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US4282354A Expired / Lapsed US ⏱️ 0.0 years remaining

Electrophoretic migration imaging process

Assignee: Eastman Kodak Co
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Filing: 1979-04-18
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Granted: 1981-08-04
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Expires: 1999-04-18
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Abstract

Abstract In general, materials having the structure ##STR1## wherein A represents phenylene, napthylene, anthracenediyl, and dibenzothien-diyl; R 1 and R 2 , which may be the same or different when taken alone represent hydrogen, cyano, alkylcarbonyl and arylcarbamoyl, arylcarbonyl, cyanoaryl; R 1 and R 2 , when taken together, represent sufficient atoms to form substituted and unsubstituted radicals selected from the group consisting of furanylidene, fluorenylidene, pyrimidinylidene, thiazolidinylidene, pyrrolinyl, and indenyl, isoxazolinylidene, pyrazolinylidene and indanylidene, wherein said substituents are selected from the group consisting of hydrogen, cyano, aryl, oxo, thioxo, nitro, alkyl, nitroaryl, carbamoyl and cyanoalkyl; and alkyl represents an alkyl group having from one to six carbon atoms; aryl represents an aromatic nucleus selected from the group consisting of benzene, napthalene or anthracene, are useful in electrophoretic migration imaging processes.

Inventors

  • 👤 James A. Van Allan
  • 👤 Louis J. Rossi
  • 👤 Melvin S. Bloom
  • 👤 Michael T. Regan
  • 👤 Hal E. Wright
  • 👤 Joseph Y. Kaukeinen

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 01:01
CPC Classifications
C; C07; C07D; C07D307/00; C07D307/02; C07D307/34; C07D307/56; C07D307/68; C09; C09B; C09B1/00; C09B23/00; C09B23/0091; C09B23/02; C09B23/04; G; G03; G03G; G03G17/00; G03G17/04

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 52 words
A material having the following structure: ##STR21## wherein A represents phenylene, naphthylene, anthracenediyl and dibenzothiendiyl; R 1 and R 2 both represent cyano or when taken together represent sufficient atoms to form a substituted or unsubstituted furanylidene and said substituents are selected from the group consisting of cyano, phenyl, nitrophenyl and oxo.
Claim 2
Dependent Claim 52 words
A material having the following structure: ##STR21## wherein A represents phenylene, naphthylene, anthracenediyl and dibenzothiendiyl; R 1 and R 2 both represent cyano or when taken together represent sufficient atoms to form a substituted or unsubstituted furanylidene and said substituents are selected from the group consisting of cyano, phenyl, nitrophenyl and oxo.
Claim 3
Dependent Claim 28 words
A material selected from the group consisting of: 5,5'-(9,10-anthracenediyldimethylidyne)bis[3-cyano-4-phenyl(5H)-furan-2-one 5,5'-(9,10-anthracenediyldimethylidyne)bis[3,4-di(p-nitrophenyl)-(5H)-furan-2-one] 9,10-bis(dicyanoethenyl)anthracene 5,5'-(9,10-anthracenediyldimethylidyne)bis(1,3-diethyl-1,3,5-trihydro-pyrimidine-2,4,6-trione) 2,2'-(9,10-anthracenediyldimethylidyne)bis(indan-1,3-dione) 5,5'-(9,10-anthracenediyldimethylidyne)bis(N-ethyl-2-thioxothiazolidin-4-one) 5,5'-(9,10-anthracenediyldimethylidyne)bis(3-carbamoyl-4-phenyl-furan-2-one) 5-(9-anthracenylmethylidyne)-3-cyano-4-phenyl-furan-5-one 4,4'-(9,10-anth4acenediyldimethylidyne)bis(3-phenyl-isoxazolin-5-one) 4-(9-anthracenylmethylidyne)-3-phenyl-isoxazolin-5-one 5,5'-(9,10-anthracenediyldimethylidyne)bis(2-thioxothiazolidin-4-one) 4,4'-(1,4-phenylenedimethylidyne)bis(3-carbamoyl-1-phenyl pyrazolin-5-one) 2,6-bis(dicyanoethenyl)naphthalene 5,5'-(2,6-naphthalenediyldimethylidyne)bis(3-cyano-4-phenylfuran-2-one) 2,6-bis[β-cyano-β-(p-cyanophenyl)ethenyl]naphthalene 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis(3-cyano-4-phenyl-furan-2-one) 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis[3,4-di(p-nitrophenyl)-furan-2-one] and 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis(3-carbamoyl-4-phenyl-furan-2-one).
Claim 4
Dependent Claim 28 words
A material selected from the group consisting of: 5,5'-(9,10-anthracenediyldimethylidyne)bis[3-cyano-4-phenyl(5H)-furan-2-one 5,5'-(9,10-anthracenediyldimethylidyne)bis[3,4-di(p-nitrophenyl)-(5H)-furan-2-one] 9,10-bis(dicyanoethenyl)anthracene 5,5'-(9,10-anthracenediyldimethylidyne)bis(1,3-diethyl-1,3,5-trihydro-pyrimidine-2,4,6-trione) 2,2'-(9,10-anthracenediyldimethylidyne)bis(indan-1,3-dione) 5,5'-(9,10-anthracenediyldimethylidyne)bis(N-ethyl-2-thioxothiazolidin-4-one) 5,5'-(9,10-anthracenediyldimethylidyne)bis(3-carbamoyl-4-phenyl-furan-2-one) 5-(9-anthracenylmethylidyne)-3-cyano-4-phenyl-furan-5-one 4,4'-(9,10-anth4acenediyldimethylidyne)bis(3-phenyl-isoxazolin-5-one) 4-(9-anthracenylmethylidyne)-3-phenyl-isoxazolin-5-one 5,5'-(9,10-anthracenediyldimethylidyne)bis(2-thioxothiazolidin-4-one) 4,4'-(1,4-phenylenedimethylidyne)bis(3-carbamoyl-1-phenyl pyrazolin-5-one) 2,6-bis(dicyanoethenyl)naphthalene 5,5'-(2,6-naphthalenediyldimethylidyne)bis(3-cyano-4-phenylfuran-2-one) 2,6-bis[β-cyano-β-(p-cyanophenyl)ethenyl]naphthalene 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis(3-cyano-4-phenyl-furan-2-one) 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis[3,4-di(p-nitrophenyl)-furan-2-one] and 5,5'-(dibenzothien-2,8-diyldimethylidyne)bis(3-carbamoyl-4-phenyl-furan-2-one).

References Cited (Backward Citations)

US3336357A Cited
US3932418A Cited
US3987060A Cited
US3915702A Cited
US4184871A Cited
US4072519A Cited
US4122114A Cited
US3992203A Cited
US4134761A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-08-03 1985-02-02 1985-08-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-08-03 1989-02-02 1989-08-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-08-03 1993-02-02 1993-08-04 $7700.00 Window Closed / Lapsed

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