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US4584258A Expired / Lapsed US ⏱️ 0.0 years remaining

Recording and information record elements comprising telluropyrlium dyes

Assignee: Eastman Kodak Co
•
Filing: 1984-11-16
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Granted: 1986-04-22
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Expires: 2004-11-16
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Abstract

Abstract Telluropyrylium dyes are useful as infrared absorbing dyes in recording elements.

Inventors

  • 👤 Michael R. Detty
  • 👤 Harold T. Thomas

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 09:57
CPC Classifications
G; G11; G11B; G11B7/00; G11B7/24; G11B7/241; G11B7/242; G11B7/244; G11B7/249; G11B7/252; G11B7/253; Y; Y10; Y10S; Y10S430/00; Y10S430/146

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 48 words
A recording element comprising a support having coated thereon an optical recording layer of an amorphous composition comprising an infrared absorbing telluropyrylium dye and a binder; wherein the dye is present in the layer in an amount of at least 50% by weight of the dye and binder.
Claim 2
Dependent Claim 48 words
A recording element comprising a support having coated thereon an optical recording layer of an amorphous composition comprising an infrared absorbing telluropyrylium dye and a binder; wherein the dye is present in the layer in an amount of at least 50% by weight of the dye and binder.
Claim 3
Dependent Claim 192 words
The element of claim 1 wherein the layer absorbs in the 700-900 nm region of the spectrum and the dye has the structure ##STR29## wherein R 1 , R 3 and R 5 each independently represents alkyl, aryl, (CR 6 ═CH) n CR 7 ═A 1 or (CH═CH) m A 2 provided that one, and only one, of R 1 , R 3 and R 5 is (CR 6 ═CH) n CR 7 ═A 1 or (CH═CH) m A 2 ; wherein R 2 and R 4 each independently represents hydrogen; or R 2 and R 3 , or R 4 and R 5 , taken together with the carbon atoms to which they are attached, form a mononuclear or polynuclear fused carbocyclic ring having from about 5 to 20 carbon atoms; R 6 and R 7 are each independently hydrogen, cyano, alkyl or aryl; A 1 represents a monocyclic or polycyclic heterocyclylidene group; A 2 represents aryl, amino, dialkylaminoaryl, alkylamino, arylamino, dialkylamino, diarylamino or a monocyclic or polycyclic heterocyclyl group; n represents a number from 0 to 5; m represents a number from 1 to 5; and X represents an anion.
Claim 4
Dependent Claim 141 words
The element of claim 2 wherein the dye has the structure ##STR30## wherein R 10 and R 8 each independently represents alkyl, aryl, (CR 6 ═CH) n CR 7 ═A 1 or (CH═CH) m A 2 provided that one, and only one, of R 10 and R 8 is (CR 6 ═CH) n CR 7 ═A 1 or (CH═CH) m A 2 ; A 1 represents a monocyclic or polycyclic heterocyclyidene group; A 2 represents aryl, amino, dialkylaminoaryl, alkylamino, arylamino, dialkylamino, diarylamino or a monocyclic or polycyclic heterocyclyl group; R 6 and R 7 are each independently hydrogen, cyano, alkyl or aryl; R 9 , R 11 , R 12 , R 13 and R 14 each independently represents hydrogen; n represents a number from 0 to 5; m represents a number from 1 to 5; and X represents an anion.
Claim 5
Dependent Claim 131 words
The element of claim 2 wherein R 1 , R 3 and R 5 each independently represents methyl, ethyl, t-butyl, phenyl, p-N,N-dimethylaminophenyl, p-anisyl and (CR 6 ═CH) n CR 7 --A 1 , (CH═CH) m A 2 ; A 1 represents a nucleus selected from the group consisting of oxazolylidene, thiazolylidene, selenazolylidene, imidazolylidene, pyranylidene, thiapyranylidene, selenapyranylidene, telluropyranylidene, oxoindolazinylidene, benzoxazolylidene, benzothiazolylidene, benzopyranylidene, benzothiapyranylidene, benzoselenapyranylidene, or benzotelluropyranylidene; A 2 represents phenyl, dimethylaminophenyl, dimethylamino or a nucleus selected from the group consisting of oxazolyl, 9-julolidyl, thiazolyl, selenazolyl, tetrahydroquinolinyl, imidazolyl, benzoxazolyl, benzothiazolyl or naphthyl; and X represents BF 4 - , ClO 4 - , CF 3 SO 3 - , FSO 3 - , PF 6 - , CH 3 SO 3 - , Cl - , Br - , or I - .
Claim 6
Dependent Claim 129 words
The element of claim 3 wherein R 8 and R 10 each independently represents methyl, ethyl, t-butyl, phenyl, p-anisyl, 2,5-dimethoxyphenyl, p-N,N-dimethylaminophenyl and (CR 6 ═CH) n CR 7 ═A 1 or (CH═CH) m A 2 ; A 1 represents a nucleus selected from the group consisting of oxazolylidene, thiazolylidene, selenazolylidene, imidazolylidene, pyranylidene, thiapyranylidene, selenapyranylidene, telluropyranylidene, oxoindolazinylidene, benzoxazolylidene, benzothiazolylidene, benzopyranylidene, benzothiapyranylidene, benzoselenapyranylidene, or benzotelluropyranylidene; A 2 represents phenyl, dimethylaminophenyl, dimethylamino or a nuclus selected from the group consisting of oxazolyl, 9-julolidyl, thiazolyl, selenazolyl, tetrahydroquinolinyl, imidazolyl, benzoxazolyl, benzothiazolyl or naphthyl; and X represents BF 4 - , ClO 4 - , CF 3 SO 3 - , FSO 3 - , PF 6 - , CH 3 SO 3 - , Cl - , Br - , or I - .
Claim 7
Dependent Claim 16 words
The element of claim 1 wherein the dye is selected from the group consisting of ##STR31##
Claim 8
Dependent Claim 18 words
The element of claim 1 wherein the optical recording layer has an absorption factor of at least 20.
Claim 9
Dependent Claim 11 words
The recording element of claim 1 wherein the support is reflecting.
Claim 10
Dependent Claim 44 words
The recording element of claim 1 wherein the binder is selected from the group consisting of __________________________________________________________________________ Mole % __________________________________________________________________________ ##STR32## 35% 30% ; 35% ##STR33## 40% 30% ; 30% ##STR34## 16.67% 50% 16.67% ; 16.67% and ##STR35## 35% 30% . 35% ##STR36## __________________________________________________________________________

References Cited (Backward Citations)

US4380769A Cited
US4318112A Cited
US4415621A Cited
US4365017A Cited
US4446223A Cited
US4501808A Cited
US4508811A Cited
US4499165A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-04-21 1989-10-21 1990-04-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-04-21 1993-10-21 1994-04-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-04-21 1997-10-21 1998-04-22 $7700.00 Window Closed / Lapsed

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