Abstract: The present invention provides a fluorine-containing ether compound represented by the following Formula. R1-[B]-[A]-CH2—R2—CH2-[C]-[D]-R3 (R2 is a perfluoropolyether chain; [A] is Formula (2-1); [B] is Formula (2-2); [C] is Formula (3-1); [D] is Formula (3-2); R3 is Formula (4); and R1 is a terminal group.

Abstract: A magnetic recording medium production method which includes forming a lubricating layer over a stack including a substrate, a magnetic recording layer over the substrate, and a protective layer over the magnetic recording layer includes applying a first lubricant and a second lubricant to the stack; burnishing a surface of the stack with an abrasive; and removing the second lubricant over the stack. The application of the second lubricant is performed through dipping or spin coating. A dissolution amount of the second lubricant in a solvent for the second lubricant used in the dipping or the spin coating is more than a dissolution amount of the first lubricant in the solvent. The burnishing includes abrading the surface of the stack by pressing a tape containing the abrasive against the surface of the stack. The removal of the second lubricant includes irradiating the stack with ultraviolet radiation, or heating the stack.

Abstract: A magnetic recording medium production method which includes forming a lubricating layer over a stack includes applying a first lubricant and a second lubricant to the stack; burnishing, with an abrasive, a surface of the stack to which the first lubricant and the second lubricant are applied; and removing the second lubricant over the stack. A vapor pressure at 120° C. of the second lubricant is higher than a vapor pressure at 120° C. of the first lubricant. The burnishing includes abrading the surface of the stack by pressing a tape containing the abrasive against the surface of the stack. The removal of the second lubricant includes irradiating the stack, to which the first lubricant and the second lubricant are applied, with ultraviolet radiation, or heating the stack, to which the first lubricant and the second lubricant are applied.

Abstract: A magnetic recording medium production method which includes forming a lubricating layer over a stack including a substrate, a magnetic recording layer over the substrate, and a protective layer over the magnetic recording layer includes applying a first lubricant and a second lubricant to the stack; burnishing, with an abrasive, a surface of the stack to which the first lubricant and the second lubricant are applied; and removing the second lubricant over the stack. The application of the second lubricant is performed through spin coating. The burnishing includes abrading the surface of the stack by pressing a tape containing the abrasive against the surface of the stack. The removal of the second lubricant includes at least one of irradiating the stack, to which the first lubricant and the second lubricant are applied, with ultraviolet radiation, or heating the stack to which the first lubricant and the second lubricant are applied.

Abstract: A magnetic recording medium production method, which includes forming a lubricating layer over a stack including a substrate, a magnetic recording layer over the substrate, and a protective layer over the magnetic recording layer, includes applying a first lubricant and a second lubricant to the stack; burnishing, with an abrasive, a surface of the stack to which the first lubricant and the second lubricant are applied; and removing the second lubricant over the stack. The burnishing includes abrading the surface of the stack by pressing a tape containing the abrasive against the surface of the stack. The removal of the second lubricant includes irradiating the stack, to which the first lubricant and the second lubricant are applied, with light emitted from an LED light source.

Abstract: A method of producing a magnetic recording medium is provided, in which a lubricating layer is formed on a stack including a magnetic recording layer and a protective layer disposed on a substrate in this order. The method includes: coating the stack with first and second lubricants; burnishing a surface of the coated stack with an abrasive material; and removing the second lubricant present on the stack. The first lubricant has a mean molecular weight greater than that of the second lubricant, and molecules of the first lubricant are more polar than molecules of the second lubricant. The burnishing includes pressing a tape including the abrasive material against the surface of the stack to rub the surface of the stack. The removing of the second lubricant includes irradiating the coated stack with ultraviolet rays, or performing a heat treatment on the coated stack.

Abstract: The present invention provides a fluorine-containing ether compound represented by the following Formula. R1-[B]-[A]-CH2—R2—CH2-[C]-[D]-R3 (R2 is a perfluoropolyether chain; [A] is Formula (2-1); [B] is Formula (2-2); [C] is Formula (3-1); [D] is Formula (3-2); R3 is Formula (4); and R1 is a terminal group.

Abstract: A fluorine-containing ether compound represented by Formula (1) is provided. R1—R2—CH2—R3—CH2—R4—R5 ??(1) (In Formula (1), R1 and R5 each represents a group having a heterocyclic ring and may be the same as or different from each other, R2 and R4 each represents a divalent linking group having a polar group and play be the same as or different from each other, and R3 represents a perfluoropolyether chain.

Abstract: The present invention relates to a fluorine-containing ether compound represented by Formula (1), R1—R2—CH2—R3—CH2—R4??(1). (In Formula (1), R1 is an end group including an organic group having at least one double bond or triple bond, R2 is a divalent linking group bonded to R1 by etheric oxygen, R3 is a perfluoropolyether chain, R4 is an end group having two or three polar groups with each polar group being bonded to different carbon atoms, and the carbon atoms, to which the polar groups are bonded, being bonded to each other via a linking group including carbon atoms to which the polar groups are not bonded.

Abstract: A fluorine-containing ether compound represented by Formula (1) is provided; R1—R2—CH2—R3—CH2—R4—R5??(1) (In Formula (1), R1 and R5 may be the same as or different from each other and each represents an alkenyl group having 2 to 8 carbon atoms or an alkynyl group having 3 to 8 carbon atoms, R2 and R4 may be the same as or different from each other and each represents a divalent linking group having a polar group, and R3 represents a perfluoropolyether chain, with a proviso that R1 and R2 are, and R4 and R5 are divided due to the presence of an atom other than the carbon atom such as an oxygen atom).

Abstract: This fluorine-containing ether compound is represented by Formula (1). R1—R2—CH2—R3—CH2—R4—R5??(1) (in Formula (1), R1 is an aryl group or an aralkyl group, R2 is a divalent linking group having 0 or 1 polar group, R3 is a perfluoropolyether chain, R4 is a divalent linking group having 2 or 3 polar groups, and R5 is an aryl group or an aralkyl group.

Abstract: A fluorine-containing ether compound of the present invention is represented by Formula (1). R1—CH2—R2—CH2—R3??(1) (In Formula (1), R1 is an organic end group having 3 or more carbon atoms which includes two or more polar groups with each polar group being bonded to different carbon atoms and the carbon atoms to which the polar groups are bonded being bonded to each other via a linking group including the carbon atoms which are not bonded to the polar groups, R2 includes a perfluoropolyether chain represented by Formula (3), and R3 is a hydroxyl group or R1) —(CF2)y?1—O—((CF2)yO)z—(CF2)y?1—??(3) (In Formula (3), y represents an integer of 2 to 4, and z represents an integer of 1 to 30).

Abstract: A fluorine-containing ether compound represented by Formula (1) is provided; R1—R2—CH2—R3—CH2—R4—R5??(1) (In Formula (1), R1 and R5 may be the same as or different from each other and each represents an alkenyl group having 2 to 8 carbon atoms or an alkynyl group having 3 to 8 carbon atoms, R2 and R4 may be the same as or different from each other and each represents a divalent linking group having a polar group, and R3 represents a perfluoropolyether chain, with a proviso that R1 and R2 are, and R4 and R5 are divided due to the presence of an atom other than the carbon atom such as an oxygen atom).

Abstract: A fluorine-containing ether compound represented by Formula (1) is provided. R1—R2—CH2—R3—CH2—R4—R5 ??(1) (In Formula (1), R1 and R5 each represents a group having a heterocyclic ring and may be the same as or different from each other, R2 and R4 each represents a divalent linking group having a polar group and play be the same as or different from each other, and R3 represents a perfluoropolyether chain.

Abstract: The present invention relates to a fluorine-containing ether compound represented by Formula (1), R1—R2—CH2—R3—CH2—R4??(1). (In Formula (1), R1 is an end group including an organic group having at least one double bond or triple bond, R2 is a divalent linking group bonded to R1 by etheric oxygen, R3 is a perfluoropolyether chain, R4 is an end group having two or three polar groups with each polar group being bonded to different carbon atoms, and the carbon atoms, to which the polar groups are bonded, being bonded to each other via a linking group including carbon atoms to which the polar groups are not bonded.

Abstract: A fluorine-containing ether compound of the present invention is represented by Formula (1). R1—CH2—R2—CH2—R3??(1) (In Formula (1), R1 is an organic end group having 3 or more carbon atoms which includes two or more polar groups with each polar group being bonded to different carbon atoms and the carbon atoms to which the polar groups are bonded being bonded to each other via a linking group including the carbon atoms which are not bonded to the polar groups, R2 includes a perfluoropolyether chain represented by Formula (3), and R3 is a hydroxyl group or R1) —(CF2)y-1—O—((CF2)yO)z—(CF2)y-1—??(3) (In Formula (3), y represents an integer of 2 to 4, and z represents an integer of 1 to 30).

Abstract: This fluorine-containing ether compound is represented by Formula (1). R1—R2—CH2—R3—CH2—R4—R5??(1) (in Formula (1), R1 is an aryl group or an aralkyl group, R2 is a divalent linking group having 0 or 1 polar group, R3 is a perfluoropolyether chain, R4 is a divalent linking group having 2 or 3 polar groups, and R5 is an aryl group or an aralkyl group.