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US5432040A Expired / Lapsed US ⏱️ 0.0 years remaining

Dye-donor element for use according to thermal dye sublimation transfer

Assignee: Agfa Gevaert NV
•
Filing: 1993-05-26
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Granted: 1995-07-11
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Expires: 2013-05-26
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Abstract

Abstract Dye-donor element comprising a support provided with a dye layer containing a cyan indoaniline dye and/or another cyan azomethine dye, together with a cyan thiazolylazoaniline dye.

Inventors

  • 👤 Geert Defieuw
  • 👤 Luc Vanmaele
  • 👤 Wilhelmus Janssens

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 23:46
CPC Classifications
B; B41; B41M; B41M5/00; B41M5/26; B41M5/382; B41M5/385; B41M5/3858; C; C09; C09B; C09B29/00; C09B29/0025; C09B29/0074; C09B29/0077; C09B29/0085; B41M5/3854; B41M5/388; B41M5/39

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 40 words
Dye-donor element for thermal dye sublimation transfer comprising a support provided with a dye layer containing a cyan indoaniline dye and/or a cyan azomethine dye and a binder, characterized in that said dye layer further contains a cyan thiazolylazoaniline dye.
Claim 2
Dependent Claim 40 words
Dye-donor element for thermal dye sublimation transfer comprising a support provided with a dye layer containing a cyan indoaniline dye and/or a cyan azomethine dye and a binder, characterized in that said dye layer further contains a cyan thiazolylazoaniline dye.
Claim 3
Dependent Claim 225 words
Dye-donor element according to claim 1, wherein said cyan thiazolylazoaniline dye corresponds to the following general formula (I): ##STR80## wherein A represents O, N--R 5 , CR 6 R 7 ; Y represents any substituent; n represents 0, 1, 2, 3 or 4, the Y substituents being the same or different when n is greater than 1; each of R 1 to R 2 independently represent hydrogen, an alkyl group, a cycloalkyl group or an aryl group, or R 1 and R 2 may be joined together to form a 5- or 6-membered heterocyclic ring system or each of R 1 and R 2 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, R 3 represents a substituent; R 4 represents hydrogen or an electron withdrawing substituent; R 5 represents H, CN, NR 8 R 9 , OR 8 , OCOR 8 , OCOOR 8 , OCONR 8 R 9 , OSO 2 R 8 , OPO(OR 8 )(OR 9 ); R 6 and R 7 independently represent an electron withdrawing group; R 8 and R 9 independently represent hydrogen, alkyl, aryl, cycloalkyl or R 8 and R 9 together represent the atoms necessary for completing a heterocyclic nucleus or heterocyclic nucleus.
Claim 4
Dependent Claim 24 words
Dye-donor element according to claim 2, wherein R 3 represents halogen, OR 10 or SR 10 with R 10 representing hydrogen, alkyl, cycloalkyl, aryl.
Claim 5
Dependent Claim 35 words
Dye-donor element according to claim 3, wherein R 1 and R 2 both represent an alkyl group, R 3 represents chlorine or methoxy, R 4 represents hydrogen, A represents C(CN) 2 and n represents 0.
Claim 6
Dependent Claim 283 words
Dye-donor element according to claim 1, wherein said cyan indoaniline dye corresponds to the following general formula (II): ##STR81## wherein: R 11 and R 12 independently represent hydrogen, an alkyl group, a cycloalkyl group, an aryl group, an allyl group or an alkenyl group, or R 11 and R 12 together with the nitrogen to which they are attached form the necessary atoms to close a 5- or 6-membered heterocyclic ring, or R 11 and/or R 12 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 13 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, a di(alkyl or aryl)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 13 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 13 substituents may be the same or different when q is greater than 1; R 14 can have any of the significances given to R 13 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 14 substituents may be the same or different when r is greater than 1.
Claim 7
Dependent Claim 351 words
Dye-donor element according to claim 1, wherein said other cyan azomethine dye corresponds to general formula (III) ##STR82## wherein: X represents OR 21 or NR 22 R 23 or CN; Z represents CN, COOR 24 or CONR 25 R 26 ; R 15 , R 16 , R 17 and R 18 each independently represent hydrogen substituted or unsubstituted alkyl, cycloalkyl, substituted or unsubstituted aryl, alkoxy, substituted or unsubstituted aryloxy, carbonamido, sulfamido, hydroxy, halogen, NH--SO 2 R 27 , NH--COR 27 , OSO 2 R 27 , OCOR 27 , or R 15 and R 16 together and/or R 17 and R 18 together represent the necessary atoms to close (a) ring(s) fused-on the benzene ring or R 16 and/or R 18 together with R 20 and/or R 19 represent the necessary atoms to close a heterocyclic ring fused-on the benzene ring; R 19 and R 20 each independently represent hydrogen, alkyl, cycloalkyl, aryl, a substituted or unsubstituted heterocyclic group or R 19 and R 20 together represent the necessary atoms to close a heterocyclic ring or R 20 and/or R 19 together with R 16 and/or R 18 represent the necessary atoms to close a heterocylic ring fused-on the benzene ring; R 21 represents hydrogen, alkyl, cycloalkyl, aryl, SO 2 R 27 , COR 27 , CSR 27 , POR 27 R 28 ; R 22 and R 23 each independently represent hydrogen, alkyl, cycloalkyl, aryl, amino SO 2 LR 27 , COR 27 , CSR 27 , POR 27 R 28 , or R 22 and R 23 together represent the necessary atoms to close a heterocyclic ring, including a heterocyclic ring with an aliphatic or aromatic ring fused-on; R 24 , R 25 and R 26 each independently represent hydrogen, alkyl, cycloalkyl, aryl, or R 25 and R 26 together represent the necessary atoms to close a heterocyclic ring; R 27 and R 28 each independently represent alkyl, cycloalkyl, alkenyl, aralkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, amino, a heterocyclic group or R 27 and R 28 together represent the necessary atoms to close a 5- or 6-membered ring.
Claim 8
Dependent Claim 26 words
Dye-donor element according to claim 1, wherein the compounding ratio of the thiazolylazoaniline dyes in the cyan dye mixture is from 5 to 60% by weight.
Claim 9
Dependent Claim 14 words
Dye-donor element according to claim 1, wherein the dye layer contains polystyrene-co-acrylonitrile as binder.
Claim 10
Dependent Claim 144 words
Dye-donor element according to claim 1, wherein said dye layer consists of a repeating sequence of yellow, magenta and cyan dye areas and wherein said yellow dye area contains a yellow dye corresponding to general formula (IV) ##STR83## wherein: R 30 and R 31 independently represent hydrogen, an alkyl group, a cycloalkyl group or an aryl group, or R 30 and R 31 may be joined together to form a 5- or 6-membered heterocyclic ring system, or each of R 30 and R 31 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 32 represents a substituent; s represents 0, 1, 2, 3 or 4, the R 32 substituents may be the same or different when s is greater than 1.
Claim 11
Dependent Claim 59 words
A method for making an image comprising the steps of (i) bringing the dye layer of a dye-donor element as defined in claim 1, 2, 3, 4, 5, 6, 7, 8 or 9 in face-to-face relationship with a dye-receiving layer of a receiver sheet and image-wise heating a thus obtained assemblage from the back of said dye donor element.

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1998-07-10 1999-01-09 1999-07-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2002-07-10 2003-01-09 2003-07-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2006-07-10 2007-01-09 2007-07-11 $7700.00 Window Closed / Lapsed

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