JP2005248154A - Norbornane polyether polymer - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To obtain a new cycloaliphatic polyether which does not contain double-bonding oxygen atoms like a carboxylic group, comprises an ether oxygen bonding which is expected to be advantageous in water resistance and especially in short wavelength optical absorption suppression, is a resin in which the ether bonding is bonded directly to an alicyclic ring region which is advantageous in heat resistance to compose the main chain, and possesses, at the same time, a transparency and a heat resistance to which a preparation process which does not need a two-step reaction process can be applied. <P>SOLUTION: The subject norbornane polyether polymer is a homopolymer which comprises the structure unit of formula (1) or a copolymer which comprises the structure unit of formula (1) and the structure unit of formula (2), and has a structure mol ratio, (1)/(2), of not less than 10/90. The weight average molecular weight of the homo- or co-polymer measured by GPC (gel permeation chromaty) is not less than 5,000, relative to polystyrene standards. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a novel norbornane-based polyether polymer having transparency.

  Transparent resins are widely used in lighting equipment, electrical parts, automobile parts, other daily necessities, and electronic and information equipment fields. One of the main reasons is that it is advantageous in terms of light weight and mass productivity as compared with glass materials, but it is required to have various characteristics other than transparency according to each application.

  Among the transparent resins, polymethyl methacrylate and polycarbonate are typical and widely used in large quantities, but in recent years there are many cases where these characteristics cannot be met depending on the application field, and hydrocarbon components are Various alicyclic thermoplastic resins, which are the main component, have been proposed and are infiltrated as essential resins.

  As these alicyclic type resins, for example, a) a hydrocarbon resin having a unitary structure of norbornane obtained by hydrogenating a polymer obtained by a metathesis ring-opening polymerization reaction (Patent Document 1); A polymer having a norbornane series hydrogenated from a polymer obtained by a ring polymerization reaction in a unit structure but having an ester group in the side chain (Patent Document 2), c) a vinyl polymer resin of a norbornene monomer (Patent Document) 3), d) vinyl copolymer resin of norbornene monomer and α-olefin, etc. (Patent Document 4), e) polyvinylcyclohexane resin in which aromatic rings of polystyrene are fully hydrogenated (Patent Document 5), or f) alcohol Examples of the component include a methacrylic acid ester polymer having a norbornane group in the side chain (Patent Document 6).

  In the alicyclic type resin exemplified above, the basic direction is that the introduction of the alicyclic group suppresses a decrease in the glass transition temperature peculiar to the acyclic aliphatic group. In terms of performance, selection according to the application is made based on a balance result of various required performances in addition to the effects.

In addition, from the viewpoint of the contained element, the alicyclic type resin illustrated above is
1) Substantially all hydrocarbon resins: a), c), d), e)
2) Carbon, hydrogen, oxygen-containing resins: b), f)
It is classified as follows.

  Among the above alicyclic type resins, 1) those substantially belonging to all hydrocarbon resins (a, c, d, e) have excellent characteristics in terms of water resistance and suppression of light absorption at short wavelengths. In some cases, it may be insufficient in terms of adhesion to the substrate, etc. 2) Carbon, hydrogen, oxygen, and those belonging to the resin containing resin (b, f) have an ester group as a functional group Therefore, it is advantageous in terms of adhesion, but since the carbonyl group of the ester group is a double bond, it is inevitable that it has a certain limit compared to the former in terms of water resistance and suppression of short-wavelength light absorption. .

  On the other hand, from the viewpoint of the production process, the method (a, b) that undergoes a metathesis polymerization reaction includes a two-stage polymer hydrogenation reaction step that substantially completely hydrogenates the double bond of the main chain after polymerization. There is a drawback that requires a process.

  As mentioned above, it is an oxygen atom introduced to improve adhesion and the like, and does not contain a disadvantageous carbonyl group in terms of suppression of short-wavelength light absorption and water resistance, and is further produced in a one-step reaction process. Resins with good balance that have both transparency and transparency have been desired.

JP 60-26024 A JP-A-1-240517 JP-A-4-63807 JP 61-292601 A JP-A-1-317728 JP-A-62-246001 J. et al. MACROMOL. SCI. -CHEM. , A11, p. 603 (1977)

  The problem of the present invention is that it contains an etheric oxygen bond that does not contain a double-bonded oxygen atom such as a carbonyl group and is expected to be advantageous in terms of water resistance, particularly in terms of suppressing light absorption at short wavelengths. A new alicyclic ring that has heat resistance and transparency that can be applied to a production method that does not require a two-step reaction process. It is to provide a formula polyether.

That is, the present invention is a homopolymer composed of a structural unit represented by the following formula (1), or a structural unit represented by the following formula (1) and a structural unit represented by the following formula (2). And having a molar ratio (1) / (2) of 10/90 or more, and the weight in terms of polystyrene measured by GPC of the homopolymer or the copolymer It is a norbornane polyether polymer having an average molecular weight of 5,000 or more.

  The polymer contains an etheric carbon-oxygen bond directly linked to the alicyclic moiety in the polymer main chain, does not contain any carbonyl group, and has a practically sufficiently high glass transition temperature and a transparent resin. It discovered that it was an alicyclic polyether resin, and came to complete this invention. The polymer can be obtained in a one-step reaction process by ring-opening polymerization of an oxirane ring.

  No resin has been disclosed so far which is a polyether-based polyether containing an etheric carbon-oxygen bond directly linked to an alicyclic moiety in the main chain and having a bicyclic (bicyclo) or higher alicyclic group. The only example is J. MACROMOL. SCI. -CHEM. A11, 603, 1977 discloses a cationic polymer of norbornene epoxide with a specific catalyst, but its weight average molecular weight is only 1500 at the highest, and is considered to belong to a so-called oligomer.

  ADVANTAGE OF THE INVENTION According to this invention, the novel transparent resin with which water resistance, especially short wavelength light absorption suppression, adhesiveness, and heat resistance was improved with sufficient balance can be provided. The resin can be produced without requiring a two-step reaction including a polymer hydrogenation reaction.

The resin of the present invention is a homopolymer composed of a structural unit represented by the following formula (1), or a structural unit represented by the following formula (1) and a structural unit represented by the following formula (2). And having a molar ratio (1) / (2) of 10/90 or more, and the weight in terms of polystyrene measured by GPC of the homopolymer or the copolymer Although it is a norbornane-based polyether polymer having an average molecular weight of 5,000 or more, the constituent molar ratio (1) / (2) is preferably 20/80 or more, and more preferably 30/70 or more. When the molar ratio (1) / (2) is less than 10/90, the glass transition temperature of the copolymer is insufficient.

  The weight average molecular weight in terms of polystyrene measured by GPC of the homopolymer and copolymer of the present invention is 5,000 or more. When the weight average molecular weight is 5,000 or less, the strength or hardness as a molded product or a film-formed product is insufficient. The upper limit of the weight average molecular weight is not particularly limited, but is preferably 1 million or less, more preferably 500,000 or less, particularly preferably 300,000 or less, and most preferably 200,000 or less.

  The homopolymer resin having the structural unit represented by the formula (1) of the present invention is obtained by ring-opening polymerization of an oxirane ring of 5,6-dihydrodicyclopentadiene epoxide (hereinafter abbreviated as DCPDO), and The copolymer composed of the structural unit represented by the formula (1) and the structural unit represented by the formula (2) is in the presence of DCPDO and cyclohexene epoxide (hereinafter abbreviated as CHO), It can be synthesized by ring-opening polymerization of the oxirane rings of both monomers. The ring-opening polymerization reaction may be performed in the presence of an oxirane ring-opening polymerization catalyst.

  The ring-opening polymerization catalyst may be a known one and is not particularly limited, and examples thereof include a catalyst called “Vandenberg catalyst” and related catalysts. More specifically, a compound having an active hydrogen bond such as water, alcohol or amine as a part of the organic aluminum compound having a carbon-aluminum bond such as alkylaluminum, alkylaluminum halide, alkylaluminum alkoxide, or alkylaluminoxane. And a catalyst obtained by further chelating the catalyst with acetylacetone or an ethylenediamine derivative, or a catalyst obtained by modifying the catalyst with a rare earth metal compound.

  Moreover, the catalyst which made the carbon-zinc bond of alkyl zinc partially react with the compound which has active hydrogen similarly to the above is also mentioned. Alternatively, for example, a composite metal cyanide complex catalyst as disclosed in JP-A-5-17569, a Sn-containing catalyst disclosed in JP-B 51-20560, or an organic compound described in JP-B 49-11639 Examples include composite metal compound-based catalysts.

  Although it is somewhat inferior as a catalyst giving a high molecular weight as compared with the above catalyst, a specific cationic polymerization catalyst such as trifluoroboron etherate can also be used.

  The amount of catalyst used is preferably 0.05 to 40% by weight, more preferably 0.5 to 20% by weight, still more preferably 0.5 to 15% by weight, based on the total amount of monomers.

  The ring-opening polymerization reaction is preferably carried out in an inert gas atmosphere in the presence of the above-exemplified catalyst in a solution in which the alicyclic epoxide monomer is dissolved in a non-proteic solvent.

Examples of preferred non-proteic solvents include acyclic or cyclic aliphatic solvents such as hexane, heptane, and cyclohexane, unsubstituted or substituted aromatic solvents such as benzene, toluene, and chlorobenzene, diethyl ether, dibutyl ether, and tetrahydrofuran. And non-cyclic or cyclic ether solvents, and halogenated hydrocarbon solvents such as chloroform and dichloromethane.
In a specific polymerization temperature or copolymerization reaction, even in the absence of a solvent, a uniform liquid may be obtained in the polymerization temperature range, and in that case, a polymerization reaction without a solvent is also possible.
A polymerization temperature in the range of −100 ° C. to 200 ° C. can be applied.

  Known methods can be applied to obtain the polymer after the polymerization reaction. That is, when the polymer is precipitated from the reaction medium, it is separated by a method such as filtration or centrifugation, and when the polymer is dissolved in the reaction medium, the reaction medium is separated by evaporation or the reaction solution is a poor solvent for the polymer, for example, A method in which a polymer is precipitated by mixing with methanol or ethanol and separated from a residual monomer or a low molecular weight polymer can be applied. At that time, it is possible to reduce or adjust the low molecular weight portion or the high molecular weight portion according to the target molecular weight distribution by fractionation by selecting the type and mixing ratio of the solvent.

  Depending on the type and amount of the selected catalyst, the reaction solution is treated with an appropriate agent before the above treatment to remove the metal-containing group derived from the catalyst from the polymer, and the reaction including the free catalyst system compound is already performed. A method of separating the metal compound derived from the catalyst from the system can also be applied. If necessary, the metal compound derived from the catalyst can be separated after the above-described precipitation and separation treatment. Suitable agents include, for example, dilute aqueous acid solutions.

[Preparation of 5,6-dihydrodicyclopentadiene epoxide]
A commercially available reagent (Tokyo Kasei) 5,6-dihydrodicyclopentadiene was synthesized by epoxidation using a hydrogen peroxide solution according to a known method. For other chemicals, commercially available reagents were used.
¹ H-NMR was measured in deuterated benzene using JNM-GS × 270 (manufactured by JEOL). The composition ratio (1) / (2) of the copolymer was determined from the peak area ratio in the region of δ (3.9 to 4.8) and δ (3.5 to 3.9).
GPC was measured by polystyrene conversion with a tetrahydrofuran eluent using a Shodex KF-806L × 3 column.
DSC measured the glass transition temperature (Tg) by using DSC7 (manufactured by PERKIN ELMER) under the following pretreatment and measuring under a temperature rising condition of 10 ° C./min.
30 ° C. (2 minutes) → 10 ° C./minute (temperature increase) → 230 ° C. (5 minutes) → 10 ° C./minute (temperature decrease) → 30 ° C. (5 minutes)

[Preparation of catalyst]
60 ml (54.4 mM) of a 15% hexane solution of triethylaluminum (hereinafter abbreviated as TEA) was added to a 100 ml glass flask equipped with a magnetic stir bar and a three-way cock under a nitrogen stream, and then dried with molecular sieve 4A. 19 ml of ether was added, ice-cooled, and 490 mg (27.2 mM) of deionized water was added dropwise over 30 minutes with stirring. Each solution was charged using a syringe under a nitrogen stream. Stirring was continued for 1 hour under ice-cooling, and the mixture was further stirred for 1 hour at room temperature.

[Example 1]
To 100 parts by weight of DCPDO, 30 parts by weight of benzene was added and dissolved to prepare a 77% by weight solution, to which molecular sieve 4A was added and dried.
The inside of a glass ampoule having a capacity of about 30 ml was purged with nitrogen, and 2.5 ml of a 77 wt% benzene solution of DCPDO [DCPDO; 2.0 g, 13 mM] was added using a syringe, and the mixture was ice-cooled. 2 ml [92 mg in terms of TEA, 0.82 mM)] was added, and after cooling with dry ice-acetone, the ampule was sealed. All the above operations were performed in a nitrogen atmosphere, and the operations were performed in a state of being substantially sealed from the air atmosphere. The ampoule was allowed to stand at room temperature (about 25 ° C.) for 4 days.

The ampoule was opened, diluted with about 8 g of benzene, and the following washing operation was performed.
A 3% aqueous hydrochloric acid solution was added to the benzene diluted solution, and the mixture was shaken with a shaker at room temperature for 30 minutes. After removing the aqueous layer and confirming that the pH of the aqueous layer was about 1, the organic layer was washed twice with 3 g of 3% hydrochloric acid aqueous solution, 3 g of 2% aqueous sodium hydrogen carbonate solution, and 3 g of deionized water. .
The obtained organic layer was poured into a large amount of methanol and shaken with a shaker at room temperature for 30 minutes.
The precipitate-precipitated mixture was filtered, washed with methanol, dried under reduced pressure at 50 ° C. for 2 hours, the resulting solid was dissolved again in about 13 g of benzene, and poured into a large amount of methanol. The deposited precipitate was filtered, washed with methanol, and then treated at 50 ° C. under reduced pressure for 2 hours to obtain 0.75 g of a polymer [referred to as (1)] (yield 38%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 2]
To 100 parts by weight of DCPDO, 234 parts by weight of benzene was added and dissolved to prepare a 30% by weight solution, to which molecular sieve 4A was added and dried.
Ampoules sealed in the same manner as in Example 1 except that 15 ml of a 30 wt% benzene solution of DCPDO [DCPDO; 4.2 g, 28 mM] and 6.9 ml of TEA catalyst [530 mg, 4.6 mM in terms of TEA] were used. Was allowed to stand at room temperature (about 25 ° C.) for 4 days.

The ampoule was opened, poured into a large amount of methanol, and a precipitate was deposited. After removing the supernatant, the remainder was centrifuged and solid-liquid separated. About 25 g of benzene is added to the sedimentation section, and the mixture is stirred and centrifuged. The sedimentation section and the benzene solution are separated, and about 25 g of benzene is added to the sedimentation section and stirred and centrifuged to separate the sedimentation section and the benzene solution. Two benzene solutions were combined.
About 14 g of benzene was added to the settled portion to swell and become turbid, and washed with 4 g of 3% hydrochloric acid aqueous solution and then 5 g, and it was confirmed that the pH of the aqueous layer portion was 1. The benzene layer became a homogeneous solution. Further, after washing twice with 3 g of 2% aqueous sodium hydrogen carbonate and 3 times with 3 g of deionized water, the mixture was poured into a large amount of methanol to precipitate the precipitate, and after removing the supernatant, the remainder was separated into solid and liquid by centrifugation. Was treated under reduced pressure at 50 ° C. for 2 hours to obtain 0.28 g of the polymer [(2-A)] (yield 7%).
The combined benzene solution was subjected to solid-liquid separation by 3% hydrochloric acid aqueous solution, 2% sodium hydrogen carbonate aqueous solution, deionized water, a large amount of methanol treatment, and centrifugation in the same manner as in Example 1. The part was treated at 50 ° C. for 2 hours to obtain 1.15 g of a polymer [referred to as (2-B)] (yield 28%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 3]
To 10 parts by weight of DCPDO, 900 parts by weight of benzene was added and dissolved to prepare a 10% by weight solution, and then molecular sieve 4A was added thereto and dried.
13.5 ml of DCPDO in 10 wt% benzene [DCPDO; 1.2 g, 8.0 mM], 62 mg of BF3.O (C2H5) 2 as a catalyst, and a sealed ampoule left at room temperature (about 25 ° C.) for 5 days Except for the above, the polymerization reaction and post-treatment were performed in the same manner as in Example 1 to obtain 0.19 g of polymer [(3)] (yield 16%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 4]
A mixture of 100 parts by weight of DCPDO and 7.7 parts by weight of CHO [DCPDO / CHO = 89/11 (M / M)] was dissolved by adding 27 parts by weight of benzene to prepare an 80% by weight solution, and molecular sieve 4A was added thereto. And dried.
2.3 ml of 80 wt% benzene solution of the above (DCPDO / CHO) monomer [monomer total; 1.89 g, 13.1 mM], 1.4 ml of TEA catalyst [107 mg in terms of TEA, 0.94 mM)], sealed ampoule Was allowed to stand at room temperature (about 25 ° C.) for 5 days to carry out the polymerization reaction and post-treatment in the same manner as in Example 1 to obtain 0.88 g of polymer [(4)] (yield 47%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 5]
A mixture of 100 parts by weight of DCPDO and 28 parts by weight of CHO [DCPDO / CHO = 70/30 (M / M)] was dissolved by adding 32 parts by weight of benzene to prepare an 80% by weight solution, and molecular sieve 4A was added thereto and dried. I let you.
2.7 ml of 80 wt% benzene solution of the above (DCPDO / CHO) monomer [monomer total; 2.20 g, 16.3 mM], 1.4 ml of TEA catalyst [107 mg in terms of TEA, 0.94 mM)], sealed ampoule Was allowed to stand at room temperature (about 25 ° C.) for 5 days, and the polymerization reaction and post-treatment were performed in the same manner as in Example 1 to obtain 1.09 g of a polymer [(5)] (yield 50%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 6]
A mixture of 100 parts by weight of DCPDO and 65.1 parts by weight of CHO [DCPDO / CHO = 50/50 (M / M)] was dissolved by adding 41.5 parts by weight of benzene to prepare a molecular sieve 4A. Was added and dried.
2.7 ml of 80 wt% benzene solution of the above (DCPDO / CHO) monomer [total monomer; 2.15 g, 17.3 mM], 1.4 ml of TEA catalyst [107 mg in terms of TEA, 0.94 mM)], sealed ampoule Was allowed to stand at room temperature (about 25 ° C.) for 5 days to carry out the polymerization reaction and post-treatment in the same manner as in Example 1 to obtain 1.10 g of a polymer [(6)] (yield 51%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 7]
A mixture of 100 parts by weight of DCPDO and 260 parts by weight of CHO [DCPDO / CHO = 20/80 (M / M)] was dissolved in 90 parts by weight of benzene to prepare an 80% by weight solution, and molecular sieve 4A was added thereto and dried. I let you.
2.7 ml of 80 wt% benzene solution of the above (DCPDO / CHO) monomer [monomer total; 2.10 g, 19.4 mM], 1.4 ml of TEA catalyst [107 mg in terms of TEA, 0.94 mM)], sealed ampoule Was allowed to stand at room temperature (about 25 ° C.) for 5 days to carry out the polymerization reaction and post-treatment in the same manner as in Example 1 to obtain 1.24 g of a polymer [(7)] (yield 59%).
Table 1 shows the properties and analysis results of the obtained polymer.

[Example 8]
60.5 parts by weight of toluene was added to 100 parts by weight of DCPDO and dissolved to prepare a 62.3% by weight solution, and molecular sieve 4A was added thereto and dried.
A 1 L glass four-necked flask equipped with a stirrer, dropping funnel, thermometer and three-way cock was set, and the inside of the system was purged with nitrogen. Thereafter, the introduction of the chemical into the system until the polymerization termination operation was substantially blocked from the outside air.
To the flask, 75.3 parts by weight of the above-prepared DCPDO toluene solution [DCPDO; 46.9 parts by weight] was added.
One of the two dropping funnels was charged with 33 parts by weight of the catalyst prepared above, and the other dropping funnel was charged with 45.7 parts by weight of dry toluene.
While stirring, the flask was cooled in a dry ice / methanol bath, and the internal temperature was cooled to -40 ° C.
The dropping of the catalyst was started, and the entire amount was dropped in about 1 hour and 30 minutes while maintaining the internal temperature of about −40 ° C. by controlling the increase in the internal temperature due to heat generation. In parallel, toluene was added dropwise to alleviate the increase in viscosity of the reaction solution, and finally the entire amount was added dropwise.
After completion of the dropwise addition of the catalyst, stirring was continued for 5 hours at an internal temperature of about −40 ° C., and then 1.5 parts by weight of methanol was added to stop the reaction.
The dry ice / methanol bath was removed, and 135 parts by weight of toluene and 135 parts by weight of a 3% aqueous hydrochloric acid solution were added with stirring, and stirring was continued until the internal temperature reached room temperature.
When the content liquid was allowed to stand, it separated into two layers, and the pH of the lower aqueous layer showed an acidity of about 1. The aqueous layer was separated, and the upper organic layer was divided into 68 parts by weight of 3% aqueous hydrochloric acid solution, 135 parts by weight of 2% aqueous sodium hydrogen carbonate solution (confirmed that the pH of the aqueous layer was about 8), and 3 times with 68 parts by weight of deionized water. , Washed and separated in the order of.
The obtained organic layer was added dropwise to 1800 parts by weight of methanol in a SUS container with high-speed stirring to precipitate a white precipitate. The white precipitate obtained after filtration was dissolved in 220 parts by weight of toluene, and the resulting solution was suction filtered with a 0.45 μm membrane filter. The filtrate was similarly added dropwise to 1800 parts by weight of methanol under high-speed stirring. A white precipitate was obtained. The obtained precipitate was dried at 140 ° C. under reduced pressure for 6 hours to obtain 31.6 parts by weight of a white powdery polymer (8) (yield 67%).
Table 2 shows the properties and analysis results of the obtained polymer.

[Example 9]
Polymerization and post-treatment were carried out in the same manner as in Example 8 except that the reaction internal temperature in Example 8 was -35 ° C to obtain 34.8 parts by weight of a white powdery polymer (9) (74% yield) ).
Table 2 shows the properties and analysis results of the obtained polymer.

[Example 10]
Instead of 45.7 parts by weight of dry toluene charged in the “other dropping funnel” in Example 8, 48.0 parts by weight of a dry toluene solution containing 2.3 parts by weight of CHO, and the reaction internal temperature was −50 ° C. In addition, the polymerization and the post-treatment were performed in the same manner as in Example 8 except that the stirring time until the methanol was added after dropping the catalyst was 3 hours to obtain 41.1 parts by weight of a white powdery polymer (10) ( Yield 84%).
Table 2 shows the properties and analysis results of the obtained polymer.

[Confirm transparency]
The polymer powder was charged into a glass tube and heated in an oil bath at 220 to 250 ° C. for 2 to 10 minutes for Examples 1 to 7 and for 45 to 1 hour for Examples 8 to 10 while maintaining the inside of the tube under reduced pressure. After confirming that the entire contents were in a molten state, the contents were cooled to room temperature.
The obtained polymer after melting was visually observed and its transparency was qualitatively determined. As a result, all the polymers obtained in Examples 1 to 10 showed the same degree of transparency as glass, and no haze was observed.

The novel norbornane-based polyether polymer transparent resin according to the present invention is suitable for lighting equipment such as luminaire covers, electrical parts such as insulating films and speaker diaphragms, automobile parts such as automobile lamps, eyeglass parts, and other transparency. It can be used for daily necessities.
In particular, it is very useful in the field of electronic and information equipment, for example, in the field of electronic equipment typified by conductive sheets, light-emitting element sealing materials, electronic element sealing materials, high-frequency circuit boards, printed wiring boards, and the like. Or an optical disk for recording / reproducing information such as images and music, an information disk substrate such as an optical disk (pigment-based disk, etc.), and a lens for picking up information such as a disk and barcode related to information, especially Next-generation DVD (so-called Blu-ray DVD) pickup lens using a short-wavelength blue laser as a medium, as well as lenses for lenses such as cameras, digital cameras, printers, copiers, OHP, projection TVs, VTRs, prisms, and translucent materials In addition, liquid crystal substrates, light guide plates, protective moisture-proof films, polarizing films, retardation films Viewing angle film, a prism sheet, a diffusion plate, can be effectively utilized in the various members, such as the information equipment fields typified of a liquid crystal display system such as a front protection plate.
In addition to the above optical fields, the present invention is useful in industries such as food and medical fields such as containers for foods, cosmetics, pharmaceuticals, medical instruments, packaging materials and equipment.

3 is an NMR chart of the polymer (1) obtained in Example 1. 4 is an NMR chart of the polymer (6) obtained in Example 6.

Claims (2)

It is a homopolymer consisting of a structural unit represented by the following formula (1), or is composed of a structural unit represented by the following formula (1) and a structural unit represented by the following formula (2), It is a copolymer having a constitutional molar ratio (1) / (2) of 10/90 or more, and the weight average molecular weight in terms of polystyrene measured by GPC of the homopolymer or the copolymer is 5,000. The norbornane-based polyether polymer as described above.

  The norbornane polyether polymer according to claim 1, wherein the homopolymer or the copolymer has a polystyrene-reduced weight average molecular weight of 5,000 or more and 1,000,000 or less as measured by GPC.

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