Thermal dye sublimation transfer donor element

Claim 2

Dye-donor element for use according to thermal dye transfer methods, said element comprising a support having thereon a dye layer comprising a dye layer carried by a polymeric binder resin, characterized in that said dye is an azo dye corresponding to the following general formula (I): ##STR65## wherein each of R 1 to R 4 independently represent hydrogen, an unsubstituted alkyl group, a cycloalkyl group or an aryl group, or R 1 and R 2 and/or R 3 and R 4 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each of R 1 to R 4 independently can be joined to the carbon atom of the aromatic ring at a position ortho to the position of attachment of the anilino nitrogen to form a 5- or 6-membered ring; X and Y independently represent a substituent; selected from the group consisting of SH, OH, halogen, NO 2 , CN, alkyl, amino, carbonamido, sulfonamido, acylamido, sulfonylamino phosphorylamino, alkoxy, thialkoxy, alkoxycarbonyl and aryloxycarbonyl; n represent 0, 1, 2, 3, or 4, X substituents may be the same or different when is greater than 1; n' represents 0, 1, 2, 3 and 4, and Y substitutents may be the same or different when n' is greater than 1.

Claim 3

Dye-donor element according to claim 1, wherein R 1 to R 4 independently represent an unsubstituted alkyl group, X represents hydroxy, carbonamido or sulfonamido, n represents 0 or 1 and n' represents 0.

Claim 4

Dye-donor element according to claim 1, wherein said dye-donor element further comprises in the same dye area or in another dye area a dye corresponding to the general formula (II): ##STR66## wherein: R 5 and R 6 independently represent hydrogen, an alkyl group, a cycloalkyl group, an aryl group, an allyl group or an alkenyl group, or R 5 and R 6 together with the nitrogen to which they are attached form the necessary atoms to close a 5- or 6-membered heterocyclic ring, or R 5 and/or R 6 together with the nitrogen to which they are attached and either or both carbon atoms of the phenyl ring ortho to said nitrogen atom form a 5- or 6-membered heterocyclic ring, R 7 represents halogen, hydroxy, cyano, an alkyl group, a cycloalkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an amino group, an alkylcarbonylamino group, an arylcarbonylamino group, an arylsulfonylamino group, an alkoxycarbonylamino group, an aryloxycarbonylamino group, an alkylthiocarbonylamino group, an arylthiocarbonylamino group, an alkylphosphoramidate group, an arylphosphoramidate group, an alkylphosphonamidate group, an arylphosphonamidate group, an alkylaminocarbonyl group or an arylaminocarbonyl group, or R 7 represents the necessary atoms to close an alicyclic or aromatic or heterocyclic ring fused-on the phenyl ene ring; q represents 0, 1, 2, 3 or 4, the R 7 substituents may be the same or different when q is greater than 1; R 8 can have any of the significances given to R 7 or can represent the necessary atoms to close an alicyclic or aromatic or heterocyclic ring fused-on the phenyl ring; r represents 0, 1, 2, 3 or 4, the R 8 substitutents may be the same or different when r is greater than 1.

Claim 5

Dye-donor element according to claim 3, wherein both dyes are contained in the same dye area that is black colored.

Claim 6

Dye-donor element according to claim 4, wherein said dye layer further comprises a magenta heterocyclic azo aniline dye or a magenta arylazoaniline dye with electron withdrawing substituents on the aryl nucleus, having an absorption maximum between 520 and 600 nm.

Claim 7

Dye-donor element according to claim 5, wherein said magenta dye is a 4-chloro,5-formylthiazol-2-ylazoaniline dye.

Claim 8

Dye-donor element according to claim 4, wherein said dye layer further comprises a yellow dye with an absorption maximum below 460 nm.

Claim 9

Dye-donor element according to claim 7, wherein said yellow dye corresponds to the following general formula (III): ##STR67## wherein: R 9 and R 10 independently represent hydrogen, an alkyl group, a cycloalkyl group or an aryl group, or R 9 and R 10 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each of R 9 and R 10 can be joined to the carbon atom of the aromatic ring at a position ortho to the position of attachment of the anilino nitrogen to form a 5- or 6-membered ring; R 11 represents substitutent selected from the group consisting of alkyl, CN, alkoxy, thioalkoxy, halogen, NO 2 and acylamino; s represents 0, 1, 2, 3 or 4, the R 11 substitutents may be the same or different when s is greater than 1.

Claim 10

Dye-donor element according to claim 4, wherein the compounding ratio of the dyes is 10 to 50% by weight for the yellow dyes according to formula (I), 20 to 60% by weight for the cyan dyes according to formula (II), 10 to 60% by weight for the magenta dyes and 0 to 40% by weight for the yellow dyes of formula (III).

Claim 11

Dye-donor element according to claim 1, wherein the binder is cellulose acetate butyrate or co-acrylonitrile-styrene.

Claim 12

Dyed receiving element comprising a support provided with a dye-image receiving layer containing dyes in imagewise distribution, formed by thermal dye sublimation transfer using a dye-donor element comprising a support having thereon a dye layer comprising a dye carried by a polymeric binder resin, characterized in that said dye in an azo dye corresponding to the following general formula (I): ##STR68## wherein each of R 1 to R 4 independently represented hydrogen, an unsubstituted alkyl group, a cycloalkyl group or an aryl group, or R 1 and R 2 and/or R 3 and R 4 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each R 1 to R 4 independently can be joined to the carbon atom of the aromatic ring at a position ortho to the position of attachment of the anilino nitrogen to form a 5- or 6-membered ring; X and Y independently represent a substituent selected from the group consisting of SH, OH, halogen, NO 2 , CN, alkyl, amino, carbonamido, sulfonamido, acylamino, sulfonylamino, phosphorylamino, alkoxy, thioalkoxy, alkoxcarbonyl and aryloxycarbonyl; n represents 0, 1, 2, 3 or 4, the X substituents may be the same of different when n is greater than 1; n' represents 0, 1, 2, 3 to 4, the Y substituents may be the same different when n' is greater than 1.

Claim 13

Dyed receiving element comprising a support provided with a dye-image receiving layer containing dyes in imagewise distribution, formed by thermal dye sublimation transfer using a dye-donor element comprising a support having thereon a dye layer comprising a dye carried by a polymeric binder resin, characterized in that said dye in an azo dye corresponding to the following general formula (I): ##STR68## wherein each of R 1 to R 4 independently represented hydrogen, an unsubstituted alkyl group, a cycloalkyl group or an aryl group, or R 1 and R 2 and/or R 3 and R 4 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each R 1 to R 4 independently can be joined to the carbon atom of the aromatic ring at a position ortho to the position of attachment of the anilino nitrogen to form a 5- or 6-membered ring; X and Y independently represent a substituent selected from the group consisting of SH, OH, halogen, NO 2 , CN, alkyl, amino, carbonamido, sulfonamido, acylamino, sulfonylamino, phosphorylamino, alkoxy, thioalkoxy, alkoxcarbonyl and aryloxycarbonyl; n represents 0, 1, 2, 3 or 4, the X substituents may be the same of different when n is greater than 1; n' represents 0, 1, 2, 3 to 4, the Y substituents may be the same different when n' is greater than 1.

Claim 14

Dyed receiving element according to claim 11 wherein said dye-donor element further comprises in the same dye area or in another dye area a dye corresponding to the general formula (II): ##STR69## wherein R 5 and R 6 independently represent hydrogen, an alkyl group, a cycloalkyl group, an aryl group, an allyl group or an alkenyl group, or R 5 and R 6 together with the nitrogen to which they are attached form the necessary atoms to close a 5- or 6-membered heterocyclic ring, or R 5 and/or R 6 together with the nitrogen to which they are attached and either or both carbon atoms of the phenyl ring ortho to said nitrogen atom form a 5- or 6-membered heterocyclic ring; R 7 represents halogen, hydroxy, cyano, an alkyl group, a cycloalkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an amino group, an alkylcarbonylamino group, an arylcarbonylamino group, an arylsulfonylamino group, an alkoxycarbonylamino group, an aryloxycarbonylamino group, an alkylthiocarbonylamino group, an arylthiocarbonylamino group, an alkylphosphoramidate group, an arylphosphoramidate group, an alkylphosphonamidate group, an arylphosphonamidate group, an alkylaminocarbonyl group or an arylaminocarbonyl group, or R 7 represents the necessary atoms to close an alicyclic or aromatic or heterocyclic ring fused-on the phenylene ring; q represents 0, 1, 2, 3 or 4, the R 7 substituents may be the same or different when q is greater than 1; R 8 can have any of the significances given to R 7 or can represent the necessary atoms to close an alicyclic or aromatic or heterocyclic ring fused-on the phenyl ring; r represents 0, 1, 2, 3 or 4, the R 8 substitutents may be the same or different when r is greater than 1.

Claim 15

Dyed receiving element according to claim 12 wherein both dyes are contained in the same dye area that is black colored.

Claim 16

Dyed receiving element according to claim 13 wherein said dye layer further comprises a magenta heterocyclic azo aniline dye or a magenta arylazoaniline dye with electron withdrawing substituents on the aryl nucleus, having an absorption maximum between 520 and 600 nm.

Claim 17

Dyed receiving element according to claim 13, said dye layer further comprises a yellow dye with an absorption maximum below 460 nm.

Claim 18

Dyed receiving element according to claim 15 wherein said yellow dye corresponds to the following general formula (III): ##STR70## wherein: R 9 and R 10 independently represent hydrogen, an alkyl group, a cycloalkyl group or an aryl group, or R 9 and R 10 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each of R 9 and R 10 can be joined to the carbon atom of the aromatic ring at a position ortho to the position of attachment of the anilino nitrogen to form a 5- or 6-membered ring R 11 represents a substituent selected from the group consisting of alkyl, CN, alkoxy, thioalkoxy, halogen, NO.sub. 2 and acylamino; s represents 0, 1, 2, 3 or 4, the R 11 substituents may be the same or different when s is greater than 1.