Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium

A compound, fluorine-containing ether technology, applied in the direction of magnetic recording layer, lubricating composition, organic chemistry, etc., can solve the problem that the durability of magnetic recording medium cannot be fully obtained, and achieve excellent adhesion, excellent reliability and durability. , chemical resistance and good wear resistance

Pending Publication Date: 2022-08-02
SHOWA DENKO KK
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the durability of the magnetic recording medium cannot be sufficiently obtained only by providing a protective layer on the recording layer.

Method used

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  • Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium
  • Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium
  • Fluorine-containing ether compound, lubricant for magnetic recording medium, and magnetic recording medium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0288] The compound represented by the said formula (A) was obtained by the method shown below.

[0289] Add HOCH to a 100 mL eggplant flask under nitrogen atmosphere 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 20 g of the compound (number average molecular weight 1000, molecular weight distribution 1.1) represented by OH (m representing the average degree of polymerization in the formula is 4.5, and n representing the average degree of polymerization is 4.5), and 2.55 g of the compound represented by the above formula (6a) g, and 20 mL of tert-butanol, and stirred at room temperature until it became homogeneous to prepare a mixture. To this mixture was added 0.90 g of potassium tert-butoxide, and the mixture was stirred at 70° C. for 16 hours to react.

[0290] In addition, the compound represented by formula (6a) is synthesized by reacting 2-cyanoethanol with epibromohydrin.

[0291] The reaction product obtained after the reaction was cooled to 25°C, transferred ...

Embodiment 2

[0300] The compound represented by the above-mentioned formula (B) was obtained by the method shown below.

[0301] The compound represented by the following formula (16) is obtained as an intermediate by reacting the compound represented by the above formula (15) with epibromohydrin.

[0302]

[0303] (In the formula (16), m representing the average degree of polymerization represents 4.5, and n representing the average degree of polymerization represents 4.5.)

[0304] Add HOCH to a 100 mL eggplant flask under nitrogen atmosphere 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 20 g of a compound (number average molecular weight 1000, molecular weight distribution 1.1) represented by OH (m representing the average degree of polymerization in the formula is 4.5, and n representing the average degree of polymerization is 4.5), and a compound represented by the following formula (6ba) 5.70 g and 20 mL of t-butanol were stirred at room temperature until it became homogen...

Embodiment 3

[0317] The compound represented by the said formula (C) was obtained by the method shown below.

[0318] Except having used the compound represented by the formula (6ca) in place of the compound represented by the formula (6ba) in Example 2, the same operation as in Example 2 was carried out to obtain the compound (C) (in the formula (C) ), mc1, mc2, nc1, and nc2 representing the average degree of polymerization are 4.5.) 8.5 g.

[0319]

[0320] (In the formula (6ca), THP represents a tetrahydropyranyl group.)

[0321] In addition, the compound represented by formula (6ca) is synthesized by carrying out a monoaddition reaction of 2-cyanoethanol after protecting the secondary hydroxyl group of glycerol diglycidyl ether with dihydropyran.

[0322] Carry out the obtained compound (C) 1 H-NMR and 19 The structure was identified by the following results by F-NMR measurement.

[0323] 1 H-NMR (acetone-D 6 ): δ[ppm]=3.40-3.60(4H), 3.65-3.85(8H), 3.85-4.10(29H)

[0324] 19...

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Abstract

A fluorine-containing ether compound represented by formula (1). R1-R2-CH2-R3-CH2-OCH2CH (OH) CH2O-CH2-R3-CH2-R4-R5 (in the formula, R3 is a perfluoropolyether chain, R2 is a perfluoropolyether chain, R3 is a perfluoropolyether chain, R3 is a perfluoropolyether chain, and R4 is a perfluoropolyether chain. R2 and R4 independently represent a divalent linking group having a polar group, and may be the same as or different from each other; r1 and R5 are terminal groups bonded to R2 or R4, and may be the same as or different from each other; and at least one of R1 and R5 is an organic group having 1-8 carbon atoms, and is a group in which at least one hydrogen atom of the organic group is substituted by a cyano group).

Description

technical field [0001] The present invention relates to a fluorine-containing ether compound, a lubricant for a magnetic recording medium, and a magnetic recording medium. [0002] This application claims priority based on Japanese Patent Application No. 2019-232037 filed in Japan on December 23, 2019, the content of which is incorporated herein by reference. Background technique [0003] In order to increase the recording density of a magnetic recording and reproducing apparatus, development of a magnetic recording medium suitable for a high recording density has been carried out. [0004] Conventionally, as a magnetic recording medium, a recording layer is formed on a substrate, and a protective layer such as carbon is formed on the recording layer. The protective layer protects the information recorded on the recording layer and improves the slidability of the magnetic head. However, the durability of the magnetic recording medium cannot be sufficiently obtained by mere...

Claims

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Application Information

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IPC IPC(8): C07C43/13C08G65/333C10N20/04C10N30/00C10N30/06C10N40/18G11B5/72C10M107/38
CPCC08G65/333C10M107/38C10N2030/06C10N2040/18C10M2213/043C10M2213/0606C07C255/13G11B5/7253C10N2050/025G11B5/7257C07C43/137C10M105/56C10M105/72C10M2215/16C10M2219/102C10N2020/04
Inventor福本直也加藤刚室伏克己柳生大辅南口晋毅芝田夏实
OwnerSHOWA DENKO KK