TW201510099A

TW201510099A - 光學基材及顯示裝置

光學基材及顯示裝置 Download PDF

Info

Publication number: TW201510099A
Authority: TW; Taiwan
Prior art keywords: group; ring; optical substrate; formula; compound
Prior art date: 2013-08-15

Application number

TW103127698A

Other languages

English (en)

Chinese (zh)

Inventor

Koutaro Okabe

Takashi Kato

Daisuke Sasaki

Soji Ishizaka

Original Assignee

Fujifilm Corp

Priority date

2013-08-15

Filing date

2014-08-13

Publication date

2015-03-16

2014-08-13 Application filed by Fujifilm Corp filed Critical Fujifilm Corp

2015-03-16 Publication of TW201510099A publication Critical patent/TW201510099A/zh

Links

230000003287 optical effect Effects 0.000 title claims abstract description 122
239000000758 substrate Substances 0.000 title claims abstract description 113
239000000463 material Substances 0.000 claims abstract description 83
238000010521 absorption reaction Methods 0.000 claims abstract description 27
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims abstract description 20
125000001424 substituent group Chemical group 0.000 claims description 116
125000004432 carbon atom Chemical group C* 0.000 claims description 88
150000001875 compounds Chemical class 0.000 claims description 85
125000000217 alkyl group Chemical group 0.000 claims description 80
125000003118 aryl group Chemical group 0.000 claims description 71
125000000623 heterocyclic group Chemical group 0.000 claims description 65
239000010410 layer Substances 0.000 claims description 43
125000003342 alkenyl group Chemical group 0.000 claims description 37
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 30
125000001072 heteroaryl group Chemical group 0.000 claims description 29
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 26
125000004429 atom Chemical group 0.000 claims description 17
125000001931 aliphatic group Chemical group 0.000 claims description 16
125000005843 halogen group Chemical group 0.000 claims description 16
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239000002184 metal Substances 0.000 claims description 13
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238000009792 diffusion process Methods 0.000 claims description 5
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230000000052 comparative effect Effects 0.000 description 8
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FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 7
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WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
239000003513 alkali Substances 0.000 description 6
125000004414 alkyl thio group Chemical group 0.000 description 6
239000012965 benzophenone Substances 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 6
125000002883 imidazolyl group Chemical group 0.000 description 6
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
239000007788 liquid Substances 0.000 description 6
125000002971 oxazolyl group Chemical group 0.000 description 6
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238000000411 transmission spectrum Methods 0.000 description 6
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238000011160 research Methods 0.000 description 4
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229910052725 zinc Inorganic materials 0.000 description 4
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 3
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RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
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PSYVYZXKAVCUSY-UHFFFAOYSA-N 10h-[1,3]oxazolo[5,4-a]carbazole Chemical group C1=CC=C2NC3=C(OC=N4)C4=CC=C3C2=C1 PSYVYZXKAVCUSY-UHFFFAOYSA-N 0.000 description 2
XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
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125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
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