KR910015560A - 비선형 광학활성을 갖는 티오펜 화합물과 이 화합물에 관련된 물질 및 장치 - Google Patents
비선형 광학활성을 갖는 티오펜 화합물과 이 화합물에 관련된 물질 및 장치 Download PDFInfo
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- KR910015560A KR910015560A KR1019900002247A KR900002247A KR910015560A KR 910015560 A KR910015560 A KR 910015560A KR 1019900002247 A KR1019900002247 A KR 1019900002247A KR 900002247 A KR900002247 A KR 900002247A KR 910015560 A KR910015560 A KR 910015560A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- compound
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- formula
- cyano
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims 11
- 239000000463 material Substances 0.000 title claims 4
- 230000003287 optical effect Effects 0.000 title claims 2
- 150000003577 thiophenes Chemical class 0.000 title claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 230000009022 nonlinear effect Effects 0.000 claims 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Divinylene sulfide Natural products C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000005110 aryl thio group Chemical group 0.000 claims 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- ZHCAAFJSYLFLPX-UHFFFAOYSA-N nitrocyclohexatriene Chemical group [O-][N+](=O)C1=CC=C=C[CH]1 ZHCAAFJSYLFLPX-UHFFFAOYSA-N 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 1
- 229930192474 thiophene Natural products 0.000 claims 1
- -1 thiophene compound Chemical class 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/08—Hydrogen atoms or radicals containing only hydrogen and carbon atoms
- C07D333/10—Thiophene
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/355—Non-linear optics characterised by the materials used
- G02F1/361—Organic materials
- G02F1/3613—Organic materials containing Sulfur
- G02F1/3614—Heterocycles having S as heteroatom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4015—Esters of acyclic unsaturated acids
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (11)
- 다음의 일반식을 가지는 것을 특징으로 하는 티오펜 화합물.{[상기식(Ⅰ)에서, n은 1내지 10사이의 정수로서, 유리하게는 1내지 4인 정수. D는 다음의 식을 가진 군들중에서 선택된 전자공여체를 나타낸다.]또는 -R2(D1)n (II)[상기식 (Ⅱ)에서 R2는 아릴기이고, 바람직하게는, 벤질리덴기이다.D1은 아미노, 알킬아미노, 디알킬아미노, 아릴아미노, 히드록실, 티올, 알킬티오, 아릴티오, 알콕시, 아릴옥시 할로게노알킬, 옥시기로 구성된 군중에서 선택된 기이다. 특히 바람직한 기들로는파라아니실들이다.A는 니트로, 시아노기들중에서 선택된 전자수용기 이거나 다음 일반식의 기를 나타낸다][상기식 (Ⅲ)에서 A1과 A2는, 동일할 수도 다를 수도 있는데, 수소, 시아노기, 니트로기, 패닐술폰기, 파라니트로페닐기 또는 -PO3(R5)2를 나타낸다. -PO3(R5)2에서 R5는 에틸 또는 프로필기와 같은 저급알킬기이다. 모든 경우에 있어서 A1과 A2군은 동시에 모두 수소일 수 없다.]}
- 제1항에서 있어서, 기 D가 다음식의 기로 구성된 군중에서 선택되는 것을 특징으로 하는 화합물.
- 제1항 또는 제2항에 없어서, 기 A1과 A2가 시아노, 니트로기로 구성된 군중에서 선택되는 것을 특징으로 하는 화합물.
- 제3항에 있어서, 식(Ⅲ)의 A1과 A2가 각각 시아노/시아노, 시아노/니트로, 또는 니트로/시아노를 나타내는 것을 특징으로하는 화합물.
- 제1항 내지 제4항중 어느 한 항에 있어서, 다음의 식을 가지는 것을 특징으로하는 화합물.
- 티오펜 유도체가 다음의 일반식으로 된것을 특징으로 하는 초편광성 화합물.[상기식에서 n은 1내지 10사이의 정수이며, 유리하게는 1내지 4사이의 정수가 좋다. A는 전자수용기이며, D는 전자공여기이다]
- 제6항에 있어서, 제1항 내지 제5항중 어느 한 항에서의 A와 D기를 함유하는 화합물.
- 광학적으로 비선형(non linear)의 활성(activity)을 갖는, 특히 제2차 하모니를 발생시키는 화합물로서, 제6항 및 제7항중 어느 한 항에서의 화합물을 적어도 한개이상 함유하는 것을 특징으로 하는 물질.
- 제8항에 있어서, 폴리머로 형성된 매질로 구성된 물질로서, 매질속에 제6항 및 제7항중 어느 한 항에서의 화합물을 적어도 한개 이상 침투시킨것을 특징으로하는 물질.
- 제8항 또는 제9항에 있어서, 필름형태로된 것을 특징으로하는 물질.
- 광학적으로 비선형의 활성을 갖는 성분으로 이루어진 광학장치 또는 전기광학장치로서, 제8항 내지 제10항 중 어느 한항에서의 물질을 함유하는 성분으로 구성된 것을 특징으로 하는 장치.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8902271A FR2643372B1 (fr) | 1989-02-22 | 1989-02-22 | Composes thiopheniques actifs en optique non lineaire, materiaux et dispositifs les contenant |
FR89/02271 | 1989-02-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910015560A true KR910015560A (ko) | 1991-09-30 |
Family
ID=9379002
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900002247A KR910015560A (ko) | 1989-02-22 | 1990-02-22 | 비선형 광학활성을 갖는 티오펜 화합물과 이 화합물에 관련된 물질 및 장치 |
Country Status (8)
Country | Link |
---|---|
US (1) | US5156774A (ko) |
EP (1) | EP0384811A1 (ko) |
JP (1) | JPH02288874A (ko) |
KR (1) | KR910015560A (ko) |
CA (1) | CA2010528A1 (ko) |
FI (1) | FI900877A0 (ko) |
FR (1) | FR2643372B1 (ko) |
IL (1) | IL93449A0 (ko) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03194519A (ja) * | 1989-12-25 | 1991-08-26 | Nippon Oil & Fats Co Ltd | 非線形光学材料 |
US5395556A (en) * | 1990-12-12 | 1995-03-07 | Enichem S.P.A. | Tricyanovinyl substitution process for NLO polymers |
US5514799A (en) * | 1993-08-02 | 1996-05-07 | Enichem S.P.A. | 1,1-vinyl substituted nonlinear optical materials |
FR2686162B1 (fr) * | 1992-01-13 | 1995-09-22 | Commissariat Energie Atomique | Modulateur spatial de lumiere a adressage optique. |
US5534201A (en) * | 1992-03-31 | 1996-07-09 | E. I. Du Pont De Nemours And Company | NLO dye compositions and use thereof in producing NLO elements |
US5594093A (en) * | 1992-07-13 | 1997-01-14 | Fujitsu Limited | Nonlinear optical material and nonlinear optical device and directional coupling type optical switch using same |
EP0585999A1 (en) * | 1992-08-14 | 1994-03-09 | ENICHEM S.p.A. | Functional heteroaromatics for NLO applications |
DE4234230C2 (de) * | 1992-10-10 | 2003-08-14 | Covion Organic Semiconductors | Substituierte Thieno[3,2-b]thiophene und ihre Verwendung |
SG90693A1 (en) * | 1993-10-06 | 2002-08-20 | Enichem Spa | Highly efficient nonlinear optical polyimides |
US5710173A (en) * | 1995-06-07 | 1998-01-20 | Sugen, Inc. | Thienyl compounds for inhibition of cell proliferative disorders |
US5834575A (en) * | 1996-11-13 | 1998-11-10 | Hitachi Chemical Company, Ltd. | Compounds and polymers, resin compositions, nonlinear optical element and nonlinear optical devices, and production process therefor |
US6652779B1 (en) | 1998-07-27 | 2003-11-25 | Pacific Wave Industries, Inc. | Polymers containing polyene-based second-order nonlinear optical chromophores and devices incorporating the same |
US6361717B1 (en) * | 1998-07-27 | 2002-03-26 | Pacific Wave Industries, Inc. | Sterically stabilized second-order nonlinear optical chromophores and devices incorporating the same |
US6555027B2 (en) | 1998-07-27 | 2003-04-29 | Pacific Wave Industries, Inc. | Second-order nonlinear optical chromophores containing dioxine and/or bithiophene as conjugate bridge and devices incorporating the same |
US6514434B1 (en) * | 2000-06-16 | 2003-02-04 | Corning Incorporated | Electro-optic chromophore bridge compounds and donor-bridge compounds for polymeric thin film waveguides |
WO2002008215A1 (en) * | 2000-07-24 | 2002-01-31 | University Of Washington | Hyperpolarizable organic chromophores |
AU2002354688A1 (en) * | 2001-07-13 | 2003-01-29 | The University Of Chicago | Novel nonlinear optical compounds and polymers |
ITMI20021456A1 (it) * | 2002-07-02 | 2004-01-02 | Santopietro Giuseppe | Dispositivo logico ottico e procedimento per la generazione di un segnale logico ottico |
US7425643B1 (en) | 2004-01-26 | 2008-09-16 | University Of Washington | Electron acceptors for nonlinear optical chromophores |
JP5086807B2 (ja) * | 2005-05-13 | 2012-11-28 | Agcセイミケミカル株式会社 | 新規アミノ基含有複素環誘導体および該複素環誘導体を含有する光電変換用増感色素 |
US8409713B2 (en) * | 2007-12-07 | 2013-04-02 | University Of Washington | Crosslinkable polymer host containing a nonlinear optical chromophore guest |
US8394499B2 (en) * | 2007-12-07 | 2013-03-12 | University Of Washington | Crosslinkable polymer host having pendant nonlinear optical chromophores and containing a nonlinear optical chromophore guest |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0268354A3 (en) * | 1986-10-07 | 1988-06-15 | Imperial Chemical Industries Plc | Substituted pyrazoline |
US4792567A (en) * | 1987-06-09 | 1988-12-20 | Fmc Corporation | Acaricidal aryl arylthien-2-yl ethenes |
-
1989
- 1989-02-22 FR FR8902271A patent/FR2643372B1/fr not_active Expired - Lifetime
-
1990
- 1990-02-16 EP EP90400428A patent/EP0384811A1/fr not_active Withdrawn
- 1990-02-19 IL IL93449A patent/IL93449A0/xx unknown
- 1990-02-21 FI FI900877A patent/FI900877A0/fi not_active IP Right Cessation
- 1990-02-21 CA CA002010528A patent/CA2010528A1/fr not_active Abandoned
- 1990-02-21 JP JP2038520A patent/JPH02288874A/ja active Pending
- 1990-02-22 US US07/482,946 patent/US5156774A/en not_active Expired - Fee Related
- 1990-02-22 KR KR1019900002247A patent/KR910015560A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
CA2010528A1 (fr) | 1990-08-22 |
IL93449A0 (en) | 1990-11-29 |
EP0384811A1 (fr) | 1990-08-29 |
FR2643372A1 (fr) | 1990-08-24 |
FR2643372B1 (fr) | 1991-04-26 |
US5156774A (en) | 1992-10-20 |
JPH02288874A (ja) | 1990-11-28 |
FI900877A0 (fi) | 1990-02-21 |
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