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

Abstract

A fluorine-containing ether compound which is represented by the formula below. R1-R2-CH2-R3-CH2-R4-R5 (In the formula, R3 represents a perfluoropolyether chain; each of R1 and R5 independently represents any one of an optionally substituted alkyl group, an organic group having a double bond or a triple bond, and a hydrogen atom; -R2-CH2-R3 is represented by –[A]-[B]-O-CH2-R3; R3-CH2-R4 is represented by R3-CH2-O-[C]-[D]-; and [A] is represented by formula (4), [B] is represented by formula (5), [C] is represented by formula (6), and [D] is represented by formula (7).)

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. This application claims priority based on Japanese Patent Application No. 2019-236885, filed on December 26, 2019, the contents of which are incorporated herein by reference. [Background technology]

[0002] In order to improve the recording density of magnetic recording and reproducing devices, development of magnetic recording media suitable for high recording density is underway. Conventionally, magnetic recording media include those in which 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 also improves the sliding properties of the magnetic head. However, the durability of the magnetic recording medium cannot be sufficiently obtained by simply providing a protective layer on the recording layer. For this reason, a lubricant is generally applied to the surface of the protective layer to form a lubricating layer.

[0003] The lubricant used in forming the lubricating layer of the magnetic recording medium is, for example, CF 2 It has been proposed to use a fluorine-based polymer having a repeating structure including the following: For example, Patent Document 1 discloses a fluoropolyether compound having amino alcohol groups at both molecular ends. Patent Document 2 discloses a polymer containing two perfluoropolyether chains linked by a divalent chain containing at least one hydroxyl group and at least two amino groups, and having a monovalent chain containing a hydroxyl group and an amino group at the end. In addition, Patent Document 3 describes a method in which an ether bond (-O-) and a methylene group (-CH) are formed between a perfluoropolyether chain and both terminal groups. 2 This paper discloses a fluorine-containing ether compound having a linking group that combines a methylene group (--CH(OH)--) in which one hydrogen atom is substituted with a hydroxyl group. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Publication No. 11-131083 [Patent Document 2] Special Publication No. 2018-521183 [Patent Document 3] International Publication No. 2019 / 054148 Summary of the Invention [Problem to be solved by the invention]

[0005] In magnetic recording and reproducing devices, there is a demand for an even smaller flying height of the magnetic head, which in turn requires a thinner lubricating layer in the magnetic recording medium. However, generally, when the thickness of the lubricating layer is reduced, the wear resistance of the magnetic recording medium tends to decrease.

[0006] The present invention has been made in consideration of the above circumstances, and an object of the present invention is to provide a fluorine-containing ether compound that can form a lubricating layer having excellent wear resistance even if it is thin, and can be suitably used as a material for a lubricant for a magnetic recording medium. Another object of the present invention is to provide a lubricant for magnetic recording media, which contains the fluorine-containing ether compound of the present invention. Another object of the present invention is to provide a magnetic recording medium having excellent reliability and durability, which has a lubricating layer containing the fluorinated ether compound of the present invention. [Means for solving the problem]

[0007] The present inventors have conducted extensive research in order to solve the above problems. As a result, there is a -CH 2The present inventors have found that a fluorine-containing ether compound having a linking group having a specific structure in which -, -O-, -NH- and -CH(OH)- are combined and bonded in a chain form can be obtained, and have arrived at the present invention. That is, the present invention relates to the following: The present invention includes the following first aspect.

[0008] [1] A fluorinated ether compound represented by the following formula (1): R 1 -R 2 -CH 2 -R 3 -CH 2 -R 4 -R 5 (1) (In formula (1), R 3 is a perfluoropolyether chain; R 1 is R 2 is an end group bonded to; R 5 is R 4 is an end group bonded to; R 1 and R 5 each independently represents an alkyl group which may have a substituent, an organic group having a double bond or a triple bond, or a hydrogen atom; -R 2 -CH 2 -R 3 is expressed by the following formula (2); R 3 -CH 2 -R 4 - is expressed by the following formula (3). -[A]-[B]-O-CH 2 -R 3 (2) R 3 -CH 2 -O-[C]-[D]- (3) (In formula (2), [A] is represented by the following formula (4), and [B] is represented by the following formula (5); [A] and [B] may be interchanged in formula (2).) (In formula (3), [C] is represented by the following formula (6), and [D] is represented by the following formula (7); [C] and [D] may be interchanged in formula (3).)

[0009] [ka]

[0010] [ka] (a in formula (4) and b in formula (5) are integers of 0 to 2; c in formula (5) is an integer of 2 to 5; d in formula (6) and e in formula (7) are integers of 0 to 2; f in formula (7) is an integer of 2 to 5; at least one of b in formula (5) and d in formula (6) is 1 or more; X is O, NH, CH 2 In the formulas (4) to (7), at least one of X is NH; R 1 or R 5 When X is NH, R 1 or R 5 is either an alkyl group which may have a substituent, or an organic group having a double bond or a triple bond.

[0011] The compound according to the first aspect of the present invention preferably includes the features described in the following items [2] to

[12] . It is also preferable to combine two or more of these features. [2] The fluorinated ether compound according to [1], wherein the number of secondary amine structures contained in the molecule is two or more. [3] The fluorinated ether compound according to [1] or [2], wherein the number of hydroxyl groups contained in the molecule is 4 or less. [4] The fluorinated ether compound according to any one of [1] to [3], wherein the total number of secondary amine structures and hydroxyl groups contained in the molecule is 7 or less. [5] The fluorine-containing ether compound according to any one of [1] to [4], wherein the number of secondary amine structures contained in the molecule is 2 or more, the number of hydroxyl groups is 4 or less, and the total number of secondary amine structures and hydroxyl groups is 7 or less.

[0012] [6] R in the above formula (1) 2 is any one of the following formulae (11-1) to (11-5):

[0013] [ka]

[0014] [7] The fluorine-containing ether compound according to any one of [1] to [6], wherein the optionally substituted alkyl group is an alkyl group having 1 to 6 carbon atoms and a hydroxyl group. [8] The fluorine-containing ether compound according to any of [1] to [7], wherein the organic group having a double bond or a triple bond is any one of a group containing an aromatic hydrocarbon, a group containing an aromatic heterocycle, an alkenyl group, and an alkynyl group.

[0015] [9] R in the above formula (1) 3 is any one of the following formulae (8) to (10): -CF 2 O-(CF 2 CF 2 O) m -(CF 2 O) n -CF 2 - (8) (In formula (8), m and n each represent an average degree of polymerization and are 0 to 30; however, m or n is 0.1 or more.) -CF(CF 3 )-(OCF(CF 3 )CF 2 ) y -OCF(CF 3 )- (9) (In formula (9), y represents the average degree of polymerization and is from 0.1 to 30.) -CF 2 CF 2 O-(CF 2 CF 2 CF 2 O) z -CF 2 CF 2 - (10) (In formula (10), z represents the average degree of polymerization and is from 0.1 to 30.)

[0016]

[10] The fluorinated ether compound according to any of [1] to [9], wherein the sum of a in said formula (4) and b in said formula (5), and the sum of d in said formula (6) and e in said formula (7) are each 1 or more.

[0017]

[11] The fluorinated ether compound according to [1], wherein the compound represented by formula (1) is any of compounds represented by the following formulae (K) to (M), (S), and (T):

[0018] [ka] (In formula (K), mk and nk represent average degrees of polymerization, mk represents 1 to 30, and nk represents 0 to 30.) (In formula (L), ml and nl represent average degrees of polymerization, ml represents 1 to 30, and nl represents 0 to 30.) (In formula (M), mm and nm represent average degrees of polymerization, mm represents 1 to 30, and nm represents 0 to 30.) (In formula (S), ms and ns represent average degrees of polymerization, ms represents 1 to 30, and ns represents 0 to 30.) (In formula (T), mt and nt represent average degrees of polymerization, mt represents 1 to 30, and nt represents 0 to 30.)

[0019]

[12] The fluorinated ether compound according to any one of [1] to

[11] , having a number average molecular weight in the range of 500 to 10,000. A second aspect of the present invention is the following lubricant.

[13] A lubricant for magnetic recording media, comprising the fluorinated ether compound according to any one of [1] to

[12] .

[0020] A third aspect of the present invention is a magnetic recording medium as follows.

[14] A magnetic recording medium comprising at least a magnetic layer, a protective layer, and a lubricating layer provided in that order on a substrate, the lubricating layer comprising a fluorine-containing ether compound according to any one of [1] to

[12] . The above magnetic recording medium preferably includes the following features.

[15] The magnetic recording medium according to

[14] , wherein the lubricating layer has an average thickness of 0.5 nm to 2.0 nm. Effect of the Invention

[0021] The fluorine-containing ether compound of the present invention is a compound represented by the above formula (1), and is suitable as a material for a lubricant for a magnetic recording medium. Since the lubricant for magnetic recording media of the present invention contains the fluorine-containing ether compound of the present invention, it is possible to form a lubricating layer that has excellent abrasion resistance even if it is thin. The magnetic recording medium of the present invention has excellent reliability and durability because it is provided with a lubricating layer having excellent wear resistance. [Brief description of the drawings]

[0022] [Figure 1] 1 is a schematic cross-sectional view showing a preferred embodiment of a magnetic recording medium of the present invention. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0023] Preferred examples of the fluorine-containing ether compound, the lubricant for magnetic recording media (hereinafter sometimes abbreviated as "lubricant") and the magnetic recording media of the present invention will be described in detail below. Note that the present invention is not limited to the following embodiments. For example, the present invention is not limited to the following examples, and the number, amount, ratio, composition, type, position, material, configuration, etc. can be added, omitted, replaced, or changed within the scope of the present invention.

[0024] [Fluorine-containing ether compounds] The fluorine-containing ether compound of the present embodiment is represented by the following formula (1). R 1 -R 2 -CH 2 -R 3 -CH 2 -R 4 -R 5 (1) (In formula (1), R 3 is a perfluoropolyether chain; R 1 is R 2 is an end group bonded to; R 5 is R 4 is an end group bonded to; R 1 and R 5 each independently represents an alkyl group which may have a substituent, an organic group having a double bond or a triple bond, or a hydrogen atom; -R 2 -CH 2 -R 3 is expressed by the following formula (2); R 3 -CH 2 -R 4 - is expressed by the following formula (3).

[0025] -[A]-[B]-O-CH 2 -R 3 (2) R 3 -CH 2 -O-[C]-[D]- (3) (In formula (2), [A] is represented by the following formula (4), and [B] is represented by the following formula (5); [A] and [B] may be interchanged in formula (2).) (In formula (3), [C] is represented by the following formula (6), and [D] is represented by the following formula (7); [C] and [D] may be interchanged in formula (3).)

[0026] [ka] (a in formula (4) and b in formula (5) are integers of 0 to 2; c in formula (5) is an integer of 2 to 5; d in formula (6) and e in formula (7) are integers of 0 to 2; f in formula (7) is an integer of 2 to 5; at least one of b in formula (5) and d in formula (6) is 1 or more; X is O, NH, CH 2 In the formulas (4) to (7), at least one of X is NH; R 1 or R 5 When X is NH, R 1 or R5 is either an alkyl group which may have a substituent, or an organic group having a double bond or a triple bond. In the above formula, a, b, d, and e may each be 0, 1, or 2, and c and f may each be 2, 3, 4, or 5.

[0027] Here, the reason why excellent wear resistance can be obtained even if the lubricating layer is thin when a lubricating layer containing the fluorine-containing ether compound of this embodiment is used to form the lubricating layer on the protective layer of a magnetic recording medium will be explained.

[0028] The fluorine-containing ether compound of the present embodiment is represented by the formula (1), 3 In the lubricating layer containing the fluorine-containing ether compound of this embodiment, the PFPE chain coats the surface of the protective layer and imparts lubricity to the lubricating layer, thereby reducing the frictional force between the magnetic head and the protective layer.

[0029] In addition, -R in formula (1) 2 -CH 2 -R 3 is expressed by the above formula (2), and R 3 -CH 2 -R 4 - is represented by the above formula (3). In formula (2), [A] is represented by the above formula (4), and [B] is represented by the above formula (5). In formula (3), [C] is represented by the above formula (6), and [D] is represented by the above formula (7). At least one of b in formula (5) and d in formula (6) is 1 or more, X in formulas (4) to (7) is a divalent linking group bonded to a carbon atom in formulas (4) to (7), and at least one of X in formulas (4) to (7) is NH. Therefore, the fluorine-containing ether compound represented by formula (1) is R 2 and R 4 R contains a total of one or more hydroxyl groups (-OH) and secondary amine structures (-NH-). 2 and R 4The hydroxyl group and secondary amine structure contained in the above improve the wear resistance by bonding the fluorine-containing ether compound and the protective layer in the lubricant containing the fluorine-containing ether compound of this embodiment.

[0030] The hydroxyl group (-OH) and secondary amine structure (-NH-) of the fluorine-containing ether compound shown in formula (1) have polarity and have an interaction (affinity) with the protective layer and an intramolecular interaction. The interaction of the secondary amine structure with the protective layer is equivalent to that of the hydroxyl group. However, the intramolecular interaction of the secondary amine structure is weaker than that of the hydroxyl group. For this reason, in the -NH- contained in the fluorine-containing ether compound shown in formula (1) on the protective layer, the interaction with the protective layer surface takes precedence over the intramolecular interaction. As a result, the fluorine-containing ether compound shown in formula (1) is less likely to aggregate on the protective layer than a fluorine-containing ether compound having the same number of hydroxyl groups as the number of -NH- instead of the -NH- contained in the fluorine-containing ether compound shown in formula (1), and can form a thin lubricating layer with a sufficient coverage. From these facts, a lubricating layer having excellent wear resistance can be obtained by using a lubricant containing the fluorine-containing ether compound shown in formula (1).

[0031] R 2 is a divalent linking group, -R 2 -CH 2 -R 3 is represented by the above formula (2). In formula (2), [A] is represented by the above formula (4), and [B] is represented by the above formula (5). In formula (2), [A] and [B] may be interchanged. a in formula (4) and b in formula (5) are integers of 0 to 2, and c in formula (5) is an integer of 2 to 5.

[0032] In order to further improve the adhesion between the fluorine-containing ether compound and the protective layer in the lubricating layer containing the fluorine-containing ether compound, it is preferable that at least one of a in formula (4) and b in formula (5) is 1 or more (i.e., formula (2) contains at least one of [A] and [B]). The sum of a in formula (4) and b in formula (5) is 4 or less, and preferably 2 or less. If the sum of a in formula (4) and b in formula (5) is 2 or less, the polarity of the fluorine-containing ether compound becomes too high, which is preferable because it can prevent the occurrence of pickup that adheres to the magnetic head as foreign matter (smear). In formula (5), c is an integer of 2 to 5, preferably an integer of 2 to 4, and most preferably 2. When c in formula (5) is an integer of 2 to 5, the hydroxyl group and R 1 and / or the distance between the hydroxyl groups in formula (5) is appropriate, which is preferable.

[0033] X in formula (4) and formula (5) is O, NH, CH 2 Either 1 When X is NH, R 1 is either an alkyl group which may have a substituent, or an organic group which has a double bond or a triple bond, and cannot be a hydrogen atom. -R in formula (1) 2 -(-[A]-[B]-O- in formula (2)) is preferably any of the structures represented by the following formulae (11-1) to (11-5) and (12-1) to (12-5). In the structures represented by formulae (11-1) to (11-5) and (12-1) to (12-5), R is added to the linking group (NH or O) located on the leftmost side. 1 are combined.

[0034] [ka]

[0035] In formulae (11-1) to (11-5) and formulae (12-1) to (12-5), a is the numerical value of a in formula (4), and b and c are the numerical values ​​of b and c in formula (5), respectively. Formulae (11-1) to (11-5) represent structures in which X is NH in formulae (4) and (5). Formulae (12-1) to (12-5) represent structures in which X is O in formulae (4) and (5). In the fluorine-containing ether compound of the present embodiment, -R 2 can be appropriately selected depending on the performance required of the lubricant containing the fluorine-containing ether compound.

[0036] R 4 is a divalent linking group, R 3 -CH 2 -R 4 - is represented by the above formula (3). In formula (3), [C] is represented by the above formula (6), and [D] is represented by the above formula (7). In formula (3), [C] and [D] may be interchanged. d in formula (6) and e in formula (7) are integers of 0 to 2, and f in formula (7) is an integer of 2 to 5.

[0037] In the lubricating layer containing a fluorine-containing ether compound, at least one of d in formula (6) and e in formula (7) is preferably 1 or more (i.e., formula (3) contains at least one of [C] and [D]) in order to further improve the adhesion between the fluorine-containing ether compound and the protective layer. The sum of d in formula (6) and e in formula (7) is 4 or less, and preferably 2 or less. If the sum of d in formula (6) and e in formula (7) is 2 or less, the polarity of the fluorine-containing ether compound becomes too high, which can prevent the occurrence of pickup that adheres to the magnetic head as foreign matter (smear), and is therefore preferable. In formula (7), f is an integer of 2 to 5, preferably an integer of 2 to 4, and most preferably 2. When f in formula (7) is an integer of 2 to 5, the hydroxyl group and R 5 and / or the distance between the hydroxyl groups in formula (7) is appropriate, which is preferable.

[0038] X in formula (6) and formula (7) is O, NH, CH2 Either 5 When X is NH, R 5 is either an alkyl group which may have a substituent, or an organic group which has a double bond or a triple bond, and cannot be a hydrogen atom. -R in formula (1) 4 -(-O-[C]-[D]- in formula (3)) is preferably any of the structures represented by the following formulae (13-1) to (13-5) and (14-1) to (14-5). In the structures represented by formulae (13-1) to (13-5) and (14-1) to (14-5), R is added to the linking group (NH or O) located on the rightmost side. 5 are combined.

[0039] [ka]

[0040] In formulae (13-1) to (13-5) and formulae (14-1) to (14-5), d is the numerical value of d in formula (6), and e and f are the numerical values ​​of e and f in formula (7), respectively. Formulae (13-1) to (13-5) represent structures in which X is NH in formulae (6) and (7). Formulae (14-1) to (14-5) represent structures in which X is O in formulae (6) and (7). In the fluorine-containing ether compound of the present embodiment, -R 4 can be appropriately selected depending on the performance required of the lubricant containing the fluorine-containing ether compound.

[0041] In the fluorine-containing ether compound of this embodiment, at least one of b in formula (5) and d in formula (6) is equal to or greater than 1. Therefore, when a in formula (4) and e in formula (7) are both 0 (zero), and one of b in formula (5) and d in formula (6) is 0 (zero) (i.e., [A] and [D] are not included, and at least one of [B] and [C] are included), R in formula (1) 2 or R 4 Among these, one of the bonds is an ether bond (-O-), resulting in a fluorine-containing ether compound.

[0042] In this embodiment, it is preferable that at least one of b in formula (5) and d in formula (6) is 1 or greater, and the sum of a in formula (4) and b in formula (5) and the sum of d in formula (6) and e in formula (7) are each 1 or greater.

[0043] In the fluorine-containing ether compound of the present embodiment, R 2 The number of hydroxyl groups (-OH) and R 4 The total number of hydroxyl groups contained in R is 1 or more, and preferably 2 or more. 2 and R 4 It is more preferable that each of R contains one or more hydroxyl groups. 2 and R 4 Each of the groups preferably contains one or more hydroxyl groups, since this improves the adhesion between the fluorine-containing ether compound and the protective layer in the lubricating layer containing the fluorine-containing ether compound. R 2 The number of hydroxyl groups in R 4 The total number of hydroxyl groups contained in R is 8 or less, preferably 6 or less, and more preferably 4 or less. 2 The number of hydroxyl groups in R 4 When the total number of hydroxyl groups contained in is 8 or less, the polarity of the fluorine-containing ether compound becomes too high, and pickup of foreign matter (smear) adhering to a magnetic head can be prevented, which is preferable.

[0044] In the fluorine-containing ether compound represented by formula (1), the total number of hydroxyl groups contained in the molecule is preferably 6 or less, more preferably 4 or less. When the total number of hydroxyl groups contained in the molecule is 6 or less, aggregation of the fluorine-containing ether compound on the protective layer due to intramolecular interaction of the hydroxyl groups is unlikely to occur. Therefore, a thin lubricating layer can be formed with a better coverage rate, and better wear resistance can be obtained.

[0045] In the fluorine-containing ether compound represented by formula (1), the total number of secondary amine structures (-NH-) contained in the molecule is preferably 2 or more, since this improves the adhesion to the protective layer. In addition, when the total number of secondary amine structures (-NH-) contained in the molecule is 2 or more, R 2 and R 4 It is more preferable that each of R contains one or more secondary amine structures (-NH-). 2 and R 4 When each of these groups contains one or more secondary amine structures (-NH-), the adhesion between the fluorine-containing ether compound and the protective layer in the lubricating layer containing the fluorine-containing ether compound is improved.

[0046] In the fluorine-containing ether compound represented by formula (1), the total number of hydroxyl groups and secondary amine structures (-NH-) contained in the molecule is preferably 7 or less, more preferably 6 or less. In this case, aggregation of the fluorine-containing ether compound on the protective layer due to intramolecular interaction of the hydroxyl groups is unlikely to occur, and a synergistic effect of interaction with the protective layer due to the inclusion of the hydroxyl groups and the secondary amine structures is obtained. As a result, better abrasion resistance is obtained.

[0047] In the fluorine-containing ether compound of the present embodiment represented by the above formula (1), R 1 is R 2 is an end group bonded to R 5 is R 4 is an end group bonded to R 1 and R 5 are each independently any one of an alkyl group which may have a substituent, an organic group having a double bond or a triple bond, and a hydrogen atom. The alkyl group which may have a substituent and the organic group having a double bond or a triple bond may contain any one of an oxygen atom, a sulfur atom, and a nitrogen atom.

[0048] The alkyl group in the alkyl group which may have a substituent is preferably an alkyl group having 1 to 8 carbon atoms, and more preferably an alkyl group having 1 to 6 carbon atoms. Specific examples include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group, and may be linear or branched.

[0049] Examples of the substituent in the alkyl group which may have a substituent include a halogeno group, an alkoxy group, a hydroxyl group, etc. When the alkyl group which may have a substituent has such a substituent, the fluorine-containing ether compound can form a lubricating layer having better wear resistance. The alkyl group having a halogeno group as a substituent is preferably an alkyl group having at least one fluoro group. Examples of the alkyl group having a fluoro group include a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, a perfluorohexyl group, an octafluoropentyl group, and a tridecafluorooctyl group.

[0050] The alkyl group having a hydroxyl group as a substituent is preferably an alkyl group having 1 to 6 carbon atoms and a hydroxyl group, and more preferably an alkyl group represented by the following formula (19-1): 1 and R 5 At least one of the groups represented by the formula (19-1) is preferably an alkyl group represented by the formula (19-1), since the affinity between the lubricating layer containing this fluorine-containing ether compound and the protective layer is further improved.

[0051] [ka] (In formula (19-1), R 6 represents an alkyl group having 1 to 4 carbon atoms or a hydrogen atom, and h represents an integer of 1 to 6.

[0052] In formula (19-1), R 6is an alkyl group having 1 to 4 carbon atoms or a hydrogen atom, and is preferably a hydrogen atom. In the structure represented by formula (19-1), the left side is R 2 or R 4 In formula (19-1), h represents an integer of 1 to 6, preferably an integer of 1 to 4, and more preferably 2 or 3. The number of carbon atoms in formula (19-1) (R 6 It is preferable that the total number of carbon atoms contained in and h is from 1 to 6, since there is no decrease in the surface free energy of the entire molecule due to a low proportion of fluorine atoms in the fluorine-containing ether compound molecule.

[0053] The organic group having a double bond or a triple bond has at least one double bond or a triple bond, and examples thereof include a group containing an aromatic hydrocarbon, a group containing an aromatic heterocycle, an alkenyl group, an alkynyl group, etc. Specifically, the organic group having a double bond or a triple bond is a phenyl group, a methoxyphenyl group, a fluorinated phenyl group, a naphthyl group, a phenethyl group, a methoxyphenethyl group, a fluorinated phenethyl group, a benzyl group, a methoxybenzyl group, a naphthylmethyl group, a methoxynaphthyl group, a pyrrolyl group, a pyrazolyl group, a methylpyrazolylmethyl group, an imidazolyl group, a furyl group, a furfuryl group, an oxazolyl group, an isoxazolyl group, a thienyl group, a thienylethyl group, a thiazolyl group, a methylthiazolylethyl group, an isothiazolyl group, a pyridyl group, a pyrimidinyl group, a pyrimidine group, a phenyl group, a methoxyphenyl group, a fluorinated phenyl group, a naphthyl group, a phenethyl group, a methoxyphenethyl group, a fluorinated phenethyl group, a benzyl group, a methoxybenzyl group, a naphthylmethyl group, a methoxynaphthyl group, a pyrrolyl group, a pyrazolyl group, a methylpyrazolylmethyl group, an imidazolyl group, a furyl group, a furfuryl group, an oxazolyl group, an isoxazolyl group, a thienyl group, a thienylethyl group, a thiazolyl group, a methylthiazolylethyl group, an isothiazolyl group, a pyridyl group, a pyrimidinyl group, a pyrimidinyl group, a pyrimidinyl group, a pyrimidinyl group, a pyrimidinyl group, a pyrimidinyl group, a pyrimidin The aryl group may be a phenyl group, a pyridazinyl group, a pyrazinyl group, an indolinyl group, a benzofuranyl group, a benzothienyl group, a benzimidazolyl group, a benzoxazolyl group, a benzothiazolyl group, a benzopyrazolyl group, a benzoisoxazolyl group, a benzoisothiazolyl group, a quinolyl group, an isoquinolyl group, a quinazolinyl group, a quinoxalinyl group, a phthalazinyl group, a cinnolinyl group, a vinyl group, an allyl group, a butenyl group, a propynyl group, a propargyl group, a butynyl group, a methylbutynyl group, a pentynyl group, a methylpentynyl group, or a hexynyl group.

[0054] As the organic group having double or triple bond, among the above, particularly, phenyl group, methoxyphenyl group, thienylethyl group, butenyl group, allyl group, propargyl group, phenethyl group, methoxyphenethyl group, fluorinated phenethyl group are preferred, and phenyl group, thienylethyl group, allyl group, butenyl group are more preferred.When the organic group having double or triple bond is phenyl group, thienylethyl group, allyl group, butenyl group, the fluorine-containing ether compound can form a lubricating layer with better wear resistance. The organic group having a double bond or a triple bond may have a substituent such as an alkyl group, an alkoxy group, a hydroxy group, a mercapto group, a carboxy group, a carbonyl group or an amino group.

[0055] In the fluorine-containing ether compound of the present embodiment represented by the above formula (1), R 3 is a perfluoropolyether chain (PFPE chain). 3 is not particularly limited and can be appropriately selected depending on the performance required for the lubricant containing the fluorine-containing ether compound, etc. Examples of the PFPE chain include perfluoromethylene oxide polymer, perfluoroethylene oxide polymer, perfluoro-n-propylene oxide polymer, perfluoroisopropylene oxide polymer, and copolymers thereof.

[0056] Specifically, R in formula (1) 3 is preferably any one of the following formulas (8) to (10). In addition, the repeating unit (CF 2 CF 2 O) and (CF 2 The order of the monomer units (CF 2 -CF 2 -O) and (CF 2 -O) may be any of a random copolymer, a block copolymer, and an alternating copolymer.

[0057] -CF 2 O-(CF2 CF 2 O) m -(CF 2 O) n -CF 2 - (8) (In formula (8), m and n each represent an average degree of polymerization and are 0 to 30; however, m or n is 0.1 or more.) -CF(CF 3 )-(OCF(CF 3 )CF 2 ) y -OCF(CF 3 )- (9) (In formula (9), y represents the average degree of polymerization and is from 0.1 to 30.) -CF 2 CF 2 O-(CF 2 CF 2 CF 2 O) z -CF 2 CF 2 - (10) (In formula (10), z represents the average degree of polymerization and is from 0.1 to 30.)

[0058] When y and z in formula (9) and formula (10) are each 0.1 to 30, and when m and n in formula (8) are each 0 to 30 and m or n is 0.1 or more, the lubricant containing them is easy to apply, and a lubricating layer having good wear resistance is obtained. Therefore, m, n, y, and z are each 30 or less, and preferably 20 or less. m, n, y, and z may be 15 or less, 10 or less, or 5 or less. m, n, y, and z may be 0.5 or more, 1 or more, or 3 or more.

[0059] R in formula (1) 3 When R is any one of the formulas (8) to (10), the synthesis of the fluorine-containing ether compound is easy, which is preferable. 3 is represented by formula (8), it is more preferable since the raw materials are easily available. Also, R 3When R is any one of formulas (8) to (10), the ratio of the number of oxygen atoms (the number of ether bonds (-O-)) to the number of carbon atoms in the perfluoropolyether chain is appropriate. This results in a fluorine-containing ether compound with appropriate hardness. Therefore, the fluorine-containing ether compound applied onto the protective layer is less likely to aggregate on the protective layer, and a thinner lubricating layer can be formed with a sufficient coverage. In addition, R 3 When is any one of the formulas (8) to (10), the fluorine-containing ether compound provides a lubricating layer having good wear resistance.

[0060] In the fluorine-containing ether compound represented by formula (1), R 1 and R 5 may be the same or different. 1 and R 5 It is preferable that the above ratios are the same because they can be easily produced. In the fluorine-containing ether compound represented by formula (1), R 2 and R 4 may be the same or different. 2 and R 4 It is preferable that the above ratios are the same because they can be easily produced. Therefore, R of the fluorine-containing ether compound represented by formula (1) 1 and R 5 is the same and R 2 and R 4 It is preferable that the number of the fluorine atoms is equal to that of the fluorine atoms, since this makes it easier to manufacture.

[0061] Specifically, the fluorine-containing ether compound represented by formula (1) is preferably any of the compounds represented by the following formulae (A) to (Z). Note that the repeat numbers ma to mw, na to nw, x, y, and z in formulae (A) to (Z) are values ​​indicating average values ​​and are not necessarily integers. The repeat numbers ma to mw represent 1 to 30, and may be 2 to 20, 3 to 15, or 5 to 10, but are not limited to these examples. The repeat numbers na to nw represent 0 to 30, and may be 0.5 to 20, 1 to 15, or 5 to 10, but are not limited to these examples. The repeat numbers x, y, and z represent 0.1 to 30, and may be 1 to 20, 3 to 15, or 5 to 10, but are not limited to these examples.

[0062] The compound represented by formula (A) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkenyl group. The compound represented by formula (A) is 1 , R 5 is the same, and R 2 , R 4 is the same. The compound represented by formula (B) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [B], X is NH, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [D], X is NH, e is 1, f is 2, and R 5 is an alkenyl group. The compound represented by formula (B) is 1 , R 5 is the same, and R 2 , R 4 is the same.

[0063] The compound represented by formula (C) is a compound represented by formula (1), 1 is an alkyl group, and R 2 has [A], X is NH, a is 1, and R3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group. The compound represented by formula (C) is 1 , R 5 is the same, and R 2 , R 4 is the same. The compound represented by formula (D) is a compound represented by formula (1), 1 is a group containing an aromatic hydrocarbon, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is a group containing an aromatic hydrocarbon. The compound represented by formula (D) is 1 , R 5 is the same, and R 2 , R 4 is the same.

[0064] The compound represented by formula (E) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 2, and R 5 is an alkenyl group. The compound represented by formula (E) is 1 , R 5 is the same, and R 2 , R 4 is the same. The compound represented by formula (F) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A] and [B], in each of which X is NH, a is 1, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C] and [D], in which X is NH, d is 1, e is 1, f is 2, and R 5 is an alkenyl group. The compound represented by formula (F) is 1 , R5 is the same, and R 2 , R 4 is the same.

[0065] The compound represented by formula (G) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (H) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [B], X is NH, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0066] The compound represented by formula (I) is a compound represented by formula (1), 1 is an alkyl group, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (J) is a compound represented by formula (1), 1 is a group containing an aromatic hydrocarbon, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0067] The compound represented by formula (K) is a compound represented by formula (1), 1 is an alkenyl group, and R 2has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (L) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A] and [B], each of X is NH, a is 1, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (M) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is O, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0068] The compound represented by formula (N) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (O) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [B], X is NH, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0069] The compound represented by formula (P) is a compound represented by formula (1),1 is an alkyl group, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (Q) is a compound represented by formula (1), 1 is a group containing an aromatic hydrocarbon, and R 2 has [A], X is NH, a is 1, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0070] The compound represented by formula (R) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is O, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (S) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (T) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A] and [B], each of X is NH, a is 1, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0071] The compound represented by formula (U) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is O, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 2, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (V) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 2, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (W) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A] and [B], each of X is NH, a is 1, b is 1, c is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 2, and R 5 is an alkyl group having a hydroxyl group at the end.

[0072] The compound represented by formula (X) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (8), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end. The compound represented by formula (Y) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (9), and R 4 has [C], X is NH, d is 1, and R 5is an alkyl group having a hydroxyl group at the end. The compound represented by formula (Z) is a compound represented by formula (1), 1 is an alkenyl group, and R 2 has [A], X is NH, a is 2, and R 3 is Equation (10), and R 4 has [C], X is NH, d is 1, and R 5 is an alkyl group having a hydroxyl group at the end.

[0073] Compounds represented by formulas (A) to (Z) are shown below.

[0074] [ka] (In formula (A), ma and na represent average degrees of polymerization, ma represents 1 to 30, and na represents 0 to 30.) (In formula (B), mb and nb represent average degrees of polymerization, mb represents 1 to 30, and nb represents 0 to 30.) (In formula (C), mc and nc represent average degrees of polymerization, mc represents 1 to 30, and nc represents 0 to 30.) (In formula (D), md and nd represent average degrees of polymerization, md represents 1 to 30, and nd represents 0 to 30.)

[0075] [ka] (In formula (E), me and ne represent average degrees of polymerization, me represents 1 to 30, and ne represents 0 to 30.) (In formula (F), mf and nf represent average degrees of polymerization, mf represents 1 to 30, and nf represents 0 to 30.) (In formula (G), mg and ng represent average degrees of polymerization, mg represents 1 to 30, and ng represents 0 to 30.) (In formula (H), mh and nh represent average degrees of polymerization, mh represents 1 to 30, and nh represents 0 to 30.)

[0076] [ka] (In formula (I), mi and ni represent average degrees of polymerization, mi represents 1 to 30, and ni represents 0 to 30.) (In formula (J), mj and nj represent average degrees of polymerization, mj represents 1 to 30, and nj represents 0 to 30.) (In formula (K), mk and nk represent average degrees of polymerization, mk represents 1 to 30, and nk represents 0 to 30.) (In formula (L), ml and nl represent average degrees of polymerization, ml represents 1 to 30, and nl represents 0 to 30.)

[0077] [ka] (In formula (M), mm and nm represent average degrees of polymerization, mm represents 1 to 30, and nm represents 0 to 30.) (In the formula (N), mn and nn represent average degrees of polymerization, mn represents 1 to 30, and nn represents 0 to 30.) (In formula (O), mo and no represent average degrees of polymerization, mo represents 1 to 30, and no represents 0 to 30.) (In formula (P), mp and np represent average degrees of polymerization, mp represents 1 to 30, and np represents 0 to 30.)

[0078] [ka] (In formula (Q), mq and nq represent average degrees of polymerization, mq represents 1 to 30, and nq represents 0 to 30.) (In formula (R), mr and nr represent average degrees of polymerization, mr represents 1 to 30, and nr represents 0 to 30.) (In formula (S), ms and ns represent average degrees of polymerization, ms represents 1 to 30, and ns represents 0 to 30.) (In formula (T), mt and nt represent average degrees of polymerization, mt represents 1 to 30, and nt represents 0 to 30.)

[0079] [ka] (In formula (U), mu and nu represent average degrees of polymerization, mu represents 1 to 30, and nu represents 0 to 30.) (In formula (V), mv and nv represent average degrees of polymerization, mv represents 1 to 30, and nv represents 0 to 30.) (In formula (W), mw and nw represent average degrees of polymerization, mw represents 1 to 30, and nw represents 0 to 30.)

[0080] [ka] (In formula (X), x represents an average degree of polymerization, and x represents 0.1 to 30.) (In formula (Y), y represents an average degree of polymerization, and y represents 0.1 to 30.) (In formula (Z), z represents an average degree of polymerization, and z represents 0.1 to 30.)

[0081] When the compound represented by formula (1) is any of the compounds represented by the above formulas (A) to (Z), the raw materials are easily available, and a lubricating layer that has excellent wear resistance even when thin can be formed, which is preferable.

[0082] The fluorine-containing ether compound of this embodiment preferably has a number average molecular weight (Mn) in the range of 500 to 10,000. When the number average molecular weight is 500 or more, the lubricant containing the fluorine-containing ether compound of this embodiment is less likely to evaporate, and the lubricant can be prevented from evaporating and transferring to the magnetic head. The number average molecular weight of the fluorine-containing ether compound is more preferably 1,000 or more. In addition, when the number average molecular weight is 10,000 or less, the viscosity of the fluorine-containing ether compound becomes appropriate, and a thin lubricating layer can be easily formed by applying a lubricant containing this. The number average molecular weight of the fluorine-containing ether compound is more preferably 3,000 or less, since the viscosity becomes easy to handle when applied to a lubricant.

[0083] The number average molecular weight (Mn) of fluorine-containing ether compounds was measured using AVANCEIII400 manufactured by Bruker Biospin. 1 H-NMR and19 This is a value measured by F-NMR. In the NMR (nuclear magnetic resonance) measurement, the sample was diluted in a single or mixed solvent such as hexafluorobenzene, d-acetone, or d-tetrahydrofuran and used for the measurement. 19 The standard for F-NMR chemical shifts is the hexafluorobenzene peak at -164.7 ppm. 1 The reference for H-NMR chemical shifts was set to the acetone peak at 2.2 ppm.

[0084] "Manufacturing method" The method for producing the fluorinated ether compound of the present embodiment is not particularly limited, and the compound can be produced by a conventionally known production method. The fluorinated ether compound of the present embodiment can be produced, for example, by the production method shown below. First, R in Equation (1) 3 At both ends of the perfluoropolyether chain corresponding to 2 A fluorine-based compound having a fluorine atom and an OH group is prepared.

[0085] Next, the hydroxyl group of the hydroxymethyl group located at one end of the fluorine-based compound is converted to R 1 -R 2 Then, the hydroxyl group of the hydroxymethyl group located at the other end is replaced with a group consisting of -R 4 -R 5 (second reaction) The first and second reactions can be carried out by a conventional method. 1 , R 2 , R 4 , R 5 The reaction time can be appropriately determined depending on the type of R. In addition, either the first reaction or the second reaction may be carried out first. 1 , R 5 is the same, and R 2 , R 4 When they are the same, the first and second reactions may be carried out simultaneously. By the above method, the compound represented by formula (1) can be obtained.

[0086] In this embodiment, -R 2 -CH 2 -R 3 is expressed by equation (2), and R 3 -CH 2 -R 4 In order to produce a fluorine-containing ether compound represented by formula (3), it is preferable to use an epoxy compound. This epoxy compound may be purchased commercially or may be synthesized. When synthesizing an epoxy compound, R of the fluorine-containing ether compound to be produced is 1 or R 5 The epoxy compound can be synthesized by using an alcohol or a protected amine having a structure corresponding to the terminal group represented by the formula (1) and any one selected from epichlorohydrin, epibromohydrin, and 2-bromoethyloxirane. The epoxy compound may also be synthesized by oxidizing an unsaturated bond.

[0087] The fluorine-containing ether compound of the present embodiment is a compound represented by the above formula (1). Therefore, when a lubricating layer is formed on a protective layer using a lubricant containing this compound, R 3 The surface of the protective layer is covered with the PFPE chain represented by the formula (I) and the frictional force between the magnetic head and the protective layer is reduced. In addition, in the lubricating layer formed using the lubricant containing the fluorine-containing ether compound of this embodiment, R 1 and R 5 and a terminal group represented by R 2 and R 4 Excellent wear resistance is achieved by intramolecular interactions between the secondary amine structure (-NH-) and the hydroxyl group contained in the polymer.

[0088] In the fluorine-containing ether compound of the present embodiment, R 1 and R 5 and an end group represented by R 2 and R 4The PFPE chain is adhered to the protective layer by the interaction between the protective layer and the hydroxyl group and the secondary amine structure contained in the total of one or more of the following. Therefore, according to the fluorine-containing ether compound of this embodiment, the lubricating layer and the protective layer are firmly bonded to each other, and a lubricating layer having excellent wear resistance can be obtained.

[0089] [Lubricants for magnetic recording media] The lubricant for a magnetic recording medium of this embodiment contains a fluorine-containing ether compound represented by formula (1). The lubricant of the present embodiment can be used by mixing, as necessary, known materials used as lubricant materials, so long as the properties resulting from the inclusion of the fluorinated ether compound represented by formula (1) are not impaired.

[0090] Specific examples of known materials include FOMBLIN (registered trademark) ZDIAC, FOMBLIN ZDEAL, FOMBLIN AM-2001 (all manufactured by Solvay Solexis), Moresco A20H (manufactured by Moresco), etc. The known material to be mixed with the lubricant of the present embodiment preferably has a number average molecular weight of 1,000 to 10,000.

[0091] When the lubricant of this embodiment contains a material other than the fluorinated ether compound represented by formula (1), the content of the fluorinated ether compound represented by formula (1) in the lubricant of this embodiment is preferably 50% by mass or more, more preferably 70% by mass or more. The upper limit can be selected arbitrarily, and may be, for example, 99% by mass or less, 95% by mass or less, 90% by mass or less, or 85% by mass or less.

[0092] The lubricant of the present embodiment contains a fluorine-containing ether compound represented by formula (1), so that even if the thickness is thin, the surface of the protective layer can be covered with a high coverage rate, and a lubricant layer having excellent adhesion to the protective layer can be formed. Therefore, according to the lubricant of the present embodiment, even if the thickness is thin, a lubricant layer having excellent wear resistance can be obtained.

[0093] In addition, since the lubricant of the present embodiment contains the fluorine-containing ether compound represented by formula (1), the fluorine-containing ether compound in the lubricant layer that is not in contact with (adsorbed on) the protective layer is less likely to aggregate, and therefore the fluorine-containing ether compound can be prevented from aggregating and adhering to the magnetic head as foreign matter (smear), suppressing pickup. In addition, since the lubricant of the present embodiment contains a fluorine-containing ether compound represented by formula (1), R 1 and R 5 and terminal groups represented by R 2 and R 4 The interaction between the protective layer and the hydroxyl group (-OH) and secondary amine structure (-NH-) contained in the rubber composition (a total of one or more of the above) forms a lubricating layer that provides excellent wear resistance.

[0094] [Magnetic recording media] The magnetic recording medium of this embodiment has at least a magnetic layer, a protective layer, and a lubricating layer provided in this order on a substrate. In the magnetic recording medium of this embodiment, one or more underlayers may be provided between the substrate and the magnetic layer, if necessary. Also, an adhesive layer and / or a soft magnetic layer may be provided between the underlayer and the substrate.

[0095] FIG. 1 is a schematic cross-sectional view showing one embodiment of a magnetic recording medium of the present invention. The magnetic recording medium 10 of this embodiment has a structure in which an adhesive layer 12, a soft magnetic layer 13, a first underlayer 14, a second underlayer 15, a magnetic layer 16, a protective layer 17, and a lubricating layer 18 are sequentially provided on a substrate 11.

[0096] "substrate" Any material can be selected for the substrate 11. As the base material 11, for example, a non-magnetic substrate in which a film made of NiP or a NiP alloy is formed on a base made of a metal or an alloy material such as Al or an Al alloy can be preferably used. In addition, the substrate 11 may be a non-magnetic substrate made of a non-metallic material such as glass, ceramics, silicon, silicon carbide, carbon, or resin, or a non-magnetic substrate having a NiP or NiP alloy film formed on a base made of these non-metallic materials.

[0097] "Adhesion layer" The adhesive layer 12 prevents the progress of corrosion of the substrate 11, which occurs when the substrate 11 and the soft magnetic layer 13 provided on the adhesive layer 12 are disposed in contact with each other. The material of the adhesive layer 12 can be arbitrarily selected, and can be appropriately selected from, for example, Cr, a Cr alloy, Ti, a Ti alloy, CrTi, NiAl, an AlRu alloy, etc. The adhesive layer 12 can be formed by, for example, a sputtering method.

[0098] "Soft magnetic layer" The soft magnetic layer 13 may be selected arbitrarily, but preferably has a structure in which a first soft magnetic film, an intermediate layer made of a Ru film, and a second soft magnetic film are laminated in this order. That is, the soft magnetic layer 13 preferably has a structure in which the intermediate layer made of a Ru film is sandwiched between two soft magnetic films, and the soft magnetic films above and below the intermediate layer are anti-ferro-coupling (AFC).

[0099] The first and second soft magnetic films may be made of a material such as a CoZrTa alloy or a CoFe alloy. It is preferable to add any one of Zr, Ta, and Nb to the CoFe alloy used in the first and second soft magnetic films, which promotes the amorphization of the first and second soft magnetic films, improves the orientation of the first underlayer (seed layer), and reduces the flying height of the magnetic head. The soft magnetic layer 13 can be formed by, for example, a sputtering method.

[0100] "First base layer" The first underlayer 14 is a layer for controlling the orientation and crystal size of the second underlayer 15 and the magnetic layer 16 provided thereon. The first underlayer 14 may be, for example, a Cr layer, a Ta layer, a Ru layer, or an alloy layer of CrMo, CoW, CrW, CrV, or CrTi. The first underlayer 14 can be formed by, for example, a sputtering method.

[0101] "Second base layer" The second underlayer 15 is a layer that controls the orientation of the magnetic layer 16 so that it is favorable. The second underlayer 15 can be selected arbitrarily, but is preferably a layer made of Ru or a Ru alloy. The second underlayer 15 may be a layer made of one layer, or may be made of multiple layers. When the second underlayer 15 is made of multiple layers, all the layers may be made of the same material, or at least one layer may be made of a different material. The second underlayer 15 can be formed by, for example, a sputtering method.

[0102] "Magnetic layer" The magnetic layer 16 is made of a magnetic film with an easy axis of magnetization oriented perpendicular or parallel to the substrate surface. The magnetic layer 16 can be selected arbitrarily, but is preferably a layer containing Co and Pt, and may be a layer containing an oxide, Cr, B, Cu, Ta, Zr, etc. to further improve the SNR characteristics. The oxide contained in the magnetic layer 16 is SiO 2 , SiO, Cr 2 O 3 , CoO, Ta 2 O 3 , TiO 2 etc.

[0103] The magnetic layer 16 may be composed of a single layer, or may be composed of multiple magnetic layers made of materials with different compositions. For example, when the magnetic layer 16 is composed of three layers, a first magnetic layer, a second magnetic layer, and a third magnetic layer, stacked in this order from the bottom, the first magnetic layer preferably has a granular structure made of a material containing Co, Cr, and Pt and further containing an oxide. As the oxide contained in the first magnetic layer, it is preferable to use oxides of Cr, Si, Ta, Al, Ti, Mg, Co, etc., among which TiO2 , Cr 2 O 3 , SiO 2 The first magnetic layer is preferably made of a composite oxide containing two or more kinds of oxides. 2 O 3 -SiO 2 , Cr 2 O 3 -TiO 2 , SiO 2 -TiO 2 etc. can be suitably used.

[0104] The first magnetic layer may contain, in addition to Co, Cr, Pt, and oxides, one or more elements selected from B, Ta, Mo, Cu, Nd, W, Nb, Sm, Tb, Ru, and Re. The second magnetic layer may be made of the same material as the first magnetic layer, and preferably has a granular structure.

[0105] The third magnetic layer preferably has a non-granular structure made of a material that contains Co, Cr, and Pt and does not contain oxides. In addition to Co, Cr, and Pt, the third magnetic layer may contain one or more elements selected from B, Ta, Mo, Cu, Nd, W, Nb, Sm, Tb, Ru, Re, and Mn.

[0106] When the magnetic layer 16 is formed of multiple magnetic layers, it is preferable to provide a nonmagnetic layer between adjacent magnetic layers. When the magnetic layer 16 is formed of three layers, a first magnetic layer, a second magnetic layer, and a third magnetic layer, it is preferable to provide a nonmagnetic layer between the first magnetic layer and the second magnetic layer and between the second magnetic layer and the third magnetic layer.

[0107] The non-magnetic layer provided between adjacent magnetic layers in the magnetic layer 16 can suitably be made of, for example, Ru, a Ru alloy, a CoCr alloy, or a CoCrX1 alloy (X1 represents one or more elements selected from Pt, Ta, Zr, Re, Ru, Cu, Nb, Ni, Mn, Ge, Si, O, N, W, Mo, Ti, V, and B).

[0108] For the non-magnetic layer provided between adjacent magnetic layers of the magnetic layer 16, it is preferable to use an alloy material containing an oxide, a metal nitride, or a metal carbide. Specifically, the oxide may be, for example, SiO 2 , Al 2 O 3 , Ta 2 O 5 , Cr 2 O 3 , MgO, Y 2 O 3 , TiO 2 Examples of metal nitrides that can be used include AlN, Si 3 N 4 , TaN, CrN, etc. can be used as the metal carbide. For example, TaC, BC, SiC, etc. can be used as the metal carbide. The nonmagnetic layer can be formed by, for example, a sputtering method.

[0109] In order to achieve higher recording density, the magnetic layer 16 is preferably a magnetic layer for perpendicular magnetic recording in which the axis of easy magnetization is oriented perpendicular to the substrate surface, but may also be a magnetic layer for in-plane magnetic recording. The magnetic layer 16 may be formed by any known method such as vapor deposition, ion beam sputtering, magnetron sputtering, etc. The magnetic layer 16 is usually formed by sputtering.

[0110] "Protective layer" The protective layer 17 protects the magnetic layer 16. The protective layer 17 may be made of a single layer or multiple layers. Examples of materials for the protective layer 17 include carbon, carbon containing nitrogen, and silicon carbide. A carbon-based protective layer, particularly an amorphous carbon protective layer, can be preferably used as the protective layer 17. When the protective layer 17 is a carbon-based protective layer, the interaction with the polar group (particularly a hydroxyl group) contained in the fluorine-containing ether compound in the lubricating layer 18 is further enhanced, which is preferable.

[0111] The adhesion between the carbon-based protective layer and the lubricating layer 18 can be controlled by making the carbon-based protective layer from hydrogenated carbon and / or nitrogenated carbon and adjusting the hydrogen content and / or nitrogen content in the carbon-based protective layer. The hydrogen content in the carbon-based protective layer is preferably 3 to 20 atomic % when measured by hydrogen forward scattering (HFS). The nitrogen content in the carbon-based protective layer is preferably 4 to 15 atomic % when measured by X-ray photoelectron spectroscopy (XPS).

[0112] The hydrogen and / or nitrogen contained in the carbon-based protective layer does not need to be uniformly contained throughout the carbon-based protective layer. The carbon-based protective layer is preferably a compositionally graded layer in which, for example, nitrogen is contained on the lubricating layer 18 side of the protective layer 17, and hydrogen is contained on the magnetic layer 16 side of the protective layer 17. In this case, the adhesion between the magnetic layer 16 and the lubricating layer 18 and the carbon-based protective layer is further improved.

[0113] The thickness of the protective layer 17 is preferably 1 nm to 7 nm. If the thickness of the protective layer 17 is 1 nm or more, sufficient performance as the protective layer 17 can be obtained. If the thickness of the protective layer 17 is 7 nm or less, it is preferable from the viewpoint of making the protective layer 17 thinner.

[0114] The protective layer 17 can be formed by a sputtering method using a target material containing carbon, a CVD (chemical vapor deposition) method using a hydrocarbon raw material such as ethylene or toluene, an IBD (ion beam deposition) method, or the like. When a carbon-based protective layer is formed as the protective layer 17, it can be deposited by, for example, a DC magnetron sputtering method. In particular, when a carbon-based protective layer is formed as the protective layer 17, it is preferable to deposit an amorphous carbon protective layer by a plasma CVD method. The amorphous carbon protective layer deposited by the plasma CVD method has a uniform surface with small roughness.

[0115] "Lubricant layer" The lubricating layer 18 prevents contamination of the magnetic recording medium 10. In addition, the lubricating layer 18 reduces the frictional force of the magnetic head of the magnetic recording and reproducing device that slides on the magnetic recording medium 10, thereby improving the durability of the magnetic recording medium 10. 1, the lubricating layer 18 is formed on and in contact with the protective layer 17. The lubricating layer 18 contains the above-mentioned fluorine-containing ether compound.

[0116] When the protective layer 17 disposed below the lubricating layer 18 is a carbon-based protective layer, the lubricating layer 18 is bonded with a high bonding strength to the protective layer 17. As a result, even if the thickness of the lubricating layer 18 is thin, it is easy to obtain a magnetic recording medium 10 in which the surface of the protective layer 17 is covered with a high coverage rate, and contamination of the surface of the magnetic recording medium 10 can be effectively prevented.

[0117] The average thickness of the lubricating layer 18 can be selected arbitrarily, but is preferably 0.5 nm (5 Å) to 2.0 nm (20 Å), and more preferably 0.5 nm (5 Å) to 1.0 nm (10 Å). When the average thickness of the lubricating layer 18 is 0.5 nm or more, the lubricating layer 18 is formed with a uniform thickness without being island-shaped or mesh-shaped. Therefore, the surface of the protective layer 17 can be covered with the lubricating layer 18 at a high coverage rate. In addition, by setting the average thickness of the lubricating layer 18 to 2.0 nm or less, the lubricating layer 18 can be made sufficiently thin, and the flying height of the magnetic head can be sufficiently reduced.

[0118] If the surface of the protective layer 17 is not covered with the lubricating layer 18 at a sufficiently high coverage rate, environmental substances adsorbed to the surface of the magnetic recording medium 10 will pass through the gaps in the lubricating layer 18 and penetrate underneath the lubricating layer 18. The environmental substances that penetrate underneath the lubricating layer 18 will be adsorbed and bonded to the protective layer 17 to generate contaminants. Then, during magnetic recording and reproduction, these contaminants (aggregated components) will adhere (transfer) to the magnetic head as smear, damaging the magnetic head or degrading the magnetic recording and reproduction characteristics of the magnetic recording and reproduction device.

[0119] Examples of environmental substances that generate pollutants include siloxane compounds (cyclic siloxanes, linear siloxanes), ionic impurities, hydrocarbons with relatively high molecular weights such as octacosane, and plasticizers such as dioctyl phthalate. Examples of metal ions contained in ionic impurities include sodium ions and potassium ions. Examples of inorganic ions contained in ionic impurities include chloride ions, bromide ions, nitrate ions, sulfate ions, and ammonium ions. Examples of organic ions contained in ionic impurities include oxalate ions and formate ions.

[0120] "Method of forming lubricating layer" A method for forming the lubricating layer 18 includes, for example, preparing a magnetic recording medium in the middle of manufacture in which all layers up to the protective layer 17 are formed on the substrate 11, applying a solution for forming a lubricating layer onto the protective layer 17, and drying the same.

[0121] The lubricant layer forming solution can be obtained by dispersing and dissolving the lubricant for magnetic recording media of the above-mentioned embodiment in a solvent as necessary, and adjusting the viscosity and concentration to be suitable for the coating method. Examples of the solvent used in the lubricant layer forming solution include fluorine-based solvents such as Vertrel (registered trademark) XF (product name, manufactured by Mitsui DuPont Fluorochemicals).

[0122] The method for applying the solution for forming the lubricating layer is not particularly limited, but examples thereof include spin coating, spraying, paper coating, and dipping. When using the dipping method, for example, the following method can be used. First, the substrate 11 on which each layer up to the protective layer 17 has been formed is immersed in the lubricant layer forming solution placed in the immersion tank of a dip coater. Next, the substrate 11 is lifted from the immersion tank at a predetermined speed. In this way, the lubricant layer forming solution is applied to the surface of the substrate 11 above the protective layer 17. By using the dipping method, the lubricant layer forming solution can be applied uniformly onto the surface of the protective layer 17, and the lubricant layer 18 can be formed on the protective layer 17 with a uniform thickness.

[0123] In this embodiment, it is preferable to perform a heat treatment on the substrate 11 on which the lubricating layer 18 is formed. By performing the heat treatment, the adhesion between the lubricating layer 18 and the protective layer 17 is improved, and the adhesive force between the lubricating layer 18 and the protective layer 17 is improved. The heat treatment temperature is preferably 100 to 180° C. If the heat treatment temperature is 100° C. or higher, the effect of improving the adhesion between the lubricating layer 18 and the protective layer 17 can be sufficiently obtained. Furthermore, by setting the heat treatment temperature to 180° C. or lower, thermal decomposition of the lubricating layer 18 can be prevented. The heat treatment time is preferably 10 to 120 minutes.

[0124] The magnetic recording medium 10 of this embodiment has at least a magnetic layer 16, a protective layer 17, and a lubricating layer 18 sequentially provided on a substrate 11. In the magnetic recording medium 10 of this embodiment, the lubricating layer 18 containing the above-mentioned fluorine-containing ether compound is formed on and in contact with the protective layer 17. Even though the lubricating layer 18 is thin, it covers the surface of the protective layer 17 with a high coverage. Therefore, the lubricating layer 18 in the magnetic recording medium 10 of this embodiment has excellent wear resistance. Furthermore, in the magnetic recording medium 10 of this embodiment, the surface of the protective layer 17 is covered with the lubricating layer 18 at a high coverage rate. This prevents environmental substances that generate contaminants such as ionic impurities from penetrating through the gaps in the lubricating layer 18. Therefore, the magnetic recording medium 10 of this embodiment has a small amount of contaminants present on its surface. Furthermore, the lubricating layer 18 in the magnetic recording medium 10 of this embodiment is less likely to generate foreign matter (smear), and can suppress pick-up. For these reasons, the magnetic recording medium 10 of this embodiment has excellent reliability and durability. EXAMPLES

[0125] The present invention will be described in more detail below with reference to examples and comparative examples, but the present invention is not limited to the following examples.

[0126] "Lubricant manufacturing" Example 1 The compound represented by the above formula (A) was produced by the method shown below. First, diallylamine and di-tert-butyl dicarbonate were reacted in methanol to obtain a compound. Then, the obtained compound was oxidized in dichloromethane using metachloroperbenzoic acid to synthesize a compound represented by the following formula (20).

[0127] [ka] (t-Bu in formula (20) represents a tertiary butyl group.)

[0128] Next, in a 200 mL eggplant flask under a nitrogen atmosphere, 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 20 g of a fluoropolyether (number average molecular weight 1000, molecular weight distribution 1.1) represented by formula (20) (wherein m indicating the average degree of polymerization is 4.5, and n indicating the average degree of polymerization is 4.5) was added, and 9.39 g of a compound represented by formula (20) (molecular weight 213.14, 44 mmol) and 20 mL of t-butanol were added and stirred at room temperature until the mixture became homogenous.

[0129] To this homogeneous liquid, 0.90 g (molecular weight 112.21, 8 mmol) of potassium tert-butoxide was added, and the mixture was stirred at 70° C. for 14 hours to react. The resulting reaction product was cooled to 25° C., neutralized with 1 mol / L hydrochloric acid, extracted with Vertrel (registered trademark) XF, and washed with water. The organic layer was dehydrated with anhydrous sodium sulfate, and the drying agent was filtered off, and the filtrate was concentrated.

[0130] To the concentrated filtrate, 15 mL of trifluoroacetic acid was added, and the mixture was stirred at 25°C for 3 hours to react. The reaction mixture was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water, and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated with anhydrous sodium sulfate. After filtering off the drying agent, the filtrate was concentrated, and the residue was purified by silica gel column chromatography to obtain 12.3 g of compound (A). In formula (A), ma, which indicates the average degree of polymerization, is 4.5, and na, which indicates the average degree of polymerization, is 4.5.

[0131] The obtained compound (A) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (A); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.9(18H), 5.1~5.2(2H), 5.2~5.3(2H), 5.8~6.0(2H)

[0132] Example 2 The same procedure as in Example 1 was carried out except that 10.6 g of a compound represented by the following formula (21) was used instead of the compound represented by formula (20), to obtain 12.8 g of compound (B). In formula (B), mb, which indicates the average degree of polymerization, is 4.5, and nb, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (21) was synthesized by protecting the amino group of dibutenylamine with di-tert-butyl dicarbonate and oxidizing the double bond.

[0133] [ka] (t-Bu in formula (21) represents a tertiary butyl group.)

[0134] The obtained compound (B) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (B); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(4H), 2.2~2.4(4H), 3.4~4.0(18H), 5.0~5.1(2H), 5.1~5.2(2H), 5.8~6.0(2H)

[0135] Example 3 The same procedure as in Example 1 was carried out except that 9.47 g of a compound represented by the following formula (22) was used instead of the compound represented by formula (20), to obtain 12.3 g of compound (C). In formula (C), mc, which indicates the average degree of polymerization, is 4.5, and nc, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (22) was synthesized by protecting the amino group of propylamine with di-tert-butyl dicarbonate and reacting it with epibromohydrin.

[0136] [ka] (t-Bu in formula (22) represents a tertiary butyl group.)

[0137] The obtained compound (C) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (C); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]0.8~1.0(6H), 1.5~1.6(4H), 3.3~4.2(18H)

[0138] Example 4 The same procedure as in Example 1 was carried out except that 12.3 g of the compound represented by formula (23) was used instead of the compound represented by formula (20), to obtain 13.6 g of compound (D). In formula (D), md, which indicates the average degree of polymerization, is 4.5, and nd, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (23) was synthesized by protecting the amino group of p-anisidine with di-tert-butyl dicarbonate and reacting it with epibromohydrin.

[0139] [ka] (t-Bu in formula (23) represents a tertiary butyl group.)

[0140] The obtained compound (D) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (D); 1 H-NMR (CD 3 COCD 3 ): δ[ppm]3.5~4.2(20H), 6.8~7.0(8H)

[0141] Example 5 The same procedure as in Example 1 was carried out except that 17.0 g of the compound represented by formula (24) was used instead of the compound represented by formula (20), to obtain 13.7 g of compound (E). In formula (E), me, which indicates the average degree of polymerization, is 4.5, and ne, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (24) was synthesized by protecting the amino group of the compound obtained by the reaction of allylamine with epichlorohydrin using di-tert-butyl dicarbonate and oxidizing the double bond.

[0142] [ka] (t-Bu in formula (24) represents a tertiary butyl group.)

[0143] The obtained compound (E) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (E); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(10H), 3.9~4.2(18H), 5.1~5.2(2H), 5.2~5.3(2H), 5.8~6.0(2H)

[0144] Example 6 The same procedure as in Example 1 was carried out except that 18.2 g of the compound represented by formula (25) was used instead of the compound represented by formula (20), to obtain 14.3 g of compound (F). In formula (F), mf, which indicates the average degree of polymerization, is 4.5, and nf, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (25) was synthesized by protecting the amino group of the compound obtained by the reaction of 3-butenylamine with epichlorohydrin using di-tert-butyl dicarbonate and oxidizing the double bond.

[0145] [ka] (t-Bu in formula (25) represents a tertiary butyl group.)

[0146] The obtained compound (F) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (F); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(4H), 2.2~2.4(4H), 3.4~4.0(28H), 5.0~5.1(2H), 5.1~5.2(2H), 5.8~6.0(2H)

[0147] Example 7 The compound represented by the above formula (G) was produced by the method shown below. Under nitrogen gas atmosphere, HOCH was added to a 100 mL eggplant flask. 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 220.0 g of fluoropolyether (number average molecular weight 1000, molecular weight distribution 1.1) represented by OH (where m indicating the average degree of polymerization is 4.5, and n indicating the average degree of polymerization is 4.5), 2.56 g of the compound represented by the above formula (20), and 12 mL of t-butanol were charged and stirred at room temperature until homogenous. 0.674 g of potassium tert-butoxide was further added to this homogenous liquid, and the mixture was reacted at 70°C for 8 hours with stirring to obtain a reaction product.

[0148] The reaction product was cooled to 25°C, neutralized with 0.5 mol / L hydrochloric acid, extracted with Vertrel (registered trademark) XF, the organic layer was washed with water and dehydrated with anhydrous sodium sulfate. After filtering off the drying agent, the filtrate was concentrated, and the residue was purified by silica gel column chromatography to obtain 9.71 g of the compound represented by the following formula (26).

[0149] [ka] (In formula (26), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0150] In a nitrogen gas atmosphere, 6.07 g of the compound represented by the above formula (26), 1.21 g of the compound represented by the following formula (27), and 50 mL of t-butanol were charged into a 200 mL recovery flask and stirred at room temperature until the mixture became homogeneous. 0.168 g of potassium tert-butoxide was added to this homogeneous liquid and reacted with stirring at 70°C for 16 hours. The compound represented by formula (27) was synthesized by reacting a compound in which one hydroxy group of ethylene glycol is protected with dihydropyran with epibromohydrin.

[0151] [ka]

[0152] The liquid after the reaction was returned to room temperature, 20 g of 10% hydrogen chloride-methanol solution (hydrogen chloride-methanol reagent (5-10%), Tokyo Chemical Industry Co., Ltd.) was added, and stirred at room temperature for 1 hour. The reaction liquid was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water, and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated with anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated.

[0153] To the concentrated filtrate, 15 mL of trifluoroacetic acid was added, and the mixture was stirred at 25°C for 3 hours to react. The reaction solution was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water, and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated with anhydrous sodium sulfate. After filtering off the drying agent, the filtrate was concentrated, and the residue was purified by silica gel column chromatography to obtain 4.31 g of compound (G). In formula (G), mg, which indicates the average degree of polymerization, is 4.5, and ng, which indicates the average degree of polymerization, is 4.5.

[0154] The obtained compound (G) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (G); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~4.2(29H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0155] Example 8 The same procedure as in Example 7 was carried out except that the compound represented by formula (21) was used instead of the compound represented by formula (20), and 4.41 g of compound (H) was obtained via the intermediate represented by formula (28). In formula (H), mh, which indicates the average degree of polymerization, is 4.5, and nh, which indicates the average degree of polymerization, is 4.5.

[0156] [ka] (In formula (28), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0157] The obtained compound (H) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (H); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(2H), 2.2~2.4(2H), 3.4~4.0(20H), 5.0~5.1(1H), 5.1~5.2(1H), 5.8~6.0(1H)

[0158] Example 9 The same procedure as in Example 7 was carried out except that the compound represented by formula (22) was used instead of the compound represented by formula (20), and 4.32 g of compound (I) was obtained via the intermediate represented by formula (29). In formula (I), mi, which indicates the average degree of polymerization, is 4.5, and ni, which indicates the average degree of polymerization, is 4.5.

[0159] [ka] (In formula (29), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0160] The obtained compound (I) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (I); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]0.8~1.0(3H), 1.5~1.6(2H), 3.3~4.2(20H)

[0161] Example 10 The same procedure as in Example 7 was carried out except that the compound represented by formula (23) was used instead of the compound represented by formula (20), and 4.57 g of compound (J) was obtained via the intermediate represented by formula (30). In formula (J), mj, which indicates the average degree of polymerization, is 4.5, and nj, which indicates the average degree of polymerization, is 4.5.

[0162] [ka] (In formula (30), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0163] The obtained compound (J) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (J); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.5~4.2(21H), 6.8~7.0(4H)

[0164] Example 11 The same procedure as in Example 7 was carried out except that the compound represented by formula (24) was used instead of the compound represented by formula (20), and 4.57 g of compound (K) was obtained via the intermediate represented by formula (31). In formula (K), mk, which indicates the average degree of polymerization, is 4.5, and nk, which indicates the average degree of polymerization, is 4.5.

[0165] [ka] (In formula (31), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0166] The obtained compound (K) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (K); 1 H-NMR (CD 3 COCD3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0167] Example 12 The same procedure as in Example 7 was carried out except that the compound represented by formula (25) was used instead of the compound represented by formula (20), and 4.67 g of compound (L) was obtained via the intermediate represented by formula (32). In formula (L), ml, which indicates the average degree of polymerization, is 4.5, and nl, which indicates the average degree of polymerization, is 4.5.

[0168] [ka] (In formula (32), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0169] The obtained compound (L) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (L); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(2H), 2.2~2.4(2H), 3.4~4.0(25H), 5.0~5.1(1H), 5.1~5.2(1H), 5.8~6.0(1H)

[0170] (Example 13) The same procedure as in Example 7 was carried out except that the compound represented by formula (24) was used instead of the compound represented by formula (20) and the compound represented by formula (33) was used instead of the compound represented by formula (27), to obtain 4.62 g of compound (M) via the intermediate represented by formula (31). In formula (M), mm, which indicates the average degree of polymerization, is 4.5, and nm, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (33) was synthesized by reacting a compound in which one hydroxy group of 1,3-propanediol is protected with dihydropyran with epibromohydrin.

[0171] [ka]

[0172] The obtained compound (M) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (M); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(2H), 3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0173] Example 14 The compound represented by the above formula (N) was produced by the method shown below. In the same manner as in Example 7, 9.71 g of the compound represented by the above formula (26) was obtained. In a 200 mL recovery flask, 6.07 g of the compound represented by formula (26), 1.64 g of the compound represented by formula (34) below, and 50 mL of t-butanol were charged under a nitrogen gas atmosphere and stirred at room temperature until the mixture became homogeneous. 0.168 g of potassium tert-butoxide was added to the homogeneous solution, and the mixture was reacted at 70°C for 16 hours with stirring. The compound represented by formula (34) was synthesized by reacting a compound represented by the following formula (35), in which the hydroxy group of 2-aminoethanol is protected with methyl tert-butyl ether and the amino group is protected with di-tert-butyl dicarbonate, with epibromohydrin.

[0174] [ka] (t-Bu in formula (34) and formula (35) represents a tertiary butyl group.)

[0175] After the reaction was completed, the liquid was returned to room temperature, and 20 g of a 10% hydrogen chloride-methanol solution (hydrogen chloride-methanol reagent (5-10%), Tokyo Chemical Industry Co., Ltd.) was added and stirred at room temperature for 1 hour. The reaction liquid was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated using anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated.

[0176] To the concentrated filtrate, 15 mL of trifluoroacetic acid was added, and the mixture was stirred at 25°C for 3 hours to react. The reaction solution was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water, and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated with anhydrous sodium sulfate. After filtering off the drying agent, the filtrate was concentrated, and the residue was purified by silica gel column chromatography to obtain 4.31 g of compound (N). In formula (N), mn, which indicates the average degree of polymerization, is 4.5, and nn, which indicates the average degree of polymerization, is 4.5.

[0177] The obtained compound (N) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (N); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~4.2(29H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0178] Example 15 The same procedure as in Example 14 was carried out except that the compound represented by formula (21) was used instead of the compound represented by formula (20), and 4.41 g of compound (O) was obtained via the intermediate represented by formula (28). In formula (O), mo, which indicates the average degree of polymerization, is 4.5, and no, which indicates the average degree of polymerization, is 4.5.

[0179] The obtained compound (O) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (O); 1 H-NMR (CD3 COCD 3 ); δ[ppm]1.6~2.0(2H), 2.2~2.4(2H), 3.4~4.0(20H), 5.0~5.1(1H), 5.1~5.2(1H), 5.8~6.0(1H)

[0180] (Example 16) The same procedure as in Example 14 was carried out except that the compound represented by formula (22) was used instead of the compound represented by formula (20), and 4.32 g of compound (P) was obtained via the intermediate represented by formula (29). In formula (P), mp, which indicates the average degree of polymerization, is 4.5, and np, which indicates the average degree of polymerization, is 4.5.

[0181] The obtained compound (P) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (P); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]0.8~1.0(3H), 1.5~1.6(2H), 3.3~4.2(20H)

[0182] (Example 17) The same procedure as in Example 14 was carried out except that the compound represented by formula (23) was used instead of the compound represented by formula (20), and 4.57 g of compound (Q) was obtained via the intermediate represented by formula (30). In formula (Q), mq, which indicates the average degree of polymerization, is 4.5, and nq, which indicates the average degree of polymerization, is 4.5.

[0183] The obtained compound (Q) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (Q); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.5~4.2(21H), 6.8~7.0(4H)

[0184] (Example 18) The same procedure as in Example 14 was carried out except that the compound represented by formula (36) was used instead of the compound represented by formula (20), and 4.57 g of compound (R) was obtained via the intermediate represented by formula (37). In formula (R), mr, which indicates the average degree of polymerization, is 4.5, and nr, which indicates the average degree of polymerization, is 4.5. The compound represented by formula (36) was synthesized by protecting the hydroxy group of 1,3-diallyloxy-2-propanol with dihydropyran and oxidizing the double bond.

[0185] [ka] (In formula (37), m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5.)

[0186] The obtained compound (R) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (R); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0187] (Example 19) The same procedure as in Example 14 was carried out except that the compound represented by formula (24) was used instead of the compound represented by formula (20), and 4.57 g of compound (S) was obtained via the intermediate represented by formula (31). In formula (S), ms, which indicates the average degree of polymerization, is 4.5, and ns, which indicates the average degree of polymerization, is 4.5.

[0188] The obtained compound (S) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (S); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0189] (Example 20) The same procedure as in Example 14 was carried out except that the compound represented by formula (25) was used instead of the compound represented by formula (20), and 4.67 g of compound (T) was obtained via the intermediate represented by formula (32). In formula (T), mt, which indicates the average degree of polymerization, is 4.5, and nt, which indicates the average degree of polymerization, is 4.5.

[0190] The obtained compound (T) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (T); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(2H), 2.2~2.4(2H), 3.4~4.0(25H), 5.0~5.1(1H), 5.1~5.2(1H), 5.8~6.0(1H)

[0191] Example 21 The compound represented by the above formula (U) was produced by the method shown below. In the same manner as in Example 18, 10.2 g of the compound represented by the above formula (37) was obtained. In a 200 mL recovery flask, 6.37 g of the compound represented by formula (37), 2.68 g of the compound represented by formula (38) below, and 50 mL of t-butanol were charged under a nitrogen gas atmosphere and stirred at room temperature until the mixture became homogeneous. 0.168 g of potassium tert-butoxide was added to the homogeneous solution, and the mixture was reacted at 70°C for 16 hours with stirring. The compound represented by formula (38) was synthesized by reacting the compound represented by formula (35) with the compound represented by formula (39) below, which was synthesized by protecting the amino group of diallylamine with di-tert-butyl dicarbonate and oxidizing the double bond.

[0192] [ka] (t-Bu in formula (38) and formula (39) represents a tertiary butyl group.)

[0193] After the reaction was completed, the liquid was returned to room temperature, and 20 g of a 10% hydrogen chloride-methanol solution (hydrogen chloride-methanol reagent (5-10%), Tokyo Chemical Industry Co., Ltd.) was added and stirred at room temperature for 1 hour. The reaction liquid was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated using anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated.

[0194] To the concentrated filtrate, 20 mL of trifluoroacetic acid was added and the mixture was stirred at 25°C for 3 hours to react. The reaction mixture was transferred to a beaker containing 70 mL of 8% sodium bicarbonate water and extracted twice with 200 mL of ethyl acetate. The organic layer was washed with water and dehydrated with anhydrous sodium sulfate. After filtering off the drying agent, the filtrate was concentrated and the residue was purified by silica gel column chromatography to obtain 4.83 g of compound (U). In formula (U), mu, which indicates the average degree of polymerization, is 4.5, and nu, which indicates the average degree of polymerization, is 4.5.

[0195] The obtained compound (U) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (U); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.9(25H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0196] Example 22 The same procedure as in Example 21 was carried out except that the compound represented by formula (24) was used instead of the compound represented by formula (36), and 4.67 g of compound (V) was obtained via the intermediate represented by formula (31). In formula (V), mv, which indicates the average degree of polymerization, is 4.5, and nv, which indicates the average degree of polymerization, is 4.5.

[0197] The obtained compound (V) 1H-NMR measurement was performed, and the structure was identified from the following results. Compound (V); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.9(25H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0198] Example 23 The same procedure as in Example 21 was carried out except that the compound represented by formula (25) was used instead of the compound represented by formula (36), and 4.92 g of compound (W) was obtained via the intermediate represented by formula (32). In formula (W), mw, which indicates the average degree of polymerization, is 4.5, and nw, which indicates the average degree of polymerization, is 4.5.

[0199] The obtained compound (W) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (W); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]1.6~2.0(2H), 2.2~2.4(2H), 3.4~4.0(25H), 5.0~5.1(1H), 5.1~5.2(1H), 5.8~6.0(1H)

[0200] (Example 24) HOCH 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 OH (wherein m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5), instead of fluoropolyether represented by HOCH 2 CF 2 O(CF 2 CF 2 O) x CF 2 CH 2The same procedure as in Example 14 was carried out except that a fluoropolyether represented by formula (24) was used instead of the compound represented by formula (20) and a compound represented by formula (24) was used, and 4.53 g of compound (X) was obtained via an intermediate represented by formula (40). In formula (X), x, which indicates the average degree of polymerization, is 7.0.

[0201] [ka] (In formula (40), x, which indicates the average degree of polymerization, is 7.0; t-Bu represents a tertiary butyl group.)

[0202] The obtained compound (X) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (X); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0203] (Example 25) HOCH 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 OH (wherein m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5), instead of fluoropolyether represented by HOCH 2 CF(CF 3 )(OCF(CF 3 )CF 2 ) y OCF(CF 3 )CH 2The same procedure as in Example 14 was carried out except that a fluoropolyether represented by OH (wherein y, which indicates the average degree of polymerization, is 4.5) was used and a compound represented by formula (24) was used instead of the compound represented by formula (20), and 4.66 g of compound (Y) was obtained via an intermediate represented by formula (41). In formula (Y), y, which indicates the average degree of polymerization, is 4.5.

[0204] [ka] (In formula (41), y, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0205] The obtained compound (Y) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (Y); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0206] (Example 26) HOCH 2 CF 2 O(CF 2 CF 2 O) m (CF 2 O) n CF 2 CH 2 OH (wherein m, which indicates the average degree of polymerization, is 4.5, and n, which indicates the average degree of polymerization, is 4.5), instead of fluoropolyether represented by HOCH 2 CF 2 CF 2 O(CF 2 CF 2 CF 2 O) z CF 2 CF 2 CH 2The same procedure as in Example 14 was carried out except that a fluoropolyether represented by formula (24) was used instead of the compound represented by formula (20) and a compound represented by formula (24) was used, and 4.66 g of compound (Z) was obtained via an intermediate represented by formula (42). In formula (Z), z, which indicates the average degree of polymerization, is 4.5.

[0207] [ka] (In formula (42), z, which indicates the average degree of polymerization, is 4.5; t-Bu represents a tertiary butyl group.)

[0208] The obtained compound (Z) 1 H-NMR measurement was performed, and the structure was identified from the following results. Compound (Z); 1 H-NMR (CD 3 COCD 3 ); δ[ppm]3.4~3.7(9H), 3.9~4.2(16H), 5.1~5.2(1H), 5.2~5.3(1H), 5.8~6.0(1H)

[0209] The compounds of Examples 1 to 26 thus obtained are represented by the formula (1) 1 The structure of R 2 (a, X in [A] in formula (2), b, c, and X in [B]), R 3 The structure of R 4 (d, X in [C] in formula (3) and e, f, X in [D]), R 5 The structure of the compound and the total number of hydroxyl groups [-OH] and secondary amine structures [-NH-] contained in the molecule are shown in Table 1.

[0210] [Table 1]

[0211] "Comparative Example 1" The compound represented by the following formula (AA) was synthesized by the method described in Patent Document 3.

[0212] [ka] (In formula (AA), jA indicating the average degree of polymerization is 4.5, and kA indicating the average degree of polymerization is 4.5.)

[0213] "Comparative Example 2" The compound represented by the following formula (AB) was synthesized by the method described in Patent Document 1.

[0214] [ka] (In formula (AB), jB indicating the average degree of polymerization is 4.5, and kB indicating the average degree of polymerization is 4.5.)

[0215] "Comparative Example 3" The compound represented by the following formula (AC) was synthesized by the method described in Patent Document 2.

[0216] [ka] (In formula (AC), jC1, kC1, jC2, and kC2, which indicate the average degree of polymerization, are 4.5.)

[0217] The number average molecular weights (Mn) of the compounds thus obtained in Examples 1 to 26 and Comparative Examples 1 to 3 are shown in Tables 2 and 3.

[0218] [Table 2]

[0219] [Table 3]

[0220] Next, a solution for forming a lubricant layer was prepared by the method described below using the compounds obtained in Examples 1 to 26 and Comparative Examples 1 to 3. Then, the obtained solution for forming a lubricant layer was used to form a lubricant layer for a magnetic recording medium by the method described below, thereby obtaining the magnetic recording media of Examples 1 to 26 and Comparative Examples 1 to 3.

[0221] "Lubricant layer forming solution" The compounds obtained in Examples 1 to 26 and Comparative Examples 1 to 3 were each dissolved in Vertrel (registered trademark) XF, and diluted with Vertrel (registered trademark) XF so that the film thickness when applied onto the protective layer would be 9 Å, to prepare a solution for forming a lubricating layer.

[0222] "Magnetic recording media" A magnetic recording medium was prepared by sequentially providing an adhesive layer, a soft magnetic layer, a first underlayer, a second underlayer, a magnetic layer, and a protective layer on a substrate having a diameter of 65 mm. The protective layer was made of carbon. On the protective layer of the magnetic recording medium on which each layer up to the protective layer had been formed, the lubricant layer forming solutions of Examples 1 to 26 and Comparative Examples 1 to 3 were applied by dipping. The dipping was performed under the conditions of an immersion speed of 10 mm / sec, an immersion time of 30 sec, and a lifting speed of 1.2 mm / sec. The magnetic recording medium coated with the lubricant layer-forming solution was then placed in a thermostatic chamber at 120°C and heated for 10 minutes to remove the solvent in the lubricant layer-forming solution, thereby forming a lubricant layer on the protective layer and obtaining the magnetic recording medium.

[0223] The thickness of the lubricating layer of each of the magnetic recording media thus obtained in Examples 1 to 26 and Comparative Examples 1 to 3 was measured using an FT-IR (product name: Nicolet iS50, manufactured by Thermo Fisher Scientific Co., Ltd.) The results are shown in Tables 2 and 3.

[0224] Next, the magnetic recording media of Examples 1 to 26 and Comparative Examples 1 to 3 were subjected to the following wear resistance test. (Wear resistance test) Using a pin-on-disk type friction and wear tester, an alumina ball with a diameter of 2 mm was slid as a contact on the lubricating layer of the magnetic recording medium at a load of 40 gf and a sliding speed of 0.25 m / sec to measure the friction coefficient of the surface of the lubricating layer. The sliding time until the friction coefficient of the surface of the lubricating layer suddenly increased was then measured. The sliding time until the friction coefficient suddenly increased was measured four times for the lubricating layer of each magnetic recording medium, and the average value (time) was used as an index of the wear resistance of the lubricant coating.

[0225] The results of the magnetic recording media using the compounds of Examples 1 to 26 and the compounds of Comparative Examples 1 to 3 are shown in Tables 2 and 3. The friction coefficient increase time was evaluated as follows. It should be noted that the larger the value of the friction coefficient increase time, the better the result. ◎(Excellent): 650sec or more ○(Good): 550sec or more, less than 650sec △ (OK): 450 sec or more, less than 550 sec × (Not acceptable): Less than 450 seconds

[0226] The time until the friction coefficient increases sharply can be used as an index of the wear resistance of the lubricating layer for the following reason. The lubricating layer of the magnetic recording medium wears away as the magnetic recording medium is used, and when the lubricating layer is worn away, the contact and the protective layer come into direct contact, causing a sharp increase in the friction coefficient. The time until the friction coefficient increases sharply is thought to be correlated with the friction test.

[0227] As shown in Table 3, the magnetic recording media of Examples 1 to 26 had a longer sliding time before the friction coefficient increased sharply and better wear resistance than the magnetic recording media of Comparative Examples 1 to 3. This is presumably because, in the magnetic recording media of Examples 1 to 26, in the fluorine-containing ether compound represented by formula (1) forming the lubricating layer, a linking group containing a hydroxyl group and a secondary amine structure is disposed between one or both of the terminal groups and the perfluoropolyether chain. In particular, in Examples 1, 2, 4, 11 to 17, 19, 20, and 24 to 26, which used compounds (A), (B), (D), (K) to (Q), (S), (T), and (X) to (Z) in which the number of secondary amine structures (-NH-) contained in the molecule is 2 or more, the number of hydroxyl groups is 4 or less, and the total number of hydroxyl groups and secondary amine structures is 7 or less, the results for the friction coefficient increase time were excellent (excellent), which was a good result. [Industrial Applicability]

[0228] By using a lubricant for magnetic recording media containing the fluorinated ether compound of the present invention, it is possible to form a lubricating layer that is thin but has excellent abrasion resistance. That is, according to the present invention, a lubricating layer having excellent wear resistance even when it is thin can be formed, and a fluorine-containing ether compound suitable as a material for a lubricant for a magnetic recording medium can be provided. [Explanation of symbols]

[0229] 10. Magnetic recording media 11... Substrate 12. Adhesion layer 13...Soft magnetic layer 14...1st base layer 15...Second base layer 16...magnetic layer 17...protective layer 18...Lubricating layer

Claims

1. A fluorine-containing ether compound represented by the following formula (1): R １ -R ２ -CH ２ -R ３ -CH ２ -R ４ -R ５ (1) (In formula (1), R ３ is a perfluoropolyether chain; R １ is R ２ is an end group bonded to ５ is R ４ is an end group bonded to １ and R ５ each independently represents an alkyl group having 1 to 6 carbon atoms, an alkyl group having 1 to 6 carbon atoms and a hydroxyl group, an allyl group, a butenyl group, or a methoxyphenyl group; -R ２ -CH ２ -R ３ is represented by the following formula (2); R ３ -CH ２ -R ４ - is expressed by the following formula (3): -[A]-[B]-O-CH ２ -R ３ (2) R ３ -CH ２ -O-[C]-[D]- (3) (In formula (2), [A] is represented by the following formula (4), and [B] is represented by the following formula (5); [A] and [B] may be interchanged in formula (2).) (In formula (3), [C] is represented by the following formula (6), and [D] is represented by the following formula (7); [C] and [D] may be interchanged in formula (3).) 【Chemistry 1】 【Chemistry 2】 (a in formula (4) and b in formula (5) are integers of 0 to 2; c in formula (5) is an integer of 2 to 5; d in formula (6) and e in formula (7) are integers of 0 to 2; f in formula (7) is an integer of 2 to 5; at least one of b in formula (5) and d in formula (6) is 1 or more; X is O, NH, CH ２ One or more of X in formulas (4) to (7) is NH.

2. 2. The fluorine-containing ether compound according to claim 1, which has two or more secondary amine structures in the molecule.

3. 3. The fluorine-containing ether compound according to claim 1, which has 4 or less hydroxyl groups in the molecule.

4. 4. The fluorine-containing ether compound according to claim 1, wherein the total number of secondary amine structures and hydroxyl groups contained in the molecule is 7 or less.

5. The fluorine-containing ether compound according to any one of claims 1 to 4, wherein the number of secondary amine structures contained in the molecule is 2 or more, the number of hydroxyl groups is 4 or less, and the total number of secondary amine structures and hydroxyl groups is 7 or less.

6. R in the formula (1) ２ The fluorine-containing ether compound according to any one of claims 1 to 5, wherein the fluorine-containing ether compound is represented by any one of the following formulas (11-1) to (11-5): 【Chemistry 3】 7. The fluorine-containing ether compound according to claim 1, wherein the alkyl group having 1 to 6 carbon atoms and a hydroxyl group is a hydroxyethyl group or a hydroxypropyl group.

8. A fluorine-containing ether compound according to any one of claims 1 to 7, wherein the alkyl group having 1 to 6 carbon atoms is a propyl group.

9. R in the formula (1) ３ The fluorine-containing ether compound according to any one of claims 1 to 8, wherein the fluorine-containing ether compound is represented by any one of the following formulas (8) to (10): -CF ２ O-(CF ２ CF ２ O) ｍ -(CF ２ O) ｎ -CF ２ - (8) (In formula (8), m and n each represent an average degree of polymerization and are 0 to 30; however, m or n is 0.1 or more.) -CF(CF ３ )-(OCF(CF ３ )CF ２ ) ｙ -OCF(CF ３ )- (9) (In formula (9), y represents the average degree of polymerization and is 0.1 to 30.) -CF ２ CF ２ O-(CF ２ CF ２ CF ２ O) ｚ -CF ２ CF ２ - (10) (In formula (10), z represents the average degree of polymerization and is 0.1 to 30.)

10. The fluorine-containing ether compound according to any one of claims 1 to 9, wherein the sum of a in said formula (4) and b in said formula (5), and the sum of d in said formula (6) and e in said formula (7) are each 1 or more.

11. The fluorine-containing ether compound according to claim 1, wherein the compound represented by formula (1) is any one of compounds represented by the following formulas (K) to (M), (S), and (T): 【Chemistry 4】 (In formula (K), mk and nk represent average degrees of polymerization, mk represents 1 to 30, and nk represents 0 to 30.) (In formula (L), ml and nl represent average degrees of polymerization, ml represents 1 to 30, and nl represents 0 to 30.) (In formula (M), mm and nm represent average degrees of polymerization, mm represents 1 to 30, and nm represents 0 to 30.) (In formula (S), ms and ns represent the average degree of polymerization, ms represents 1 to 30, and ns represents 0 to 30.) (In formula (T), mt and nt represent average degrees of polymerization, mt represents 1 to 30, and nt represents 0 to 30.)

12. The fluorine-containing ether compound according to any one of claims 1 to 11, having a number average molecular weight in the range of 500 to 10,000.

13. A lubricant for magnetic recording media, comprising the fluorine-containing ether compound according to any one of claims 1 to 12.

14. A magnetic recording medium comprising at least a magnetic layer, a protective layer, and a lubricating layer provided in this order on a substrate, the lubricating layer comprising the fluorine-containing ether compound according to any one of claims 1 to 12.

15. 15. The magnetic recording medium according to claim 14, wherein the lubricating layer has an average thickness of 0.5 nm to 2.0 nm.

Images