WO2019039493A1 - 新規重合体及びジアミン化合物 - Google Patents
新規重合体及びジアミン化合物 Download PDFInfo
- Publication number
- WO2019039493A1 WO2019039493A1 PCT/JP2018/030918 JP2018030918W WO2019039493A1 WO 2019039493 A1 WO2019039493 A1 WO 2019039493A1 JP 2018030918 W JP2018030918 W JP 2018030918W WO 2019039493 A1 WO2019039493 A1 WO 2019039493A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- reaction
- mmol
- added
- acid
- Prior art date
Links
- 0 Cc1ccc(*)cc1 Chemical compound Cc1ccc(*)cc1 0.000 description 4
- YMKCHVDAAZJDTM-UHFFFAOYSA-N CC(CC1)CCN1c1ccc(C)cc1 Chemical compound CC(CC1)CCN1c1ccc(C)cc1 YMKCHVDAAZJDTM-UHFFFAOYSA-N 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Cc1ccc(C)cc1 Chemical compound Cc1ccc(C)cc1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- QABPCLAGAWPETB-UHFFFAOYSA-N CC(C(C1(C)C(N2c(cc3)ccc3OCOc(cc3)ccc3N)=O)C(N3c(cc4)ccc4O)=O)(C1C2=O)C3=O Chemical compound CC(C(C1(C)C(N2c(cc3)ccc3OCOc(cc3)ccc3N)=O)C(N3c(cc4)ccc4O)=O)(C1C2=O)C3=O QABPCLAGAWPETB-UHFFFAOYSA-N 0.000 description 1
- LBCZLAVMELJZIY-UHFFFAOYSA-N CC(C(C1(C)C(O2)=O)C(O3)=O)(C1C2=O)C3=O Chemical compound CC(C(C1(C)C(O2)=O)C(O3)=O)(C1C2=O)C3=O LBCZLAVMELJZIY-UHFFFAOYSA-N 0.000 description 1
- YVYDFSIJDLHFCR-UHFFFAOYSA-N CC(C)(C)OC(Nc(cc1)ccc1OCOc(cc1)ccc1N(C(C(C1(C)C(N2Cc3cc(OCOc(cc4)ccc4NC(OC(C)(C)C)=O)ccc3)=O)C3(C)C1C2=O)=O)C3=O)=O Chemical compound CC(C)(C)OC(Nc(cc1)ccc1OCOc(cc1)ccc1N(C(C(C1(C)C(N2Cc3cc(OCOc(cc4)ccc4NC(OC(C)(C)C)=O)ccc3)=O)C3(C)C1C2=O)=O)C3=O)=O YVYDFSIJDLHFCR-UHFFFAOYSA-N 0.000 description 1
- RICSNUYFOZZWNN-UHFFFAOYSA-N CC(C)(C)OC(Nc(cc1)ccc1OCOc(cc1)ccc1N)=O Chemical compound CC(C)(C)OC(Nc(cc1)ccc1OCOc(cc1)ccc1N)=O RICSNUYFOZZWNN-UHFFFAOYSA-N 0.000 description 1
- TVSMLBGFGKLKOO-UHFFFAOYSA-N CC1CCN(C)CC1 Chemical compound CC1CCN(C)CC1 TVSMLBGFGKLKOO-UHFFFAOYSA-N 0.000 description 1
- SXAUQPOPQIFGMU-UHFFFAOYSA-N CCCN(CCNC)c1ccc(C)cc1 Chemical compound CCCN(CCNC)c1ccc(C)cc1 SXAUQPOPQIFGMU-UHFFFAOYSA-N 0.000 description 1
- GYBMIIMARPGPOJ-UHFFFAOYSA-N Cc(cc1)ccc1N1CCN(C)CC1 Chemical compound Cc(cc1)ccc1N1CCN(C)CC1 GYBMIIMARPGPOJ-UHFFFAOYSA-N 0.000 description 1
- ZRZCNDIPIZYLSC-UHFFFAOYSA-N Nc(cc1)ccc1OCOc(cc1)ccc1N Chemical compound Nc(cc1)ccc1OCOc(cc1)ccc1N ZRZCNDIPIZYLSC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
Definitions
- the present invention relates to a novel diamine compound (in the present invention, also simply referred to as "diamine") useful as a raw material of a polymer used for a liquid crystal alignment film, and a polymer obtained using the diamine. More specifically, the present invention relates to, for example, a polyimide suitable for electronic materials and a diamine compound which is a raw material monomer thereof.
- polyimide resins are widely used as electronic materials such as protective materials, insulation materials, and color filters in liquid crystal display devices and semiconductors because of their high mechanical strength, heat resistance, insulation properties, and solvent resistance. It is used. Further, recently, applications as materials for optical communication such as materials for optical waveguides are also expected.
- polyimides in particular all aromatic polyimide resins
- PMDA acid anhydride
- ODA 4,4'-dioxyaniline
- polyamic acid because it has poor solubility and can not be used as a solution. It is obtained by heating and dehydration reaction via a precursor.
- amide-based or lactone-based organic solvents such as N-methyl-2-pyrrolidone (NMP) and ⁇ -butyrolactone having high solubility that have been widely used conventionally have high boiling points Therefore, high temperature baking was inevitable to remove the solvent.
- the present invention can easily impart various properties which can not be obtained unless the polymer of the polyamic acid obtained from the diamine and the acid dianhydride is imidized by using an inexpensive and highly available commercial raw material. It is an object of the present invention to provide a process for producing a highly soluble diamine and the resulting diamine, as well as a novel polymer obtainable therefrom.
- the inventors of the present invention conducted intensive studies to solve the above problems, and as a result, using existing diamine compounds having linear or branched alkylene groups and commercially available compounds that are inexpensive and highly available as raw materials, The inventors have found a method for producing a polymer capable of easily imparting various properties which can not be obtained unless the polymer of a polyamic acid obtained from a diamine and an acid dianhydride is imidized, and completed the invention.
- the present invention is based on such findings and has the following gist.
- R 1 , R 2 , R 3 and R 4 each independently represent H, CH 3 or CF 3 , provided that one of R 1 , R 2 , R 3 and R 4 is always CH 3 or CF 4
- W 1 represents a single bond or phenylene
- phenylene is a halogen group, a linear or branched alkyl group having 1 to 10 carbon atoms, a linear or branched alkoxy group having 1 to 10 carbon atoms, a hydroxyl group, A cyano group, a dialkylamino group (the alkyl group is each independently a linear or branched alkyl group having 1 to 10 carbon atoms), a linear or branched ester group having 1 to 10 carbon atoms, the carbon number It may be substituted by a substituent selected from the first group consisting of 1 to 10 linear or branched acyl group, carboxyl group, aldehyde group, nitro group, Boc protected amino group, and two W 1
- the present invention relates to a diamine compound represented by the formula (1) (hereinafter sometimes referred to as a specific diamine), and a polymer obtained from the diamine compound.
- the liquid crystal aligning agent of the present invention is a liquid crystal aligning agent containing a polymer obtained from a diamine having a structure represented by the above formula (1) (hereinafter, also referred to as a specific polymer). Each condition will be described in detail below.
- R 1 , R 2 , R 3 and R 4 each independently represent H, CH 3 or CF 3 , provided that one of R 1 , R 2 , R 3 and R 4 is always CH 3 or CF 3
- W 1 represents a single bond or phenylene
- phenylene is a halogen group, a linear or branched alkyl group having 1 to 10 carbon atoms, a linear or branched alkoxy group having 1 to 10 carbon atoms, a hydroxyl group, A cyano group, a dialkylamino group (the alkyl group is each independently a linear or branched alkyl group having 1 to 10 carbon atoms), a linear or branched ester group having 1 to 10 carbon atoms, the carbon number It may be substituted by a substituent selected from the first group consisting of 1 to 10 linear or branched acyl group, carboxyl group, aldehyde group, nitro group, Boc protected amino group, and two W 1 are They may be identical to or
- R 1 , R 2 , R 3 and R 4 each independently represent H, CH 3 or CF 3 , provided that one of R 1 , R 2 , R 3 and R 4 is always CH 3 or CF 3
- R 1 and R 4 represents CH 3 or CF 3
- R 2 and R 3 represents a hydrogen atom
- R 1 and R 4 represent a methyl group
- R 2 and R What 3 represents a hydrogen atom is preferable from the point that solubility is high.
- W 1 a single bond or a 1,4-phenylene group is preferable.
- W 2 a 1,4-phenylene group is preferable.
- the alkylene having 1 to 10 carbon atoms of L may be linear or branched, and is a linear alkylene represented by-(CH 2 ) n- (wherein n is 1 to 10). Or 1-methylmethane-1,1-diyl, 1-ethylmethane-1,1-diyl, 1-propylmethane-1,1-diyl, 1-methylethane-1,2-diyl, 1-ethylethane-1, 2-diyl, 1-propylethane-1,2-diyl, 1-methylpropane-1,3-diyl, 1-ethylpropane-1,3-diyl, 1-propylpropane-1,3-diyl, 2- Methylpropane-1,3-diyl, 2-ethylpropane-1,3-diyl, 2-propylpropane-1,3-diyl, 1-methylbutane-1,4-diyl, 1-e
- groups selected from the second group may be adjacent to each other under the condition that the same atoms do not bond except carbon atoms.
- the bond between the groups selected from the second group is bonded at the same atom excluding carbon atoms, In such a case, the groups selected from the second group can not be adjacent to each other.
- the bond between the groups selected from the second group is a carbon atom or bonds with mutually different atoms, then the groups selected from the second group can bond. .
- the bond between groups selected from the second group is a carbon atom
- groups selected from the second group can be bonded.
- the groups selected from the second group are not adjacent to each other.
- Preferred structures of W 1 -L-W 2 include, but are not limited to, the following structures.
- R 1 , R 2 , R 3 , R 4 , W 1 , W 2 and L have the above meanings, and Q represents NO 2 or a protected amino group (NHPro).
- a protecting group (Pro) for an amino group acetyl group, trifluoroacetyl group, pivaloyl group, tert-butoxycarbonyl group, ethoxycarbonyl group, isopropoxycarbonyl group, 2,2,2-trichloroethoxycarbonyl group, benzyloxy Carbonyl, trimethylsilyl, triethylsilyl, dimethylphenylsilyl, tert-butyldimethylsilyl, tert-butyldiethylsilyl, 9-fluorenylmethyloxycarbonyl, phthaloyl, allyloxycarbonyl, p-toluene
- a sulfonyl group, o-nitrobenzene sulfonyl group etc. can be used, limitation is not carried out to these.
- the amount of the compound represented by the formula (B) to be used is preferably 2 to 4 moles, more preferably 2 to 2.5 moles, relative to 1 mole of the compound represented by the formula (A) Is more preferred.
- the reaction is preferably carried out in a solvent.
- the solvent can be used without limitation as long as it does not react with each raw material.
- aprotic polar organic solvents such as DMF, DMSO, DMAc, NMP; Et 2 O, i-Pr 2 O, THF (tetrahydrofuran), TBME (tert-butyl methyl ether), CPME (cyclopentyl methyl ether), dioxane
- Aliphatic hydrocarbons such as pentane, hexane, heptane and petroleum ether; aromatic hydrocarbons such as benzene, toluene, xylene, mesitylene, chlorobenzene, dichlorobenzene, nitrobenzene and tetralin; chloroform, dichloromethane, etc.
- Halogenated hydrocarbons such as carbon tetrachloride and dichloroethane; lower fatty acid esters such as methyl acetate, ethyl acetate, butyl acetate and methyl propionate; nitriles such as acetonitrile, propionitrile and butyronitrile And so on.
- solvents can be appropriately selected in consideration of the easiness of reaction and the like, and can be used singly or in combination of two or more. If necessary, the solvent can be dried using a suitable dehydrating agent or desiccant and used as a non-aqueous solvent.
- the amount of the solvent used is not particularly limited, but is 0.1 to 100 times by mass that of the bismaleimide compound.
- the amount is preferably 0.5 to 30 times by mass, more preferably 1 to 10 times by mass.
- the reaction temperature is not particularly limited, but is in the range of -100 ° C to the boiling point of the solvent used, preferably -50 to 150 ° C.
- the reaction time is generally 0.05 to 350 hours, preferably 0.5 to 100 hours.
- inorganic bases such as sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium hydrogencarbonate, potassium hydrogencarbonate, potassium phosphate, sodium carbonate, potassium carbonate, lithium carbonate, cesium carbonate and the like;
- tert-butoxy Bases such as sodium, tert-butoxy potassium, sodium hydride and potassium hydride;
- amines such as trimethylamine, triethylamine, tripropylamine, triisopropylamine, tributylamine, tributylamine, diisopropylethylamine, pyridine, quinoline and collidine can be used.
- triethylamine, pyridine, tert-butoxy sodium, tert-butoxy potassium, sodium hydride, potassium hydride and the like are preferable.
- the amount of the base used is not particularly limited, but is 0.1 to 100 times by mass that of the bismaleimide compound.
- the amount is preferably 0 to 30 times by mass, more preferably 0 to 10 times by mass.
- the compound represented by Formula (D) can be obtained by imidating the compound represented by Formula (C).
- imidization chemical imidization in which a catalyst is added to a solution of a compound represented by the formula (C) obtained by the reaction of an amine component and a bismaleimide compound is convenient.
- Chemical imidization is preferable because the imidization reaction proceeds at a relatively low temperature and decomposition of the Pro group hardly occurs in the imidization process.
- Chemical imidization can be carried out by stirring a compound to be imidized in an organic solvent in the presence of a basic catalyst and an acid anhydride.
- the organic solvent used for this reaction is preferably N, N-dimethylformamide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone or the like from the viewpoint of solubility, and one or more of these may be mixed and used.
- the concentration of the compound is preferably 1 to 30% by mass, and more preferably 5 to 20% by mass, from the viewpoint that precipitation of the compound hardly occurs.
- Examples of basic catalysts include pyridine, triethylamine, trimethylamine, tributylamine and trioctylamine. Among them, pyridine is preferable because it has a suitable basicity to allow the reaction to proceed. Further, as the acid anhydride, acetic anhydride, trimellitic anhydride, pyromellitic anhydride and the like can be mentioned, and it is preferable to use acetic anhydride among them because purification after completion of the reaction becomes easy.
- the temperature at which the imidization reaction is carried out is -20 to 140 ° C, preferably 0 to 100 ° C, and the reaction time can be 1 to 100 hours.
- the amount of the basic catalyst is 0.5 to 30 times mol, preferably 2 to 20 times the mol of the amic acid group, and the amount of acid anhydride is 1 to 50 times mol, preferably 3 to 30 times the mol of the amic acid group. It is a mole.
- the catalyst used for the reduction reaction is preferably a commercially available activated carbon-supported metal, and examples thereof include palladium-activated carbon, platinum-activated carbon, and rhodium-activated carbon.
- palladium hydroxide, platinum oxide, Raney nickel, etc. may not necessarily be a metal catalyst of the activated carbon support type.
- palladium-activated carbon is preferred because good results can be obtained.
- These reactions are carried out under hydrogen atmosphere, at normal pressure or under pressure.
- metals such as iron, tin and zinc or metal salts thereof may be used together with a proton source to carry out reduction of the nitro group.
- the metal and the metal salt may be used alone or in combination of two or more.
- acids such as hydrochloric acid, ammonium salts such as ammonium chloride, and protic solvents such as methanol and ethanol can be used.
- reaction may be carried out in the presence of activated carbon.
- the amount of activated carbon to be used is not particularly limited, but it is preferably in the range of 1 to 30% by mass, more preferably 10 to 20% by mass with respect to the dinitro compound (D).
- reaction may be implemented under pressure. In this case, in order to avoid the reduction of the benzene nucleus, it is performed at a pressure range up to 20 atm. The reaction is preferably carried out in the range up to 10 atmospheres.
- the solvent can be used without limitation as long as it does not react with each raw material.
- aprotic polar organic solvents such as DMF, DMSO, DMAc, NMP; Et 2 O, i-Pr 2 O, TBME, CPME, CPME, THF, ethers such as dioxane; pentane, hexane, heptane, petroleum ether, etc.
- Aliphatic hydrocarbons such as benzene, toluene, xylene, mesitylene, chlorobenzene, dichlorobenzene, nitrobenzene and tetralin; Halogenated hydrocarbons such as chloroform, dichloromethane, carbon tetrachloride and dichloroethane; Methyl acetate And lower fatty acid esters such as ethyl acetate, butyl acetate and methyl propionate; nitriles such as acetonitrile, propionitrile and butyronitrile; alcohols such as methanol and ethanol; These solvents can be appropriately selected in consideration of the easiness of reaction and the like, and can be used singly or in combination of two or more. If necessary, the solvent can be dried using a suitable dehydrating agent or desiccant and used as a non-aqueous solvent.
- the amount of the solvent used is not particularly limited, but is 0.1 to 100 times by mass that of the dinitro compound.
- the amount is preferably 0.5 to 30 times by mass, more preferably 1 to 10 times by mass.
- the reaction temperature is not particularly limited, but is in the range of -100 ° C to the boiling point of the solvent used, preferably -50 to 150 ° C.
- the reaction time is generally 0.05 to 350 hours, preferably 0.5 to 100 hours.
- the method for deprotecting the protective group is not particularly limited, but it is possible to obtain the desired product by neutralization after hydrolysis in the presence of an acid or a base.
- the acid to be used include inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid and hydrobromic acid, and organic acids such as formic acid, acetic acid, oxalic acid and trifluoroacetic acid
- bases to be used include hydroxide Inorganic bases such as sodium, sodium hydrogencarbonate, potassium hydrogencarbonate, potassium phosphate, sodium carbonate, potassium carbonate, lithium carbonate, cesium carbonate etc., trimethylamine, triethylamine, tripropylamine, triisopropylamine, tributylamine, tributylamine, diisopropylethylamine, pyridine, quinoline And organic amines such as collidine may be used.
- deprotection may be performed using aluminum chloride or a Lewis acid compound such as trifluoroborane-diethyl ether complex.
- debenzylation reaction may be performed under a hydrogen atmosphere.
- a fluorine-containing acid such as hydrofluoric acid, cesium fluoride, potassium fluoride, tetrabutylammonium fluoride or the like, an inorganic base, an ammonium salt or the like may be used.
- any solvent which does not interfere with hydrolysis can be used, and aprotic polar organic solvents such as DMF, DMSO, DMAc, NMP, Et 2 O, i-Pr 2 O, TBME, CPME, THF , Ethers such as dioxane, aliphatic hydrocarbons such as pentane, hexane, heptane, petroleum ether, benzene, toluene, xylene, mesitylene, chlorobenzene, dichlorobenzene, nitrobenzene, tetralin, aromatic hydrocarbons such as tetralin, chloroform, dichloromethane , Halogenated hydrocarbons such as carbon tetrachloride and dichloroethane, methyl acetate, ethyl acetate, butyl acetate, methyl propionate etc., nitriles (lower fatty acid esters such as acetonitrile,
- the above-mentioned solvent is 1
- These can be used alone or in combination of two or more, and can also be used as a non-aqueous solvent using an appropriate dehydrating agent or drying agent in consideration of the use of a Lewis acid, etc.
- the reaction temperature may be any temperature in the range of ⁇ 100 ° C. to the boiling point of the solvent used, preferably in the range of ⁇ 50 to 150 ° C.
- the reaction time can be arbitrarily selected in the range of 0.1 to 1000 hours.
- the compound (B1) in which Q is NHPro is a diamine represented by the following formula (B1-1) and an acid chloride or acid of an amine protecting group (Pro) or It is obtained by reacting with an anhydride or the like.
- the diamine (B1-1) is preferably a symmetrical diamine.
- W 1 , W 2 , L and Pro represent the above meanings.
- Examples of (Pro) 2 O include, but are not limited to, dimethyl dicarbonate, diethyl dicarbonate, di-t-butyl dicarbonate, dibenzyl dicarbonate and the like.
- the reaction for obtaining the compound represented by the above formula (B1) is preferably carried out in the presence of a base.
- a base inorganic bases such as sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium hydrogencarbonate, potassium hydrogencarbonate, potassium phosphate, sodium carbonate, potassium carbonate, lithium carbonate, cesium carbonate and the like; trimethylamine, triethylamine, tripropylamine And amines such as triisopropylamine, tributylamine, diisopropylethylamine, pyridine, quinoline and collidine; sodium hydride, potassium hydride, sodium tert-butoxy, potassium tert-butoxy and the like can be used.
- the use of amines is preferred in consideration of the operability of the post-treatment of the reaction.
- any solvent which is stable under the reaction conditions, is inert and does not interfere with the intended reaction can be used.
- aprotic polar organic solvents such as dimethylformamide, dimethylsulfoxide, dimethylacetate, N-methylpyrrolidone; diethylether, isopropylether, THF, TBME, CPME, ethers such as dioxane; pentane, hexane, heptane, petroleum ether
- Aliphatic hydrocarbons such as; aromatic hydrocarbons such as benzene, toluene, xylene, mesitylene, chlorobenzene, dichlorobenzene, nitrobenzene, tetralin; halogen based hydrocarbons such as chloroform, dichloromethane, carbon tetrachloride, dichloroethane; methyl acetate, acetic acid Lower fatty acid esters such as ethyl, butyl acetate and
- solvents can be appropriately selected in consideration of the easiness of reaction and the like, and can be used singly or in combination of two or more.
- the above-mentioned solvent can also be used as a water-free solvent using a suitable dehydrating agent or desiccant.
- the reaction temperature is preferably in the range of -100 ° C. or higher to the temperature of the boiling point of the reaction solvent used, but is more preferably -50 to 150 ° C., particularly preferably 0 to 60 ° C. .
- the reaction time is 0.1 to 1000 hours, more preferably 0.5 to 50 hours.
- the compound represented by the formula 2 obtained by the above reaction formula (1) may be purified by distillation, recrystallization, column chromatography such as silica gel, etc., but it may be used as it is in the next step without purification. Good.
- the compound (B2) in which Q is NO 2 can be obtained by deprotecting the compound represented by the following formula (B2-1).
- the conditions for deprotection the above-mentioned methods can be used.
- W 1 , W 2 , L and Pro represent the above meanings.
- the compound represented by the formula (B2-1) is a halogenated and sulfonylated compound represented by the following formula (B2-3) ⁇ methanesulfonyl (OMs), ethanesulfonyl (OEs), p-toluenesulfonyl (OTs) ), Trifluoromethanesulfonyl (OTf) and the like ⁇ and the compound is obtained by reacting with a nitrated phenol represented by the following formula (B2-4).
- W 1 and W 2 represent the above-mentioned meanings
- L 1 represents alkylene from which one CH 2 (strictly speaking, CH 2 replaced by oxygen atom) has been removed.
- the compound represented by the formula (B2-3) used as the starting material in the reaction of this step and the nitrated phenol represented by the formula (B2-4) are commercially available or are produced by known methods. You can do it.
- the reaction system may be either rotary (batch system) or flow system.
- the reaction is preferably carried out in the presence of a base.
- the base include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, alkali metal carbonates such as sodium carbonate and potassium carbonate, alkali metal bicarbonates such as sodium hydrogencarbonate and potassium hydrogencarbonate, potassium phosphate
- An organic base such as 1,8-diazabicyclo [5,4,0] -7-undecene or the like can be used at 1 to 4 equivalents relative to the compound represented by formula (B2-3).
- alkali metal carbonates such as sodium carbonate and potassium carbonate are preferable.
- finely powdered potassium carbonate it is preferable to use finely powdered potassium carbonate because the reactivity is improved.
- examples of commercially available finely powdered potassium carbonate include FG-F20 (manufactured by Asahi Glass Co., Ltd.) (registered trademark).
- the reaction solvent is preferably dimethylformamide (DMF), dimethylacetamide (DMAc), 1,3-dimethyl-2-imidazolidinone (DMI), dimethylsulfoxide (DMSO), N-methylpyrrolidone, N-methylpyrrolidone Particularly preferred.
- DMF dimethylformamide
- DMAc dimethylacetamide
- DMI 1,3-dimethyl-2-imidazolidinone
- DMSO dimethylsulfoxide
- N-methylpyrrolidone N-methylpyrrolidone
- N-methylpyrrolidone Particularly preferred.
- the reaction temperature is, for example, -10 to 100 ° C, preferably 0 to 80 ° C.
- the reaction time is 0.5 to 20 hours, preferably 1 to 15 hours in the case of batch processing.
- the reaction is preferably carried out in a solvent. Preferred solvents and reaction conditions are the same as the production conditions of the above compound (1).
- the target substance in each step obtained by each of the above reactions may be purified by distillation, recrystallization, column chromatography such as silica gel or the like, or the reaction liquid may be used as it is for the next step without purification. You can also.
- the polymer of the present invention is a polymer obtained by using the above diamine. Specific examples include polyamic acid, polyamic acid ester, polyimide, polyurea, polyamide and the like.
- ⁇ Diisocyanate component As a diisocyanate component which gives polyamide by reaction with the diamine represented by the said General formula (1), aromatic diisocyanate, aliphatic diisocyanate etc. are mentioned, for example.
- Preferred diisocyanate components are aromatic diisocyanates and aliphatic diisocyanates.
- the aliphatic diisocyanate means that the group Y of the isocyanate structure is composed of a cyclic or non-cyclic aliphatic structure.
- aromatic diisocyanate examples include o-phenylene diisocyanate, m-phenylene diisocyanate, p-phenylene diisocyanate, toluene diisocyanates (eg, tolylene 2,4-diisocyanate), and 2-methoxybenzene 1,4-diisocyanate 2,5-diisocyanate xylenes, 2,2'-bis (4-diisocyanatophenyl) propane, 4,4'-diisocyanate diphenylmethane, 4,4'-diisocyanate diphenyl ether, 4,4'-diisocyanate Examples thereof include diphenyl sulfone, diphenyl sulfone 3,3'-diisocyanate and benzophenone 2,2'-diisocyanate.
- the aromatic diisocyanate preferably includes m-phenylene diisocyanate, p-phenylene diisocyanate, and to
- aliphatic diisocyanates include isophorone diisocyanate, hexamethylene diisocyanate, tetramethylethylene diisocyanate and the like.
- the aliphatic diisocyanate preferably includes isophorone diisocyanate.
- isophorone diisocyanate and tolylene 2,4-diisocyanate are preferable from the viewpoint of polymerization reactivity, and isophorone diisocyanate is more preferable from the viewpoint of availability and polymerization reactivity.
- X 1 is a tetravalent organic group derived from a tetracarboxylic acid derivative, and its structure is not particularly limited.
- X 1 in the polyimide precursor is the solubility of the polymer in the solvent, the coatability when used as a liquid crystal aligning agent, the alignment of liquid crystal when used as a liquid crystal alignment film, voltage holding ratio, accumulated charge, etc. It may be appropriately selected according to the degree of properties required, and may be one type in the same polymer, or two or more types may be mixed.
- a monomer compound for constructing a dicarboxylic acid component giving a polyamide by reaction with a diamine represented by the above general formula (1) include terephthalic acid, isophthalic acid, 2-methyl-isophthalic acid, 4-methyl -Isophthalic acid, 5-methyl-isophthalic acid, 5-allyloxy isophthalic acid, 5-allyloxycarbonyl isophthalic acid, 5-propargyloxy isophthalic acid, 5-acetyloxy isophthalic acid, 5-benzoylamido isophthalic acid, tetrafluoro Isophthalic acid, methylterephthalic acid, tetrafluoroterephthalic acid, 2,6-naphthalenedicarboxylic acid, 1,6-naphthalenedicarboxylic acid, 2,6-anthracenedicarboxylic acid, 1,6-anthracenedicarboxylic acid, 4,4'-di Carboxybipheny
- a known synthesis method can be used. Generally, at least one selected from a diisocyanate component, a dicarboxylic acid component and a tetracarboxylic acid component is reacted with a diamine component in an organic solvent.
- the reaction of the diamine component with at least one selected from the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component is advantageous in that it proceeds relatively easily in the organic solvent and no by-products are generated.
- the organic solvent used for the reaction of the diamine component with at least one selected from the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component is not particularly limited as long as the produced polymer can be dissolved.
- the example is given below.
- Organic solvents which can be used here include N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, N-methylcaprolactam, dimethyl sulfoxide, tetramethyl Urea, pyridine, dimethyl sulfone, ⁇ -butyrolactone, isopropyl alcohol, methoxymethyl pentanol, dipentene, ethyl amyl ketone, methyl nonyl ketone, methyl ethyl ketone, methyl isoamyl ketone, methyl isopropyl ketone, methyl cellosolve, ethyl cellosolve, methyl cellosolve acetate , Ethyl cellosolve acetate, butyl carbitol, ethyl carbitol, ethylene glycol, ethylene glycol monoacetate, ethylene glycol monoiso
- the organic solvent which has been dehydrated and dried as much as possible.
- the Of the method may be used.
- at least one selected from the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component or the diamine component is composed of a plurality of compounds, they may be reacted in a mixed state in advance, or may be reacted individually one after another Further, low molecular weight products individually reacted may be mixed and reacted to form a high molecular weight product.
- the polymerization temperature in this case can be selected from any temperature from -20 ° C to 150 ° C, preferably from -5 ° C to 100 ° C.
- the reaction can be carried out at any concentration, but if the concentration is too low, it will be difficult to obtain a polymer of high molecular weight, if the concentration is too high the viscosity of the reaction solution will be too high and uniform stirring will be difficult
- the total concentration in the reaction solution of at least one selected from the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component and the diamine component is preferably 1 to 50% by mass, more preferably 5 to 30% by mass. is there.
- the initial stage of the reaction is carried out at a high concentration, and then an organic solvent can be added.
- the ratio of the total number of moles of at least one selected from the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component to the total number of moles of the diamine component is 0.8 to 1.2. Is preferred. Similar to a normal polycondensation reaction, the molecular weight of the produced polymer increases as the molar ratio approaches 1.0.
- the reaction solution may be introduced into a poor solvent and precipitated.
- the poor solvent used for precipitation include methanol, acetone, hexane, butyl cellosolve, heptane, methyl ethyl ketone, methyl isobutyl ketone, ethanol, toluene, benzene, water and the like.
- the polymer precipitated by being put into a poor solvent and precipitated can be collected by filtration and then dried by heating at normal temperature or under normal pressure or reduced pressure.
- impurities in the polymer can be reduced.
- a poor solvent for example, alcohols, ketones, hydrocarbons and the like can be mentioned, and it is preferable to use three or more poor solvents selected from these, because the efficiency of purification is further enhanced.
- polyurea is, for example, a polymer having a repeating unit represented by the following formula [1].
- a 1 is a divalent organic group
- a 2 is a divalent group represented by the following formula (A 2 )
- R 1 , R 2 , R 3 , R 4 , W 1 , W 2 and L each have the above-mentioned meanings, and C 1 and C 2 each represent a hydrogen atom or an alkyl group having 1 to 3 carbon atoms And may be the same or different.
- a 1 and A 2 may be polymers of one type and having the same repeating unit, or polymers of A 1 and A 2 having plural types of repeating units having different structures. May be.
- a 1 is a group derived from a diisocyanate component as a raw material.
- a 2 is a group derived from a diamine component as a raw material.
- a group derived from the preferred diisocyanate components listed above is preferable as A 1.
- the polyimide precursor is, for example, a polymer having a repeating unit represented by the following formula [2].
- each A 3 is independently a tetravalent organic group
- a 2 is a divalent group represented by the above Formula (A 2 ).
- R 11 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms
- C 1 to C 2 each independently represent a hydrogen atom, or an alkyl group having 1 to 10 carbon atoms which may have a substituent
- It is an alkenyl group having 2 to 10 carbon atoms or an alkynyl group having 2 to 10 carbon atoms.
- R 11 Specific examples of the above alkyl group in R 11 include methyl group, ethyl group, propyl group, i-propyl group, n-butyl group, i-butyl group, s-butyl group, t-butyl group, n-pentyl group Etc. From the viewpoint of ease of imidation by heating, R 11 is preferably a hydrogen atom or a methyl group.
- the polyamide is, for example, a polymer having a repeating unit represented by the following formula [3].
- a 4 is a divalent organic group each independently derived from a dicarboxylic acid, and A 2 , C 1 and C 2 are as described above.
- two or three of the diisocyanate component, the dicarboxylic acid component and the tetracarboxylic acid component may be reacted simultaneously or sequentially.
- the diisocyanate component and the tetracarboxylic acid When the component is reacted, polyureapolyamic acid which is a polymer having the repeating unit represented by the above formula [1] and the repeating unit represented by the above formula [2] is obtained.
- the polyamic acid which is a polyimide precursor used for this invention can be synthesize
- the organic solvent used for the above reaction is preferably N, N-dimethylformamide, N-methyl-2-pyrrolidone, ⁇ -butyrolactone, etc. in view of solubility of monomers and polymers, and one or more of these may be mixed You may use it.
- the concentration of the polymer is preferably 1 to 30% by mass, and more preferably 5 to 20% by mass, from the viewpoint that precipitation of the polymer hardly occurs and a polymer can be easily obtained.
- the polyamic acid obtained as described above can be recovered by precipitating a polymer by pouring the reaction solution into a poor solvent while well stirring it. Further, precipitation is carried out several times, and after washing with a poor solvent, it is possible to obtain a purified polyamic acid powder by normal temperature or heat drying.
- the poor solvent is not particularly limited, and water, methanol, ethanol, 2-propanol, hexane, butyl cellosolve, acetone, toluene and the like can be mentioned, and water, methanol, ethanol, 2-propanol and the like are preferable.
- the polyimide used in the present invention can be produced by imidizing the polyamic acid.
- chemical imidization which adds a catalyst to the solution of the said polyamic acid obtained by reaction of a diamine component and tetracarboxylic dianhydride is simple.
- Chemical imidization is preferable because the imidization reaction proceeds at a relatively low temperature, and molecular weight reduction of the polymer does not easily occur in the imidization process.
- Chemical imidization can be carried out by stirring a polymer to be imidized in an organic solvent in the presence of a basic catalyst and an acid anhydride.
- a basic catalyst include pyridine, triethylamine, trimethylamine, tributylamine and trioctylamine.
- pyridine is preferable because it has a suitable basicity to allow the reaction to proceed.
- acid anhydride acetic anhydride, trimellitic anhydride, pyromellitic anhydride and the like can be mentioned, and it is preferable to use acetic anhydride among them because purification after completion of the reaction becomes easy.
- the temperature at which the imidization reaction is carried out is -20 to 140 ° C, preferably 0 to 100 ° C, and the reaction time can be 1 to 100 hours.
- the amount of basic catalyst is 0.5 to 30 times mol, preferably 2 to 20 times mol of polyamic acid group, and the amount of acid anhydride is 1 to 50 times mol, preferably 3 to 30 times mol of polyamic acid group. It is a mole.
- the imidation ratio of the resulting polymer can be controlled by adjusting the amount of catalyst, temperature and reaction time. Since the added catalyst and the like remain in the solution after the imidization reaction of the polyamic acid, the obtained imidized polymer is recovered by the means described below, and redissolved in an organic solvent to obtain the present invention. It is preferable to use as the liquid crystal aligning agent of
- the solution of the polyimide obtained as mentioned above can precipitate a polymer by inject
- the poor solvent is not particularly limited, and methanol, 2-propanol, acetone, hexane, butyl cellosolve, heptane, methyl ethyl ketone, methyl isobutyl ketone, ethanol, toluene, benzene and the like can be mentioned, and methanol, ethanol, 2-propanol, Acetone is preferred.
- the polyamic acid ester which is a polyimide precursor to be used in the present invention can be produced by the following production method (i), (ii) or (iii).
- Polyamic acid ester can be manufactured by esterifying the polyamic acid manufactured as mentioned above. Specifically, the polyamic acid and the esterifying agent are reacted in the presence of an organic solvent at -20 ° C to 150 ° C, preferably 0 ° C to 50 ° C, for 30 minutes to 24 hours, preferably 1 to 4 hours. It can be manufactured.
- esterifying agent those which can be easily removed by purification are preferable, and N, N-dimethylformamide dimethyl acetal, N, N-dimethylformamide diethyl acetal, N, N-dimethylformamide dipropyl acetal, N, N-dimethylformamide Dineopentyl butyl acetal, N, N-dimethylformamide di-t-butyl acetal, 1-methyl-3-p-tolyltriazene, 1-ethyl-3-p-tolyltriazene, 1-propyl-3-p -Tolyltriazene, 4- (4,6-dimethoxy-1,3,5-triazin-2-yl) -4-methylmorpholinium chloride and the like.
- the addition amount of the esterifying agent is preferably 2 to 6 molar equivalents relative to 1 mole of the repeating unit of the polyamic acid.
- organic solvent for example, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone or ⁇ -butyrolactone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide or 1,3-dimethyl- And imidazolidinone.
- solvent solubility of the polyimide precursor is high, methyl ethyl ketone, cyclohexanone, cyclopentanone, 4-hydroxy-4-methyl-2-pentanone, or the following formula [D-1] to formula [D-3]
- the indicated solvents can be used.
- D 1 represents an alkyl group having 1 to 3 carbon atoms
- D 2 represents an alkyl group having 1 to 3 carbon atoms
- Formula [D-3] among, D 3 is an alkyl group having 1 to 4 carbon atoms.
- solvents may be used alone or in combination. Furthermore, even if it is a solvent which does not dissolve a polyimide precursor, it may be used by mixing with the above-mentioned solvent in the range which the generated polyimide precursor does not precipitate. Further, since water in the solvent inhibits the polymerization reaction and causes hydrolysis of the formed polyimide precursor, it is preferable to use the solvent which has been dehydrated and dried.
- the solvent used for the above reaction is preferably N, N-dimethylformamide, N-methyl-2-pyrrolidone, or ⁇ -butyrolactone in view of the solubility of the polymer, and these may be used alone or in combination of two or more. Good.
- the concentration at the time of production is preferably 1 to 30% by mass, and more preferably 5 to 20% by mass, from the viewpoint that precipitation of a polymer hardly occurs and a polymer can be easily obtained.
- Polyamic acid ester can be manufactured from tetracarboxylic acid diester dichloride and diamine. Specifically, tetracarboxylic acid diester dichloride and diamine in the presence of a base and an organic solvent at -20 ° C to 150 ° C, preferably 0 ° C to 50 ° C, for 30 minutes to 24 hours, preferably 1 to 4 hours It can be produced by reacting.
- pyridine triethylamine, 4-dimethylaminopyridine and the like can be used, but pyridine is preferable because the reaction proceeds mildly.
- the addition amount of the base is preferably 2 to 4 times the molar amount of the tetracarboxylic acid diester dichloride from the viewpoint of easy removal and high molecular weight.
- the solvent used for the above reaction is preferably N-methyl-2-pyrrolidone or ⁇ -butyrolactone in view of the solubility of monomers and polymers, and these may be used alone or in combination of two or more.
- the polymer concentration at the time of production is preferably 1 to 30% by mass, and more preferably 5 to 20% by mass from the viewpoint that precipitation of the polymer hardly occurs and a polymer can be easily obtained.
- the solvent used for producing the polyamic acid ester is preferably dehydrated as much as possible, and it is preferable to prevent mixing of the outside air in a nitrogen atmosphere.
- Polyamic acid ester can be manufactured by polycondensing tetracarboxylic acid diester and diamine. Specifically, a tetracarboxylic acid diester and a diamine in the presence of a condensing agent, a base and an organic solvent at 0 ° C. to 150 ° C., preferably 0 ° C. to 100 ° C., for 30 minutes to 24 hours, preferably 3 to 15 It can be produced by reacting for time.
- the condensing agent examples include triphenyl phosphite, dicyclohexyl carbodiimide, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride, N, N′-carbonyldiimidazole, dimethoxy-1,3,5-triadidi Nylmethylmorpholinium, O- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium tetrafluoroborate, O- (benzotriazol-1-yl) -N, N And N ′, N′-tetramethyluronium hexafluorophosphate, diphenyl (2,3-dihydro-2-thioxo-3-benzoxazolyl) phosphonate and the like can be used.
- the addition amount of the condensing agent is preferably 2 to 3 moles per mol of the tetracarboxylic acid die
- tertiary amines such as pyridine and triethylamine can be used.
- the amount of the base added is preferably 2 to 4 moles per mole of the diamine component, in terms of easy removal and high molecular weight.
- the reaction proceeds efficiently by adding a Lewis acid as an additive.
- the Lewis acid lithium halides such as lithium chloride and lithium bromide are preferable.
- the addition amount of the Lewis acid is preferably 0 to 1.0 times the molar amount with respect to the diamine component.
- the polyamic acid ester having a high molecular weight can be obtained, and therefore the production method of the above (i) or the above (ii) is particularly preferable.
- the solution of the polyamic acid ester obtained as described above can precipitate the polymer by pouring it into a poor solvent while stirring well. Precipitation is carried out several times, and after washing with a poor solvent, it is possible to obtain a purified polyamic acid ester powder at room temperature or by heating and drying.
- the poor solvent is not particularly limited, and water, methanol, ethanol, hexane, butyl cellosolve, acetone, toluene and the like can be mentioned.
- the diamine represented by the formula (1) may be used as the diamine in the above production method. Moreover, in that case, things other than what is represented by Formula (1) as diamine can also be used. If a specific example is given by daringly, the diamine which two amino groups couple
- the polymer of the present invention obtained in this manner can be used as a paint, and can also be used for applications such as an insulating film, a film substrate, a liquid crystal alignment film, a protective film, and the like.
- DA-1 to DA-8 and DA-10 to DA-15 are novel compounds which have not been published in the literature or the like, and their synthesis methods will be described in detail in the following synthesis examples 1 to 14.
- DA-9 was synthesized by the synthesis method described in the patent document (WO 2017-057854).
- FT-NMR Fourier transform type superconducting nuclear magnetic resonance apparatus
- INOVA-400 manufactured by Varian 400 MHz.
- Solvent deuterated chloroform (CDCl 3 ) or deuterated N, N-dimethyl sulfoxide ([D 6 ] -DMSO).
- Reference material tetramethylsilane (TMS).
- [DA-3-1] (48.0 g, 120 mmol) and NMP (480 g) were added to a 3 L four-necked flask, and 1,3-DMCBDA (13.4 g, 60 mmol) was added in a water bath, then at room temperature. Stir for 6 h. Subsequently, pyridine (28.4 g, 360 mmol) and acetic anhydride (18.4 g, 180 mmol) were added to the reaction solution, and the mixture was stirred at 60 ° C. After completion of the reaction, the reaction system was poured into pure water (3 L), and the precipitate was separated by filtration. To the resulting crude product was added MeOH (400 ml), and repulped at room temperature to obtain 42.5 g of [DA-3-2].
- [DA-4-2] (84.3 g, 226 mmol), 6 N aqueous hydrochloric acid solution (200 g) and ethyl acetate (600 g) were charged into a 2 L four-necked flask, and the mixture was stirred at 60 ° C. After completion of the reaction, the reaction system was poured into pure water (1.2 L) and neutralized with 1N aqueous sodium hydroxide solution. The aqueous layer was removed and the organic layer was washed with pure water (2 L). The washed organic layer was dried over anhydrous magnesium sulfate, dried over anhydrous magnesium sulfate, and filtered. The solvent of the obtained filtrate was distilled off with a rotary evaporator to obtain 60.8 g of [DA-4-3].
- [DA-4-3] (60.8 g, 235 mmol) and NMP (600 g) were added to a 2 L four-necked flask, and 1,3-DMCBDA (24.8 g, 111 mmol) was added in a water bath, then at room temperature Stir for 6 h. Subsequently, pyridine (55.8 g, 705 mmol) and acetic anhydride (35.9 g, 352 mmol) were added to the reaction solution, and the mixture was stirred at 60 ° C. After completion of the reaction, the reaction system was poured into pure water (3 L), and the precipitate was separated by filtration. EtOH (1000 g) was added to the obtained crude product, and repulped at room temperature to obtain 79.1 g of [DA-4-4].
- [DA-4-2] (80.6 g, 216 mmol), THF (300 g) and EtOH (100 g) are charged into a 1 L four-necked flask, and after replacing with nitrogen, 5 wt% Pd / C (8.0 g) is added. It was replaced with hydrogen and stirred at room temperature. After completion of the reaction, the reaction solution was filtered through a 0.45 ⁇ m membrane filter to remove Pd / C. The solvent of the obtained filtrate was distilled off with a rotary evaporator to obtain 73.9 g of [DA-5-1].
- [DA-5-1] (73.9 g, 225 mmol) and NMP (700 g) were added to a 2 L four-necked flask, and 1,3-DMCBDA (23.7 g, 106 mmol) was added in a water bath, then at room temperature Stir for 6 h. Subsequently, pyridine (53.4 g, 675 mmol) and acetic anhydride (34.5 g, 338 mol) were added to the reaction solution, and the mixture was stirred at 60 ° C. After completion of the reaction, the reaction system was poured into pure water (3 L), and the precipitate was separated by filtration. EtOH (1000 g) was added to the obtained crude product, and repulping was performed at room temperature to obtain 85.4 g of [DA-5-2].
- [DA-6-3] (62.6 g, 230 mmol) and NMP (900 g) were added to a 2 L four-necked flask, and 1,3-DMCBDA (25.5 g, 114 mmol) was added in a water bath, then at room temperature Stir for 6 h. Subsequently, pyridine (54.5 g, 690 mmol) and acetic anhydride (35.2 g, 345 mmol) were added to the reaction solution, and the mixture was stirred at 60 ° C. After completion of the reaction, the reaction system was poured into pure water (4 L), and the precipitate was separated by filtration. MeOH (500 g) was added to the obtained crude product, and repulping was performed at room temperature to obtain 82.0 g of [DA-6-4].
- [DA-8-1] (67.2 g, 121 mmol) and acetic acid (400 g) were charged into a 1 L four-necked flask and stirred at 100 ° C. After completion of the reaction, the reaction system was poured into pure water (1.5 L), and the precipitate was separated by filtration. MeOH (60 g) was added to the obtained crude product, and repulping was performed at room temperature to obtain 30.4 g of [DA-8-2].
- a 1- (4-nitrophenyl) -4-piperidine amine (39.0 g, 116 mmol) and NMP (400 g) are charged into a 500 mL four-necked flask and after adding 1,3DMCBDA (12.8 g, 47 mmol) in a water bath The mixture was stirred at 50 ° C. for 6 h. Subsequently, pyridine (27.6 g, 349 mmol) and acetic anhydride (17.8 g, 175 mol) were added to the reaction solution, and the mixture was stirred at 50 ° C. After completion of the reaction, the reaction system was poured into pure water (2 L), and the precipitate was separated by filtration. Subsequently, MeOH (250 g) was added to the obtained crude product, and repulping was performed at room temperature to obtain 32.1 g of [DA-12-1].
- [DA-13-1] (92.0 g, 170 mmol) and CHCl 3 (920 g) were charged in a 2 L four-necked flask, trifluoroacetic acid (193.3 g, 1700 mol) was added dropwise in a water bath, and the mixture was stirred at 50 ° C. did. After completion of the reaction, the precipitate was separated by filtration, ethyl acetate (300 g) was added to the obtained crude product, and repulped at room temperature to obtain 97.8 g of [DA-13-2].
- Example 1 The diamine compound [DA-1] was added to NMP (2 g) heated to 60 ° C. until a residue remained, and the mixture was stirred at 60 ° C. for 1 hour. After heating, it was allowed to cool at room temperature for 6 hours, the precipitate was removed, and an NMP saturated solution of [DA-1] at room temperature was prepared. Subsequently, a 1 wt% [DA-1] NMP solution was prepared as a standard, and the peak area was measured using HPLC. Finally, NMP (39 g) was added to the prepared saturated solution (1 g) to measure the peak area, and the saturation solubility of [DA-1] in NMP at room temperature was calculated.
- the saturation solubility in NMP of the diamine compounds (DA-1 to DA-8, DA-11) of the present invention of Examples 1 to 9 at room temperature is similar to that of the diamine compound of Comparative Example 1 (DA- It was confirmed to show good solubility compared to 9).
- the saturated solubility in NMP of the diamine compound (DA-8) of Example 8 at room temperature shows better solubility than the diamine compound (DA-10) of Comparative Example 2.
- the solubility improvement with respect to NMP is possible by making a diamine compound into the structure of this invention.
- the molecular weights of the polyimide, polyamic acid and polyamic acid ester in the examples are as follows: room temperature gel permeation chromatography (GPC) apparatus (GPC-101) manufactured by Shodex Co., Ltd .; columns (KD-803, KD-805) manufactured by Shodex Co. It measured as follows.
- Example 10 BCS is added to 3 g of a polyamic acid-polyimide polymerization solution (PI-1) and stirred, and the solution (A-1) is made to have 6 mass% of polyamic acid-polyimide, 54 mass% of NMP, and 40 mass% of BCS. It was prepared, and the solubility of polyamic acid-polyimide at room temperature and freezing ( ⁇ 20 ° C.) was confirmed.
- Example 11 to 19 Comparative examples 3 to 4.
- solubility is shown by the following reference
- the polyimide solution was confirmed to exhibit good solubility, with no turbid varnish, no precipitate, no gelation, etc. even at room temperature and when frozen ( ⁇ 20 ° C.).
- the varnish became turbid, precipitates, gelation and the like were confirmed at room temperature and when frozen ( ⁇ 20 ° C.). From the above, it was suggested that the solubility of the polymer can be improved by making the diamine compound at the time of polymerizing the polyamic acid-polyimide into the structure of the present invention.
- the diamine of the present invention and the polymer obtained therefrom can be easily imparted with various properties using inexpensive raw materials, and therefore, they are expected to be useful in the fields of paints, electronic materials, etc., for example, liquid crystal alignment films etc. .
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Polyamides (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Abstract
Description
しかしながら、ポリイミド、特に全芳香族ポリイミド樹脂の代表例として多用されているピロメリット酸無水物(PMDA)と4,4’-ジオキシアニリン(ODA)から製造されるポリイミド(カプトン:商品名)においては、溶解性が乏しく、溶液として用いることは出来ないため、ポリアミック酸と呼ばれる前駆体を経て、加熱し脱水反応させることで得ている。
一方で、高い溶媒溶解性を示すポリアミック酸では十分な液晶表示特性が得られずイミド化に起因した体積変化も起こりやすいという問題点もあり、沸点の低い有機溶媒類に対して可溶であるポリイミドが望まれるようになってきた。
その解決策として、有機溶媒溶解性に有利な脂環式ジカルボン酸無水物を利用したテトラカルボン酸二無水物の合成法が考えられる。その一例として、無水トリメリット酸クロライドや、無水核水添トリメリット酸クロライドを原料として用いることにより、さまざまな酸二無水物を製造することが知られている(例えば、特許文献1)。
本発明は、安価で入手性の高い市販の原料を用いることにより、ジアミンと酸二無水物から得られるポリアミック酸のポリマーをイミド化しなければ得られない各種特性を容易に付与することが可能な高溶解性のジアミンの製造方法及び得られるジアミン、ならびに、それから得られる新規重合体を提供することを目的とする。
本発明は、かかる知見に基づくものであり、下記を要旨とするものである。
R1、R2、R3及びR4はそれぞれ独立に、H、CH3またはCF3を表し、但し、R1、R2、R3及びR4の内、必ず一つはCH3またはCF3を表し、
W1は、単結合またはフェニレンを表し、フェニレンは、ハロゲン基、炭素数1~10の直鎖又は分岐鎖のアルキル基、炭素数1~10の直鎖又は分岐鎖のアルコキシ基、ヒドロキシル基、シアノ基、ジアルキルアミノ基(アルキル基は、各々独立に、炭素数1~10の直鎖又は分岐鎖のアルキル基である)、炭素数1~10の直鎖又は分岐鎖のエステル基、炭素数1~10の直鎖又は分岐鎖のアシル基、カルボキシル基、アルデヒド基、ニトロ基、Boc保護したアミノ基からなる第1の群から選ばれる置換基で置換されてもよく、2つのW1は互いに同一でも異なっていてもよく、
W2はフェニレンを表し、フェニレンは、上記第1の群から選ばれる置換基で置換されてもよく、2つのW2は互いに同一でも異なっていてもよく、
Lは、上記第1の群から選ばれる置換基で置換されていてもよい炭素数1~10の直鎖又は分岐鎖のアルキレン基を表し、L内の-CH2-は、-CH=CH-、-C≡C-、-CF2-、-C(CF3)2-、-O-、-NHCO-、-CONH-、-COO-、-OCO-、-NH-、-N(CH3)-、-NHCONH-、-N(Boc)CONH-、-NHCON(Boc)-、-N(Boc)CON(Boc)-、-NHCOO-、-OCONH-、-CO-、-S-、-SO2-、-N(Boc)-、-Si(CH3)2OSi(CH3)2-、-Si(CH3)2OSi(CH3)2OSi(CH3)2-、ピペリジン環及びピペラジン環からなる第2の群から選ばれる基で置き換えられていてもよく、ただし、第2の群から選ばれる基同士は、炭素原子を除く同じ原子同士が結合しない条件で互いに隣り合ってもよい。
<2> 上記式(1)で表されるジアミン化合物から得られる、重合体。
また、本発明の液晶配向剤は、上記式(1)で表される構造を有するジアミンから得られる重合体(以下、特定重合体とも言う)を含有する液晶配向剤である。
以下、各条件につき詳述する。
前記したように、本発明によるジアミン化合物は、式(1)で表される。ここで式(1)の各置換基は下記の通り定義される。
W1は、単結合またはフェニレンを表し、フェニレンは、ハロゲン基、炭素数1~10の直鎖又は分岐鎖のアルキル基、炭素数1~10の直鎖又は分岐鎖のアルコキシ基、ヒドロキシル基、シアノ基、ジアルキルアミノ基(アルキル基は、各々独立に、炭素数1~10の直鎖又は分岐鎖のアルキル基である)、炭素数1~10の直鎖又は分岐鎖のエステル基、炭素数1~10の直鎖又は分岐鎖のアシル基、カルボキシル基、アルデヒド基、ニトロ基、Boc保護したアミノ基からなる第1の群から選ばれる置換基で置換されてもよく、2つのW1は互いに同一でも異なっていてもよく、
W2はフェニレンを表し、フェニレンは、上記第1の群から選ばれる置換基で置換されてもよく、2つのW2は互いに同一でも異なっていてもよく、
Lは、上記第1の群から選ばれる置換基で置換されていてもよい炭素数1~10の直鎖又は分岐鎖のアルキレン基を表し、L内の-CH2-は、-CH=CH-、-C≡C-、-CF2-、-C(CF3)2-、-O-、-NHCO-、-CONH-、-COO-、-OCO-、-NH-、-N(CH3)-、-NHCONH-、-N(Boc)CONH-、-NHCON(Boc)-、-N(Boc)CON(Boc)-、-NHCOO-、-OCONH-、-CO-、-S-、-SO2-、-N(Boc)-、-Si(CH3)2OSi(CH3)2-、-Si(CH3)2OSi(CH3)2OSi(CH3)2-、ピペリジン環及びピペラジン環からなる第2の群から選ばれる基で置き換えられていてもよく、ただし、第2の群から選ばれる基同士は、炭素原子を除く同じ原子同士が結合しない条件で互いに隣り合ってもよい。
なかでも、R1及びR4がCH3またはCF3を表し、R2及びR3が水素原子を表すことが好ましく、より好ましくは、R1及びR4がメチル基を表し、R2及びR3が水素原子を表すものは溶解性が高いという点から好ましい。
W2としては、1,4-フェニレン基が好ましい。
本発明の別の態様によれば、第2の群から選ばれる基同士が互いに隣り合うことはない。
以下に、前述したジアミンを得る方法について説明する。
本発明の特定ジアミンを合成する方法は特に限定されないが、例えば、下記式(A)で表されるビスマレイミド化合物と、下記式(B)で表される化合物とを反応させて下記式(C)で表される化合物を得たのちに、これをイミド化して下記式(D)で表される化合物を得たのち、これを式(1)で表される化合物に変換する方法を挙げることができる。
溶媒は、各原料と反応しない溶媒であれば、制限なく使用することができる。例えば、DMF、DMSO、DMAc、NMPなどの非プロトン性極性有機溶媒;Et2O、i-Pr2O、THF(テトラヒドロフラン)、TBME(tert-ブチルメチルエーテル)、CPME(シクロペンチルメチルエーテル)、ジオキサンなどのエーテル類;ペンタン、へキサン、ヘプタン、石油エーテルなどの脂肪族炭化水素類;ベンゼン、トルエン、キシレン、メシチレン、クロロベンゼン、ジクロロベンゼン、ニトロベンゼン、テトラリンなどの芳香族炭化水素類;クロロホルム、ジクロロメタン、四塩化炭素、ジクロロエタンなどのハロゲン系炭化水素類;酢酸メチル、酢酸エチル、酢酸ブチル、プロピオン酸メチルなどの低級脂肪酸エステル類;アセトニトリル、プロピオニトリル、ブチロニトリルなどのニトリル類;などが使用できる。
反応に使用する塩基としては、水酸化ナトリウム、水酸化カリウム、水酸化リチウム、炭酸水素ナトリウム、炭酸水素カリウム、燐酸カリウム、炭酸ナトリウム、炭酸カリウム、炭酸リチウム、炭酸セシウムなどの無機塩基;tert-ブトキシナトリウム、tert-ブトキシカリウム、水素化ナトリウム、水素化カリウムなどの塩基;トリメチルアミン、トリエチルアミン、トリプロピルアミン、トリイソプロピルアミン、トリブチルアミン、ジイソプロピルエチルアミン、ピリジン、キノリン、コリジンなどのアミンを使用できる。なかでも、トリエチルアミン、ピリジン、tert-ブトキシナトリウム、tert-ブトキシカリウム、水素化ナトリウム、水素化カリウムなどが好ましい。
イミド化する場合、アミン成分とビスマレイミド化合物との反応で得られた式(C)で表される化合物の溶液に触媒を添加する化学的イミド化が簡便である。化学的イミド化は、比較的低温でイミド化反応が進行し、イミド化の過程でPro基の分解が起こりにくいので好ましい。
イミド化反応を行うときの温度は、-20~140℃、好ましくは0~100℃であり、反応時間は1~100時間で行うことができる。塩基性触媒の量はアミック酸基の0.5~30倍モル、好ましくは2~20倍モルであり、酸無水物の量はアミック酸基の1~50倍モル、好ましくは3~30倍モルである。
これらの反応は、水素雰囲気下、常圧、または加圧条件下で行なわれる。また、鉄, スズ, 亜鉛などの金属、もしくはこれらの金属塩をプロトン源と共に使用してニトロ基の還元を行ってもよい。金属と金属塩は単体で、もしくは2種類以上を混合して使用しても良い。
反応温度は特に限定されないが、-100℃から使用する溶媒の沸点までの範囲、好ましくは、-50~150℃である。反応時間は、通常0.05~350時間、好ましくは0.5~100時間である。
式(B)で表される化合物のうち、QがNHProである化合物(B1)は、下記式(B1-1)で表されるジアミンと、アミンの保護基(Pro)の酸クロリドもしくは、酸無水物等とを反応させることにより得られる。このとき、ジアミン(B1-1)としては、反応の複雑化を抑制する観点から、対称なジアミンであることが好ましい。式中、W1、W2、L、Proは前記の意味を表す。
反応は、塩基存在下で行うことが好ましい。塩基としては、例えば水酸化ナトリウム、水酸化カリウム等のアルカリ金属水酸化物、炭酸ナトリウム、炭酸カリウム等のアルカリ金属炭酸塩、炭酸水素ナトリウム、炭酸水素カリウム等のアルカリ金属重炭酸塩、リン酸カリウム、1,8-ジアザビシクロ[5,4,0]-7-ウンデセン等の有機塩基等を式(B2-3)で表される化合物に対して1~4当量用いることができる。
中でも、炭酸ナトリウム、炭酸カリウム等のアルカリ金属炭酸塩が好ましい。特に、微粉末炭酸カリウムを用いると、反応性が向上するので好ましい。市販されている微粉末炭酸カリウムとしては、FG-F20(旭硝子株式会社製)(登録商標)等がある。
反応時間は、バッチ処理の場合には0.5~20時間、好ましくは1~15時間である。
本反応は、好ましくは溶媒中で行われる。好ましい溶媒や反応条件は、上記化合物(1)の製造条件と同様である。
上記各反応により得られた各段階における目的物は、蒸留、再結晶、又はシリカゲルなどのカラムクロマトグラフィーなどで精製してもよいし、精製せずに、反応液のまま次の段階に供することもできる。
本発明の重合体は、上記ジアミンを用いて得られる重合体である。具体例としては、ポリアミック酸、ポリアミック酸エステル、ポリイミド、ポリウレア、ポリアミドなどが挙げられる。
上記一般式(1)で表されるジアミンとの反応によりポリアミドを与えるジイソシアネート成分として、例えば、芳香族ジイソシアネート、脂肪族ジイソシアネートなどが挙げられる。好ましいジイソシアネート成分は、芳香族ジイソシアネート、脂肪族ジイソシアネートである。
上記一般式(1)で表されるジアミンとの反応によりポリイミド(前駆体)を与える成分であるテトラカルボン酸二無水物は、下記式(X)で表される。
上記一般式(1)で表されるジアミンとの反応によりポリアミドを与えるジカルボン酸成分を構築するためのモノマー化合物の具体例としては、テレフタル酸、イソフタル酸、2-メチル-イソフタル酸、4-メチル-イソフタル酸、5-メチル-イソフタル酸、5-アリルオキシイソフタル酸、5-アリルオキシカルボニルイソフタル酸、5-プロパギルオキシイソフタル酸、5-アセチルオキシイソフタル酸、5-ベンゾイルアミドイソフタル酸、テトラフルオロイソフタル酸、メチルテレフタル酸、テトラフルオロテレフタル酸、2,6-ナフタレンジカルボン酸、1,6-ナフタレンジカルボン酸、2,6-アントラセンジカルボン酸、1,6-アントラセンジカルボン酸、4,4’-ジカルボキシビフェニル、3,4’-ジカルボキシビフェニル、2,3’-ジカルボキシビフェニル、2,4’-ジカルボキシビフェニル、4,4’-ジカルボキシジフェニルエーテル、3,4’-ジカルボキシジフェニルエーテル、2,3’-ジカルボキシジフェニルエーテル、2,4’-ジカルボキシジフェニルエーテル、3,3’-ジカルボキシジフェニルエーテル、3,3’-ジメチル-4,4’-ジカルボキシビフェニル、4,4’-ジメチル-3,3’-ジカルボキシビフェニル、2,2’-ジメチル-4,4’-ジカルボキシビフェニル、3,3’-ジメトシキ-4,4’-ジカルボキシビフェニル、4,4’-ジメトシキ-3,3’-ジカルボキシビフェニル、2,2’-ジメトシキ-4,4’-ジカルボキシビフェニル、4,4’-ジカルボキシベンゾフェノン、3,4’-ジカルボキシベンゾフェノン、3,3’-ジカルボキシベンゾフェノン、4,4’-ジカルボキシジフェニルメタン、3,4’-ジカルボキシジフェニルメタン、3,3’-ジカルボキシジフェニルメタン、4,4’-ジカルボキシジフェニルアミド、3,4-ジカルボキシジフェニルアミド、4,4’-ジカルボキシジフェニルスルホン、3,4’-ジカルボキシジフェニルスルホン、3,3’-ジカルボキシジフェニルスルホン、2,2’-ジカルボキシジフェニルプロパン、1,4-ビス(4-カルボキシフェノキシ)ベンゼン、1,3-ビス(4-カルボキシフェノキシ)ベンゼン、N-[3{(4-カルボキシフェニル)カルボニルアミノ}フェニル](4-カルボキシフェニル)ホルムアミド、N-[4{(4-カルボキシフェニル)カルボニルアミノ}フェニル](4-カルボキシフェニル)ホルムアミド、4,4’-(4-カルボキシフェノキシフェニル)メタン、4,4’-ビス(4-カルボキシフェノキシ)ジフェニルスルホン、2,2’-ビス[4-(4-カルボキシフェノキシ)フェニル]プロパン、2,2-ビス(4-カルボキシフェニル)ヘキサフルオロプロパン、2,2’-ビス[4-(4-カルボキシフェノキシ)フェニル]ヘキサフルオロプロパン、1,5-ビス(4-カルボキシフェニル)ペンタン、1,4-ビス(4-カルボキシフェニル)ブタン、1,3-ビス(4-カルボキシフェニル)プロパン、4,4’-ジ(カルボキシフェニル)ペンタン-1,5-ジオエート、4,4’-ジ(カルボキシフェニル)ヘキサン-1,6-ジオエート、4,4’-ジ(カルボキシフェニル)ヘプタン-1,7ジオエート等の芳香族あるいは芳香族含有ジカルボン酸及びこれらの酸ハロゲン化物並びにアルキルエステル化物が挙げられる。
本発明に用いられるポリイミド前駆体であるポリアミック酸は、以下に示す方法により合成することができる。
具体的には、テトラカルボン酸二無水物とジアミンとを有機溶媒の存在下で-20~150℃、好ましくは0~70℃において、30分~24時間、好ましくは1~12時間反応させることによって合成できる。
本発明に用いられるポリイミドは、前記ポリアミック酸をイミド化することにより製造することができる。
ポリアミック酸からポリイミドを製造する場合、ジアミン成分とテトラカルボン酸二無水物との反応で得られた前記ポリアミック酸の溶液に触媒を添加する化学的イミド化が簡便である。化学的イミド化は、比較的低温でイミド化反応が進行し、イミド化の課程で重合体の分子量低下が起こりにくいので好ましい。
ポリアミック酸のイミド化反応後の溶液には、添加した触媒等が残存しているので、以下に述べる手段により、得られたイミド化重合体を回収し、有機溶媒で再溶解して、本発明の液晶配向剤とすることが好ましい。
本発明に用いられるポリイミド前駆体であるポリアミック酸エステルは、以下に示す(i)、(ii)又は(iii)の製法で製造することができる。
ポリアミック酸エステルは、前記のように製造されたポリアミック酸をエステル化することによって製造できる。具体的には、ポリアミック酸とエステル化剤を有機溶剤の存在下で-20℃~150℃、好ましくは0℃~50℃において、30分~24時間、好ましくは1~4時間反応させることによって製造することができる。
上記の反応に用いる溶媒は、ポリマーの溶解性からN,N-ジメチルホルムアミド、N-メチル-2-ピロリドン、又はγ-ブチロラクトンが好ましく、これらは1種又は2種以上を混合して用いてもよい。製造時の濃度は、ポリマーの析出が起こりにくく、かつ高分子量体が得やすいという点から、1~30質量%が好ましく、5~20質量%がより好ましい。
ポリアミック酸エステルは、テトラカルボン酸ジエステルジクロリドとジアミンから製造することができる。
具体的には、テトラカルボン酸ジエステルジクロリドとジアミンとを塩基と有機溶剤の存在下で-20℃~150℃、好ましくは0℃~50℃において、30分~24時間、好ましくは1~4時間反応させることによって製造することができる。
ポリアミック酸エステルは、テトラカルボン酸ジエステルとジアミンを重縮合することにより製造することができる。
具体的には、テトラカルボン酸ジエステルとジアミンを縮合剤、塩基、及び有機溶剤の存在下で0℃~150℃、好ましくは0℃~100℃において、30分~24時間、好ましくは3~15時間反応させることによって製造することができる。
また、上記反応において、ルイス酸を添加剤として加えることで反応が効率的に進行する。ルイス酸としては、塩化リチウム、臭化リチウムなどのハロゲン化リチウムが好ましい。ルイス酸の添加量はジアミン成分に対して0~1.0倍モルが好ましい。
上記3つのポリアミック酸エステルの製造方法の中でも、高分子量のポリアミック酸エステルが得られるため、上記(i)又は上記(ii)の製法が特に好ましい。
<ジアミン化合物>
DA-9は特許文献(WO2017-057854)に記載の合成法にて合成した。
NMP: N-メチル-2-ピロリドン。
BCS: ブチルセロソルブ。
THF: テトラヒドロフラン。
DMF: N,N-ジメチルホルムアミド。
CH2Cl2: ジクロロメタン。
CHCl3: クロロホルム。
MeOH: メタノール。
EtOH: エタノール。
IPA: イソプロピルアルコール。
1,3-DMCBDA:1,3-ジメチル-1,2,3,4-シクロブタンテトラカルボン酸二無水物
装置:フーリエ変換型超伝導核磁気共鳴装置(FT-NMR)「INOVA-400」(Varian製)400MHz。
溶媒:重水素化クロロホルム(CDCl3)又は重水素化N,N-ジメチルスルホキシド([D6]-DMSO)。
標準物質:テトラメチルシラン(TMS)。
[DA-1]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.35-7.37 (d,4H), 7.21-7.23 (d,4H), 6.78-6.80 (d,4H), 6.50-6.52 (d,4H), 5.71 (s,4H), 4.79 (s,4H), 3.54 (s,2H), 1.38 (s,6H)
[DA-2]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.30-7.33 (d,4H), 7.08-7.11 (d,4H), 6.66-6.70 (d,4H), 6.48-6.52 (d,4H), 4.62 (s,2H), 4.15-4.18 (t,4H), 3.98-4.01 (t,4H), 3.51 (s,2H), 2.10-2.16 (t,4H), 1.38 (s,6H)
[DA-3]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.29-7.31 (d,4H), 7.06-7.08 (d,4H), 6.63-6.65 (d,4H), 6.48-6.50 (d,4H), 4.59 (s,4H), 4.01-4.04 (t,4H), 3.80-3.84 (t,4H), 3.52 (s,2H), 1.74-1.76 (t,4H), 1.66-1.70 (t,4H), 1.46-1.48 (m,8H), 1.38 (s,6H)
[DA-4]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.46-7.48 (d,4H), 7.33-7.35 (d,4H), 6.65-6.68(d,4H), 6.49-6.51 (d,4H), 4.61 (s,4H), 4.07-4.10 (t,4H), 3.54 (s,2H), 3.02-3.05 (t,4H), 1.39 (s,6H)
[DA-5]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.29-7.31 (d,4H), 7.05-7.08 (d,4H), 6.97-6.99 (d,4H), 6.51-6.53 (d,4H), 4.90 (s,4H), 4.11-4.14 (t,4H), 3.51 (s,2H), 2.86-2.89 (t,4H), 1.37 (s,6H)
[DA-6]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.38-7.40 (d,4H), 7.31-7.33 (d,4H), 6.65-6.67 (d,4H), 6.49-6.51 (d,4H), 4.60 (d,4H), 3.83-3.86 (t,4H), 3.54 (s,2H), 2.73-2.80 (t,4H), 1.97-2.01 (t,4H), 1.39 (s,6H)
[DA-7]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.29-7.32 (d,4H), 7.05-7.07 (d,4H), 6.87-6.89 (d,4H), 6.49-6.51 (d,4H), 4.86 (d,4H), 3.97-4.00 (t,4H), 3.52 (s,2H), 2.56-2.60 (t,4H), 1.93-1.97 (t,4H), 1.38 (s,6H)
[DA-8]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ6.82-6.84 (d,4H), 6.46-6.48 (d,4H), 4.91 (s,4H), 3.50-3.66 (m,4H), 2.96 (s,2H), 2.66-2.73 (t,4H), 0.94 (d,1H)
[DA-10]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ6.81-6.83 (d,4H), 6.46-6.48 (d,4H), 4.90 (s,4H), 3.54-3.57 (t,4H), 3.08 (s,2H), 2.63-2.67 (t,4H)
1H NMR (400 MHz, [D6]-DMSO):δ7.32-7.38 (m,8H), 6.83-6.85 (d,4H), 6.48-6.50 (d,4H), 5.92-5.95 (t,2H), 5.81-5.84 (t,2H), 4.87 (s,4H), 3.55 (s,2H), 3.24-3.29 (m,4H), 3.10-3.15 (m,4H), 2.72-2.76 (m,4H), 2.47-2.51 (m,4H), 1.39 (s,6H)
[DA-12]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ6.71-6.73 (m,4H), 6.47-6.50 (m,4H), 4.68 (s,4H), 3.95-4.01 (m,2H), 3.42-3.45 (d,4H), 3.13 (s,2H), 2.51-2.59 (m,4H), 2.39-2.50 (m,4H), 1.62-1.71 (q,4H), 1.17 (s,6H)
[DA-13]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ6.84-6.86 (d,4H), 6.46-6.48 (d,4H), 4.82 (s,4H), 3.83-3.89 (m,2H), 3.10 (s,2H), 2.99-3.01 (d,4H), 2.49-2.56 (m,4H), 2.39-2.43 (m,4H), 2.26-2.32 (m,4H), 1.94-1.99 (t,4H), 1.52-1.61 (q,4H), 1.14 (s,6H)
[DA-14]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.38-7.43 (d,4H), 7.31-7.33 (d,4H), 6.86-6.88 (d,4H), 6.47-6.49 (d,4H), 4.83 (s,4H), 3.53 (s,2H), 3.04-3.06 (d,4H), 2.52-2.58 (m,6H), 2.45-2.50 (m,4H), 2.03-2.08 (t,4H), 1.67-1.77 (m,8H), 1.39 (s,6H)
[DA-15]の合成:
1H NMR (400 MHz, [D6]-DMSO):δ7.19-7.22 (d,4H), 7.04-7.06 (d,4H), 6.87-6.89 (d,4H), 6.47-6.49 (d,4H), 4.84 (s,4H), 3.48 (s,2H), 3.34 (s,6H), 3.21 (s,8H), 2.58 (s,10H), 1.36 (s,6H)
(実施例1)
ジアミン化合物[DA-1]を60℃に加熱したNMP(2g)に溶け残りができるまで加え、60℃で1時間撹拌した。加熱後、室温で6時間放冷し、沈殿物を除去して、室温時における[DA-1]のNMP飽和溶液を作製した。続いて、標品として、1wt%の[DA-1]のNMP溶液を作製し、HPLCを用いて、ピーク面積を測定した。最後に、作製した飽和溶液(1g)にNMP(39g)を加えてピーク面積を測定し、[DA-1]の室温時におけるNMPに対する飽和溶解度を算出した。
表1に示すように、実施例1と同様の方法を用いて実施例2~9も算出した。また、比較例1~2も同様の方法で算出した。
実施例におけるポリイミド、ポリアミック酸、ポリアミック酸エステルの分子量は、(株)Shodex社製常温ゲル浸透クロマトグラフィー(GPC)装置(GPC-101)、Shodex社製カラム(KD―803、KD-805)を用い以下のようにして測定した。
カラム温度:50℃
溶離液:DMF(添加剤として、臭化リチウム-水和物(LiBr・H2O)が30mmol/L、リン酸・無水結晶(o―リン酸)が30mmol/L、THFが10mL/L)
流速:1.0mL/分
検量線作成用標準サンプル:東ソー社製 TSK 標準ポリエチレンオキサイド(分子量 約900,000、150,000、100,000、30,000)、及び、ポリマーラボラトリー社製 ポリエチレングリコール(分子量 約12,000、4,000、1,000)。
CBDAを0.18g(0.93mol)gとDA-1を0.64g(1.0mmol)をNMP(7.48g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-1)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約29500であった。
CBDAを0.18g(0.93mol)gとDA-2を0.70g(1.0mmol)をNMP(7.98g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-2)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約30000であった。
CBDAを0.18g(0.93mol)gとDA-3を0.78g(1.0mmol)をNMP(8.74g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-3)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約32000であった。
CBDAを0.18g(0.93mol)gとDA-4を0.64g(1.0mmol)をNMP(7.44g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-4)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約14800であった。
CBDAを0.18g(0.93mol)gとDA-5を0.64g(1.0mmol)をNMP(7.44g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-5)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約9900であった。
CBDAを0.18g(0.93mol)gとDA-6を0.67g(1.0mmol)をNMP(7.69g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-6)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約8700であった。
CBDAを0.18g(0.93mol)gとDA-7を0.67g(1.0mmol)をNMP(7.69g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-7)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約16900であった。
CBDAを0.18g(0.93mol)gとDA-8を0.46g(1.0mmol)をNMP(5.78g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-8)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約8900であった。
CBDAを0.18g(0.93mol)gとDA-9を0.40g(1.0mmol)をNMP(5.28g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-9)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約13600であった。
CBDAを0.18g(0.93mol)gとDA-10を0.43g(1.0mmol)をNMP(5.53g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-10)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約8500であった。
CBDAを0.18g(0.93mol)gとDA-11を0.78g(1.0mmol)をNMP(8.71g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-11)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約9600であった。
CBDAを0.18g(0.93mol)gとDA-12を0.57g(1.0mmol)をNMP(6.78g)中、室温で16時間反応させ、ポリアミック酸-ポリイミド重合溶液(PI-12)を調製した。このポリアミック酸-ポリイミドは、数平均分子量が約11200であった。
(実施例10)
ポリアミック酸-ポリイミド重合溶液(PI-1)3gにBCSを加えて攪拌し、ポリアミック酸-ポリイミドが6質量%、NMPが54質量%、BCSが40質量%になるよう溶液(A-1)を調製し、室温、冷凍(-20℃)時でのポリアミック酸-ポリイミドの溶解性を確認した。
表2に示すように、実施例10と同様の方法を用いて、実施例11~19の溶解性を確認した。また、比較例3~4も同様の方法で溶解性を確認した。なお、溶解性を下記の基準で示す。
○:濁り、析出物、ゲル化なし
△:少量の濁りあり
×:濁り、析出物、ゲル化あり
Claims (2)
- 下記一般式(1)で表されるジアミン化合物。
R1、R2、R3及びR4はそれぞれ独立にH、CH3またはCF3を表し、但し、R1、R2、R3及びR4の内、必ず一つはCH3またはCF3を表し、
W1は、単結合またはフェニレンを表し、フェニレンは、ハロゲン基、炭素数1~10の直鎖又は分岐鎖のアルキル基、炭素数1~10の直鎖又は分岐鎖のアルコキシ基、ヒドロキシル基、シアノ基、ジアルキルアミノ基(アルキル基は、各々独立に、炭素数1~10の直鎖又は分岐鎖のアルキル基である)、炭素数1~10の直鎖又は分岐鎖のエステル基、炭素数1~10の直鎖又は分岐鎖のアシル基、カルボキシル基、アルデヒド基、ニトロ基、Boc保護したアミノ基からなる第1の群から選ばれる置換基で置換されてもよく、2つのW1は互いに同一でも異なっていてもよく、
W2はフェニレンを表し、フェニレンは、上記第1の群から選ばれる置換基で置換されてもよく、2つのW2は互いに同一でも異なっていてもよく、
Lは、上記第1の群から選ばれる置換基で置換されていてもよい炭素数1~10の直鎖又は分岐鎖のアルキレン基を表し、L内の-CH2-は、-CH=CH-、-C≡C-、-CF2-、-C(CF3)2-、-O-、-NHCO-、-CONH-、-COO-、-OCO-、-NH-、-N(CH3)-、-NHCONH-、-N(Boc)CONH-、-NHCON(Boc)-、-N(Boc)CON(Boc)-、-NHCOO-、-OCONH-、-CO-、-S-、-SO2-、-N(Boc)-、-Si(CH3)2OSi(CH3)2-、-Si(CH3)2OSi(CH3)2OSi(CH3)2-、ピペリジン環及びピペラジン環からなる第2の群から選ばれる基で置き換えられていてもよく、ただし、第2の群から選ばれる基同士は、炭素原子を除く同じ原子が結合しない条件で互いに隣り合ってもよい。 - 請求項1記載の上記式(1)で表されるジアミン化合物から得られる、重合体。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020207007850A KR102613111B1 (ko) | 2017-08-23 | 2018-08-22 | 신규 중합체 및 디아민 화합물 |
JP2019537645A JP7279637B2 (ja) | 2017-08-23 | 2018-08-22 | 新規重合体及びジアミン化合物 |
CN201880068774.4A CN111263761B (zh) | 2017-08-23 | 2018-08-22 | 新型聚合物和二胺化合物 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2017-160471 | 2017-08-23 | ||
JP2017160471 | 2017-08-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2019039493A1 true WO2019039493A1 (ja) | 2019-02-28 |
Family
ID=65439056
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2018/030918 WO2019039493A1 (ja) | 2017-08-23 | 2018-08-22 | 新規重合体及びジアミン化合物 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP7279637B2 (ja) |
KR (1) | KR102613111B1 (ja) |
CN (1) | CN111263761B (ja) |
TW (1) | TWI823863B (ja) |
WO (1) | WO2019039493A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021215280A1 (ja) * | 2020-04-20 | 2021-10-28 | 日産化学株式会社 | 新規ジアミン、重合体、液晶配向剤、液晶配向膜、及びそれを用いた液晶表示素子 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113930247A (zh) * | 2020-07-13 | 2022-01-14 | 奇美实业股份有限公司 | 液晶配向剂、液晶配向膜及液晶显示元件 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4340715A (en) * | 1981-05-26 | 1982-07-20 | Lord Corporation | Epoxy resin compositions cured with imide-amines |
JPS62108862A (ja) * | 1985-11-06 | 1987-05-20 | Mitsui Toatsu Chem Inc | イミド環含有ジアミン類およびその製造方法 |
JPH0616629A (ja) * | 1992-07-03 | 1994-01-25 | Mitsui Toatsu Chem Inc | イミド環含有ジアミン類およびその製造方法 |
JPH08504197A (ja) * | 1992-12-07 | 1996-05-07 | コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガニゼイション | 重合性モノマー反応体(pmr)タイプの樹脂 |
JPH09185064A (ja) * | 1995-12-28 | 1997-07-15 | Japan Synthetic Rubber Co Ltd | イミド基含有ポリアミック酸およびその製造方法並びに液晶配向剤 |
JP2006070096A (ja) * | 2004-08-31 | 2006-03-16 | New Japan Chem Co Ltd | イミド基含有ジアミン、該イミド基含有ポリイミド前駆体、該前駆体を含有してなるポジ型感光性樹脂組成物、ポジ型パターンの製造方法及び電子部品 |
JP2008273934A (ja) * | 2007-03-30 | 2008-11-13 | Jsr Corp | 新規ジアミン化合物、それを使用して製造されるポリアミック酸及びイミド化重合体 |
WO2017057854A1 (ko) * | 2015-10-02 | 2017-04-06 | 주식회사 엘지화학 | 광배향막의 제조 방법 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100145002A1 (en) | 2005-06-01 | 2010-06-10 | Mitsubishi Chemical Corporation | Tetracarboxylic acid or polyesterimide thereof, and process for production of the same |
KR100851787B1 (ko) * | 2007-04-11 | 2008-08-13 | 제일모직주식회사 | 3,4-디카르복시-1,2,3,4-테트라하이드로-6-터셔리부틸-1-나프탈렌숙신산이무수물 및 그를 이용하여 제조한 폴리이미드중합체를 포함하는 액정 배향제 |
WO2013015407A1 (ja) | 2011-07-27 | 2013-01-31 | 日産化学工業株式会社 | 液晶配向剤、液晶配向膜及び液晶表示素子 |
JP6304492B2 (ja) * | 2012-03-30 | 2018-04-04 | 日産化学工業株式会社 | トリアジノン化合物及びt型カルシウムチャネル阻害剤 |
CN105492965B (zh) * | 2013-06-25 | 2019-04-09 | 日产化学工业株式会社 | 液晶取向剂、液晶取向膜、液晶表示元件 |
CN105659156B (zh) * | 2013-10-23 | 2019-02-01 | 日产化学工业株式会社 | 液晶取向剂、液晶取向膜和液晶表示元件 |
KR101809650B1 (ko) * | 2015-10-02 | 2017-12-15 | 주식회사 엘지화학 | 광배향막의 제조 방법 |
CN106565613B (zh) * | 2016-10-25 | 2018-11-20 | 上海交通大学 | 液晶单元协同偶氮取向的聚酰亚胺定向膜及其制备方法 |
JP7259328B2 (ja) * | 2016-11-18 | 2023-04-18 | 日産化学株式会社 | 液晶配向剤、液晶配向膜、及び液晶表示素子 |
KR102593074B1 (ko) * | 2016-12-21 | 2023-10-23 | 닛산 가가쿠 가부시키가이샤 | 액정 배향제, 액정 배향막, 및 액정 표시 소자 |
KR102514165B1 (ko) * | 2017-07-28 | 2023-03-24 | 닛산 가가쿠 가부시키가이샤 | 액정 배향제, 액정 배향막 및 액정 표시 소자 |
-
2018
- 2018-08-22 TW TW107129325A patent/TWI823863B/zh active
- 2018-08-22 WO PCT/JP2018/030918 patent/WO2019039493A1/ja active Application Filing
- 2018-08-22 JP JP2019537645A patent/JP7279637B2/ja active Active
- 2018-08-22 KR KR1020207007850A patent/KR102613111B1/ko active IP Right Grant
- 2018-08-22 CN CN201880068774.4A patent/CN111263761B/zh active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4340715A (en) * | 1981-05-26 | 1982-07-20 | Lord Corporation | Epoxy resin compositions cured with imide-amines |
JPS62108862A (ja) * | 1985-11-06 | 1987-05-20 | Mitsui Toatsu Chem Inc | イミド環含有ジアミン類およびその製造方法 |
JPH0616629A (ja) * | 1992-07-03 | 1994-01-25 | Mitsui Toatsu Chem Inc | イミド環含有ジアミン類およびその製造方法 |
JPH08504197A (ja) * | 1992-12-07 | 1996-05-07 | コモンウェルス・サイエンティフィック・アンド・インダストリアル・リサーチ・オーガニゼイション | 重合性モノマー反応体(pmr)タイプの樹脂 |
JPH09185064A (ja) * | 1995-12-28 | 1997-07-15 | Japan Synthetic Rubber Co Ltd | イミド基含有ポリアミック酸およびその製造方法並びに液晶配向剤 |
JP2006070096A (ja) * | 2004-08-31 | 2006-03-16 | New Japan Chem Co Ltd | イミド基含有ジアミン、該イミド基含有ポリイミド前駆体、該前駆体を含有してなるポジ型感光性樹脂組成物、ポジ型パターンの製造方法及び電子部品 |
JP2008273934A (ja) * | 2007-03-30 | 2008-11-13 | Jsr Corp | 新規ジアミン化合物、それを使用して製造されるポリアミック酸及びイミド化重合体 |
WO2017057854A1 (ko) * | 2015-10-02 | 2017-04-06 | 주식회사 엘지화학 | 광배향막의 제조 방법 |
Non-Patent Citations (3)
Title |
---|
BHUVANA, S. ET AL.: "Synthesis and Characterization of processable heat resistant poly (amide-imides) for high temperature applications", POLYMER BULLETIN, vol. 57, no. 1, 2006, pages 61 - 72, XP019334854, ISSN: 0170-0839, DOI: doi:10.1007/s00289-006-0530-6 * |
MALLAKPOUR, SHADPOUR: "Synthesis of soluble poly(amide-ether-imide-urea)s bearing amino acid moieties in the main chain under green media (ionic liquid", AMINO ACIDS, vol. 40, no. 2, 2011, pages 487 - 492, XP019873238, ISSN: 0939-4451, DOI: doi:10.1007/s00726-010-0660-x * |
SRIVIDHYA, M. ET AL.: "Soluble Rigid Poly(Imide-Siloxane)s: Synthesis, Characterization, and Structure-Property Relations", JOURNAL OF APPLIED POLYMER SCIENCE, vol. 109, no. 1, January 2008 (2008-01-01), pages 565 - 576, XP055579681, ISSN: 0021-8995 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021215280A1 (ja) * | 2020-04-20 | 2021-10-28 | 日産化学株式会社 | 新規ジアミン、重合体、液晶配向剤、液晶配向膜、及びそれを用いた液晶表示素子 |
Also Published As
Publication number | Publication date |
---|---|
JP7279637B2 (ja) | 2023-05-23 |
JPWO2019039493A1 (ja) | 2020-10-01 |
TW201920100A (zh) | 2019-06-01 |
CN111263761A (zh) | 2020-06-09 |
TWI823863B (zh) | 2023-12-01 |
KR102613111B1 (ko) | 2023-12-12 |
CN111263761B (zh) | 2022-11-04 |
KR20200044036A (ko) | 2020-04-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5733340B2 (ja) | ビスアミノフェニル若しくはビスアミノフェノキシアルキルウレア | |
KR101514861B1 (ko) | 액정 배향 처리제, 및 그것을 사용한 액정 표시 소자 | |
JP5663876B2 (ja) | 液晶配向処理剤、及びそれを用いた液晶表示素子 | |
US6111059A (en) | Diaminobenzene derivatives, polyimides prepared therefrom, and alignment film for liquid crystals | |
WO2005105892A1 (ja) | 液晶配向剤並びにそれを用いた液晶配向膜及び液晶表示素子 | |
WO2001002466A1 (fr) | Derive diaminobenzene, polyimide obtenu a partir dudit derive, et film d'orientation pour cristaux liquides | |
JP2020021081A (ja) | 液晶配向剤、液晶配向膜、及び液晶表示素子 | |
JP7279637B2 (ja) | 新規重合体及びジアミン化合物 | |
TWI626259B (zh) | Liquid crystal alignment agent, and liquid crystal alignment film using the same | |
US7635746B2 (en) | Diamine compound containing triazine group, polyamic acid synthesized from the diamine compound and LC alignment film prepared from the polyamic acid | |
KR20200079315A (ko) | 액정 배향제, 액정 배향막, 및 액정 표시 소자 | |
TWI810169B (zh) | 新穎聚合物及二胺化合物、液晶配向劑、液晶配向膜及液晶顯示元件 | |
JP2001072770A (ja) | ジアミノベンゼン誘導体及びそれを用いたポリイミド並びに液晶配向膜 | |
TW202124682A (zh) | 液晶配向劑、液晶配向膜及液晶顯示元件 | |
KR100802576B1 (ko) | 낮은 선경사각을 갖는 액정배향막용 폴리아믹산 조성물 및이로부터 제조된 가용성 폴리이미드 수지 | |
KR100774616B1 (ko) | 낮은 선경사각을 갖는 액정배향막용 폴리아믹산 조성물 및이로부터 제조된 가용성 폴리이미드 수지 | |
JP3956034B2 (ja) | オリゴアニリンユニットを有するジアミン及びポリイミド | |
TW202144320A (zh) | 化合物、聚合物、液晶配向劑、液晶配向膜、液晶顯示元件、以及製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18847715 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2019537645 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 20207007850 Country of ref document: KR Kind code of ref document: A |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 18847715 Country of ref document: EP Kind code of ref document: A1 |