NC=CC2=CC=CC=C12.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O Chemical compound [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C(CCCCC)C1=CC=C(C=C1)C1=NC=CC2=CC=CC=C12.C(CCCCC)C1=CC=C(C=C1)C1=NC=CC2=CC=CC=C12.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O PWTLNDQMJGFIJE-UHFFFAOYSA-K 0.000 description 1
FDVDQIIBRIPRCZ-UHFFFAOYSA-K [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C1(=CC=CC=C1)C1=NC2=CC=CC=C2C=C1.C1(=CC=CC=C1)C1=NC2=CC=CC=C2C=C1.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O Chemical compound [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C1(=CC=CC=C1)C1=NC2=CC=CC=C2C=C1.C1(=CC=CC=C1)C1=NC2=CC=CC=C2C=C1.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O FDVDQIIBRIPRCZ-UHFFFAOYSA-K 0.000 description 1
HYYWHKOBMBWFCR-UHFFFAOYSA-K [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O Chemical compound [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O HYYWHKOBMBWFCR-UHFFFAOYSA-K 0.000 description 1
JUPMUQIISWHFNV-UHFFFAOYSA-K [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.CC1(C2=CC=CC=C2C=2C=CC(=CC12)C1=NC2=CC=CC=C2C=C1)C.CC1(C2=CC=CC=C2C=2C=CC(=CC12)C1=NC2=CC=CC=C2C=C1)C.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O Chemical compound [Ir+3].C(C)(=O)NCC(C(=O)[O-])=O.CC1(C2=CC=CC=C2C=2C=CC(=CC12)C1=NC2=CC=CC=C2C=C1)C.CC1(C2=CC=CC=C2C=2C=CC(=CC12)C1=NC2=CC=CC=C2C=C1)C.C(C)(=O)NCC(C(=O)[O-])=O.C(C)(=O)NCC(C(=O)[O-])=O JUPMUQIISWHFNV-UHFFFAOYSA-K 0.000 description 1
DPKNTSQFNICHPC-UHFFFAOYSA-K [Ir+3].C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12.C(CCCCC)C1=CC=C(C=C1)C1=NC2=CC=CC=C2C=C1.C(CCCCC)C1=CC=C(C=C1)C1=NC2=CC=CC=C2C=C1.C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12.C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12 Chemical compound [Ir+3].C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12.C(CCCCC)C1=CC=C(C=C1)C1=NC2=CC=CC=C2C=C1.C(CCCCC)C1=CC=C(C=C1)C1=NC2=CC=CC=C2C=C1.C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12.C(C)C(C(C(=O)[O-])=O)C1=CC=CC=2C3=CC=CC=C3CC12 DPKNTSQFNICHPC-UHFFFAOYSA-K 0.000 description 1
WZRGYFHTQGBSQC-UHFFFAOYSA-K [Ir+3].C(C)C=1C(=NC=CC1)C(=O)[O-].C1(=CC=CC=C1)C1=NC=CC=C1.C1(=CC=CC=C1)C1=NC=CC=C1.C(C)C=1C(=NC=CC1)C(=O)[O-].C(C)C=1C(=NC=CC1)C(=O)[O-] Chemical compound [Ir+3].C(C)C=1C(=NC=CC1)C(=O)[O-].C1(=CC=CC=C1)C1=NC=CC=C1.C1(=CC=CC=C1)C1=NC=CC=C1.C(C)C=1C(=NC=CC1)C(=O)[O-].C(C)C=1C(=NC=CC1)C(=O)[O-] WZRGYFHTQGBSQC-UHFFFAOYSA-K 0.000 description 1
XRKLHXYZRLNFFU-UHFFFAOYSA-K [Ir+3].C(C)CC(C(=O)[O-])=O.CC1=NC2=C3C(=C4C(=C2N=C1)C=CC=C4)C=CC=C3.CC3=NC4=C1C(=C2C(=C4N=C3)C=CC=C2)C=CC=C1.C(C)CC(C(=O)[O-])=O.C(C)CC(C(=O)[O-])=O Chemical compound [Ir+3].C(C)CC(C(=O)[O-])=O.CC1=NC2=C3C(=C4C(=C2N=C1)C=CC=C4)C=CC=C3.CC3=NC4=C1C(=C2C(=C4N=C3)C=CC=C2)C=CC=C1.C(C)CC(C(=O)[O-])=O.C(C)CC(C(=O)[O-])=O XRKLHXYZRLNFFU-UHFFFAOYSA-K 0.000 description 1
PTEVGHSDUOFADP-UHFFFAOYSA-N [Ir+3].C(C1=CC=CC=C1)C1=C(C=CC=C1)P(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])C1=CC=CC=C1.FC(F)(F)C1=NNC(=C1OP(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])(C1=CC=CC=C1)C1=C(C=CC=C1)CC1=CC=CC=C1)C1=NC=CC=C1.FC(F)(F)C1=NNC(=C1OP(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])(C1=CC=CC=C1)C1=C(C=CC=C1)CC1=CC=CC=C1)C1=NC=CC=C1 Chemical compound [Ir+3].C(C1=CC=CC=C1)C1=C(C=CC=C1)P(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])C1=CC=CC=C1.FC(F)(F)C1=NNC(=C1OP(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])(C1=CC=CC=C1)C1=C(C=CC=C1)CC1=CC=CC=C1)C1=NC=CC=C1.FC(F)(F)C1=NNC(=C1OP(OC=1C(=NNC1C1=NC=CC=C1)C(F)(F)F)([O-])(C1=CC=CC=C1)C1=C(C=CC=C1)CC1=CC=CC=C1)C1=NC=CC=C1 PTEVGHSDUOFADP-UHFFFAOYSA-N 0.000 description 1
QMWPUBKGLDUDGZ-UHFFFAOYSA-N [Ir+3].CC1=CC=C(C=C1)C1=NC=CC=C1 Chemical compound [Ir+3].CC1=CC=C(C=C1)C1=NC=CC=C1 QMWPUBKGLDUDGZ-UHFFFAOYSA-N 0.000 description 1
PJCOFQAWZLOKCL-UHFFFAOYSA-N [Ir].C(C)CC(C(=O)OC1=CC=CC2=C1N=C(S2)C2=CC=CC=C2)=O Chemical compound [Ir].C(C)CC(C(=O)OC1=CC=CC2=C1N=C(S2)C2=CC=CC=C2)=O PJCOFQAWZLOKCL-UHFFFAOYSA-N 0.000 description 1
WOWBANCMFNFOKK-UHFFFAOYSA-N [Ir].C1(=CC=CC=C1)C1=NC2=CC=CC=C2C(=C1)C Chemical compound [Ir].C1(=CC=CC=C1)C1=NC2=CC=CC=C2C(=C1)C WOWBANCMFNFOKK-UHFFFAOYSA-N 0.000 description 1
AOUDMVNHWSXAHA-UHFFFAOYSA-N [Li].Oc1cccc2ccc(=O)[nH]c12 Chemical compound [Li].Oc1cccc2ccc(=O)[nH]c12 AOUDMVNHWSXAHA-UHFFFAOYSA-N 0.000 description 1
JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
GBKYFASVJPZWLI-UHFFFAOYSA-N [Pt+2].N1C(C=C2C(=C(CC)C(C=C3C(=C(CC)C(=C4)N3)CC)=N2)CC)=C(CC)C(CC)=C1C=C1C(CC)=C(CC)C4=N1 Chemical compound [Pt+2].N1C(C=C2C(=C(CC)C(C=C3C(=C(CC)C(=C4)N3)CC)=N2)CC)=C(CC)C(CC)=C1C=C1C(CC)=C(CC)C4=N1 GBKYFASVJPZWLI-UHFFFAOYSA-N 0.000 description 1
GQLKOYLFMGFHLU-UHFFFAOYSA-N [Ru+3].C(C)(C)(C)C1=CC(=NC=C1)C1=NC=CC(=C1)C(C)(C)C Chemical compound [Ru+3].C(C)(C)(C)C1=CC(=NC=C1)C1=NC=CC(=C1)C(C)(C)C GQLKOYLFMGFHLU-UHFFFAOYSA-N 0.000 description 1
FWCIDQRZZWZNQG-UHFFFAOYSA-N [Ru].FC(C1=NNC(=C1C=1C(=C(C=CC1)P(C1=CC=CC=C1)C)C=1C(=NNC1C1=NC=CC2=CC=CC=C12)C(F)(F)F)C1=NC=CC2=CC=CC=C12)(F)F Chemical compound [Ru].FC(C1=NNC(=C1C=1C(=C(C=CC1)P(C1=CC=CC=C1)C)C=1C(=NNC1C1=NC=CC2=CC=CC=C12)C(F)(F)F)C1=NC=CC2=CC=CC=C12)(F)F FWCIDQRZZWZNQG-UHFFFAOYSA-N 0.000 description 1
CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
229920000109 alkoxy-substituted poly(p-phenylene vinylene) Polymers 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
MPJHCHQZABSXMJ-UHFFFAOYSA-N aluminum;quinolin-8-ol Chemical compound [Al+3].C1=CN=C2C(O)=CC=CC2=C1 MPJHCHQZABSXMJ-UHFFFAOYSA-N 0.000 description 1
125000002078 anthracen-1-yl 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 description 1
125000000748 anthracen-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([H])=C([*])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
125000005577 anthracene group Chemical group 0.000 description 1
230000003466 anti-cipated effect Effects 0.000 description 1
VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 1
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229910052785 arsenic Inorganic materials 0.000 description 1
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
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QVKVWMHPXFPWGT-UHFFFAOYSA-N benzhydryl-bis[5-(4-tert-butylpyridin-2-yl)-3-(trifluoromethyl)-1,2,4-triazol-1-yl]phosphane osmium(2+) Chemical compound FC(C1=NN(C(=N1)C1=NC=CC(=C1)C(C)(C)C)P(C(C1=CC=CC=C1)C1=CC=CC=C1)N1N=C(N=C1C1=NC=CC(=C1)C(C)(C)C)C(F)(F)F)(F)F.[Os+2] QVKVWMHPXFPWGT-UHFFFAOYSA-N 0.000 description 1
BNBQRQQYDMDJAH-UHFFFAOYSA-N benzodioxan Chemical compound C1=CC=C2OCCOC2=C1 BNBQRQQYDMDJAH-UHFFFAOYSA-N 0.000 description 1
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ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
150000003519 bicyclobutyls Chemical group 0.000 description 1
150000005350 bicyclononyls Chemical group 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
QJXVCEINEQQSPK-UHFFFAOYSA-N bis(2-methylphenyl)-diphenylsilane Chemical compound CC1=CC=CC=C1[Si](C=1C(=CC=CC=1)C)(C=1C=CC=CC=1)C1=CC=CC=C1 QJXVCEINEQQSPK-UHFFFAOYSA-N 0.000 description 1
FCDNEESKPPIAJZ-UHFFFAOYSA-N bis[3,5-di(carbazol-9-yl)phenyl]-diphenylsilane Chemical compound C1=CC=CC=C1[Si](C=1C=C(C=C(C=1)N1C2=CC=CC=C2C2=CC=CC=C21)N1C2=CC=CC=C2C2=CC=CC=C21)(C=1C=C(C=C(C=1)N1C2=CC=CC=C2C2=CC=CC=C21)N1C2=CC=CC=C2C2=CC=CC=C21)C1=CC=CC=C1 FCDNEESKPPIAJZ-UHFFFAOYSA-N 0.000 description 1
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JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
MRKVYAQCIIPPFP-UHFFFAOYSA-N c1ccc(cc1)-c1cccc2-c3ccccc3C(c12)(c1ccccc1)c1ccccc1 Chemical compound c1ccc(cc1)-c1cccc2-c3ccccc3C(c12)(c1ccccc1)c1ccccc1 MRKVYAQCIIPPFP-UHFFFAOYSA-N 0.000 description 1
HFUZCVTVOQHYBZ-UHFFFAOYSA-N c1ccc2c(cccc2c1)-c1c2ccccc2c(-c2ccc(cc2)-c2ccc(cc2)-c2c3ccccc3c(-c3cccc4ccccc34)c3ccccc23)c2ccccc12 Chemical group c1ccc2c(cccc2c1)-c1c2ccccc2c(-c2ccc(cc2)-c2ccc(cc2)-c2c3ccccc3c(-c3cccc4ccccc34)c3ccccc23)c2ccccc12 HFUZCVTVOQHYBZ-UHFFFAOYSA-N 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
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XSVXWCZFSFKRDO-UHFFFAOYSA-N triphenyl-(3-triphenylsilylphenyl)silane Chemical compound C1=CC=CC=C1[Si](C=1C=C(C=CC=1)[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 XSVXWCZFSFKRDO-UHFFFAOYSA-N 0.000 description 1
DETFWTCLAIIJRZ-UHFFFAOYSA-N triphenyl-(4-triphenylsilylphenyl)silane Chemical compound C1=CC=CC=C1[Si](C=1C=CC(=CC=1)[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 DETFWTCLAIIJRZ-UHFFFAOYSA-N 0.000 description 1
LNQMQGXHWZCRFZ-UHFFFAOYSA-N triphenyl-[4-(4-triphenylsilylphenyl)phenyl]silane Chemical group C1=CC=CC=C1[Si](C=1C=CC(=CC=1)C=1C=CC(=CC=1)[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 LNQMQGXHWZCRFZ-UHFFFAOYSA-N 0.000 description 1
HITRWHKLCHWBNZ-UHFFFAOYSA-N triphenyl-[4-(9-phenylfluoren-9-yl)phenyl]silane Chemical compound C1=CC=CC=C1C1(C=2C=CC(=CC=2)[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)C2=CC=CC=C2C2=CC=CC=C21 HITRWHKLCHWBNZ-UHFFFAOYSA-N 0.000 description 1
KIGXXTRUJYDDKP-UHFFFAOYSA-N triphenyl-[4-[4-(4-triphenylsilylphenyl)phenyl]phenyl]silane Chemical group C1=CC=CC=C1[Si](C=1C=CC(=CC=1)C=1C=CC(=CC=1)C=1C=CC(=CC=1)[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 KIGXXTRUJYDDKP-UHFFFAOYSA-N 0.000 description 1
238000001132 ultrasonic dispersion Methods 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1
VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
HTPBWAPZAJWXKY-UHFFFAOYSA-N zinc;quinolin-8-ol Chemical compound [Zn+2].C1=CN=C2C(O)=CC=CC2=C1.C1=CN=C2C(O)=CC=CC2=C1 HTPBWAPZAJWXKY-UHFFFAOYSA-N 0.000 description 1
229910052726 zirconium Inorganic materials 0.000 description 1