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US4444869A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for using positive-working resist materials to form negative resist pattern on substrate

Assignee: Fujitsu Ltd
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Filing: 1981-11-25
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Granted: 1984-04-24
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Expires: 2001-11-25
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Abstract

Abstract An improved positive-working resist material capable of forming on a substrate either a positive resist pattern or a negative resist pattern. The positive-working resist material comprises a positive-working resist resin having incorporated therein one or more photochromic compounds, such as spiropyrans, triphenylmethane dyes, anils and the like. A positive or negative resist pattern having a remarkably improved definition can be obtained. The use of such a positive-working resist material in the formation of a negative resist pattern on the substrate is also disclosed.

Inventors

  • 👤 Tsunehiro Chonan
  • 👤 Akira Morishige

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 22:07
CPC Classifications
G; G03; G03F; G03F7/00; G03F7/004; G03F7/09; G03F7/105; G03F7/20; G03F7/2022; Y; Y10; Y10S; Y10S430/00; Y10S430/163

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 50 words
A process for forming a negative resist with a desired pattern on a substrate, comprising the steps of: (1) coating on the substrate a resist material consisting of a mixture of a positive-working resist resin which is napthoquinonediazide or benzoquinonediazide and at least one spiropyran compound which is: 1,3,3-trimethyl-6'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-nitro-8'-methoxyspiro(indoline-2,2'-benzopyran),
Claim 2
Dependent Claim 50 words
A process for forming a negative resist with a desired pattern on a substrate, comprising the steps of: (1) coating on the substrate a resist material consisting of a mixture of a positive-working resist resin which is napthoquinonediazide or benzoquinonediazide and at least one spiropyran compound which is: 1,3,3-trimethyl-6'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-nitro-8'-methoxyspiro(indoline-2,2'-benzopyran),
Claim 3
Dependent Claim 203 words
3,3-trimethyl-5'-chloro-6'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-bromo-8'-bromospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-methoxy-8'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-5'-nitro-8'-methoxy-spiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-8'-carboxyspiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-nitro-8'-hydroxyspiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-hydroxyspiro(indoline-2,2'-benzopyran), 1', 3', 3'-trimethyl-6'-hydroxyspiro(2H-1-benzopyran-2,2'-indoline), 1',3',3'-trimethyl-6'-nitrospiro(2H-1-benzopyran-2,2'-indoline), or 1', 3', 3'-trimethyl-6'-nitro-8'-hydroxy-spiro(2H-1-benzopyran-2,2'-indoline), wherein said at least one spiropyran compound is mixed with the positive-working resist resin in an amount of 1 through 4 parts by weight of said at least one spiropyran compound per 100 parts by weight of the positive-working resist resin; (2) prebaking the coated resist material; (3) exposing the coated resist material to radiation with said desired pattern, so as to allow the exposed part to be selectively hardened in a subsequent heating step; (4) subsequently heating the coated resist material at a temperature of from 95° to 150° C. for time between 5 through 60 minutes, to provide said selective hardening of said exposed part of said coated resist material, so as to render said exposed part insoluble to an alkaline developer for said positive-working resist resin; (5) subsequently subjecting the coated resist material to a blanket exposure by further radiation, so as to decompose the non-exposed part of said coated resist material; and (6) subsequently developing the coated resist material by removing said non-exposed part of said coated resist material with said alkaline developer, so as to form said negative resist with said desired pattern.
Claim 4
Dependent Claim 203 words
3,3-trimethyl-5'-chloro-6'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-bromo-8'-bromospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-methoxy-8'-nitrospiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-5'-nitro-8'-methoxy-spiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-8'-carboxyspiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-nitro-8'-hydroxyspiro(indoline-2,2'-benzopyran), 1,3,3-trimethyl-6'-hydroxyspiro(indoline-2,2'-benzopyran), 1', 3', 3'-trimethyl-6'-hydroxyspiro(2H-1-benzopyran-2,2'-indoline), 1',3',3'-trimethyl-6'-nitrospiro(2H-1-benzopyran-2,2'-indoline), or 1', 3', 3'-trimethyl-6'-nitro-8'-hydroxy-spiro(2H-1-benzopyran-2,2'-indoline), wherein said at least one spiropyran compound is mixed with the positive-working resist resin in an amount of 1 through 4 parts by weight of said at least one spiropyran compound per 100 parts by weight of the positive-working resist resin; (2) prebaking the coated resist material; (3) exposing the coated resist material to radiation with said desired pattern, so as to allow the exposed part to be selectively hardened in a subsequent heating step; (4) subsequently heating the coated resist material at a temperature of from 95° to 150° C. for time between 5 through 60 minutes, to provide said selective hardening of said exposed part of said coated resist material, so as to render said exposed part insoluble to an alkaline developer for said positive-working resist resin; (5) subsequently subjecting the coated resist material to a blanket exposure by further radiation, so as to decompose the non-exposed part of said coated resist material; and (6) subsequently developing the coated resist material by removing said non-exposed part of said coated resist material with said alkaline developer, so as to form said negative resist with said desired pattern.
Claim 5
Dependent Claim 26 words
The process of claim 1, comprising less than 2 parts by weight of said spiropyran compound per 100 parts by weight of said positive-working resist resin.
Claim 6
Dependent Claim 35 words
The process of claim 1, wherein the coated resist material is not subjected to a liquid as part of said heating of said coated resist material after said exposing to radiation with said desired pattern.
Claim 7
Dependent Claim 25 words
The process of claim 1, comprising forming said negative resist with said desired pattern with a resolution of as fine as 1 micron line width.
Claim 8
Dependent Claim 31 words
The process according to claim 1, wherein said step of prebaking is carried out at a temperature of from 50° to 110° C. for a period between 5 through 30 minutes.
Claim 9
Dependent Claim 27 words
The process of claim 1, 5 or 4, wherein said radiation of said blanket exposure is of the same type as said radiation of said desired pattern.
Claim 10
Dependent Claim 27 words
The process of claim 6, wherein different doses of said same type of radiation are used for said blanket exposure and said exposing to said desired pattern.
Claim 11
Dependent Claim 32 words
The process of claim 1, 5 or 4, said radiation of said desired pattern and said radiation of said blanket exposure each being selectively electron, gamma, X, ultraviolet, visible and infrared radiation.
Claim 12
Dependent Claim 24 words
The process of claim 8, wherein said radiation of said blanket exposure is of the same type as said radiation of said desired pattern.
Claim 13
Dependent Claim 27 words
The process of claim 9, wherein different doses of said same type of radiation are used for said blanket exposure and said exposing to said desired pattern.

References Cited (Backward Citations)

US3264104A Cited
US4028111A Cited
US4007047A Cited
JPS526528A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-04-24 1987-10-24 1988-04-24 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-04-24 1991-10-24 1992-04-24 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-04-24 1995-10-24 1996-04-24 $7700.00 Window Closed / Lapsed

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