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US3907569A Expired / Lapsed US ⏱️ 0.0 years remaining

Ultraviolet holdback of nonsilver photosensitive systems by incorporating therein certain organic additives

Assignee: Horizons Inc
•
Filing: 1973-01-31
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Granted: 1975-09-23
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Expires: 1993-01-31
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Abstract

Abstract A non-silver, photosensitive composition comprising: at least one aminoaryl ethylene color forming compound and at least one activator for said color forming compound, wherein the composition includes in addition at least one organic compound the addition of which produces imagery having improved ultraviolet holdback, such compounds being selected from the group consisting of heterocyclic compounds, quinone compounds, multifunctional aromatic hydroxy compounds and aromatic carbonyl containing compounds.

Inventors

  • 👤 Andrew C Hazy
  • 👤 John E Shirey
  • 👤 Lothar Ramins

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 12:32
CPC Classifications
G; G03; G03C; G03C1/00; G03C1/675

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 18 words
IN A NON-SILVER PHOTOSENSITIVE COMPOSITION COMPRISING: (1) AT LEAST ONE COLOR FORMING COMPOUND REPRESENTED BY THE GENERAL FORMULA
Claim 2
Dependent Claim 18 words
IN A NON-SILVER PHOTOSENSITIVE COMPOSITION COMPRISING: (1) AT LEAST ONE COLOR FORMING COMPOUND REPRESENTED BY THE GENERAL FORMULA
Claim 3
Dependent Claim 30 words
The composition of claim 1 in which the relative proportions of said color forming ethylene compound and said compound producing imagery having improved U.V. holdback is between 50:1 and 1:2.
Claim 4
Dependent Claim 178 words
at least one activator for said color forming compound, said activator being selected from the group consisting of (a) organic halogen compounds represented by the general formula Q-C-Hal3 wherein Q is selected from the group consisting of H, Cl, Br, I, alkyl, substituted alkyl, aryl, substituted aryl, aroyl, and arylalkyl; and each Hal represents a halogen atom selected from the group consisting of Cl, Br or I; (b) sulfur containing compounds represented by either R-SH or R-S-S-R wherein each R represents an aryl or heterocyclic ring; and (c) compounds containing both halogen and sulfur selected from the group consisting of sulfonyl and sulfenyl halides; the improvement which consists in the incorporation in said composition of (3) at least one organic compound which produces imagery having improved ultraviolet holdback, said compound being selected from the group consisting of heterocyclic compounds selected from the group consisting of acridine, phenothiazine, acridan, carbazole, N-vinylcarbazole, and benzolflavine; quinone compounds selected from the group consisting of naphthoquinones and 9,10 anthraquinones; and multifunctional aromatic hydroxy compounds selected from the group consisting of 1,2,4-trihydroxybenzene and 1,4,9,10-tetrahydroxy-9,10-dihydroanthracene.
Claim 5
Dependent Claim 178 words
at least one activator for said color forming compound, said activator being selected from the group consisting of (a) organic halogen compounds represented by the general formula Q-C-Hal3 wherein Q is selected from the group consisting of H, Cl, Br, I, alkyl, substituted alkyl, aryl, substituted aryl, aroyl, and arylalkyl; and each Hal represents a halogen atom selected from the group consisting of Cl, Br or I; (b) sulfur containing compounds represented by either R-SH or R-S-S-R wherein each R represents an aryl or heterocyclic ring; and (c) compounds containing both halogen and sulfur selected from the group consisting of sulfonyl and sulfenyl halides; the improvement which consists in the incorporation in said composition of (3) at least one organic compound which produces imagery having improved ultraviolet holdback, said compound being selected from the group consisting of heterocyclic compounds selected from the group consisting of acridine, phenothiazine, acridan, carbazole, N-vinylcarbazole, and benzolflavine; quinone compounds selected from the group consisting of naphthoquinones and 9,10 anthraquinones; and multifunctional aromatic hydroxy compounds selected from the group consisting of 1,2,4-trihydroxybenzene and 1,4,9,10-tetrahydroxy-9,10-dihydroanthracene.
Claim 6
Dependent Claim 178 words
AT LEAST ONE ACTIVATOR FOR SAID COLOR FORMING COMPOUND SAID ACTIVATOR BEING SELECTED FROM THE GROUP CONSISTING OF (A) ORGANIC HALOGEN COMPOUNDS REPRESENTED BY THE GENERAL FORMULA Q-C-HAL3 WHEREIN Q IS SELECTED FROM THE GROUP CONSISTING OF H, CL, BR, L, ALKYL, SUBSTITUTED ALKYL, ARYL, SUBSTITUTED ARYL, AROYL, AND ARYLALKYL, AND EACH HAL REPRESENTS A HALOGEN ATOM SELECTED FROM THE GROUP CONSISTING OF CL, BR OR I, (B) SULFUR CONTAINING COMPOUNDS REPRESENTED BY EITHER R-SH OR R-S-S-R WHEREIN EACH R REPRESENTS AN ARYL OR HETEROCYCLIC RING, AND (C) COMPOUNDS CONTAINING BOTH HALOGEN AND SULFUR SELECTED FROM THE GROUP CONSISTING OF SULFONYL AND SULFENYL HALIDES THE IMPROVEMENT WHICH CONSISTS IN THE INCORPORTION IN SAID COMPOSITION OF (3) AT LEAST ONE ORGANIC COMPOUND WHICH PRODUCES IMAGERY HAVING IMPROVED ULTRAVIOLET HOLDBACK, SAID COMPOUND BEING SELECTED FROM THE GROUP CONSISTING OF HETEROCYCLIC COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF ACRIDINE, PHENOTHIAZINE, ACRIDAN, CARBAZOLE, N-VINYLCARBAZOLE, AND BENZOLFLAVINE, QUINONE COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF NAPHTHOQUINONES AND 9,10 ANTHRAQUINONES, AND MULTIFUNCTIONAL AROMATIC HYDROXY COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF 1,2,4-TRIHYDROXYBENZENE AND 1,4,9.10-TETRAHYDROXY-9,10-DIHYDROAANTHRACENE.
Claim 7
Dependent Claim 178 words
AT LEAST ONE ACTIVATOR FOR SAID COLOR FORMING COMPOUND SAID ACTIVATOR BEING SELECTED FROM THE GROUP CONSISTING OF (A) ORGANIC HALOGEN COMPOUNDS REPRESENTED BY THE GENERAL FORMULA Q-C-HAL3 WHEREIN Q IS SELECTED FROM THE GROUP CONSISTING OF H, CL, BR, L, ALKYL, SUBSTITUTED ALKYL, ARYL, SUBSTITUTED ARYL, AROYL, AND ARYLALKYL, AND EACH HAL REPRESENTS A HALOGEN ATOM SELECTED FROM THE GROUP CONSISTING OF CL, BR OR I, (B) SULFUR CONTAINING COMPOUNDS REPRESENTED BY EITHER R-SH OR R-S-S-R WHEREIN EACH R REPRESENTS AN ARYL OR HETEROCYCLIC RING, AND (C) COMPOUNDS CONTAINING BOTH HALOGEN AND SULFUR SELECTED FROM THE GROUP CONSISTING OF SULFONYL AND SULFENYL HALIDES THE IMPROVEMENT WHICH CONSISTS IN THE INCORPORTION IN SAID COMPOSITION OF (3) AT LEAST ONE ORGANIC COMPOUND WHICH PRODUCES IMAGERY HAVING IMPROVED ULTRAVIOLET HOLDBACK, SAID COMPOUND BEING SELECTED FROM THE GROUP CONSISTING OF HETEROCYCLIC COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF ACRIDINE, PHENOTHIAZINE, ACRIDAN, CARBAZOLE, N-VINYLCARBAZOLE, AND BENZOLFLAVINE, QUINONE COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF NAPHTHOQUINONES AND 9,10 ANTHRAQUINONES, AND MULTIFUNCTIONAL AROMATIC HYDROXY COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF 1,2,4-TRIHYDROXYBENZENE AND 1,4,9.10-TETRAHYDROXY-9,10-DIHYDROAANTHRACENE.
Claim 8
Dependent Claim 21 words
The composition of claim 1 in which the color forming compound is 1,1-bis(4-dimethylaminophenyl)-ethylene and the ultraviolet holdback compound is a quinone.
Claim 9
Dependent Claim 11 words
The composition of claim 3 wherein the quinone is a naphthoquinone.
Claim 10
Dependent Claim 12 words
The composition of claim 4 in which the naphthoquinone is 1, 2-naphthoquinone.
Claim 11
Dependent Claim 16 words
A photosensitive member comprising a support and a coating therein comprising the composition of claim 1.
Claim 12
Dependent Claim 12 words
The composition of claim 1 wherein the U.V. hold-back compound is acridan.
Claim 13
Dependent Claim 13 words
The composition of claim 1 wherein the U.V. hold-back compound is an anthraquinone.
Claim 14
Dependent Claim 12 words
The composition of claim 1 wherein the U.V. hold-back compound is acridine.

References Cited (Backward Citations)

US3351467A Cited
US3527639A Cited
US3502476A Cited
US3620748A Cited
US3560216A Cited
US3510304A Cited
US3533792A Cited
US3579342A Cited
US3708297A Cited
US3642479A Cited
US3712817A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-09-22 1979-03-24 1979-09-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-09-22 1983-03-24 1983-09-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-09-22 1987-03-24 1987-09-23 $7700.00 Window Closed / Lapsed

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