KR900004807A - 비선형 광학 활성 중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조 방법 및 그를 포함하는 전기 광학 장치 - Google Patents

비선형 광학 활성 중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조 방법 및 그를 포함하는 전기 광학 장치 Download PDF

Info

Publication number
KR900004807A
KR900004807A KR1019890013301A KR890013301A KR900004807A KR 900004807 A KR900004807 A KR 900004807A KR 1019890013301 A KR1019890013301 A KR 1019890013301A KR 890013301 A KR890013301 A KR 890013301A KR 900004807 A KR900004807 A KR 900004807A
Authority
KR
South Korea
Prior art keywords
polymer
group
compound
electron
optically active
Prior art date
Application number
KR1019890013301A
Other languages
English (en)
Inventor
미냐니 제라르
바르뗄르미 빠스깔
메이뤼이 레미
Original Assignee
쟝-삐에르 에송
롱-쁠랑 쉬미
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9370052&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR900004807(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 쟝-삐에르 에송, 롱-쁠랑 쉬미 filed Critical 쟝-삐에르 에송
Publication of KR900004807A publication Critical patent/KR900004807A/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G83/00Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL 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
    • G02F1/00Devices 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
    • G02F1/35Non-linear optics
    • G02F1/355Non-linear optics characterised by the materials used
    • G02F1/361Organic materials
    • G02F1/3615Organic materials containing polymers
    • G02F1/3617Organic materials containing polymers having the non-linear optical group in a side chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/675Low-molecular-weight compounds
    • C08G18/676Low-molecular-weight compounds containing the unsaturation at least partially in a non-aromatic carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/675Low-molecular-weight compounds
    • C08G18/677Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups
    • C08G18/678Low-molecular-weight compounds containing heteroatoms other than oxygen and the nitrogen of primary or secondary amino groups containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/38Polymers
    • C09K19/3833Polymers with mesogenic groups in the side chain
    • C09K19/3885Polyurethanes
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL 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
    • G02F1/00Devices 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
    • G02F1/35Non-linear optics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Materials Engineering (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Light Receiving Elements (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Organic Insulating Materials (AREA)
  • Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
  • Polymerisation Methods In General (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

내용 없음

Description

비선형광학 활성중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조방법 및 그를 포함하는 전기광학장치.
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (14)

  1. 하나이상의 이작용성 화합물이 하나이상의 전자 수용기와 하나이상의 전자공여기를 함유하는 전하이동극성기를 포함하는 첫번째 이작용성 화합물과 두번째 이작용성 화합물의 반응에 의해 수득되며, 중합반응 작용이 상기 하나이상의 전자공여기에 의해 실시됨을 특징으로 하는 비선형광학 활성 중합체.
  2. 제1항에 있어서, 하기식(I)의 구조를 가진 전하 이동극성기를 포함하는 이작용성 화합물이며, 중합용 반응기가 전자공여기 D에 의해 전달됨을 특징으로 하는 중합체.
    D-(π전자비편재화 라디칼)-A
  3. 제1 또는 2항에 있어서, 이작용성 화합물의 중합용 반응기가 알콜, 아민, 이소시아네이트, 알릴, 비닐, 산기를 포함하는 군중에서 선택됨을 특징으로 하는 중합체.
  4. 제1 내지 3항중 어느 한 항에 있어서, 첫번째 및 두번째 작용성 화합물이 동일한 중합용 반응기를 전달함을 특징으로 하는 중합체.
  5. 제1 내지 3항중 어느 한 항에 있어서, 첫번째 이 작용성 화합물의 중합용 반응기가 두번째 이작용성 화합물에 의해 전달되는 기와는 상이함을 특징으로 하는 중합체.
  6. 제1 내지 5항중 어느 한 항에 있어서, 이작용성 화합물의 혼합물에 삼작용성 화합물을 첨가하여 망상화시킴을 특징으로 하는 중합체.
  7. 제2 내지 6항중 어느 한 항에 있어서, π전자 비편재화 라디칼이 하기 구조의 라디칼을 포함하는 군중에서 선택됨을 특징으로 하는 중합체.
    (식중, R3,R4및 R6은 동일 또는 상이하며, 수소 또는 내부 알킬라디칼을 나타낸다).
  8. 제1 내지 7항중 어느 한 항에 있어서, 전자수용 라디칼(A)이 하기 라디칼중에서 선택됨을 특징으로 하는 중합체. 니트로, 시아노, -CO2R5,PO3(R5)2(R5는 저급알킬 라디칼이다).
  9. 제1 내지 8항중 어느 한 항에 있어서, 전자공여 라디칼(D)이 다음식
    (식중, R7및 R8은 동일 또는 상이하며, 중합용 반응기를 포함하는 라디칼이다)의 라디칼이며, 바람직하게는 다음의 구조
    -(CH2)m-OH; -(CH2)p-CH=CH2
    (식중, m 및 p는 정수이며, m은 1 내지 6, p는 0 내지 6이다)를 가짐을 특징으로 하는 중합체.
  10. 전기장 효과에 의해 편향되어 비중심대칭의 전하가 수득되는 제1 내지 9항중 어느 한 항에 따른 중합체를 포함함을 특징으로 하는 비선형 광학활성 재료.
  11. 재료를 중합체의 유리전이 온도 이상의 온도로 가열하고, 가열된 재료를 전기장으로 처리한후, 냉각 시키는 것으로 구성됨을 특징으로 하는 제10항에 따른 비선형 광학 활성재료의 제조방법.
  12. 이작용성 화합물과 다작용성 화합물을 포함하는 혼합물을 부분적으로 중합시키고, 이렇게 수득된 예비중합체를 그의 연화온도 또는 그의 유리전이온도를 초과하는 온도로 가열하고, 가열된 예비중합체를 전기장으로 처리한후, 중합체로 완전 중합하는 것으로 구성됨을 특징으로 하는 제10항에 따른 비선형 광학 활성 재료의 제조방법.
  13. 제11 또는 12항에 있어서, 중합체 또는 재료의 중합 또는 예비중합이 열, 라디칼, 이온에 의해, 또는 복사에 의한 충격에 의해 실시됨을 특징으로 하는 제조방법.
  14. 제10항에 따른 재료를 포함함을 특징으로 하는 광학장치.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890013301A 1988-09-16 1989-09-12 비선형 광학 활성 중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조 방법 및 그를 포함하는 전기 광학 장치 KR900004807A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8812080A FR2636745B1 (fr) 1988-09-16 1988-09-16 Polymeres et materiaux les contenant, actifs en optique non lineaire, procedes de fabrication de ces polymeres et materiaux et dispositif optoelectrique les contenant
FR88-12080 1988-09-16

Publications (1)

Publication Number Publication Date
KR900004807A true KR900004807A (ko) 1990-04-13

Family

ID=9370052

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019890013301A KR900004807A (ko) 1988-09-16 1989-09-12 비선형 광학 활성 중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조 방법 및 그를 포함하는 전기 광학 장치

Country Status (15)

Country Link
US (1) US5189134A (ko)
EP (1) EP0363237B2 (ko)
JP (1) JPH071361B2 (ko)
KR (1) KR900004807A (ko)
CN (1) CN1042164A (ko)
AT (1) ATE98382T1 (ko)
AU (1) AU4149589A (ko)
DE (1) DE68911258T3 (ko)
DK (1) DK456189A (ko)
FI (1) FI894375A (ko)
FR (1) FR2636745B1 (ko)
IL (1) IL91645A0 (ko)
NO (1) NO893694L (ko)
PT (1) PT91729A (ko)
ZA (1) ZA897046B (ko)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2646671B1 (fr) * 1989-05-03 1993-01-22 Rhone Poulenc Chimie Materiau organique actif en optique non lineaire
US5173546A (en) * 1989-11-27 1992-12-22 The Dow Chemical Company Nonlinear optical materials
MY105844A (en) * 1989-11-27 1995-01-30 Dow Chemical Co Novel nonlinear optical materials.
ES2060281T3 (es) * 1990-03-06 1994-11-16 Akzo Nobel Nv Sistema nlo termicamente curable y componentes opticos integrados preparados a partir del mismo.
DE4040471A1 (de) * 1990-08-01 1992-02-06 Bayer Ag Haertbare mischungen zur herstellung von epoxidnetzwerken, verfahren zu deren herstellung und verwendung
EP0473935A3 (en) * 1990-08-03 1992-09-09 The Dow Chemical Company Curable mixture of mesogenic epoxy resins and mesogenic polyamines and cured compositions
EP0477667A3 (en) * 1990-09-24 1993-01-27 Siemens Aktiengesellschaft Cured epoxy resins having nonlinear optical properties
US5187234A (en) * 1990-10-23 1993-02-16 Hoechst Celanese Corp. Vinyl polymers exhibiting nonlinear optical response
AU3120393A (en) * 1991-06-04 1993-01-12 Hoechst Celanese Corporation Vinyl polymers exhibiting nonlinear optical response
FR2678613B1 (fr) * 1991-07-02 1993-09-17 Thomson Csf Materiaux reticulables thermiquement pour application en optique non lineaire.
JPH06509188A (ja) * 1991-07-19 1994-10-13 イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー 非線形光学要素の製造
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
JPH06175172A (ja) * 1992-07-13 1994-06-24 Fujitsu Ltd 非線形光学材料、その製造方法並びにそれを用いた非線形光学デバイス及び方向性結合型光スイッチ
US5288816A (en) * 1992-08-10 1994-02-22 The Dow Chemical Company Nonlinear optical aminoaryl hydrazones and nonlinear optical polymers thereof
DE4244195A1 (de) * 1992-12-24 1994-06-30 Basf Ag Verfahren zur Herstellung von strukturierten Polymerschichten mit nichtlinear optischen Eigenschaften
US5670603A (en) * 1993-03-08 1997-09-23 Alliedsignal Inc. Polymers exhibiting nonlinear optical properties
EP0647874A1 (en) * 1993-10-06 1995-04-12 ENICHEM S.p.A. Highly efficient nonlinear optical polyimides
DE4335541A1 (de) * 1993-10-19 1995-04-20 Basf Ag Azo- oder Stilbenfarbstoffgruppierungen und Urethangruppen enthaltendes Polyaddukt und dessen Verwendung in der nicht-linearen Optik
TW243501B (en) * 1994-07-22 1995-03-21 Akzo Nobel Nv Bleachable optical waveguide component
US5688896A (en) * 1994-09-26 1997-11-18 Akzo Nobel N.V. Non-linear optically active polycarbonate
WO2006102603A2 (en) * 2005-03-24 2006-09-28 Medtronic, Inc. Modification of thermoplastic polymers
CN102482504B (zh) 2009-08-24 2016-01-20 独立行政法人情报通信研究机构 二阶非线性光学化合物及含有它的非线性光学元件

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2530809C2 (de) * 1975-07-10 1983-08-11 Bayer Ag, 5090 Leverkusen Verfahren zur Herstellung von gefärbten, gegebenenfalls verschäumten Polyurethankunststoffen
US4719281A (en) * 1986-04-21 1988-01-12 Hoechst Celanese Corporation Pendant quinodimethane-containing polymer
US4757130A (en) * 1987-07-01 1988-07-12 Hoechst Celanese Corporaton Condensation polymers with pendant side chains exhibiting nonlinear optical response
US4922003A (en) * 1987-12-21 1990-05-01 Hoechst Celanese Corp. Bisacrylate monomers and polymers exhibiting nonlinear optical response
US5001209A (en) * 1988-07-04 1991-03-19 Akzo N.V. Non-linear optical active diols and polyurethanes prepared therefrom
FR2636634B1 (fr) * 1988-09-16 1992-11-27 Rhone Poulenc Chimie Polyurethannes, actifs en optique non lineaire et materiaux les contenant, dispositif optique les contenant et procedes de fabrication de ces composes et materiaux

Also Published As

Publication number Publication date
EP0363237B2 (fr) 1997-06-18
NO893694L (no) 1990-03-19
DE68911258T3 (de) 1998-01-15
DE68911258T2 (de) 1994-06-30
DE68911258D1 (de) 1994-01-20
FR2636745A1 (fr) 1990-03-23
FI894375A0 (fi) 1989-09-15
IL91645A0 (en) 1990-04-29
EP0363237A2 (fr) 1990-04-11
ZA897046B (en) 1990-06-27
EP0363237A3 (en) 1990-05-16
US5189134A (en) 1993-02-23
FI894375A (fi) 1990-03-17
DK456189D0 (da) 1989-09-15
AU4149589A (en) 1990-03-22
JPH02115827A (ja) 1990-04-27
DK456189A (da) 1990-03-17
FR2636745B1 (fr) 1990-11-09
CN1042164A (zh) 1990-05-16
JPH071361B2 (ja) 1995-01-11
PT91729A (pt) 1990-03-30
EP0363237B1 (fr) 1993-12-08
NO893694D0 (no) 1989-09-15
ATE98382T1 (de) 1993-12-15

Similar Documents

Publication Publication Date Title
KR900004807A (ko) 비선형 광학 활성 중합체, 그를 포함하는 재료, 상기 중합체 및 재료의 제조 방법 및 그를 포함하는 전기 광학 장치
Choi et al. Poly (1, 6-heptadiyne)-based materials by metathesis polymerization
Chen et al. Thermosetting polyurethanes with stable and large second-order optical nonlinearity
Catala et al. Living radical polymerization: kinetic results
KR900004793A (ko) 비선형 광학 활성 폴리 우레탄, 그를 포함하는 재료, 광학 장치 및 상기 화합물 및 재료의 제조 방법
Hoogenboom et al. Microwave‐assisted polymer synthesis: recent developments in a rapidly expanding field of research
Jullien et al. Polyurethane curing by a pulsed microwave field
Zhu et al. Synthesis and photopolymerization of hyperbranched polyurethane acrylates applied to UV curable flame retardant coatings
Chesnokov et al. Photopolymerization of poly (ethylene glycol) dimethacrylates: The influence of ionic liquids on the formulation and the properties of the resultant polymer materials
US5447662A (en) Optically non-linear polymeric coatings
EP0348220A2 (en) Optical waveguides
Broer et al. Temperature effects on the kinetics of photoinitiated polymerization of dimethacrylates
Silinski et al. Synthesis under microwaves (2.45 GHz) of polyurethane polymers—I. Model study from diisocyanate and polyethertriol prepolymers
Vakhonina et al. Synthesis and nonlinear optical properties of branched copolymers with covalently attached azochromophores
Masere et al. Optical gradient materials produced via low‐temperature isothermal frontal polymerization
Chodák et al. Effect of the type of radical initiator on crosslinking of polypropylene
Viner et al. Effects of thiols, lithium chloride, and ethoxylated monomers on the frontal polymerization of a triacrylate
Chen et al. Facile synthesis of poly (hydroxyethyl acrylate) by frontal free‐radical polymerization
Mukherjee et al. Radiation‐Induced graft copolymerization of methacrylic acid onto polypropylene fibers. IV. Thermal behavior
CA1341183C (en) Nonlinear optical medium with a stable noncentrosymmetric polymeric structure
Binici et al. Spherically propagating thermal polymerization fronts
Nizam El‐Din et al. Chelating polymer granules prepared by radiation‐induced homopolymerization. I—Kinetic study of radiation polymerization process
Thompson et al. Electron beam effects on polymers: Structure–property behavior of radiation‐cured bis‐GMA
Jovanovic et al. Comparison of the kinetics of conventional and microwave methyl methacrylate polymerization
US5053168A (en) Nonlinear optical medium with a stable noncentrosymmetric polymeric structure

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E601 Decision to refuse application