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JPS56152830A - High-molecular liquid crystal - Google Patents

High-molecular liquid crystal

Info

Publication number
JPS56152830A
JPS56152830A JP5696880A JP5696880A JPS56152830A JP S56152830 A JPS56152830 A JP S56152830A JP 5696880 A JP5696880 A JP 5696880A JP 5696880 A JP5696880 A JP 5696880A JP S56152830 A JPS56152830 A JP S56152830A
Authority
JP
Japan
Prior art keywords
molecular
liquid crystal
molecular liquid
alkanediol
molded
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP5696880A
Other languages
Japanese (ja)
Other versions
JPS6251292B2 (en
Inventor
Masatami Takeda
Kazuyoshi Iimura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Soda Co Ltd
Original Assignee
Nippon Soda Co Ltd
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
Application filed by Nippon Soda Co Ltd filed Critical Nippon Soda Co Ltd
Priority to JP5696880A priority Critical patent/JPS56152830A/en
Publication of JPS56152830A publication Critical patent/JPS56152830A/en
Publication of JPS6251292B2 publication Critical patent/JPS6251292B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Liquid Crystal Substances (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

PURPOSE: To produce a high-molecular substance having a polyurethane bond, which can be molded and processed into film, fiber, etc. and yet shows a liquid crystal behavior, by the polymerization reaction of o-toluidine isocyanate and an α,ω-alkanediol.
CONSTITUTION: o-Toluidine isocyanate is dissolved in a solvent, such as purified anisole. To this solution is added an α,ω-alkanediol of formula I (n≥5), e.g., 1,6-hexanediol or 1,12-dodecanediol, and the mixture is reacted with heating. The resultant is then cooled, and a diluting solvent, such as acetone, is added so as to separate the reaction product in the form of a solid, which is collected by separation from the liquid phase. Subsequently, the product is further purified by reprecipitation or other means to give the object high-molecular liquid crystals with their main chain structure composed of repeating units of formula II. The resulting high- molecular liquid crystals can readily be molded and processed into film, fiber, etc. and have the possibility for extensive application in the field of electronics, etc.
COPYRIGHT: (C)1981,JPO&Japio
JP5696880A 1980-04-28 1980-04-28 High-molecular liquid crystal Granted JPS56152830A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5696880A JPS56152830A (en) 1980-04-28 1980-04-28 High-molecular liquid crystal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5696880A JPS56152830A (en) 1980-04-28 1980-04-28 High-molecular liquid crystal

Publications (2)

Publication Number Publication Date
JPS56152830A true JPS56152830A (en) 1981-11-26
JPS6251292B2 JPS6251292B2 (en) 1987-10-29

Family

ID=13042316

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5696880A Granted JPS56152830A (en) 1980-04-28 1980-04-28 High-molecular liquid crystal

Country Status (1)

Country Link
JP (1) JPS56152830A (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4745137A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from solutions or dispersions of polymers of rigid polyaromatic monomers in polyols
US4745136A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from dispersions or solutions of cholesterol or cholestanol-containing polymers in a polyol
US4745135A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from liquid crystal-containing polyols
US4798849A (en) * 1986-06-25 1989-01-17 The Dow Chemical Company Organic polymers containing dispersed liquid crystalline filler polymers
US4861803A (en) * 1986-06-25 1989-08-29 The Dow Chemical Company Organic polymers reinforced with rigid rod micro fillers
US4962163A (en) * 1989-01-17 1990-10-09 The Dow Chemical Company Vinyl ester resins containing mesogenic/rigid rodlike moieties
US5024785A (en) * 1989-01-17 1991-06-18 The Dow Chemical Company Liquid crystal/rigid rodlike polymer modified epoxy/vinyl ester resins
US5164464A (en) * 1989-01-17 1992-11-17 The Dow Chemical Company Vinyl ester resins containing mesogenic/rigid rodlike moieties
US5262509A (en) * 1990-08-03 1993-11-16 The Dow Chemical Company Mesogenic glycidyl amines
US5276184A (en) * 1990-08-03 1994-01-04 The Dow Chemical Company Sulfonamide compounds containing mesogenic moieties
US5296570A (en) * 1990-08-03 1994-03-22 The Dow Chemical Company Curable mixtures of mesogenic epoxy resins and mesogenic polyamines and cured compositions
US5360884A (en) * 1990-08-03 1994-11-01 The Dow Chemical Company Mesogenic glycidyl amine blends
US5362822A (en) * 1990-08-03 1994-11-08 The Dow Chemical Company Mesogenic adducts
US5391651A (en) * 1990-08-03 1995-02-21 The Dow Chemical Company Curable mixtures of mesogenic epoxy resins and mesogenic polyamines and cured compositions
US5414125A (en) * 1990-08-03 1995-05-09 The Dow Chemical Company Diamino-alpha-alkylstilbenes

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4745137A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from solutions or dispersions of polymers of rigid polyaromatic monomers in polyols
US4745136A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from dispersions or solutions of cholesterol or cholestanol-containing polymers in a polyol
US4745135A (en) * 1986-06-25 1988-05-17 The Dow Chemical Company Polyurethanes prepared from liquid crystal-containing polyols
US4798849A (en) * 1986-06-25 1989-01-17 The Dow Chemical Company Organic polymers containing dispersed liquid crystalline filler polymers
US4861803A (en) * 1986-06-25 1989-08-29 The Dow Chemical Company Organic polymers reinforced with rigid rod micro fillers
US4962163A (en) * 1989-01-17 1990-10-09 The Dow Chemical Company Vinyl ester resins containing mesogenic/rigid rodlike moieties
US5024785A (en) * 1989-01-17 1991-06-18 The Dow Chemical Company Liquid crystal/rigid rodlike polymer modified epoxy/vinyl ester resins
US5164464A (en) * 1989-01-17 1992-11-17 The Dow Chemical Company Vinyl ester resins containing mesogenic/rigid rodlike moieties
US5262509A (en) * 1990-08-03 1993-11-16 The Dow Chemical Company Mesogenic glycidyl amines
US5276184A (en) * 1990-08-03 1994-01-04 The Dow Chemical Company Sulfonamide compounds containing mesogenic moieties
US5296570A (en) * 1990-08-03 1994-03-22 The Dow Chemical Company Curable mixtures of mesogenic epoxy resins and mesogenic polyamines and cured compositions
US5360884A (en) * 1990-08-03 1994-11-01 The Dow Chemical Company Mesogenic glycidyl amine blends
US5362822A (en) * 1990-08-03 1994-11-08 The Dow Chemical Company Mesogenic adducts
US5391651A (en) * 1990-08-03 1995-02-21 The Dow Chemical Company Curable mixtures of mesogenic epoxy resins and mesogenic polyamines and cured compositions
US5414125A (en) * 1990-08-03 1995-05-09 The Dow Chemical Company Diamino-alpha-alkylstilbenes
US5602211A (en) * 1990-08-03 1997-02-11 The Dow Chemical Company Adducts of epoxy resins and active hydrogen containing compounds containing mesogenic moieties

Also Published As

Publication number Publication date
JPS6251292B2 (en) 1987-10-29

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