KR940014280A - 트리플루오로페닐렌 화합물, 이의 제조방법 및 액정 혼합물중의 이의 용도 - Google Patents
트리플루오로페닐렌 화합물, 이의 제조방법 및 액정 혼합물중의 이의 용도 Download PDFInfo
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- KR940014280A KR940014280A KR1019930028165A KR930028165A KR940014280A KR 940014280 A KR940014280 A KR 940014280A KR 1019930028165 A KR1019930028165 A KR 1019930028165A KR 930028165 A KR930028165 A KR 930028165A KR 940014280 A KR940014280 A KR 940014280A
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- -1 Trifluorophenylene Compounds Chemical class 0.000 title claims abstract 23
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract 9
- 239000000203 mixture Substances 0.000 title claims abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 12
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 claims 2
- 125000005714 2,5- (1,3-dioxanylene) group Chemical group [H]C1([H])OC([H])([*:1])OC([H])([H])C1([H])[*:2] 0.000 claims 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000005407 trans-1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])[C@]([H])([*:2])C([H])([H])C([H])([H])[C@@]1([H])[*:1] 0.000 claims 2
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 claims 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims 1
- JECYNCQXXKQDJN-UHFFFAOYSA-N 2-(2-methylhexan-2-yloxymethyl)oxirane Chemical group CCCCC(C)(C)OCC1CO1 JECYNCQXXKQDJN-UHFFFAOYSA-N 0.000 claims 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 claims 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229930188620 butyrolactone Natural products 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910052798 chalcogen Inorganic materials 0.000 claims 1
- 150000001787 chalcogens Chemical class 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
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Abstract
본 발명은 트리플루오로페닐렌 화합물, 이의 제조방법 및 액정 혼합물중의 이의 용도에 관한 것이다.
일반식(Ⅰ)의 트리플루오로페닐렌 화합물은 액정 혼합물에 유용한 성분이다.
상기식에서,
는 메소제닉(mesogenic) 라디칼이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 일반식(Ⅰ)의 트리플루오로페닐렌 화합물.상기식에서, R1및 R2는 각각 독립적으로 수소, -CN, -CF3, -OCF3, -OCF2H, -F, -Cl 또는 탄소수 1 내지 20의 직쇄 또는 측쇄 알킬 라디칼[비대칭 탄소원자는 존재하거나 존재하지 않으며, 하나 이상의 CH2그룹은, 산소원자 및 황원자(이후, 칼코겐이라고 함)가 서로 직접 결합하지 않는 조건하에서, -O-, -S-, -CO--, -CH=CH-., -C≡C-, Δ, -Si(CH3)2-, 1,4-페닐렌, 트란스-1,4-사이클로헥실렌 또는 트란스-1,3-사이클로펜틸렌에 의해 치환될 수도 있고/거나, 알킬 라디칼 중의 하나 이상의 H원자는 -F, -Cl, -Br 또는 -OR3에 의해 치환될 수 있다]이거나, 라디칼중의 하나이고 ; R3, R4, R5, R6및 R7은 각각 독립적으로 수소 또는 탄소수 1 내지 16의 직쇄 또는 측쇄 알킬[비대칭 탄소 원자는 존재하거나 존재하지 않으며, 하나 이상의 CH2그룹은, 산소원자들이 서로 직접 결합하지 않는 조건하에서, -O- 또는 -CH=CH-에 의해 치환될 수도 있고/거나 알킬 라디칼 중의 하나 이상의 H원자는 -F 또는 -Cl에 의해 치환될 수 있다]이고, R4및 R5는 함께 이들이 옥시란, 디옥솔란, 테트라하이드로푸란, 테트라하이드로피란, 부티로락톤 또는 발레로락톤 시스템에 결합되는 경우, -(CH2)4또는 -(CH2)5-일수도 있으며 ; M1, M2, M3및 M4는 동일하거나 상이하며,는 동일하거나 상이하며, 1,4-페닐렌(여기서,1 내지 4개의 H원자는 F,Cl 및/또는 CN에 의해 치환될 수 있다), 피라진-2,5-디일, 피라진-3,6디일, 피리딘-2,5-디일(여기서, 하나의 H원자는 F에 의해 치환될 수도 있다), 피리미딘-2,5-디일(여기서, 하나의 H원자는 F에 의해 치환될 수도 있다), 트란스-1,4-사이클로헥실렌(여기서, 1 또는 2개의 H원자는 CN 및/또는 CH3에 의해 치환될 수 있다), 1,3,4-티아디아졸-2,5-디일, 1,3-디옥산-2,5-디일, 1,3-티아졸-2,4-디일, 1,3-티아졸,2,5-디일,티오펜-2,4디일, 티오펜-2,5-디일, 피페라진-1,4-디일, 피페라진-2,5-디일, 나프탈렌-2,6-디일, 비사이클로[2.2.2]옥산-1,4-디일 또는 1,3-디옥사보리난-2,5-디일이며 ; k, l, m 및 n은 0 또는 1 이며, 단 k+l+m+n의 합은 1,2 또는 3이다.
- 제 1 항에 있어서, R1및 R2가 각각 독립적으로 H 또는 탄소수 1 내지 20의 알킬(여기서, 하나 이상의 CH2그룹은 -O-, -CH=CH-, -CO-, -C≡C- 또는 -Si(CH3)2-에 의해 치환될 수 있고, 하나이상의 H원자는 F에 의해 치환될 수 있다)이거나, 그룹중의 하나이고 ; M1, M2, M3및 M4가 -CO-, -O-CO-, -CH2-O-, -OCH2-, -C≡C- 또는 단일결합이며 ;가 1,4-페닐렌(여기서, 1 내지 3개의 H원자는 F에 치환될 수 있다.), 피리미딘-2,5-디일, 피리딘-2, 5-디일(여기서, 하나의 H원자는 또한 F에 의해 치환될 수 있다), 1,4-사이클로헥실렌 1,3-디옥산-2, 5-디일 1,3,4-티아디아졸 또는 나프탈렌-2,6-디일이고 ; k+l+m+n이 1 또는 2인 화합물.
- 제 1 항 또는 제 2 항에 있어서, R1및 R2가 탄소수 1 내지 16의 알킬(여기서, 하나 이상의 -CH2-그룹은 -O-, -CH=CH- 또는 -Si(CH3)2-에 의해 치환될 수도 있고, 하나 이상의 H원자는 F에 의해 치환될 수도 있다)이고 ; M1, M2, M3및 M4가 -CO-O-, -O-CO- 또는 단일결합이며,가 1,4-페닐렌(여기서, 1 내지 3개의 H원자는 F에 치환될 수 있다.), 피리미딘-2,5-디일, 피리딘-2, 5-디일(하나의 H원자는 또한 F에 의해 치환될 수 있다), 1,4-사이클로헥실렌 또는 나프탈렌 2, 6-디일이고 ; k+l+m+n이 1 또는 2인 화합물.
- 2내지 35개의 성분을 포함하여, 이들 중의 하나 이상의 제 1 항 내지 제 3 항 중의 어느 한 항에 따른 트리플루오로페닐렌 유도체인 액정 혼합물.
- 제 4 항에 있어서, 제 1 항 내지 제 3 항 중의 어느 한항에 따른 화합물이 0.01 내지 80중량%로 존재하는 액정 혼합물.
- 제 4 항 또는 제 5 항에 있어서, 강유전성인 액정 혼합물.
- 제 4 항 또는 제 5 항에 있어서, 네마틱인 액정 혼합물.
- 전자-광학 스위칭 소자 및/또는 디스플레이 소자에 있어서의 제 1 항 내지 제 3 항 중의 어느 한 항에 따른 화합물의 용도.
- 전자-광학 스위칭 소자 및/또는 디스플레이 소자에 있어서의 제 4 항 내지 제 6 항 중의 한 항에 따른 액정 혼합물의 용도.
- 제 4 항 내지 제 7 항중의 어느 한 항에 따른 액정 혼합물을 함유하는 전자-광학 스위칭 소자 및/또는 디스플레이 소자.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4242695.2 | 1992-12-17 | ||
DE4242695 | 1992-12-17 | ||
DEP4320755.3 | 1993-06-23 | ||
DE4320755 | 1993-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR940014280A true KR940014280A (ko) | 1994-07-18 |
Family
ID=25921445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930028165A KR940014280A (ko) | 1992-12-17 | 1993-12-17 | 트리플루오로페닐렌 화합물, 이의 제조방법 및 액정 혼합물중의 이의 용도 |
Country Status (5)
Country | Link |
---|---|
US (1) | US5525258A (ko) |
EP (1) | EP0602596B1 (ko) |
JP (1) | JPH06263662A (ko) |
KR (1) | KR940014280A (ko) |
DE (1) | DE59307644D1 (ko) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19546520A1 (de) * | 1995-12-13 | 1997-06-19 | Hoechst Ag | Neue Derivate des 2,3,6-Trifluorphenols und ein Verfahren zu ihrer Herstellung |
JP4415456B2 (ja) * | 2000-05-30 | 2010-02-17 | チッソ株式会社 | シリコン誘導体、液晶組成物および液晶表示素子 |
JP4826005B2 (ja) * | 2000-09-28 | 2011-11-30 | Dic株式会社 | 液晶性化合物の精製方法 |
TWI306114B (en) * | 2002-04-09 | 2009-02-11 | Chisso Corp | Liquid cryatal compound having one terminal group being hydrogen atom, liquid crystal composition containing the same, and lcd device using the liquid crystal composition |
CN103242860B (zh) * | 2013-05-15 | 2014-11-05 | 江苏和成显示科技股份有限公司 | 液晶组合物及液晶显示器件 |
CN104371743B (zh) * | 2013-08-16 | 2017-05-03 | 江苏和成显示科技股份有限公司 | 液晶组合物及液晶显示器件 |
CN104371746B (zh) * | 2013-08-16 | 2016-05-25 | 江苏和成显示科技股份有限公司 | 液晶组合物及液晶显示器件 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3209178A1 (de) * | 1982-03-13 | 1983-09-15 | Merck Patent Gmbh, 6100 Darmstadt | Polyhalogenaromaten |
EP0329752B1 (en) * | 1987-09-09 | 1993-03-17 | MERCK PATENT GmbH | Fluorinated oligophenyls and their use in liquid crystal materials |
DE68902443T2 (de) * | 1988-01-14 | 1993-01-28 | Merck Patent Gmbh | Fluorinierte oligophenylderivate. |
GB8807572D0 (en) * | 1988-03-30 | 1988-05-05 | Merck Patent Gmbh | Octafluorobiphenyls |
US5213710A (en) * | 1990-09-26 | 1993-05-25 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Benzene derivatives and a liquid-crystalline medium |
DE4111765A1 (de) * | 1990-09-26 | 1992-04-02 | Merck Patent Gmbh | Penta- oder tetrafluorbenzolderivate und fluessigkristallines medium |
DE4037519A1 (de) * | 1990-11-26 | 1992-05-27 | Merck Patent Gmbh | Tetrafluorphenylester |
EP0500210A3 (en) * | 1991-01-19 | 1992-10-21 | Sanyo Chemical Industries, Ltd. | Liquid crystal compounds and compositions |
DE4127450B4 (de) * | 1991-03-26 | 2005-06-02 | Merck Patent Gmbh | Lateral fluorierte Benzolderivate |
-
1993
- 1993-12-14 EP EP93120134A patent/EP0602596B1/de not_active Expired - Lifetime
- 1993-12-14 DE DE59307644T patent/DE59307644D1/de not_active Expired - Fee Related
- 1993-12-17 KR KR1019930028165A patent/KR940014280A/ko not_active Application Discontinuation
- 1993-12-17 JP JP5318520A patent/JPH06263662A/ja active Pending
-
1995
- 1995-04-18 US US08/425,260 patent/US5525258A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE59307644D1 (de) | 1997-12-11 |
EP0602596B1 (de) | 1997-11-05 |
US5525258A (en) | 1996-06-11 |
JPH06263662A (ja) | 1994-09-20 |
EP0602596A1 (de) | 1994-06-22 |
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