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US4030926A Expired / Lapsed US ⏱️ 0.0 years remaining

Light-sensitive material containing a dye-forming combination of a heterocyclic compound and a cyclic dihalodicarbonyl compound in a polymeric binder

Assignee: Agfa Gevaert AG
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Filing: 1975-07-07
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Granted: 1977-06-21
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Expires: 1995-07-07
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Abstract

Abstract A storage medium for optical data recording comprises a dye-forming combination which on exposure to light within a first range of wavelengths reacts irreversibly to form a dye, but is substantially insensitive to light within a second range of wavelengths which is capable of energizing the dye to produce luminescence. The dye-forming combination consists of a heterocyclic compound of the formula I and of a cyclic dihalodicarbonyl compound of the formula II ##STR1## The symbols are defined in the specification. An example of formula I is benzofuran and an example of formula II is dibromomaleic anhydride.

Inventors

  • 👤 Kurt-Rainer Stahlke
  • 👤 Werner Krafft
  • 👤 Rudolf Meyer
  • 👤 Hans Jurgen Rosenkranz

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 09:12
CPC Classifications
G; G03; G03C; G03C1/00; G03C1/675

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 278 words
A light sensitive storage material for optical data recording comprising in a supported or self-supporting layer comprised of a polymeric hydrophobic binder selected from the group consisting of homopolymers and copolymers of monomers which have copolymerizable olefinic double bonds, polyvinyl acetals and cellulose esters and a dye-forming combination of a heterocyclic compound of the formula ##STR5## X represents oxygen, sulfur or the group >N--R 3 , Y represents nitrogen or the group ≧C--R 4 , R 1 and R 2 , which may be the same or different represent hydrogen or an alkyl or aryl group of may together represent the group required for completing a condensed benzene or naphthalene ring which may be substituted, R 3 represents hydrogen or an alkyl or aryl group and R 4 represents hydrogen or an alkyl group; and of a cyclic dihalodicarbonyl compound of the formula ##STR6## in which Z represents oxygen or the group >N--R 6 or ##STR7## R 5 represents chlorine or bromine, R 6 represents hydrogen or an alkyl group and R 7 and R 8 , which may be the same or different represent hydrogen or an alkyl group said heterocyclic compound of formula I and said cyclic dihalodicarbonyl compound of formula II being in amounts effective to provide said dye-forming combination upon exposure to ultraviolet light in a first range of wavelengths with capability of forming an image which is in a state of luminescence upon exposure to ultraviolet light in a second range of wavelengths not including said first range, and in a proportion of said heterocyclic compound of formula I being in at least double the molar quantity of the compound of formula II.
Claim 2
Dependent Claim 278 words
A light sensitive storage material for optical data recording comprising in a supported or self-supporting layer comprised of a polymeric hydrophobic binder selected from the group consisting of homopolymers and copolymers of monomers which have copolymerizable olefinic double bonds, polyvinyl acetals and cellulose esters and a dye-forming combination of a heterocyclic compound of the formula ##STR5## X represents oxygen, sulfur or the group >N--R 3 , Y represents nitrogen or the group ≧C--R 4 , R 1 and R 2 , which may be the same or different represent hydrogen or an alkyl or aryl group of may together represent the group required for completing a condensed benzene or naphthalene ring which may be substituted, R 3 represents hydrogen or an alkyl or aryl group and R 4 represents hydrogen or an alkyl group; and of a cyclic dihalodicarbonyl compound of the formula ##STR6## in which Z represents oxygen or the group >N--R 6 or ##STR7## R 5 represents chlorine or bromine, R 6 represents hydrogen or an alkyl group and R 7 and R 8 , which may be the same or different represent hydrogen or an alkyl group said heterocyclic compound of formula I and said cyclic dihalodicarbonyl compound of formula II being in amounts effective to provide said dye-forming combination upon exposure to ultraviolet light in a first range of wavelengths with capability of forming an image which is in a state of luminescence upon exposure to ultraviolet light in a second range of wavelengths not including said first range, and in a proportion of said heterocyclic compound of formula I being in at least double the molar quantity of the compound of formula II.
Claim 3
Dependent Claim 20 words
Storage material according to claim 1, characterised in that the heterocyclic compound of formula I contained in it is benzofuran.
Claim 4
Dependent Claim 24 words
Storage material according to claim 1, characterised in that the cyclic dihalodicarbonyl compound contained in it is dibromomaleic acid anhydride or dibromomaleic acid imide.
Claim 5
Dependent Claim 43 words
Storage material according to claim 1, characterised in that it contains, as binder for the dye forming combination of formulas I and II, a homopolymer or copolymer of methacrylic acid alkyl esters in which the alkyl group contains 1 to 4 carbon atoms.
Claim 6
Dependent Claim 17 words
Storage material according to claim 4, characterised in that it contains polyacrylamide or polycarbonate as additional binder.

References Cited (Backward Citations)

US3394395A Cited
US3502476A Cited
US3671239A Cited
US3745004A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-20 1980-12-20 1981-06-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-20 1984-12-20 1985-06-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-20 1988-12-20 1989-06-21 $7700.00 Window Closed / Lapsed

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