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US4496794A Expired / Lapsed US ⏱️ 0.0 years remaining

Flexible base materials, their preparation and their use for printed circuits

Assignee: Novartis Corp
•
Filing: 1984-06-04
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Granted: 1985-01-29
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Expires: 2004-06-04
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Abstract

Abstract Flexible base materials consisting of a metal foil and a film of a polyamide, polyamide-imide and/or polyimide, firmly adhering thereto without an intermediate layer, the film being obtained by heating a polyamide, polyamide-amidoacid and/or polyamide-acid containing the structural units of the formulae I and II. The individual symbols are as defined in claim 1. The base materials according to the invention are useful for the production of flexible printed circuits.

Inventors

  • 👤 Roland Darms
  • 👤 Harry Beyeler
  • 👤 Theobald Haug

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 12:53
CPC Classifications
H; H05; H05K; H05K1/00; H05K1/02; H05K1/03; H05K1/0313; H05K1/032; H05K1/0346; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31678; Y10T428/31681; Y10T428/31721; Y10T428/31725

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 231 words
A flexible, printed circuit with excellent adhesion of the printed circuit tracks, which is obtained by coating one side of a metal foil without any interlayer with a polymer consisting of a polyamide, polyamide-imide or polyimide, obtained by heating a polyamide, polyamide-amidoacid or polyimide-acid having 1 to 100 mol % of structural units of the formula I ##STR5## and of 0 to 99 mol % of structural units of the formula II ##STR6## in which the NH groups in formula I are, independently of one another, bonded to the o-, m- or p-position of the benzene nucleus and the individual symbols or radicals m, n, R and R 1 , independently of one another, are defined as follows: m and n are each 1 or 2, R is a carbocyclic-aromatic or heterocyclic-aromatic radical, in which the carboxamide groups and carboxyl groups are bonded to different carbon atoms and the carboxyl groups, if R is a cyclic radical and at least one of m and n is 2, are each in the ortho-position to a carboxamide group, and R 1 is a carbocyclic-aromatic or heterocyclic-aromatic radical, heating the coated metal foil in the temperature range from 50° to 350° C. till a track-free coating is obtained, exposing the opposite side of the coated metal foil, which side is provided with a photolacquer, through a photo mask, and developing the exposed metal foil.
Claim 2
Dependent Claim 231 words
A flexible, printed circuit with excellent adhesion of the printed circuit tracks, which is obtained by coating one side of a metal foil without any interlayer with a polymer consisting of a polyamide, polyamide-imide or polyimide, obtained by heating a polyamide, polyamide-amidoacid or polyimide-acid having 1 to 100 mol % of structural units of the formula I ##STR5## and of 0 to 99 mol % of structural units of the formula II ##STR6## in which the NH groups in formula I are, independently of one another, bonded to the o-, m- or p-position of the benzene nucleus and the individual symbols or radicals m, n, R and R 1 , independently of one another, are defined as follows: m and n are each 1 or 2, R is a carbocyclic-aromatic or heterocyclic-aromatic radical, in which the carboxamide groups and carboxyl groups are bonded to different carbon atoms and the carboxyl groups, if R is a cyclic radical and at least one of m and n is 2, are each in the ortho-position to a carboxamide group, and R 1 is a carbocyclic-aromatic or heterocyclic-aromatic radical, heating the coated metal foil in the temperature range from 50° to 350° C. till a track-free coating is obtained, exposing the opposite side of the coated metal foil, which side is provided with a photolacquer, through a photo mask, and developing the exposed metal foil.
Claim 3
Dependent Claim 15 words
A circuit according to claim 1, wherein the coated metal foil is a copper foil.
Claim 4
Dependent Claim 64 words
A circuit according to claim 1, wherein the polymer is obtained from a polyamide, a polyamide-amidoacid on a polyamide-acid containing the structural units of the formulae I and II, in which, in formula I, the two NH groups are bonded to the benzene nucleus in the p-position, R and R 1 are aromatic radicals and m and n are as defined in claim 1.
Claim 5
Dependent Claim 84 words
A circuit, according to either of claims 1, wherein the polymer is obtained from a polyamide, a polyamide-amidoacid or polyamide-acid containing structural units of the formulae I and II, in which R, if m and n=2, is a benzene ring or the benzophenone ring system and, if m and n=1, is a benzene ring, and R 1 is a 1,3- or 1,4-phenylene group, or a 4,4'-diphenyl-ether, 4,4'-diphenylmethane or 4,4'-diphenyl-sulfone radical, or from a derivative which has been obtained by cyclising to the corresponding imide.
Claim 6
Dependent Claim 38 words
A circuit, according to either of claim 1, wherein the polymer consists of a polyamide containing 100 mol % of the structural units of the formula I, in which m and n=1 and R is 1,3- and/or 1,4-phenylene.
Claim 7
Dependent Claim 61 words
A circuit, according to either of claims 1, wherein the polymer consists of a polyamide which contains 1 to 40 mol % of structural units of the formula I and 60 to 99 mol % of structural units of the formula II, in which m and n=1, R is a benzene ring and R 1 is a 1,3- or 1,4-phenylene group.
Claim 8
Dependent Claim 84 words
A circuit, according to either of claims 1, wherein the polymer is obtained from a polyamide-acid which consists of 1 to 20 mol % of structural units of the formula I and of 80 to 99 mol % of structural units of the formula II, in which m and n=2, R is a benzene ring or the benzophenone ring system and R 1 is a 4,4'-diphenyl-ether, 4,4'-diphenylmethane or 4,4'-diphenyl-sulfone radical or from the derivative which has been obtained by cyclising to the corresponding imide.

References Cited (Backward Citations)

US3682960A Cited
GB1366490A Cited
US3809591A Cited
US4148969A Cited
DE2726541A1 Cited
US4196144A Cited
US4239880A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-01-29 1988-07-30 1989-01-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-01-29 1992-07-30 1993-01-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-01-29 1996-07-30 1997-01-29 $7700.00 Window Closed / Lapsed

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