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US4684599A Expired / Lapsed US ⏱️ 0.0 years remaining

Photoresist compositions containing quinone sensitizer

Assignee: Eastman Kodak Co
•
Filing: 1986-07-14
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Granted: 1987-08-04
•
Expires: 2006-07-14
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Abstract

Abstract Positive-working imaging compositions comprise a polymeric binder and a quinone sensitizer which provides alkali solubility to the composition when exposed to activating radiation.

Inventors

  • 👤 Thap DoMinh
  • 👤 James C. Fleming
  • 👤 Michael J. Lindstrom

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 05:22
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/0045; Y; Y10; Y10S; Y10S430/00; Y10S430/1053; Y10S430/1055; Y10S430/114; Y10S430/12; Y10S430/124

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 167 words
A positive-working imaging composition comprising a polymer binder and a sensitizer effective, when exposed to activating radiation, to provide alkali solubility to said composition, characterized in that said sensitizer comprises a quinone having the structural formula: ##STR26## wherein Q is ##STR27## R 1 is H, halo, akyl, alkoxy, aryl, aralkyl, alkaryl, cyano, or a heterocyclic ring, R 2 and R 3 are individually H, aryl, alkaryl, ##STR28## where each Ar is individually aryl, aralkyl, or alkaryl or together R 2 and R 3 comprise the number of carbon atoms that complete 1 or 2 fused carbocyclic rings, R 4 and R 5 are individually alkyl, alkaryl, aralkyl, aryl, or together R 4 and R 5 comprise the number of atoms that complete a heterocyclic ring, Z is ═0 or ═NSO 2 --Ar, where Ar is defined above, R 6 and R 7 are individually H, alkyl, aryl, alkaryl, aralkyl, --OH, or together R 6 and R 7 comprise the atoms that complete a carbocyclic or heterocyclic ring.
Claim 2
Dependent Claim 167 words
A positive-working imaging composition comprising a polymer binder and a sensitizer effective, when exposed to activating radiation, to provide alkali solubility to said composition, characterized in that said sensitizer comprises a quinone having the structural formula: ##STR26## wherein Q is ##STR27## R 1 is H, halo, akyl, alkoxy, aryl, aralkyl, alkaryl, cyano, or a heterocyclic ring, R 2 and R 3 are individually H, aryl, alkaryl, ##STR28## where each Ar is individually aryl, aralkyl, or alkaryl or together R 2 and R 3 comprise the number of carbon atoms that complete 1 or 2 fused carbocyclic rings, R 4 and R 5 are individually alkyl, alkaryl, aralkyl, aryl, or together R 4 and R 5 comprise the number of atoms that complete a heterocyclic ring, Z is ═0 or ═NSO 2 --Ar, where Ar is defined above, R 6 and R 7 are individually H, alkyl, aryl, alkaryl, aralkyl, --OH, or together R 6 and R 7 comprise the atoms that complete a carbocyclic or heterocyclic ring.
Claim 3
Dependent Claim 38 words
The composition of claim 1 wherein said sensitizer comprises a quinone having the structural formula ##STR29## wherein R 1 , R 2 , R 3 , R 4 , and R 5 are as defined in claim 1.
Claim 4
Dependent Claim 45 words
A composition of claim 1 wherein said sensitizer comprises a quinone having the structural formula: ##STR30## wherein R 1 is as defined in claim 1; and Z 1 is the number of atoms necessary to complete a heterocyclic ring containing 5 to 6 ring atoms.
Claim 5
Dependent Claim 27 words
A composition as defined in claim 1, wherein said quinone is selected from the group consisting of: 2-Benzylethylamino-3-chloro-1,4-naphthoquinone, 2-Dibenzylamino-3-chloro-1,4-naphthoquinone, 2-Diethylamino-3-chloro-1,4-naphthoquinone, 2-Diethylamino-3-cyano-1,4-naphthoquinone, 2-Benzylethylamino-3-bromo-1,4-naphthoquinone, 2-Diethylamino-3-methyl-1,4-naphthoquinone, 2-Chloro-3-isopropoxy-1,4-anthraquinone, 2-Bromo-3-isopropoxy-1,4-anthraquinone, and 2-Chloro-3-(3-pyrrolyl)-1,4-naphthoquinone.
Claim 6
Dependent Claim 39 words
The composition of claim 1 wherein said sensitizer comprises a quinone having the structural formula ##STR31## wherein R 1 , R 2 , R 3 , R 4 , R 5 and Ar are as defined in claim 1.
Claim 7
Dependent Claim 37 words
The composition of claim 1 wherein said sensitizer comprises a quinone having the structural formula: ##STR32## wherein R 1 , R 2 , R 3 , R 6 and R 7 are as defined in claim 1.

References Cited (Backward Citations)

US3462267A Cited
GB1286879A Cited
US3779778A Cited
US3782939A Cited
US4284704A Cited
US4552830A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-08-03 1991-02-02 1991-08-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-08-03 1995-02-02 1995-08-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-08-03 1999-02-02 1999-08-04 $7700.00 Window Closed / Lapsed

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