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Thermal transfer printing: hetero-aromatic azo dye

Assignee: Imperial Chemical Industries Ltd
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Filing: 1986-08-13
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Granted: 1988-08-16
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Expires: 2006-08-13
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Abstract

Abstract A thermal transfer printing sheet comprising a substrate having a coating comprising at least one azo dye of the formula: A-N=N-E I wherein : A is the residue of a diazotizable heteroaromatic amine, A-NH2, in which A is selected from imidazolyl, pyrazolyl, thiazolyl, benzothiazolyl, isothiazolyl, benzoisothiazolyl, pyridoisothiazolyl and thienyl; and E is the residue of an aromatic coupling component, E-X wherein X is a group displaceable by a diazotized aromatic amine and E is optionally substituted aminophenyl, tetra- hydroquinolinyl, julolidyl or aminoquinolinyl, and a process for the transfer of dye from the transfer sheet to a receiver sheet by the selective application of heat to the transfer sheet while it is contact with the receiver sheet.

Inventors

  • 👤 Peter Gregory
  • 👤 Raymond L. White

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 11:32
CPC Classifications
B; B41; B41M; B41M5/00; B41M5/26; B41M5/382; B41M5/385; B41M5/388; C; C09; C09B; C09B29/00; C09B29/0025; C09B29/06; C09B29/08; C09B29/0805; C09B29/0807; C09B29/0809; C09B29/34; C09B29/36; C09B29/3604; C09B29/3617; C09B29/3643; C09B29/3695; Y; Y10; Y10S; Y10S428/00; Y10S428/913; Y10S428/914; Y10S8/00; Y10S8/92; Y10S8/922; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31971; Y10T428/31993

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 136 words
A thermal transfer printing sheet comprising a substrate having a coating comprising at least one azo dye of the formula: A--N═N--E I wherein: A is the residue of a diazotisable heteroaromatic amine, A--NH 2 , in which A is selected from imidazolyl, pyrazolyl, isothiazolyl, pyridoisothiazolyl and thienyl, substituted by groups selected only from cyano, thiocyano, nitro, halogen, C 1-4 -alkoxy, formyl, cyano-C 1-4 -alkyl, C 1-4 -alkylsulphonyl, trifluoromethyl, fluorosulphonyl, C 1-4 -alkylcarbonyl and C 1-4 -alkoxycarbonyl; and E is a group of the formula: ##STR4## wherein R 1 is selected from H, chloro, C 1-4 -alkyl and C 1-4 -alkylcarbonylamino; and R 2 and R 3 are selected from H, C 1-4 -alkyl and C 1-4 -alkyl, substituted by a group selected from phenyl chloro, cyano, C 1-4 -alkoxy, C 1-4 -alkoxycarbonyl and C 1-4 -alkycarbonyloxy.
Claim 2
Dependent Claim 136 words
A thermal transfer printing sheet comprising a substrate having a coating comprising at least one azo dye of the formula: A--N═N--E I wherein: A is the residue of a diazotisable heteroaromatic amine, A--NH 2 , in which A is selected from imidazolyl, pyrazolyl, isothiazolyl, pyridoisothiazolyl and thienyl, substituted by groups selected only from cyano, thiocyano, nitro, halogen, C 1-4 -alkoxy, formyl, cyano-C 1-4 -alkyl, C 1-4 -alkylsulphonyl, trifluoromethyl, fluorosulphonyl, C 1-4 -alkylcarbonyl and C 1-4 -alkoxycarbonyl; and E is a group of the formula: ##STR4## wherein R 1 is selected from H, chloro, C 1-4 -alkyl and C 1-4 -alkylcarbonylamino; and R 2 and R 3 are selected from H, C 1-4 -alkyl and C 1-4 -alkyl, substituted by a group selected from phenyl chloro, cyano, C 1-4 -alkoxy, C 1-4 -alkoxycarbonyl and C 1-4 -alkycarbonyloxy.
Claim 3
Dependent Claim 73 words
A thermal transfer printing sheet according to claim 1 wherein A, is selected form 1-cyanomethyl-4-5-dicyanoimidazol-2-yl; 4-cyanoisothiazol-5-yl; 3-methyl-4-cyanoisothiazol-5-yl; 1-cyanomethyl-3,4-dicyanopyrazol-5-yl; pyrido-(2-,3-c)-isothiazol-3-yl substituted in the 5, 6 or 5 and 6 positions by a group selected from cyano, nitro, methyl and methoxy; and thien-2-yl, substituted in the 3, 5 or 3 and 5 positions by a group selected from cyano, nitro, methylaminocarbonyl and in the 4 position by a group selected from H, methyl and methoxy.
Claim 4
Dependent Claim 134 words
A transfer printing sheet according to claim 1 wherein the azo dye conforms to the formula: ##STR5## wherein A is selected from 1-cyanomethyl-4,5-dicyanomidazol-2 yl; 4-cyanoisothiazol-5-yl; 3-methyl-4-cyanoisothiazol-5-yl; 1-cyanomethyl-3,4-dicyanopyrazol-5-yl; pryido(2,3-c)isothiazol-3-yl substituted in the 5, 6 or 5 and 6 positions by a group selected from cyano, nitro, methyl and methoxy; and thien-2-yl, substituted in the 3, 5 or 3 and 5 positions by one or more groups selected from methylaminocarbonyl, cyano and nitro and in the 4 position by a group selected from H, methyl and methoxy; R 1 is selected from H, chloro, C 1-4 -alkyl, C 1-4 -alkylcarbonyl-amino; and R 2 and R 3 are each independently selected from H; C 1-4 -alkyl, C 1-4 -alky substituted by a group selected from C 1-4 -alkoxy, C 1-4 -alkoxycarbonyl, C 1-4 -alkylcarbonyloxy, cyano and chloro.
Claim 5
Dependent Claim 75 words
A transfer printing process which comprises contacting a transfer sheet coated with a dye according to claim 1 with a receiver sheet, so that the dye is adjacent to the receiver sheet, and selectively heating areas of the transfer sheet to a temperature from >300° C. to 400° C. for a period from 2 to 10 milliseconds whereby dye in the heated areas of the transfer sheet may be selectively transferred to the receiver sheet.
Claim 6
Dependent Claim 31 words
A thermal transfer printing sheet according to claim 1 wherein the azo dye is selected from 3-methyl-4-(3-cyanomethyl-4,5-dicyanoimidazol-2-ylazo)-N-n-butyl-N-(3-(methoxycarbonyl)-propyl)-aniline, 3-methyl-4-(1-cyanomethyl-3,4-dicyanopyrazol-5-ylazo)-N-n-butyl-N-(2-(ethoxycarbonyl)ethyl)aniline, 3-methyl-4-(1-cyanomethyl-3,4-dicyanopyrazol-5-ylazo)-N-n-butyl-N-ethyl-aniline, 3-acetylamino-4-(1-cyanomethyl-3,4-dicyanopyrazol-5-ylazo)-N-n-butyl-N-ethylaniline, 3-methyl-4-(1-cyanomethyl-3,4-dicyanopyrazol-5-ylazo)-N,N-diethylaniline, 3-methyl-4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N,N-diethylaniline, 4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N,N-diethylaniline, 4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N-ethyl-N-(2-ethoxyethyl)aniline, 3-methyl-4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N,N-di(2-acetoxyethyl)-aniline, 3-methyl-4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N-n-butyl-N-(2-(ethoxycarbonyl)ethyl)aniline, 3-methyl-4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N-n-ethyl-N-(2-(ethoxy-carbonyl)ethyl)aniline, 3-methyl-4-(3-methyl-4-cyanoisothiazol-5-ylazo)-N-n-ethyl-N-(2-ethoxyethyl)aniline, 3-methyl-4-(3,5-dinitrothien-2-ylazo)-N,N-diethylaniline and 3-methyl-4-(3,5-dicyano-4-methylthien-2-ylazo)-N,N-di(2-acetoxyethyl)aniline.

References Cited (Backward Citations)

GB1504705A Cited
GB1539513A Cited
GB2036809A Cited
EP0030028A1 Cited
EP0030695A1 Cited
US4527171A Cited
JPS6030394A Cited
JPS6030392A Cited
JPS60239292A Cited
JPS60239291A Cited
JPS6112392A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-08-16 1992-02-15 1992-08-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-08-16 1996-02-15 1996-08-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-08-16 2000-02-15 2000-08-16 $7700.00 Window Closed / Lapsed

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