US4477556A
Expired / Lapsed
US
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Acidic o-nitroaromatics as photoinhibitors of polymerization in positive working films
Assignee: EIDP Inc
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Filing: 1982-08-18
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Granted: 1984-10-16
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Expires: 2002-08-18
Abstract
Abstract A photopolymerizable coating composition comprising (1) a nongaseous, ethylenically unsaturated, polymerizable compound, (2) a specified acidic o-nitroaromatic compound, and (3) an organic, radiation-sensitive, free-radical generating system which is useful for making a positive or negative polymeric image on a substrate.
Inventors
- 👤 Thomas E. Dueber
- 👤 William J. Nebe
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 16:35
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/027; C; C07; C07C; C07C205/00; C07C205/27; C07C205/35; C07C205/36; C07C205/37; C07C205/44; C07C205/49; C07C205/56; Y; Y10; Y10S; Y10S430/00; Y10S430/1053; Y10S430/1055; Y10S430/114; Y10S430/118
Claims Analysis
Total Claims: 16
Claim 1
Independent Claim
129 words
An acidic o-nitroaromatic compound of the formula ##STR9## wherein at least on of R 1 , R 2 , R 3 or R 4 must have a carboxyl group as indicated below; R 1 , R 2 , alike or different, are selected from alkoxy in which the alkyl is of 1 to 12 carbons, and -(CH 2 )×CO 2 H where x=1 to 12; R 1 and R 2 , taken together, are --OCH 2 O--, R 3 is selected from H, lower alkyl, OH, and alkoxy in which the alkyl portion is of 1 to 6 carbons; R 4 is aryloxy of 6 carbons substituted with carboxyl, or --(CH 2 ) ×CO 2 H where x=2 to 12, and x≠2 or 3 when R 3 is OH.
Claim 2
Dependent Claim
129 words
An acidic o-nitroaromatic compound of the formula ##STR9## wherein at least on of R 1 , R 2 , R 3 or R 4 must have a carboxyl group as indicated below; R 1 , R 2 , alike or different, are selected from alkoxy in which the alkyl is of 1 to 12 carbons, and -(CH 2 )×CO 2 H where x=1 to 12; R 1 and R 2 , taken together, are --OCH 2 O--, R 3 is selected from H, lower alkyl, OH, and alkoxy in which the alkyl portion is of 1 to 6 carbons; R 4 is aryloxy of 6 carbons substituted with carboxyl, or --(CH 2 ) ×CO 2 H where x=2 to 12, and x≠2 or 3 when R 3 is OH.
Claim 3
Dependent Claim
3 words
##STR10## 2-nitro-4,5-dimethoxybenzyl-m-carboxyphenyl ether
Claim 4
Dependent Claim
3 words
##STR10## 2-nitro-4,5-dimethoxybenzyl-m-carboxyphenyl ether
Claim 5
Dependent Claim
3 words
##STR11## 10-(2'-nitro-4',5'-dimethoxyphenyl)10-hydroxydecanoic acid
Claim 6
Dependent Claim
3 words
##STR11## 10-(2'-nitro-4',5'-dimethoxyphenyl)10-hydroxydecanoic acid
Claim 7
Dependent Claim
3 words
##STR12## 6-(2'-nitro-4',5'-dimethoxyphenyl)-6-hydroxyhexanoic acid
Claim 8
Dependent Claim
3 words
##STR12## 6-(2'-nitro-4',5'-dimethoxyphenyl)-6-hydroxyhexanoic acid
Claim 9
Dependent Claim
3 words
##STR13## 3-nitro-4-formyl-6-methoxyphenoxyacetic acid
Claim 10
Dependent Claim
3 words
##STR13## 3-nitro-4-formyl-6-methoxyphenoxyacetic acid
Claim 11
Dependent Claim
103 words
A photopolymerizable composition which consists essentially of (a) a normally nongaseous, ethylenically unsaturated compound capable of addition polymerization by free-radical initiated chain propagation, (b) about 0.004 to about 0.7 parts by weight, per part of component (a), of the acidic o-nitroaromatic compound of claim 2, 3, 4, 5, or 6 (c) about 0.001 to about 10 parts by weight, per part of component (a), of organic, radiation-sensitive, free-radical generating system, activatable by actinic radiation that does not significantly rearrange the acidic o-nitroaromatic compound to an inhibitor of free-radial polymerization. (d) 0 to 85% by weight of the total composition of a polymeric binder.
Claim 12
Dependent Claim
14 words
A photographic film composed of the composition of claim 6 coated upon a support.
Claim 13
Dependent Claim
128 words
A process for producing a positive polymeric image on a substrate which comprises (1) coating the substrate with the photopolymerizable composition of claim 6, (2) imagewise exposing a portion of the photopolymerizable coating through an image-bearing transparency to radiation, at least about 20% of which has a wavelength of about 200 to about 380 nm, thereby rearranging at least some of the acidic o-nitroaromatic compound to polymerization-inhibiting nitrosoaromatic compound, and (3) subjecting the coating to a second exposure whereby a greater portion of the coating, including the portion exposed during the imagewise exposure, is exposed to radiation substantially limited to wavelengths greater than about 38 nm, whereby a positive polymeric image is formed in the areas exposed during the second exposure, but not exposed during the imagewise exposure.
Claim 14
Dependent Claim
48 words
The process of claim 8 wherein the image formed in step (3) is developed by removing the unpolymerized portion of the photopolymerizable coating in the areas exposed to the imagewise exposure radiation, or by differential adhesion of a pigment toner to the said unpolymerized portion of the coating.
Claim 15
Dependent Claim
62 words
A process for producing negative polymeric images on a substrate, which comprises (1) coating the substrate with the photopolymerizable composition of claim 6, and (2) imagewise exposing a portion of the photopolymerizable coating through an image-bearing transparency to radiation substantially limited to wavelengths greater than about 380 nm, whereby a negative polymeric image is formed in the areas exposed to the radiation.
Claim 16
Dependent Claim
48 words
The process of claim 10 wherein the image formed in step (2) is developed by removing the unpolymerized portion of the photopolymerizable coating in the areas exposed to the imagewise exposure radiation, or by differential adhesion of a pigment toner to the said unpolymerized portion of the coating.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1987-10-16 | 1988-04-16 | 1988-10-16 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1991-10-16 | 1992-04-16 | 1992-10-16 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1995-10-16 | 1996-04-16 | 1996-10-16 | $7700.00 | Window Closed / Lapsed |