KR930010017A - 액정 혼합물에서 사용하기 위한 화합물 - Google Patents
액정 혼합물에서 사용하기 위한 화합물 Download PDFInfo
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- KR930010017A KR930010017A KR1019920020648A KR920020648A KR930010017A KR 930010017 A KR930010017 A KR 930010017A KR 1019920020648 A KR1019920020648 A KR 1019920020648A KR 920020648 A KR920020648 A KR 920020648A KR 930010017 A KR930010017 A KR 930010017A
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- 150000001875 compounds Chemical class 0.000 title claims abstract 12
- 239000000203 mixture Substances 0.000 title claims abstract 5
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract 4
- -1 cyclic lactone Chemical class 0.000 claims abstract 35
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 9
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims abstract 5
- 125000005714 2,5- (1,3-dioxanylene) group Chemical group [H]C1([H])OC([H])([*:1])OC([H])([H])C1([H])[*:2] 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 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
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
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Abstract
본 발명은 일반식(I)의 화합물에 관한 것이다.
R1-(A1)a(-M1)b-(-A2)c-(-M2)d(-A3)e(-M3)f(-A4)g-H (I)
상기식에서, R1은 H또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(비대칭 탄소원자가 존재하거나 존재하지 않음)(여기서, 하나 또는 두 개의 비-인접, CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될 수 있으며, 또한 상기 알킬 라디칼의 하나 이상의 수소원자는 F, Cl, Br또는 CN으로 치환될 수 있다)이거나, 키랄 그룹, 예를 들어, 에폭시드 디옥솔란 또는 사이클릭 락톤이고; -(A1)a(-M1)b-(-A2)c(-M2)d(-A3)e(-M3)f(-A4)g-H는 1 내지 4개의 환을 포함하는 시스템(방향족 또는 헤테로 사이클릭 사이클로헥산)이고, 상기 시스템은 상이한 방법으로 연결될 수 있다. 본 발명에 따른 화합물은 액정 혼합물의 반응 속도를 증가시킨다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (7)
- 일반식(I)의 화합물.R1-(A1)a(-M1)b-(-A2)c-(-M2)d(-A3)e(-M3)f(-A4)g-H (I)상기식에서, R1은 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(비대칭 탄소원자가 존재하거나 존재하지 않음)(여기서, 하나 또는 두 개의 비-인접, CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-, -S-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될 수 있으며, 또한 상기 알킬 라디칼의 하나 이상의 수소원자는 F, Cl, Br또는 CN으로 치환될 수 있다)이거나, 하기 키랄 그룹:중 하나이고; R2, R3, R4및 R5는 서로 독립적으로 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(여기서, 하나 또는 두 개의 비인접-CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, R2및 R3은 함께 치환체로서 디옥솔란 시스템에 결합되는 경우 또한 -(CH2)4- 또는 -(CH2)5-일수 있으며; A1, A2, A3및 A4는 동일하거나 상이하고, 1,4-페닐렌(여기서, 하나 또는 두 개의 수소원자는 F, Cl 및/또는 CN으로 대체될 수 있다), 피라진-2,5-디일, 피리다진-3,6-디일, 피리딘-2,5-디일, 피리미딘-2,5-디일(여기서, 하나 또는 두 개의 수소원자는 F로 대체될 수 있다), 트란스-1,4-사이클로 헥실렌(여기서, 하나 또는 두 개의 수소원자는 -CN 및/또는 -CH3로 대체될 수 있다), 1,3,4-티아디아졸-2,5-디일, 1,3-디옥산-2,5-디일, 1,3-디티안-2,5-디일, 1,3-티아졸-2,4-디일, 1,3-티아졸-2,5-디일, 티오펜-2,4-디일, 티오펜-2,5-디일, 피페라진-1,4-디일, 피페라진-2,5-디일, 나프탈렌-2,6-디일, 바이사이클로[2.2.2]옥탄-1,4-디일, 1,3-디옥사 보리난-2,5-디일 또는 트란스-데칼린-2,6-디일이고; M1, M2및 M3은 동일하거나 상이하며 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH2-O-, -O-CH2-, -CH2CH2-, -CH=CH- 또는 -C=C-이고; M4는 -CH2-O-,-O-CH2-, -CO-O-, -O-CO- 또는 단일결합이고; 단, a+b+c+e+g의 합이 1, 2, 3 또는 4라는 조건하에서, a, b, c, d, e, f 및 g는 0또는 1이고; *는 키랄 중심이고; 단, R1-(A1)a(-M1)b-(-A2)c-(-M2)d(-A3)e(-M3)f(-A4)g-H 그룹은
- 제1항에 있어서, R1이 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(비대칭 탄소원자가 존재하거나 존재하지 않음)(여기서, 하나 또는 두 개의 비인접, CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될 수 있다)이거나, 하기 키랄 그룹:중 하나이고; R2, R3, R4및 R5는 서로 독립적으로 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(여기서, 하나 또는 두 개의 비인접-CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, R2및 R3은 함께 치환체로서 디옥솔란 시스템에 결합되는 경우 또한 -(CH2)4- 또는 -(CH2)5-일수 있으며; A1, A2, A3및 A4는 동일하거나 상이하고, 1,4-페닐렌, 피라진-2,5-디일, 피리다진-3,6-디일, 피리딘-2,5-디일, 피리미딘-2,5-디일 트란스-1,4-사이클로 헥실렌 1,3,4-티아디아졸-2,5-디일, 1,3-디옥산-2,5-디일, 나프탈렌-2,6-디일 또는 바이사이클로[2.2.2]옥탄-1,4-디일이고; M1, M2 및 M3은 동일하거나 상이하며 -O-, -CO-, -CO-O-, -O-CO-, -CH2-O-, -CH2CH2-, -CH=CH- 또는 -C=C-이고; M4는 -CH2-O-, -O-CH2-, -CO-O-, -O-CO- 또는 단일결합인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 H또는 탄소수 1내지 22의 직쇄 또는 측쇄 알킬 라디칼(비대칭 탄소원자가 존재하거나 존재한지 않음)(여기서, 하나 또는 두 개의 비인접-CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, 하기 키랄 그룹:중 하나이고; R2, R3, R4및 R5는 서로 독립적으로 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(여기서, 하나 또는 두 개의 비인접-CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, R2및 R3은 함께 치환체로서 디옥솔란 시스템에 결합되는 경우 또한 -(CH2)4- 또는 -(CH2)5-일수 있고; A1, A2, A3및 A4는 동일하거나 상이하고, 1,4-페닐렌, 피라진-2,5-디일, 피리다진-3,6-디일, 피리딘-2,5-디일, 피리미딘-2,5-디일 트란스-1,4-사이클로 헥실렌 1,3,4-티아-디아졸-2,5-디일, 나프탈렌-2,6-디일 또는 1,3-디옥산-2,5-디일이고;M1, M2및 M3은 동일하거나 상이하며 -O-, -CO-, -CO-O-, -O-CO-, -CH2-O-, -CH2CH2-, -CH=CH- 또는 -C=C-이고; M4는 -CH2O-O-, -O-CH2-, -CO-O-, -O-CO- 또는 단일결합인 일반식(I)의 화합물.
- 제1항에 있어서, R1이 H 또는 탄소소 1 내지 22의 알킬 라디칼(여기서, 하나의 -CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, 하기 키랄 그룹.R1-(A1)a(-M1)b-(-A2)c-(-M2)d(-A3)e(-M3)f(-A4)g-H 그룹이일반식(I)의 화합물.
- 액정 혼합물중 일반식(I)의 화합물의 용도.R1-(A1)a(-M1)b-(-A2)c-(-M2)d(-A3)e(-M3)f(-A4)g-H (I)상기식에서, R1은 H또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(비대칭 탄소원자가 존재하거나 존재하지 않음)(여기서, 하나 또는 두 개의 비-인접, CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될 수 있으며, 상기 알킬 라디칼의 하나 이상의 수소원자는 F, Cl, Br또는 CN으로 치환될 수 있다)이거나, 키랄 그룹,중 하나이고; R2, R3, R4및 R5는 서로 독립적으로 H 또는 탄소수 1 내지 22의 직쇄 또는 측쇄 알킬 라디칼(여기서, 하나 또는 두 개의 비인접-CH2-그룹은 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH=CH-, -C=C-, Δ 또는 -Si(CH3)2로 대체될수 있다)이거나, R2및 R3은 함께 치환체로서 디옥솔란 시스템에 결합되는 경우 또한 -(CH2)4- 또는 -(CH2)5-일수 있고; A1, A2, A3및 A4는 동일하거나 상이하고, 1,4-페닐렌(여기서, 하나 또는 두 개의 수소원자는 F, Cl 및/또는 CN으로 대체될 수 있다) 피라진-2,5-디일, 피리다진-3,6-디일, 피리딘-2,5-디일, 피리미딘-2,5-디일(여기서, 하나 또는 두 개의 수소원자는 F로 대체될 수 있다), 트란스-1,4-사이클로 헥실렌(여기서, 하나 또는 두 개의 수소원자는 -CN및/또는 -CH3로 대체될 수 있다), 1,3,4-티아디아졸-2,5-디일, 1,3-디옥산-2,5-디일, 1,3-디티안-2,5-디일,피페라진-2,5-디일, 나프탈렌-2,6-디일, 바이사이클로 [2.2.2]옥탄-1,4-디일, 1,3-디옥사 보리난-2,5-디일 또는 트란스-데칼린-2,6-디일이고; M1, M2및 M3은 동일하거나 상이하며 -O-, -S-, -CO-, -CO-O-, -O-CO-, -CO-S-,-S-CO-, -O-CO-O, -CH2-O-, -O-CH2-, -CH2CH2-, -CH=CH- 또는 -C=C-이고; M4는 -CH2-O-,-O-CH2-, -CO-O-, -O-CO- 또는 단일결합이고; 단, a+b+c+e+g의 합이 1, 2, 3 또는 4라는 조건하에서, a, b, c, d, e, f 및 g는 0또는 1이고; *는 키랄 중심이다.
- 제5항에 있어서, 액정 혼합물이 강유전성인 용도.
- 제5항에 있어서, 일반식(I)의 화합물이 LC혼합물에 0.01 내지 60중량%의 농도로 첨가되는 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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DEP4136627.1 | 1991-11-07 | ||
DE4136627 | 1991-11-07 |
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KR930010017A true KR930010017A (ko) | 1993-06-21 |
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KR1019920020648A KR930010017A (ko) | 1991-11-07 | 1992-11-05 | 액정 혼합물에서 사용하기 위한 화합물 |
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US (1) | US5849216A (ko) |
EP (1) | EP0541081B1 (ko) |
JP (1) | JP3441477B2 (ko) |
KR (1) | KR930010017A (ko) |
AT (1) | ATE215939T1 (ko) |
CA (1) | CA2082304A1 (ko) |
DE (1) | DE59209949D1 (ko) |
TW (1) | TW211581B (ko) |
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1992
- 1992-10-20 TW TW081108353A patent/TW211581B/zh active
- 1992-11-05 EP EP92118951A patent/EP0541081B1/de not_active Expired - Lifetime
- 1992-11-05 KR KR1019920020648A patent/KR930010017A/ko not_active Application Discontinuation
- 1992-11-05 AT AT92118951T patent/ATE215939T1/de not_active IP Right Cessation
- 1992-11-05 DE DE59209949T patent/DE59209949D1/de not_active Expired - Lifetime
- 1992-11-06 CA CA002082304A patent/CA2082304A1/en not_active Abandoned
- 1992-11-09 JP JP29881692A patent/JP3441477B2/ja not_active Expired - Lifetime
-
1995
- 1995-05-31 US US08/454,995 patent/US5849216A/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102506573B1 (ko) * | 2022-03-08 | 2023-03-06 | 신수용 | 모터 코일 테이핑장치 |
KR102592567B1 (ko) * | 2022-11-07 | 2023-10-23 | 김도영 | 다곡선 부스바 테이핑용 텝핑헤드가 구비된 부스바 테이핑장치 |
KR102643811B1 (ko) * | 2023-01-17 | 2024-03-06 | 예랑테크 주식회사 | 부스바 절연테이핑 장치 |
KR102706957B1 (ko) * | 2024-02-28 | 2024-09-13 | 예랑테크 주식회사 | 부스바 절연테이핑 장치 |
Also Published As
Publication number | Publication date |
---|---|
TW211581B (ko) | 1993-08-21 |
EP0541081A3 (ko) | 1994-04-20 |
CA2082304A1 (en) | 1993-05-08 |
EP0541081A2 (de) | 1993-05-12 |
EP0541081B1 (de) | 2002-04-10 |
US5849216A (en) | 1998-12-15 |
JP3441477B2 (ja) | 2003-09-02 |
ATE215939T1 (de) | 2002-04-15 |
JPH05286905A (ja) | 1993-11-02 |
DE59209949D1 (de) | 2002-05-16 |
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