A fluorine-containing ether compound represented by R.sup.1—R.sup.2—CH.sub.2—R.sup.3—CH.sub.2—R.sup.4—R.sup.5 is provided. (R.sup.3 is a perfluoropolyether chain; R.sup.1 and R.sup.5 are each independently any one of an alkyl group that may have a substituent, an organic group having at least one double bond or at least one triple bond, and a hydrogen atom; and —R.sup.2—CH.sub.2—R.sup.3 is represented by Formula (2), and R.sup.3—CH.sub.2—R.sup.4— is represented by Formula (3))
-[A]-[B]—O—CH.sub.2—R.sup.3  (2)
R.sup.3—CH.sub.2—O—[C]-[D]-  (3)
([A] is represented by Formula (4), [B] is represented by Formula (5), [C] is represented by Formula (6), [D] is represented by Formula (7), and in the formula, a and b are integers of 0 to 2, c is an integer of 2 to 5, d and f are integers of 0 to 2, and e is an integer of 2 to 5, and at least one of b and d in the formula is 1 or more) ##STR00001##

The fluorine-containing ether compound is represented by the following formula (1): R.sup.1—R.sup.2—CH.sub.2—R.sup.3—CH.sub.2—R.sup.4. In the formula (1), R.sup.1 is represented by the following formula (2), R.sup.2 is represented by the following formula (3), R.sup.3 is a perfluoropolyether chain, and R.sup.4 is an organic end group different from R.sup.1—R.sup.2— and contains two or three polar groups, wherein each polar group is bonded to a different carbon atom, and the carbon atoms to which the polar groups are bonded are bonded to one another via a linking group containing a carbon atom to which the polar group is not bonded. In the formula (2), R.sup.5 is an alkoxy group selected from the group consisting of a methoxy, an ethoxy and a propoxy group. In the formula (3), w is 2 or 3.

##STR00001##

The fluorine-containing ether compound is represented by the following formula (1): R.sup.1-R.sup.2—CH.sub.2—R.sup.3—CH.sub.2—R.sup.4. In the formula (1), R.sup.1 is represented by the following formula (2), R.sup.2 is represented by the following formula (3), R.sup.3 is a perfluoropolyether chain, and R.sup.4 is an organic end group different from R.sup.1-R.sup.2- and contains two or three polar groups, wherein each polar group is bonded to a different carbon atom, and the carbon atoms to which the polar groups are bonded are bonded to one another via a linking group containing a carbon atom to which the polar group is not bonded. In the formula (2), r is 1 to 3. In the formula (3), w is 2 or 3.

##STR00001##

Provided is a compound which has heat resistance and decomposition resistance and with which a monomolecular film having a reduced thickness can be obtained. A fluoropolyether compound in accordance with an aspect of the present invention is represented by R.sup.1—C.sub.6H.sub.4O—CH.sub.2CH(OH)CH.sub.2OCH.sub.2—R.sup.2—CH.sub.2—O—CH.sub.2CH(OH)CH.sub.2—OC.sub.6H.sub.4—R.sup.1 where R.sup.1 is a hydrogen atom, an alkoxy group having 1 to 4 carbon atoms, an amino group, or an amide group, R.sup.2 is —CF.sub.2O(CF.sub.2CF.sub.2O).sub.xCF.sub.2—, and x is a real number of 1 to 35.

Polymers used as rolling lubricating agents, to compositions including said polymers, and to alkali metal films including the polymers or compositions on the surface(s) thereof. The use of said polymers and compositions is also described for strip-rolling alkali metals or alloys thereof in order to obtain thin films. Methods for producing said thin films, which are suitable for use in electrochemical cells, are also described. An improved lubricant according to formula I, which, for example, achieves enhanced conductivity, and/or enables the production of electrochemical cells having an improved life span in cycles.

A sliding member includes a substrate, a first coating film layer which is provided on the substrate, and a second coating film layer which is provided on the first coating film layer. The first coating film layer including a coating film including a composition for a sliding member. The composition for a sliding member contains a binder resin, a solid lubricant, and at least one type of resin beads selected from the group consisting of amino resin beads and urethane resin beads. The second coating film layer includes the binder resin and the solid lubricant.

The invention relates to a lubricant coating (5) for a medical injection device (1), comprising successively: —a bottom layer (50) in contact with the medical device surface (21) of the container to be lubricated, comprising a mixture of cross-linked and non-cross-linked poly-(dimethylsiloxane), —an intermediate layer (51) consisting essentially of oxidized poly-(dimethylsiloxane) and having a thickness comprised between 10 and 30 nm and, —a top layer (52) consisting essentially of non-cross-linked poly-(dimethylsiloxane) and having a thickness of at most 2 nm. The invention also relates to a medical injection device comprising such a lubricant coating, and a manufacturing process for said coating.

The invention concerns coating composition comprising hydrophobic polymer for use as a photoreactive basecoat for a medical device or implant comprising a polymer made from monomers comprising: (a) 1 to 12 mol % of at least one photoactive monomer that is a hydrogen atom abstracter and (b) 99 to 88 mol % of one or more of acrylamides, methacrylamides, acrylates, methacrylates, and N-vinylpyrrolidone; wherein the polymer has a glass transition temperature (Tg) of less than 40° C.

A magnetic recording medium that can exhibit good traveling performance during use is provided. This magnetic recording medium is a tape-shaped magnetic recording medium, and includes a substrate including a polyester as a main component, a base layer disposed on the substrate, and a magnetic layer disposed on the base layer. The kurtosis of the surface of the magnetic layer is 3.0 or more. The base layer and the magnetic layer each include a lubricant including a fatty acid and a fatty acid ester. In the lubricant, a ratio of the content of the fatty acid to the content of the fatty acid ester is less than 0.6.

A fluorine-containing ether compound represented by formula (1) shown below.
R.sup.4—CH.sub.2—R.sup.3—CH.sub.2—R.sup.2—CH.sub.2—R.sup.1—CH.sub.2—R.sup.2—CH.sub.2—R.sup.3—CH.sub.2—R.sup.4  (1)
(In formula (1), R.sup.1 and R.sup.3 represent different perfluoropolyether chains, R.sup.2 represents a linking group containing one or more polar groups, and R.sup.4 represents a terminal group containing two or more polar groups.)