A lubricant, which includes an ionic liquid including a conjugate base and a conjugate acid, wherein the conjugate acid is represented by General Formula (A) below, and wherein a pKa of an acid that is a source of the conjugate base in acetonitrile is 10 or less,

##STR00001##

where, in General Formula (A), R.sub.1, R.sub.2, and R.sub.3 are each independently a group including a hydrocarbon group, with the proviso that at least one of the hydrocarbon groups in R.sub.1, R.sub.2, and R.sub.3 is a straight-chain hydrocarbon group having 6 or greater carbon atoms.

This invention provides a non-aqueous electrolyte magnesium secondary battery comprising a positive electrode, a negative electrode, a separator, and a non-aqueous electrolyte, the non-aqueous electrolyte comprising [N(SO.sub.2CF.sub.3).sub.2].sup.− as an anion, and Mg.sup.2+ and/or an organic onium cation as a cation.

This invention provides a non-aqueous electrolyte magnesium secondary battery comprising a positive electrode, a negative electrode, a separator, and a non-aqueous electrolyte, the non-aqueous electrolyte comprising [N(SO.sub.2CF.sub.3).sub.2].sup.− as an anion, and Mg.sup.2+ and/or an organic onium cation as a cation.

A monomer has the structure

##STR00001##

wherein R is an organic group comprising a polymerizable carbon-carbon double bond or carbon-carbon triple bond; X and Y are independently at each occurrence hydrogen or a non-hydrogen substituent; EWG1 and EWG2 are independently at each occurrence an electron-withdrawing group; p is 0, 1, 2, 3, or 4; n is 1, 2, 3, or 4; and M.sup.+ is an organic cation. A polymer prepared from monomer is useful as a component of a photoresist composition.

In an approach to improve the field of photoacid generators (PAGs) through a new photoacid generator, in particular to a photoacid generator comprising a new polycyclic aromatic photoacid generator compound anion, and a photoresist composition, comprising said photoacid generator. Embodiments the present invention relate to a method of generating an acid using said photoresist composition and a method of forming a patterned materials feature on a substrate.

A salt represented by formula (I): ##STR00001##
wherein R.sup.1 and R.sup.2 independently represent a hydrogen atom, a hydroxy group or a C.sub.1 to C.sub.12 hydrocarbon group in which a methylene group may be replaced by a —O— or —CO—; m and n independently represent 1 or 2; Ar represents an optionally substituted phenyl group; Q.sup.1 and Q.sup.2 independently represent a fluorine atom or a C.sub.1 to C.sub.6 perfluoroalkyl group, A.sup.1 represents a single bond, a C.sub.1 to C.sub.24 alkanediyl group or the like, and Y represents an optionally substituted C.sub.1 to C.sub.18 alkyl group or monovalent C.sub.3 to C.sub.18 alicyclic hydrocarbon group, and a methylene group therein may be replaced by a —O—, O— or —SO.sub.2—, provided that the alkyl group or the alicyclic hydrocarbon group has at least one substituent, or at least one methylene group contained therein is replaced by a —O—, —CO— or —SO.sub.2—.

A salt represented by formula (I): ##STR00001##
wherein R.sup.1 and R.sup.2 independently represent a hydrogen atom, a hydroxy group or a C.sub.1 to C.sub.12 hydrocarbon group in which a methylene group may be replaced by a —O— or —CO—; m and n independently represent 1 or 2; Ar represents an optionally substituted phenyl group; Q.sup.1 and Q.sup.2 independently represent a fluorine atom or a C.sub.1 to C.sub.6 perfluoroalkyl group, A.sup.1 represents a single bond, a C.sub.1 to C.sub.24 alkanediyl group or the like, and Y represents an optionally substituted C.sub.1 to C.sub.18 alkyl group or monovalent C.sub.3 to C.sub.18 alicyclic hydrocarbon group, and a methylene group therein may be replaced by a —O—, O— or —SO.sub.2—, provided that the alkyl group or the alicyclic hydrocarbon group has at least one substituent, or at least one methylene group contained therein is replaced by a —O—, —CO— or —SO.sub.2—.

An azine compound represented by the formula (1), a method for its production and an organic electroluminescent device containing it as a constituent component. ##STR00001##
wherein Ad each independently represents a 1-adamantyl group, etc., p and q are each independently 0 or 1, Ar.sup.1 and Ar.sup.2 are each independently a single bond (but only when p is 1, or q is 1), or a pyridyl group which may be substituted by a phenyl group, etc., incidentally, Ad groups on Ar.sup.1 and Ar.sup.2 are each independently bonded to said pyridyl group, etc., Ar.sup.2 is each independently a C.sub.3-13 heteroaromatic group which may be substituted by a fluorine atom, etc., X.sup.1, X.sup.2, X.sup.3 and X.sup.4 are each independently a single bond, etc., m and n are each independently 0, 1 or 2, Z is a nitrogen atom, etc., n+p+q is 1, 2 or 3.

An azine compound represented by the formula (1), a method for its production and an organic electroluminescent device containing it as a constituent component. ##STR00001##
wherein Ad each independently represents a 1-adamantyl group, etc., p and q are each independently 0 or 1, Ar.sup.1 and Ar.sup.2 are each independently a single bond (but only when p is 1, or q is 1), or a pyridyl group which may be substituted by a phenyl group, etc., incidentally, Ad groups on Ar.sup.1 and Ar.sup.2 are each independently bonded to said pyridyl group, etc., Ar.sup.2 is each independently a C.sub.3-13 heteroaromatic group which may be substituted by a fluorine atom, etc., X.sup.1, X.sup.2, X.sup.3 and X.sup.4 are each independently a single bond, etc., m and n are each independently 0, 1 or 2, Z is a nitrogen atom, etc., n+p+q is 1, 2 or 3.

The preparation is described of a compound of formula (I) comprising an —SO.sub.2F function by reacting a compound of formula (II) with a fluorinating agent selected from hydrofluoric acid and an ionic fluoride of a monovalent or divalent cation:
R—SO.sub.2F  (I)
R′—SO.sub.2X  (II)
where R is selected from the groups R1, R2 and R3: R1=—C.sub.nH.sub.aF.sub.b with n=1-10, a+b=2n+1, b≧1; R2=—C.sub.xH.sub.yF.sub.z—SO.sub.2F with x=1-10, y+z=2x and z≧1; R3=φ-C.sub.cH.sub.hF.sub.f with c=1-10; h+f=2c and f≧1;
where R′ is selected from the following groups R′1, R′2 and R′3: R′1=—C.sub.nH.sub.aX.sub.b with n=1-10, a+b=2n+1, b≧1; R′2=—C.sub.xH.sub.yX.sub.z—SO.sub.2X with x=1-10, y+z=2x and z≧1; R′3=φ-C.sub.cH.sub.hX.sub.f with c=1-10; h+f=2c and f≧1; φ denoting a phenyl group; X═Cl, Br.