KR910002767A - (4-아릴부틸)사이클로헥산 유도체 - Google Patents
(4-아릴부틸)사이클로헥산 유도체 Download PDFInfo
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- KR910002767A KR910002767A KR1019900011245A KR900011245A KR910002767A KR 910002767 A KR910002767 A KR 910002767A KR 1019900011245 A KR1019900011245 A KR 1019900011245A KR 900011245 A KR900011245 A KR 900011245A KR 910002767 A KR910002767 A KR 910002767A
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- 하기 일반식(I)의 화합물 :상기식에서, n은 0또는 1을 나타내고, R1은 그룹 R3또는 R3-A3-Z2-를 나타내며, R2은 그룹 R4또는 R4-A4-Z3-그룹을 나타내고, 고리 A1은 비치환되거나 할로겐-, 시아노- 및/또는 메틸-치환된 1,4-페닐렌 (여기에서, 임의로 한개의 CH 그룹 또는 두개의 CH 그룹들이 질소로 대체된다)을 나타내고, A3, A4및 고리 A2는 각각 독립적으로 비치환되거나 할로겐-, 시아노- 및/또는 메틸-치환된 1,4-페닐렌 (여기에서, 임의로 한개의 CH 그룹 또는 두개의 CH 그룹들이 질소로 대체된다)이거나 또는 트랜지스터 1, 4-사이클로헥실렌, 트랜스-1, 3-디옥산-2, 5-디일, 1-시아노-트랜스-1, 4-사이클로헥실렌, 바이사이클로[2, 2, 2]옥탄-1, 4-디일, 나프탈렌-2, 6-디일, 테트랄린-2, 6-디일 또는 트랜스-데칼린-2, b-디일을 나타내며, Z1, Z2및 Z3은 각각 독립적으로 단일 공유결합, -COO-, -OOC-, CH2O-, -OCH2-, -CH2CH2-, -C=C-, -(CH2)3O-, -O(CH2)3-, (CH2)4-, 또는 -CH=CH-CH2O- 또는 -OCH2-CH=CH-의 트랜스 형태이고, R3및 R4는 각각 독립적으로 할로겐, 시아노, -NCS, -CF3,-OCF3또는 알킬(여기에서, 임의로 한개의 >CH-CH<는>C=C<로 대체되고/되거나 임의로 한개의 메틸렌 그룹 또는 두개의 인접되지 않은 메틸렌 그룹들은 -O-, -COO- 및/또는 -OOC-로 대체되고/되거나 임의로 한개의 메틸렌 그룹을 -CHX-로 대체된다)을 나타내며, X는 할로겐, 시아노 또는 메틸을 나타낸다.
- 제1항에 있어서, 하기 일반식(I-1)의 화합물 :상기식에서, n, R1, R2, Z1및 고리 A2는 제1항에서 주어진 의미를 갖고, X1및 X2는 각각 독립적으로 수소, 할로겐, 시아노 또는 메틸을 나타낸다.
- 제1항 또는 제2항에 있어서, A3및 A1가 각각 독립적으로 트랜스-1, 4-사이클로헥실렌 또는 비치환되거나 할로겐-, 시아노-및/또는 메틸-치환된 1,4-페닐렌을 나타내는 화합물.
- 제1항 내지 제3항중 어느 한 항에 있어서, 고리 A2가 비치환된 1,4-페닐렌, 할로겐, 시아노 및/또는 메틸에 의해 일치환되거나 2,3-이치환된 1,4-페닐렌, 또는 트랜스-1, 4-사이클로헥실렌, 트랜스-1, 3-디옥산-2, 5-디일, 1-시아노-트랜스-1, 4-사이클로헥실렌, 바이사이클로[2,2,2]옥탄-1, 4-디일, 나프탈렌-2, 6-디일, 테트랄린-2,6-디일, 트랜스-데칼린-2, 6-디일, 피리딘-2, 5-디일, 피리미딘-2, 5-디일 또는 피라진-2, 5-디일을 나타내는 화합물.
- 제1항 내지 제4항중 어느 한 항에 있어서, Z1, Z2및 Z3은 각각 단일 공유결합을 나타내거나, Z1, Z2및 Z3그룹들중의 하나가 또한 -COO-, -OOC-, CH2O-, -OCH2-, -CH2CH2-, -C≡C-, -(CH2)3O-, -O(CH2)3-, -(CH2)4-, 또는 -CH=CH-CH2O- 또는 -OCH2-CH=CH-의 트랜스형태를 나타내는 화합물.
- 제1항 내지 제5항중 어느 한 항에 있어서, 하기 일반식들의 화합물 :상기식들에서, R3, R4및 Z3는 제1항에 주어진 의미를 갖고 : X1, X2, X3및 X4는 각각 독립적으로 수소, 할로겐, 시아노 또는 메틸을 나타내며, Z4는 단일 공유결합, -COO-, -OOC-,또는 -C≡C-를 나타내고, Z5는 단일 공유결합, -COO-, -OCH2, -CH2CH2-,-C≡C-, -O(CH2)3-, (CH2)4-, 또는 -OCH2-CH=CH-의 트랜스 형태를 나타내며, 고리 A5는 피리딘-2, 5-디일, 피리미딘-2, 5-디일, 피라진-2, 5-디일, 트랜스-1, 3-디옥산-2,5-디일, 바이사이클로[2,2,2]옥탄-1, 4-디일, 나프탈렌-2, 6-디일, 테트랄린-2, 6-디일 또는 트랜스-데칼린-2, 6-디일을 나타낸다.
- 제2항 또는 제6항에 있어서, X1, X2, X3및 X4는 각각 독립적으로 수소 또는 불소를 나타내는 화합물.
- 제1항 내지 제7항중 어느 한 항에 있어서, R3및 R4가 각각 독립적으로 임의로 한개의 >CH-CH<가>C=C<로 대체되고/되거나 임의로 한개의 메틸렌 그룹 또는 두개의 인접되지 않은 메틸렌 그룹들이 -O-, -COO- 및/또는 -OOC- 로 대체되고/되거나 임의로 한개의 메틸렌 그룹을 -CHX-에 의해 대체된 알킬을 나타내거나, 또는 R4가 또한 할로겐, 시아노, -NCS, -CF3또는 -OCF3를 나타내는 화합물.
- 제1항 내지 제8항중 어느 한 항에 있어서, R3및 R4가 최대 18개, 바람직하게는 최대 12개의 탄소원자를 갖는 화합물.
- 제1항 내지 제9항중 어느 한 항에 있어서, R3이 알킬, 알케닐, 알케닐옥시, 알콕시 카보닐, 알케닐 옥시카보닐, 알카노일옥시 또는 알케노일옥시, 바람직하게는 알킬 또는 알케닐을 나타내는 화합물.
- 제1항 내지 제10항중 어느 한 항에 있어서, R4가 알킬, 알케닐, 알콕시, 알케닐옥시, 알콕시 카보닐, 알케닐옥시카보닐, 알카노일옥시, 알케노일옥시, 할로겐, 시아노, -NCS, -CF3또는 -OCF3를 나타내는 화합물.
- 적어도 한 성분이 제1항에서 정의된 일반식(I)의 화합물인, 적어도 두개의 성분들을 함유하는 액정 혼합물.
- 전기-광학적 목적을 위한 제1항에서 정의된 일반식 (I)의 화합물의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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CH277989 | 1989-07-25 | ||
CH2779/89 | 1989-07-25 | ||
CH123990 | 1990-04-10 | ||
CH1239/90 | 1990-04-10 |
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Publication Number | Publication Date |
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KR910002767A true KR910002767A (ko) | 1991-02-26 |
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Application Number | Title | Priority Date | Filing Date |
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KR1019900011245A KR910002767A (ko) | 1989-07-25 | 1990-07-24 | (4-아릴부틸)사이클로헥산 유도체 |
Country Status (4)
Country | Link |
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EP (1) | EP0410233B1 (ko) |
JP (1) | JPH0366632A (ko) |
KR (1) | KR910002767A (ko) |
DE (1) | DE59009872D1 (ko) |
Families Citing this family (8)
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WO1992005230A2 (en) * | 1990-09-26 | 1992-04-02 | MERCK Patent Gesellschaft mit beschränkter Haftung | Fluorobenzene derivatives |
JP3137208B2 (ja) * | 1992-04-28 | 2001-02-19 | チッソ株式会社 | シクロヘキサン誘導体 |
JP2952141B2 (ja) * | 1993-01-08 | 1999-09-20 | キヤノン株式会社 | 液晶性化合物、それを含む液晶組成物、及びこれを用いた液晶素子 |
AU5413198A (en) | 1996-12-16 | 1998-07-15 | Chisso Corporation | Difluorophenyl derivatives, liquid-crystal compounds, and liquid-crystal composition |
JP2004256791A (ja) | 2003-02-03 | 2004-09-16 | Chisso Corp | 液晶組成物および液晶表示素子 |
CN102596874A (zh) | 2009-09-09 | 2012-07-18 | 三菱瓦斯化学株式会社 | 环状化合物、其制造方法、辐射敏感组合物及抗蚀图案形成方法 |
JP6616595B2 (ja) | 2015-06-15 | 2019-12-04 | 東芝機械株式会社 | バレルブロック |
JP6821417B2 (ja) | 2016-12-16 | 2021-01-27 | 芝浦機械株式会社 | 搬送装置および搬送ヘッド |
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DE3225290A1 (de) * | 1982-07-07 | 1984-01-12 | Merck Patent Gmbh | Ringverbindungen |
US5238600A (en) * | 1988-06-01 | 1993-08-24 | Hoffmann-La Roche Inc. | Ibimethylenoxy containing liquid crystal compounds |
-
1990
- 1990-07-13 DE DE59009872T patent/DE59009872D1/de not_active Expired - Fee Related
- 1990-07-13 EP EP90113459A patent/EP0410233B1/de not_active Expired - Lifetime
- 1990-07-24 KR KR1019900011245A patent/KR910002767A/ko not_active Application Discontinuation
- 1990-07-25 JP JP2195075A patent/JPH0366632A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0410233B1 (de) | 1995-11-15 |
JPH0366632A (ja) | 1991-03-22 |
EP0410233A3 (en) | 1991-04-17 |
EP0410233A2 (de) | 1991-01-30 |
DE59009872D1 (de) | 1995-12-21 |
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