Multilayer films for electronic circuit applications

Abstract

In a first embodiment, a multilayer film includes a first outer layer comprising a first thermoplastic polyimide, a core layer comprising a polyimide, and a second outer layer comprising a second thermoplastic polyimide. The polyimide of the core layer includes a first aromatic dianhydride comprising 3,3',4,4'-biphenyltetracarboxylic dianhydride and a first aromatic diamine comprising p-phenylenediamine. The multilayer film has a total thickness ranging from 5 to 150 μm. The thickness of the core layer is in the range of 35 to 73% of the total thickness of the multilayer film. The minimum peel strength for at least one of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B. In a second embodiment, a metal-clad laminate includes the multilayer film of the first embodiment and a first metal layer bonded to the outer surface of the first outer layer of the multilayer film.

Description

[Technical Field]

[0001] The field of this disclosure is multilayer films used in electronic circuit applications. [Background technology]

[0002] Polyimide films are used in the manufacture of flexible printed circuit boards due to their excellent electrical insulation properties, mechanical strength, high-temperature stability, and chemical resistance. Polyimide films are bonded to metal foils to form metal-clad laminates and have found a wide range of applications, including flexible printed circuit boards, packaging materials for semiconductor devices or chip-scale packages, die-pad bonding of chip-on-flex, chip-on-lead, lead-on-chip, multi-chip modules, ball grid arrays (or micro-ball grid arrays), and / or tape-automated bonding.

[0003] U.S. Patent No. 7,285,321 describes a low glass transition temperature (T g ) Polyimide layer and high T g This document describes a multilayer laminate having a polyimide layer and a conductive layer. g The polyimide layer is a thermosetting polyimide, low T g The polyimide layer is thermoplastic polyimide. U.S. Patent No. 6,379,784 describes an aromatic polyimide composite film and an aromatic polyimide laminate consisting of a metal film and a release film. The aromatic polyimide composite film consists of an aromatic polyimide substrate film and two thermoplastic aromatic polyimide layers. The metal film and release film are bonded to the opposite side of the aromatic polyimide laminate without the use of an additional adhesive layer.

[0004] Some electronics manufacturing processes require good optical clarity, for example, when optical registration is used to align various layers on printed circuit boards. In these applications, high transmittance and low cloudiness can be critically important for circuit designs with extremely fine features. In addition, it is important to maintain optical clarity and good adhesion even during high-temperature curing, which may be used to stabilize materials subjected to higher-temperature post-lamination processes. Metal-clad laminates may undergo hot-bar processing or spot welding at temperatures exceeding 300°C. Under these conditions, low T g Thermoplastic polyimide layers are susceptible to loss of adhesion, delamination, distortion, and blistering, which can be accompanied by a decrease in optical transmittance and an increase in cloudiness. [Overview of the project] [Means for solving the problem]

[0005] In the first embodiment, the multilayer film comprises a first outer layer containing a first thermoplastic polyimide, a core layer containing polyimide, and a second outer layer containing a second thermoplastic polyimide. The polyimide in the core layer comprises a first aromatic dianhydride containing 3,3',4,4'-biphenyltetracarboxylic acid dianhydride and a first aromatic diamine containing p-phenylenediamine. The multilayer film has a total thickness in the range of 5 to 150 μm. The thickness of the core layer is in the range of 35 to 73% of the total thickness of the multilayer film. The minimum peel strength for at least one of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B.

[0006] In a second embodiment, the metal-clad laminate includes the multilayer film of the first embodiment and a first metal layer bonded to the outer surface of the first outer layer of the multilayer film.

[0007] The above summary and the following detailed description are illustrative and descriptive only and do not limit the invention as defined in the attached claims. [Modes for carrying out the invention]

[0008] In the first embodiment, the multilayer film comprises a first outer layer containing a first thermoplastic polyimide, a core layer containing polyimide, and a second outer layer containing a second thermoplastic polyimide. The polyimide in the core layer comprises a first aromatic dianhydride containing 3,3',4,4'-biphenyltetracarboxylic acid dianhydride and a first aromatic diamine containing p-phenylenediamine. The multilayer film has a total thickness in the range of 5 to 150 μm. The thickness of the core layer is in the range of 35 to 73% of the total thickness of the multilayer film. The minimum peel strength for at least one of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B.

[0009] In one embodiment of the first aspect, the first thermoplastic polyimide comprises an aromatic dianhydride selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride and mixtures thereof; and an aromatic diamine selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, 2,2-bis(4-[4-aminophenoxy]phenyl)propane and mixtures thereof. In a particular embodiment, the aromatic dianhydride comprises pyromellitic acid dianhydride and 4,4'-oxydiphthalic acid dianhydride; and the aromatic diamine comprises 1,3-bis(4-aminophenoxy)benzene.

[0010] In another embodiment of the first aspect, the second thermoplastic polyimide comprises an aromatic dianhydride selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride and mixtures thereof; and an aromatic diamine selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, hexamethylenediamine and mixtures thereof. In a particular embodiment, the aromatic dianhydride comprises pyromellitic acid dianhydride and 4,4'-oxydiphthalic acid dianhydride; and the aromatic diamine comprises 1,3-bis(4-aminophenoxy)benzene.

[0011] In another embodiment of the first aspect, the first thermoplastic polyimide and the second thermoplastic polyimide are the same.

[0012] In yet another embodiment of the first aspect, the core layer further comprises a second aromatic dianhydride. In a particular embodiment, the second aromatic dianhydride is selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, bisphenol A dianhydride, 1,2,5,6-naphthalenetetracarboxylic acid dianhydride, 1,4,5,8-naphthalenetetracarboxylic acid dianhydride, and 2,3,6,7-naphthalenetetracarboxylic acid dianhydride.

[0013] In a further embodiment of the first aspect, the core layer further comprises a second aromatic diamine. In a particular embodiment, the second aromatic diamine is selected from the group consisting of 4,4'-diaminodiphenyl ether, 3,4'-diaminodiphenyl ether, 2,2'-bis(trifluoromethyl)benzidine, m-phenylenediamine, and 4,4'-diaminodiphenylmethane.

[0014] In a further embodiment of the first aspect, the core layer further comprises both a second aromatic dianhydride and a second aromatic diamine.

[0015] In a further embodiment of the first aspect, the polyimide of the core layer contains at least 80 mol% of 3,3’,4,4’-biphenyltetracarboxylic dianhydride based on the total dianhydride content of the polyimide and at least 80 mol% of p-phenylenediamine based on the total diamine content of the polyimide.

[0016] In yet a further embodiment of the first aspect, the multilayer film has a coefficient of thermal expansion of less than 25 μm / (meter-°C) over a temperature range of 50 to 400 °C.

[0017] In yet an even further embodiment of the first aspect, the first thermoplastic polyimide and the second thermoplastic polyimide each have a T in the range of 150 to 320 °C. g having.

[0018] In another embodiment of the first aspect, the multilayer film has a transmittance of at least 50% and a haze of less than 30%.

[0019] In yet another embodiment of the first aspect, the multilayer film has an overall thickness in the range of 5 to 75 μm.

[0020] In yet another further embodiment of the first aspect, the minimum peel strength of each of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm).

[0021] In yet an even further another embodiment of the first aspect, the thickness of the core layer is in the range of 55 to 73% of the overall thickness of the multilayer film.

[0022] In the second aspect, the metal-clad laminate includes the multilayer film of the first aspect and a first metal layer adhered to the outer surface of the first outer layer of the multilayer film.

[0023] In one embodiment of the second aspect, the metal-clad laminate further includes a second metal layer adhered to the outer surface of the second outer layer of the multilayer film.

[0024] Although many aspects and embodiments have been described above, they are merely illustrative and not limiting. After reading this specification, those skilled in the art will fully understand that other aspects and embodiments are possible without departing from the scope of the present invention. Other features and advantages of the present invention will be apparent from the following detailed description and from the claims.

[0025] In one embodiment, the core layer for the multilayer film comprises a polyimide synthesized by a polycondensation reaction involving the reaction of a first aromatic dianhydride containing 3,3',4,4'-biphenyltetracarboxylic dianhydride and a first aromatic diamine containing p-phenylenediamine. In one embodiment, the polyimide can include one or more additional aromatic dianhydrides, one or more additional aromatic diamines, or both an additional aromatic dianhydride and an additional aromatic diamine. In one embodiment, the second aromatic dianhydride can be selected from the group consisting of 4,4'-oxydiphthalic dianhydride, pyromellitic dianhydride, 3,3',4,4'-benzophenone tetracarboxylic dianhydride, bisphenol A dianhydride, 1,2,5,6-naphthalene tetracarboxylic dianhydride, 1,4,5,8-naphthalene tetracarboxylic dianhydride, and 2,3,6,7-naphthalene tetracarboxylic dianhydride. In one embodiment, the second aromatic diamine can be selected from the group consisting of 4,4'-diaminodiphenyl ether (ODA), 3,4'-diaminodiphenyl ether, 2, two'-bis(trifluoromethyl)benzidine (TFMB), m-phenylenediamine (MPD), and 4,4'-diaminodiphenylmethane (MDA). In one embodiment, the polyimide can include an aliphatic diamine. In one embodiment, the core layer can be a thermosetting polyimide. In one embodiment, the core layer can include a polyimide having some thermoplastic properties.

[0026] In one embodiment, the first outer layer for a multilayer film comprises a first thermoplastic polyimide. In one embodiment, the first thermoplastic polyimide can be synthesized by a polycondensation reaction involving the reaction of an aromatic dianhydride with an aromatic diamine. In one embodiment, the first thermoplastic polyimide may contain one or more additional aromatic dianhydrides, one or more additional aromatic diamines, or both additional aromatic dianhydrides and additional aromatic diamines. In one embodiment, the second outer layer for a multilayer film comprises a second thermoplastic polyimide. In one embodiment, the second thermoplastic polyimide can be synthesized by a polycondensation reaction involving the reaction of an aromatic dianhydride with an aromatic diamine. In one embodiment, the second thermoplastic polyimide may contain one or more additional aromatic dianhydrides, one or more additional aromatic diamines, or both additional aromatic dianhydrides and additional aromatic diamines. In one embodiment, the first outer layer, the second outer layer, or both the first and second outer layers may have a T layer if necessary. g It may contain one or more aliphatic diamines that may be useful in reducing the coefficient of oxidation. In one embodiment, the first thermoplastic polyimide and the second thermoplastic polyimide may be the same or different.

[0027] As used herein, “aromatic diamine” is intended to mean a diamine having at least one aromatic ring, either alone (i.e., a substituted or unsubstituted, functionalized or unfunctionalized benzene or similar type of aromatic ring) or linked to another (aromatic or aliphatic) ring, and such amines should be considered aromatic regardless of any non-aromatic moieties that may also be components of the diamine. Therefore, an aromatic diamine skeleton chain segment is intended to mean at least one aromatic moiety between two adjacent imide bonds. As used herein, “aliphatic diamine” is intended to mean any organic amine that does not meet the definition of an aromatic diamine.

[0028] Depending on the context, as used herein, “diamine” is intended to mean (i) an unreacted form (i.e., a diamine monomer); (ii) a partially reacted form (i.e., a portion or more of an oligomer or other polyimide precursor derived from or resulting therefrom) or (iii) a fully reacted form (a portion or more of a polyimide derived from or resulting therefrom). Diamines can be functionalized in one or more portions depending on the particular embodiment selected in the implementation of the present invention.

[0029] In practice, the term “diamine” is not intended to be restrictive (or to be interpreted literally) with respect to the number of amine moieties in the diamine component. For example, (ii) and (iii) above include polymer materials that may have two, one, or zero amine moieties. Alternatively, the diamine may be functionalized with additional amine moieties (in addition to the amine moieties at the monomer termini that react with dianhydrides to increase the polymer chain). Such additional amine moieties may be used to crosslink the polymer or to provide the polymer with other functionalities.

[0030] Similarly, the term “dianhydride” as used herein is intended to mean a component that can react with (preferably with) and in combination with a diamine to form an intermediate polyamic acid (which can then be cured into a polyimide). Depending on the context, “anhydride” as used herein may mean not only the anhydride moiety itself, but also precursors of the anhydride moiety, such as (i) a pair of carboxylic acid groups (which can be converted to an anhydride by dehydration or a similar type of reaction); or (ii) an acid halide (e.g., chloride) ester functionality (or any other functionality currently known or to be developed in the future that can be converted to anhydride functionality).

[0031] Depending on the context, “dianhydride” can mean (i) an unreacted form (i.e., a dianhydride monomer, whether the anhydride functionality is in a true anhydride form or a precursor anhydride form, as considered in the preceding paragraph); (ii) a partially reacted form (i.e., an oligomer reacted with or otherwise derived from a dianhydride monomer, or a portion or more of another partially reacted or precursor polyimide composition); or (iii) a fully reacted form (a portion or more of a polyimide derived with or otherwise derived from a dianhydride monomer).

[0032] Dianhydrides can be functionalized with one or more moieties depending on the specific embodiment selected in the implementation of the present invention. In fact, the term “dianhydride” is not intended (or should not be interpreted literally) to be limiting with respect to the number of anhydride moieties in a dianhydride component. For example, (i), (ii), and (iii) (in the above paragraph) include organic substances that may have two, one, or zero anhydride moieties, depending on whether the anhydride is in a precursor state or a reacted state. Alternatively, a dianhydride component may be functionalized with additional anhydride type moieties (in addition to the anhydride moieties that react with diamines to provide polyimides). Such additional anhydride moieties could be used to crosslink the polymer or to provide the polymer with other functionalities.

[0033] Any one of numerous polyimide manufacturing processes can be used to prepare multilayer films. It would be impossible to consider or describe all possible polyimide manufacturing processes useful in carrying out the present invention. It should be fully understood that the monomer systems of the present invention can provide the above-mentioned advantageous properties in various manufacturing processes. The compositions of the present invention can be manufactured as described herein and can be readily manufactured by those skilled in the art in any one of many (perhaps countless) methods using any conventional or unconventional polyimide (and multilayer) manufacturing techniques.

[0034] Methods and materials similar to or equivalent to those described herein may be used in carrying out or testing the present invention, but preferred methods and materials are described herein.

[0035] Where quantities, concentrations, or other values ​​or parameters are presented as a range, a preferred range, or a list of upper and lower preferred values, this should be understood to specifically disclose all ranges formed by any upper limit or preferred value and any pair of any lower limit or preferred value, regardless of whether the ranges are disclosed individually. Where numerical values ​​of a range are enumerated herein, unless otherwise specified, that range is intended to encompass its endpoint and all integers and fractions within that range. The range of the present invention is not intended to be limited to the specific values ​​enumerated when defining the range.

[0036] When describing a particular polymer, it should be understood that, in some cases, applicants may refer to the polymer by the monomers used to manufacture them or the amount of monomers used to manufacture them. Such a description does not have to include a specific nomenclature used to describe the final polymer or contain product-by-process terminology, on the other hand, any such reference to monomers and amounts should be interpreted as meaning that the polymer is manufactured from those monomers or that amount of monomers, and the corresponding polymer and its composition.

[0037] The materials, methods, and examples described herein are illustrative only and are not intended to be limiting unless expressly stated otherwise. Where used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having,” or any other variation thereof are intended to encompass non-exclusive inclusion. For example, a method, process, article, or apparatus that includes a list of elements may not necessarily be limited to those elements alone, and may include other elements not expressly listed or that are inherent to such method, process, article, or apparatus. Furthermore, unless expressly stated otherwise, “or” means comprehensive or not, not exclusive or. For example, condition A or B is satisfied by any one of the following: A is true (or exists) and B is false (or does not exist); A is false (or does not exist) and B is true (or exists); and both A and B are true (or exist).

[0038] Furthermore, the use of “one (a)” or “one (an)” is used to describe the elements and components of the present invention. This is done solely for convenience and to give a general meaning to the invention. This description should be read as including one or at least one, and the singular form also includes the plural form unless it is clearly meant not to.

[0039] Organic solvents A useful organic solvent for the synthesis of the polyimide of the present invention is preferably capable of dissolving the polyimide precursor material. Such a solvent should also have a relatively low boiling point, such as below 225°C, so that the polymer can be dried at a moderate (i.e., more convenient and less costly) temperature. Boiling points below 210, 205, 200, 195, 190, or 180°C are preferred.

[0040] The solvents of the present invention can be used alone or in combination with other solvents (i.e., cosolvents). Useful organic solvents include: N-methylpyrrolidone (NMP), dimethylacetamide (DMAc), N,N'-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), tetramethylurea (TMU), diethylene glycol diethyl ether, 1,2-dimethoxyethane (monoglyme), diethylene glycol dimethyl ether (diglyme), 1,2-bis(2-methoxyethoxy)ethane (triglyceride), bis[2-(2-methoxyethoxy)ethyl)] ether (tetraglyceride), gamma-butyrolactone, and bis(2-methoxyethyl) ether and tetrahydrofuran. In one embodiment, preferred solvents include N-methylpyrrolidone (NMP) and dimethylacetamide (DMAc).

[0041] Cosolvents are generally used in amounts of 5 to 50 weight percent of the total solvent, and useful such cosolvents include xylene, toluene, benzene, "Cerosolve" (glycol ethyl ether), and "Cerosolve acetate" (hydroxyethyl acetate glycol monoacetate).

[0042] Aromatic diamines The core layer contains p-phenylenediamine (PPD) as the first aromatic diamine, but in one embodiment, it contains m-phenylenediamine (MPD), 2,5-dimethyl-1,4-diaminobenzene, trifluoromethyl-2,4-diaminobenzene, trifluoromethyl-3,5-diaminobenzene, 2,5-dimethyl-1,4-phenylenediamine (DPX), 2,2-bis(4-aminophenyl)propane, 4,4'-diaminobiphenyl, and 4,4'-diaminobenzo Phenone, 4,4'-diaminodiphenylmethane (MDA), 4,4'-diaminodiphenyl sulfide, 4,4'-diaminodiphenyl sulfone, 3,3'-diaminodiphenyl sulfone, bis(4-(4-aminophenoxy)phenyl sulfone (BAPS), 4,4'-bis(aminophenoxy)biphenyl (BAPB), 4,4'-diaminodiphenyl ether (ODA), 3,4'-diaminodiphenyl ether, 4,4'-diaminobenzophenone, 4,4 '-Isopropylidenedianiline, 2,2'-bis(3-aminophenyl)propane, N,N-bis(4-aminophenyl)-n-butylamine, N,N-bis(4-aminophenyl)methylamine, 1,5-diaminonaphthalene, 3,3'-dimethyl-4,4'-diaminobiphenyl, m-aminobenzoyl-p-aminoanilide, 4-aminophenyl-3-aminobenzoate, N,N-bis(4-aminophenyl)aniline, 2,4-diaminotoluene, 2,5 Any number of suitable aromatic diamines, such as -diaminotoluene, 2,6-diaminotoluene, 2,4-diamine-5-chlorotoluene, 2,4-diamine-6-chlorotoluene, 2,4-bis(beta-amino-t-butyl)toluene, bis(p-beta-amino-t-butylphenyl) ether, p-bis-2-(2-methyl-4-aminopentyl)benzene, m-xylylenediamine, and p-xylylenediamine, may also be included in the core layer polyimide.

[0043] Other useful aromatic diamines include 2,2'-bis(trifluoromethyl)benzidine (TFMB), 1,2-bis(4-aminophenoxy)benzene, 1,3-bis(4-aminophenoxy)benzene, 1,2-bis(3-aminophenoxy)benzene, 1,3-bis(3-aminophenoxy)benzene, 1-(4-aminophenoxy)-3-(3-aminophenoxy)benzene, and 1,4-bis(4-aminophenoxy)ben Zen, 1,4-bis(3-aminophenoxy)benzene, 1-(4-aminophenoxy)-4-(3-aminophenoxy)benzene, 2,2-bis(4-[4-aminophenoxy]phenyl)propane (BAPP), 2,2'-bis(4-aminophenyl)-hexafluoropropane (6F-diamine), 2,2'-bis(4-phenoxyaniline)isopropylidene, 2,4,6-trimethyl-1,3-diaminobenzene, 4,4 Examples include '-diamino-2,2'-trifluoromethyldiphenyl oxide, 3,3'-diamino-5,5'-trifluoromethyldiphenyl oxide, 4,4'-trifluoromethyl-2,2'-diaminobiphenyl, 2,4,6-trimethyl-1,3-diaminobenzene, 4,4'-oxy-bis-[2-trifluoromethyl)benzeneamine](1,2,4-OBABTF), 4,4'-oxy-bis-[3-trifluoromethyl)benzeneamine], 4,4'-thio-bis-[(2-trifluoromethyl)benzeneamine], 4,4'-thiobis[(3-trifluoromethyl)benzeneamine], 4,4'-sulfoxyl-bis-[(2-trifluoromethyl)benzeneamine], 4,4'-sulfoxyl-bis-[(3-trifluoromethyl)benzeneamine], and 4,4'-keto-bis-[(2-trifluoromethyl)benzeneamine].

[0044] In one embodiment, useful aromatic diamines include bis-aminophenoxybenzene (APB), aminophenoxyphenylpropane (BAPP), dimethylphenylenediamine (DPX), isomers of bisaniline P, and combinations thereof. The use of these particular aromatic diamines can lower the lamination temperature of polyimide and increase the peel strength of polyimide when bonded to other materials, particularly metals.

[0045] In one embodiment, the outer thermoplastic polyimide may contain one or more of the aromatic diamines listed above for the core layer, such as p-phenylenediamine.

[0046] aromatic dianhydride The core layer contains 3,3',4,4'-biphenyltetracarboxylic dianhydride (BPDA) as the first aromatic dianhydride, but in one embodiment, any aromatic dianhydride or combination of aromatic dianhydrides can be used as additional dianhydrides when forming the core layer polyimide. The dianhydrides can be used in their tetracarboxylic acid form (or as mono, di, tri, or tetraesters of tetra acids) or as their diester acid halides (chlorides). However, in some embodiments, the dianhydride form may be preferred because it is generally more reactive than acids or esters.

[0047] Suitable examples of aromatic dianhydrides include 1,2,5,6-naphthalenetetracarboxylic dianhydride, 1,4,5,8-naphthalenetetracarboxylic dianhydride, 2,3,6,7-naphthalenetetracarboxylic dianhydride, 2-(3',4'-dicarboxyphenyl)5,6-dicarboxybenzimidazole dianhydride, 2-(3',4'-dicarboxyphenyl)5,6-dicarboxybenzoxazole dianhydride, 2-(3',4'-dicarboxyphenyl)5,6-dicarboxybenzothiazole dianhydride, and 2,2',3,3'-benzophen Nontetracarboxylic dianhydride, 2,3,3',4'-benzophenonetetracarboxylic dianhydride, 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTDA), 2,2',3,3'-biphenyltetracarboxylic dianhydride, 2,3,3',4'-biphenyltetracarboxylic dianhydride, bicyclo-[2,2,2]-octen-(7)-2,3,5,6-tetracarboxylic-2,3,5,6-dianhydride, 4,4'-thio-diphthalic anhydride, bis(3,4-dicarboxyphenyl)sulfone dianhydride, bis(3,4-dicarboxyphenyl) Bis(3,4-dicarboxyphenyl) sulfoxide dianhydride (DSDA), bis(3,4-dicarboxyphenyloxadiazole-1,3,4) p-phenylene dianhydride, bis(3,4-dicarboxyphenyl)2,5-oxadiazole 1,3,4-dianhydride, bis2,5-(3',4'-dicarboxydiphenyl ether)1,3,4-oxadiazole dianhydride, 4,4'-oxydiphthalic anhydride (ODPA), bis(3,4-dicarboxyphenyl) thioether dianhydride, bisphenol A dianhydride (BPADA), bisphenol S dianhydride Water, 2,2-bis(3,4-dicarboxyphenyl)1,1,1,3,3,3,-hexafluoropropane dianhydride (6FDA), 5,5-[2,2,2]-trifluoro-1-(trifluoromethyl)ethylidene, bis-1,3-isobenzofranion, 1,4-bis(4,4'-oxyphthalic anhydride)benzene, bis(3,4-dicarboxyphenyl)methane dianhydride, cyclopentadienyltetracarboxylic dianhydride, cyclopentanetetracarboxylic dianhydride, ethylenetetracarboxylic dianhydride, perylene-3,4,9,Examples include 10-tetracarboxylic dianhydride, pyromellitic acid dianhydride (PMDA), tetrahydrofurantetracarboxylic dianhydride, 1,3-bis(4,4'-oxydiphthalic acid anhydride)benzene, 2,2-bis(3,4-dicarboxyphenyl)propane dianhydride, 2,6-dichloronaphthalene-1,4,5,8-tetracarboxylic dianhydride, 2,7-dichloronaphthalene-1,4,5,8-tetracarboxylic dianhydride, 2,3,6,7-tetrachloronaphthalene-1,4,5,8-tetracarboxylic dianhydride, phenanthrene-1,8,9,10-tetracarboxylic dianhydride, pyrazine-2,3,5,6-tetracarboxylic dianhydride, benzene-1,2,3,4-tetracarboxylic dianhydride; and thiophene-2,3,4,5-tetracarboxylic dianhydride.

[0048] In one embodiment, the outer thermoplastic polyimide may contain one or more of the aromatic dianhydrides listed above for the core layer, such as 3,3',4,4'-biphenyltetracarboxylic dianhydride.

[0049] multilayer film The polyimide film layer according to the present invention can be produced by combining a diamine and a dianhydride (monomer or other polyimide precursor form) with a solvent to form a polyamic acid (also called polyamic acid) solution. The dianhydride and diamine can be combined in a molar ratio of about 0.90 to 1.10. The molecular weight of the polyamic acid formed therefrom can be adjusted by adjusting the molar ratio of the dianhydride to the diamine.

[0050] In one embodiment, the polyamic acid casting solution is derived from a polyamic acid solution. The polyamic acid casting solution preferably comprises a polyamide solution and can optionally be combined with i) one or more dehydrating agents, such as aliphatic acid anhydrides (e.g., acetic anhydride) and / or aromatic acid anhydrides; and ii) one or more conversion chemicals, such as catalysts, such as aliphatic tertiary amines (e.g., triethylamine), aromatic tertiary amines (e.g., dimethylaniline), and heterocyclic tertiary amines (e.g., pyridine, picoline, isoquinoline). The anhydride dehydrating agent is often used in molar excess compared to the amount of amide acid groups in the polyamic acid. The amount of acetic anhydride used is typically about 2.0 to 4.0 moles per equivalent (repeating unit) of polyamic acid. Generally, a comparable amount of tertiary amine catalyst is used.

[0051] In one embodiment, the polyamic acid solution and / or the polyamic acid casting solution are dissolved in an organic solvent at concentrations ranging from about 5.0 or 10% by weight to about 15, 20, 25, 30, 35 and 40% by weight.

[0052] Polyamic acids (and casting solutions) may further contain one of a number of additives, such as processing aids (e.g., oligomers), antioxidants, light stabilizers, flame retardants, antistatic agents, heat stabilizers, UV absorbers, inorganic fillers, or various reinforcing agents. These inorganic fillers include thermally conductive fillers such as metal oxides, inorganic nitrides, and metal carbides, as well as conductive fillers such as metals, graphite carbon, and carbon fibers, and conductive polymers. Common inorganic fillers include alumina, silica, silicon carbide, diamond, clay, boron nitride, aluminum nitride, titanium dioxide, dicalcium phosphate, and fumed metal oxides. Common organic fillers include polyaniline, polythiophene, polypyrrole, polyphenylene vinylene, polydialkylfluorene, carbon black, graphite, multi-walled and single-walled carbon nanotubes, and carbon nanofibers.

[0053] Next, a solvation mixture (polyamic acid casting solution) can be cast or applied onto a support such as an endless belt or a rotating drum to obtain a film. Then, the solvent-containing film can be converted into a self-supporting film by heating it at an appropriate temperature with a conversion chemical reactant (chemical curing) (thermosetting). Next, the film can be separated from the support, oriented by widening or other means, and a polyimide film can be provided while continuing thermal and chemical curing.

[0054] Useful methods for producing polyimide films in accordance with the present invention can be found in U.S. Patent No. 5,166,308 and U.S. Patent No. 5,298,331, all of which are incorporated herein by reference. (a) A method in which the diamine component and the dianhydride component are mixed together beforehand, and then the mixture is gradually added to the solvent while stirring. (b) A method in which the solvent is added to a stirred mixture of the diamine component and the dianhydride component. (Conversely to (a) above) (c) A method in which a diamine is exclusively dissolved in a solvent, and then a dianhydride is added thereto in a ratio that allows control of the reaction rate. (d) A method in which a dianhydride component is exclusively dissolved in a solvent, and then an amine component is added thereto in a ratio that allows control of the reaction rate. (e) A method in which the diamine component and the dianhydride component are dissolved separately in a solvent, and then these solutions are mixed in a reactor. (f) A method in which a polyamic acid having an excess amine component and another polyamic acid having an excess dianhydride component are formed in advance and then reacted with each other in a reactor in a manner that particularly produces a non-random copolymer or a block copolymer. (g) A method in which a specific portion of the amine component and the dianhydride component is reacted first, followed by the residual diamine component, or vice versa. (h) A method in which a conversion chemical is mixed with polyamic acid to form a polyamic acid casting solution, which is then cast to form a gel film. (i) A method in which components are added to some or all of a solvent, either partially or whole, in any order, and any part or all of any component may be added as a solution in some or all of the solvent. (j) A method comprising: first reacting one of the dianhydride components with one of the diamine components to produce a first polyamic acid; then reacting another dianhydride component with another amine component to produce a second polyamic acid; and finally, bonding the amide acids by one of several methods before film formation. Numerous other variations are also possible.

[0055] The thickness of each polyimide layer can be adjusted according to the intended purpose or end-use specifications of the film. In one embodiment, the multilayer film has a total thickness of about 5 to about 150 μm. In another embodiment, the multilayer film has a total thickness of about 5 to about 75 μm. In one embodiment, the thickness of the core layer is in the range of about 35 to about 73% of the total thickness of the multilayer film. For example, the multilayer film may have a total thickness of 30 μm with a 22 μm core layer and 4 μm first and second outer layers on both sides of the core layer. In another example, for a thicker film, the multilayer film may have a total thickness of 50 μm with a 34 μm core layer and 7 μm first and second outer layers on both sides of the core layer. In yet another example, for a very thin film, the multilayer film may have a total thickness of 5 μm with a 2 μm core layer and 1.5 μm first and second outer layers on both sides of the core layer. In one embodiment, the thickness of the core layer is in the range of about 55 to about 73% of the total thickness of the multilayer film. Those skilled in the art will fully understand that the minimum thickness of the thermoplastic polyimide outer layer is required to provide sufficient adhesion to the metal layer to form useful metal-clad laminates for electronic circuit applications. In addition, the minimum thickness of the core layer is required to maintain the mechanical integrity of the multilayer film.

[0056] In one embodiment, both the first thermoplastic polyimide and the second thermoplastic polyimide of the multilayer film are rated at temperatures in the range of approximately 150 to approximately 320°C. ghas. In certain embodiments, both the first thermoplastic polyimide and the second thermoplastic polyimide of the multilayer film have a T in the range of about 230 to about 320 °C g has. In more particular embodiments, both the first thermoplastic polyimide and the second thermoplastic polyimide of the multilayer film have a T in the range of about 270 to about 320 °C g has. Having a thermoplastic polyimide with a higher T g in the outer layer improves the thermal durability of the multilayer film. The metal-clad laminate may be subjected to post-lamination processes such as hot-bar processing or spot welding at temperatures above 300 °C. Under these conditions, a low-T g thermoplastic polyimide layer is susceptible to adhesion loss and delamination, distortion and blistering, which may be accompanied by a decrease in optical transmittance and an increase in haze. Maintaining good optical transparency can be extremely important for some electronics manufacturing processes, for example when optical registration is used to align various layers in a printed circuit board. In these applications, high transmittance and low haze can be critically important for circuit designs with very fine features. It is important to maintain optical transparency even during high-temperature curing that may be used to stabilize materials subjected to higher-temperature post-lamination processes. In one embodiment, the multilayer film has a transmittance of at least 50% and a haze of less than 30%.

[0057] In one embodiment, the core layer and the outer layer can be solution cast simultaneously by coextrusion. At the time of casting, the polyimide can be in the form of a polyamic acid solution. The casting solution forms an uncured polyamic acid film that is later cured to polyimide. The adhesive strength of such a laminate can be improved by using various techniques to enhance the adhesive strength.

[0058] In some embodiments, the resulting polyamic acid solution is filtered and pumped to a slot die, where the flow is divided in such a way that it forms the first and second outer layers of a three-layer co-extruded film. In some embodiments, the second flow of polyimide is filtered and then pumped to a casting die in such a way that it forms the central polyimide core layer of a three-layer co-extruded film. The flow rate of the solution can be adjusted to achieve the desired layer thickness.

[0059] In some embodiments, the multilayer film is prepared by simultaneously extruding a first outer layer, a core layer, and a second outer layer. In some embodiments, the layers are extruded by a single-cavity or multi-cavity extrusion die. In another embodiment, the multilayer film is manufactured using a single-cavity die. When a single-cavity die is used, the laminar flow should have a viscosity high enough to prevent flow mixing and provide uniform lamination. In some embodiments, the multilayer film is prepared by casting from a slot die onto a moving stainless steel belt. In one embodiment, the belt is then passed through a convection oven to evaporate the solvent and partially imidize the polymer to produce a "green" film. The green film can be peeled from the casting belt and wound up. The green film can then be passed through a tenter oven to produce a fully cured polyimide film. In some embodiments, during tentering, shrinkage can be minimized by constraining the film along the edges (i.e., using clips or pins).

[0060] In one embodiment, the outer layer of the present invention can also be applied to the core layer during an intermediate manufacturing stage in which the polyimide film is converted into a gel film or a green film, etc.

[0061] The term "gel film" refers to a polyamic acid sheet that can be formed by a chemical transformation process, filled with volatile substances, primarily solvents, until the polyamic acid is in a gel-expanded or rubbery state. The volatile substance content of the gel film is typically in the range of 70–90% by weight, and the polymer content is typically in the range of 10–30% by weight. The final film becomes "self-supporting" at the gel film stage. It can then be separated from the support cast on it and heated to the final curing temperature. Gel films generally have an amide acid to imide ratio of 10:90–50:50, and most often 30:70.

[0062] The gel membrane structure can be prepared by the method described in U.S. Patent No. 3,410,826. This patent discloses the mixing of chemical converters and catalysts, such as lower fatty acid anhydrides and tertiary amines, into a polyamic acid solution at low temperature. This is followed by the step of casting the polyamic acid solution in membrane form onto a casting drum. After casting, the membrane is gently heated, for example, at 100°C, to activate the converters and catalysts to transform the cast membrane into a polyamic acid / polyimide gel membrane.

[0063] Another type of polyimide-based film is a “green film,” which is partly polyamic acid and partly polyimide, and can be formed by a thermal conversion process. Green films generally contain about 50–75% by weight of polymer and 25–50% by weight of solvent. Generally, they should be strong enough to be substantially self-supporting. Green films can be prepared by casting a polyamic acid solution into film form onto a suitable support such as a casting drum or belt, and gently heating it at 150°C or below. A low percentage of the polymer, for example, less than 25% of amidic acid units, can be converted into imide units.

[0064] The application of the polyimide film of the present invention can be achieved in any number of ways. Such methods include the use of a slot die, immersion coating of the film, or kiss-roll coating, followed by metering and feeding with a doctor knife, doctor roll, compression roll, or air knife. The coating may also be applied by brushing or spraying. By using such techniques, it is possible to prepare both single-sided and double-sided coated laminates. In the preparation of double-sided coated structures, the coating can be applied to both sides of the polyimide either simultaneously or subsequently before proceeding to the curing and drying stages of the polyimide.

[0065] In one embodiment, the multilayer film has a coefficient of thermal expansion (CTE) of less than 25 μm / (meter-°C) over a temperature range of about 50 to about 400°C. Maintaining a low CTE over a wide temperature range can be used to stabilize materials subjected to higher temperature post-lamination processes, allowing the multilayer film to maintain good adhesion even during high-temperature curing. Metal-clad laminates may undergo hot bar processing or spot welding at temperatures above 300°C. Under these conditions, multilayer films with a CTE greater than 25 μm / (meter-°C) over a temperature range of about 50 to about 400°C are susceptible to loss of adhesion and delamination, distortion, and blistering.

[0066] Metal clad laminate In one embodiment, the conductive layer of the present invention is i. Metal sputtering (optionally followed by electroplating); ii. Foil lamination; and / or iii. Any conventional or unconventional method for applying a thin metal layer to a substrate. It can be produced by [this method].

[0067] In one embodiment, a lamination process may be used to form a metal-clad laminate having a multilayer film. In one embodiment, a first outer layer containing a first thermoplastic polyimide is placed between a first conductive layer and a core layer, and a second outer layer containing a second thermoplastic polyimide is placed on the opposite side of the core layer. In one embodiment, the second conductive layer is placed in contact with the second outer layer on the opposite side of the core layer. One advantage of this type of construction is that the lamination temperature of the multilayer film is lowered to the lamination temperature required for the thermoplastic polyimide of the outer layer to bond to the conductive layer. In one embodiment, the conductive layer is a metal layer.

[0068] For example, a polyimide film can be subjected to a pretreatment step before applying the multilayer film of the present invention onto a metal foil. The pretreatment step may include heat treatment, corona treatment, plasma treatment under atmospheric pressure, plasma treatment under reduced pressure, treatment with coupling agents such as silanes and titanates, sandblasting, alkali treatment, acid treatment, and coating with polyamic acid. To improve adhesive strength, it is also generally possible to add various metal compounds, such as those disclosed in U.S. Patents No. 4,742,099; No. 5,227,244; No. 5,218,034; and No. 5,543,222, which are incorporated herein by reference.

[0069] In addition, conductive metal surfaces can be treated with various organic and inorganic treatments (for the purpose of improving adhesion). These treatments include the use of silanes, imidazoles, and triazoles; oxide treatment and reduced oxide treatment; tin oxide treatment; and surface cleaning / roughening (known as micro-etching) with acid or alkaline reagents.

[0070] In further embodiments, the polyamic acid precursor (of the polyimide film of the present invention) may be coated onto a fully cured polyimide base film or directly onto a metal substrate and subsequently imidized by heat treatment. The polyimide base film may be prepared by either a chemical or thermal conversion process and may be surface-treated, for example, by chemical etching, corona treatment, or laser etching, to improve adhesion.

[0071] As used herein, the terms “conductive layer” and “conductive foil” mean a metal layer or metal foil (a thin composition having at least 50% of the conductivity of high-grade copper). Conductive foil is typically a metal foil. Metal foils do not have to be used as elements in their pure form; they can also be used as metal foil alloys, such as copper alloys containing nickel, chromium, iron, and other metals. Conductive layers can also be metal alloys and are typically applied to the polyimide of the present invention by a sputtering process followed by an electroplating process. In these types of processes, a metal seed coat layer is first sputtered onto the polyimide film. Finally, a thicker coating of metal is applied to the seed coat by electroplating or electrodeposition. Such sputtered metal layers can also be hot-pressed above the glass transition temperature of the polymer for enhanced peel strength.

[0072] Particularly preferred metal substrates are foils of rolled annealed copper or rolled annealed copper alloys. In many cases, it has been found to be advantageous to pre-treat the metal substrate before coating. This pre-treatment may include, but is not limited to, electrodeposition or immersion deposition of thin layers of copper, zinc, chromium, tin, nickel, cobalt, other metals, and alloys of these metals onto the metal. The pre-treatment may consist of chemical treatment or mechanical roughening. This pre-treatment has been found to allow for a further increase in the adhesion of the polyimide layer, and therefore, the peel strength. Apart from surface roughening, chemical pre-treatment also leads to the formation of metal oxide groups, allowing for a further increase in the adhesion of the metal to the polyimide layer. This pre-treatment can be applied to both sides of the metal and allows for enhanced adhesion to the substrate on both sides. In one embodiment, the multilayer film, when bonded to a copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B, has a minimum peel strength greater than 0.9 kgf / cm (0.88 N / mm) for at least one of the first and second outer layers. In a particular embodiment, the multilayer film has a minimum peel strength greater than 0.9 kgf / cm (0.88 N / mm) for each of the first and second outer layers.

[0073] In one embodiment, the metal-clad laminate may include a multilayer film and a first metal layer bonded to the outer surface of a first outer layer of the multilayer film. In one embodiment, the metal-clad laminate may include a second metal layer bonded to the outer surface of a second outer layer of the multilayer film. In one embodiment, the first metal layer, the second metal layer, or both metal layers may be copper. In one embodiment, the metal-clad laminate of the present invention, which includes double-sided copper cladding, can be prepared by laminating copper foil on both sides of a multilayer film.

[0074] In addition, the polyimide films of the present invention generally also have low loss tangent values. Loss tangent is typically measured at 10 GHz and is used to measure the degradation of a dielectric of a neighboring digital signal passing through a metal circuit trace. Different loss tangent values ​​exist for different dielectrics. The lower the loss tangent value for a given dielectric, the better the material is for digital circuit applications. The polyimides of the present invention exhibit excellent, low loss tangent values. In one embodiment, the loss tangent value for a polyimide layer was less than 0.010, about 0.004, at 10 GHz. The polyimides of the present invention can also be used in applications in the range of 1 to 100 GHz, most commonly 1 to 20 GHz.

[0075] In another embodiment, the multilayer film of the present invention is used as a material for constructing planar transformer components. These planar transformer components are commonly used in power supply devices.

[0076] Furthermore, in another embodiment, the polyimide film of the present invention may be used together with a thick metal foil to form a flexible heater. These heaters are typically used in automotive and aerospace applications.

[0077] The multilayer film of the present invention exhibits excellent attenuation. The polyimide of the present invention can often exhibit an attenuation value of approximately 0.3 decibels per inch at 10 GHz using a 50-ohm microstrip.

[0078] In one embodiment, polyimide precursors for the core layer and polyimide precursors for the first and second outer layers are cast simultaneously (using a multiport die) to form a multilayer polyimide film (after curing of the polyamic acid layer). This multilayer film is then bonded to a metal layer using the outer thermoplastic polyimide as a bonding layer to the metal layer. Thus, the formed multilayer metal-clad laminate comprises the multilayer film and at least one conductive layer. Bonding of the multilayer polyimide / metal-clad laminate can occur in a double-belt press in roll-to-roll processing or in an autoclave in sheet-to-sheet processing, when the metal foil is used as the conductive layer.

[0079] The polyimide of the present invention is particularly useful for packaging materials for flexible printed circuit boards or semiconductor devices or CSPs (chip-scale packages), die-pad bonding of chip-on-flex (COF), COL (chip-on-lead), LOC (lead-on-chip), multi-chip modules ("MCM"), ball grid arrays ("BGA") or micro-ball grid arrays, and / or tape-bonded ("TAB").

[0080] In another embodiment, the multilayer film of the present invention is used for wafer-level integrated circuit packaging, where the composite material is manufactured using the multilayer film according to the present invention placed between a conductive layer (typically metal) having a thickness of less than 100 μm and a wafer containing multiple integrated circuit dies. In one embodiment (wafer-level integrated circuit packaging), conductive passages are connected to the dies by conductive passages such as wire bonds, conductive metals, solder bumps, etc.

[0081] The advantageous properties of the present invention can be seen by referring to the following examples, which illustrate but do not limit the present invention. All parts and percentages are by weight unless otherwise specified.

[0082] Test method Peel strength To measure the peel strength, roll-clad laminates were manufactured by continuous lamination onto copper foil using a high-temperature nip-roll lamination apparatus heated to 350°C. The adhesion strength or "peel strength" of the multilayer film laminated onto copper was measured according to ASTM Method IPC-TM-650, Method No. 2.4.9B, and measurements were taken on both sides of the multilayer film.

[0083] transparency Transparency was measured using Haze-Guard Plus (BYK-Gardner GmbH, Germany). Total transmittance (normal light and diffuse transmitted light) was recorded over the wavelength range of 400-700 nm and reported as percentage transmittance.

[0084] Cloudiness The degree of haze was measured using Haze-Guard Plus, with the haze being measured in transmittance units by collecting forward scattered light using the method described in ASTM1003. Percent haze was determined by measuring the amount of light that, on average, deviated from the incident beam by more than 2.5 degrees. [Examples]

[0085] Polyamic acid solutions for producing the core and outer layers were prepared separately by chemical reactions between appropriate molar equivalents of monomers in dimethylacetamide (DMAc) solvent. Typically, a diamine dissolved in DMAc was stirred under nitrogen, and a dianhydride was added as a solid over a period of several minutes. Stirring was continued until the maximum viscosity of the polyamic acid was obtained. The viscosity was adjusted by controlling the amount of dianhydride in the polyamic acid composition.

[0086] Multilayer films were cast by co-extrusion. Three separate streams of polyamic acid polymer were simultaneously extruded onto a heated moving belt through a multi-port extrusion die to form a co-extruded three-layer polyimide film. The thickness of the polyimide core layer and the top and bottom thermoplastic polyimide outer layers was adjusted by varying the amount of polyamic acid supplied to the extruder.

[0087] The extruded multilayer film was dried in an oven at a temperature in the range of approximately 95 to 150°C. The self-supporting film was peeled off the belt and completely dried by heating with a radiant heater in a tenter oven at a temperature of approximately 110 to 805°C (radiant heater surface temperature), thereby imidizing the polymer.

[0088] Example 1 For Example 1(E1), the radiant heating setpoint temperature used to cure the film was 805°C. The core layer polymer composition contained polyimide derived from dianhydride to diamine in a ratio of approximately 1:1 molars. The dianhydride composition contained monomers BPDA / PMDA in a 95:5 molar ratio, and the diamine composition contained monomers PPD / ODA in a 92:8 molar ratio.

[0089] The thermoplastic outer layer also contained a polyimide derived from dianhydride to diamine in a molar ratio of approximately 1:1. The dianhydride composition contained monomers PMDA and ODPA in a 20:80 molar ratio, and the diamine composition contained 100 mol% RODA monomer. By adjusting the flow rate of the polyamic acid solution, the thermoplastic outer layer yielded a three-layer film with thicknesses of approximately 8.1 and 7.1 μm, respectively.

[0090] Cross-sectional scanning electron microscope (SEM) images of a three-layer film were obtained to measure the thickness of the multilayer film and the individual core and outer layers. To obtain these images, the film sample was cut, embedded in epoxy, and dried overnight. Next, the sample was polished using a Buehler variable-speed grinder / polisher and placed in a desiccator for approximately 2 hours to ensure complete drying. Images were taken using a Hitachi S-3400 SEM (Hitachi High Technologies America, Inc., Schaumburg, IL) under variable pressure. The total thickness of the multilayer film was 48.1 μm. The core layer thickness, as a percentage of the total multilayer film thickness, was 68.4%. Two samples were prepared and the transmittance, 62.4% and 63.4%, and the haze, 22.1% and 23.3%, of the multilayer film were measured.

[0091] A copper-clad laminate was prepared using a portion of a multilayer film to measure its peel strength. Cu foil was laminated on both sides of the multilayer film. Roll clads were manufactured by continuous lamination of adhesive-coated dielectric films onto copper foil using a high-temperature nip roll laminating apparatus with one surface heated to 350°C. The adhesive strength, i.e., peel strength, of the polyimide copper-clad laminate was measured according to ASTM Method IPC-TM-650, Method No. 2.4.9B, resulting in peel strengths of 1.0 kgf / cm (0.98 N / mm) and 1.13 kgf / cm (1.1 N / mm).

[0092] The physical properties are summarized in Table 1.

[0093] Comparative Example 1 For Comparative Example 1 (CE1), a three-layer film was formed by co-extrusion using a method similar to that of E1. The compositions of the core layer and outer layers were the same as those used in E1. By adjusting the flow rate of the polyamic acid solution, a three-layer structure was obtained in which the two outer layers were approximately 6.6 and 6.1 μm thick, respectively.

[0094] The total thickness of the multilayer film was 48.7 μm, and the core layer thickness, as a percentage of the total multilayer film thickness, was 73.9%. The transmittance of CE1, 46.1%, was significantly lower than that of E1, while the haze, 35.2%, was noticeably higher.

[0095] Example 2 In Example 2 (E2), a three-layer film was formed by co-extrusion using a method similar to that of E1. The compositions of the core layer and outer layer were the same as those in E1. By adjusting the flow rate of the polyamic acid solution, a three-layer structure was obtained in which the two outer layers each had a thickness of approximately 1.8 μm.

[0096] The total thickness of the multilayer film was 12.4 μm. The core layer thickness, as a percentage of the total multilayer film thickness, was 71.1%. The transmittance (87.2%), cloudiness (1.48%), and peel strengths (0.91 kgf / cm (0.89 N / mm) and 0.96 kgf / cm (0.94 N / mm)) were all very good.

[0097] Comparative Example 2 For Comparative Example 2 (CE2), a three-layer film was formed by co-extrusion using a method similar to that of E1. The compositions of the core layer and outer layers were the same as those used in E1. By adjusting the flow rate of the polyamic acid solution, a three-layer structure was obtained in which the two outer layers had thicknesses of approximately 3.0 and 4.6 μm, respectively.

[0098] The total thickness of the multilayer film was 31.4 μm. The core layer thickness, as a percentage of the total multilayer thickness, was 76.0%. The transmittance of CE2, 87.2%, and the haze, 1.48%, were very good, but the peel strengths, 0.85 kgf / cm (0.83 N / mm) and 0.87 kgf / cm (0.85 N / mm), were lower than desired.

[0099] Comparative Example 3 For Comparative Example 3 (CE3), a three-layer film was formed by co-extrusion using a method similar to that of E1. The core layer polymer composition contained polyimide derived from dianhydride (BPDA) and diamine (PPD) in a 1:1 molar ratio. The outer layer composition was the same as that used in E1. By adjusting the flow rate of the polyamic acid solution, a three-layer structure was obtained in which the two outer layers were approximately 4.6 and 5.8 μm thick, respectively.

[0100] The total thickness of the multilayer film was 54.9 μm. The core layer thickness, as a percentage of the total multilayer thickness, was 81.1%. The transmittance of CE3, 66.9%, and the cloudiness, 5.2%, were both good, but the peel strength of CE3, 0.82 kgf / cm (0.80 N / mm) and 0.85 kgf / cm (0.83 N / mm), were noticeably lower than that of E1.

[0101] [Table 1]

[0102] It should be noted that not all of the activities listed above are required, some of the activities may not be necessary, and additional activities may be performed in addition to those listed. Furthermore, the order in which the activities are listed is not necessarily the order in which they are performed. A person skilled in the art will be able to determine which activities can be used for their specific needs or requirements by reading this specification.

[0103] In the aforementioned specification, the present invention has been described in relation to specific embodiments. However, those skilled in the art will fully understand that various modifications and changes can be made without departing from the scope of the invention, as described in the following claims. All features disclosed herein may be replaced by alternative features that serve the same, equivalent, or similar purposes. Accordingly, this specification and the figures should be considered in an illustrative rather than restrictive sense, and all such modifications are intended to fall within the scope of the invention.

[0104] Benefits, other advantages, and solutions to problems have been described above in relation to specific embodiments. However, benefits, advantages, solutions to problems, and any elements that may produce or make more prominent any benefits, advantages, or solutions should not be construed as important, necessary, or essential features or elements of any or all of the claims.

[0105] Where quantities, concentrations, or other values ​​or parameters are presented as a range, a preferred range, or a list of upper and lower values, this should be understood to specifically disclose all ranges formed by any pair of any upper limit or preferred values ​​and any lower limit or preferred values, regardless of whether the ranges are disclosed individually. Where numerical values ​​of a range are enumerated herein, unless otherwise specified, that range is intended to encompass its endpoint, as well as all integers and fractions within that range. The scope of application of the present invention is not intended to be limited to the specific values ​​enumerated when defining a range. The present invention includes the following embodiments. 1. A first outer layer comprising a first thermoplastic polyimide; A core layer comprising a polyimide, wherein the polyimide comprises a first aromatic dianhydride containing 3,3',4,4'-biphenyltetracarboxylic acid dianhydride and a first aromatic diamine containing p-phenylenediamine; A second outer layer containing a second thermoplastic polyimide and A multilayer film comprising, The multilayer film has a total thickness in the range of 5 to 150 μm; The thickness of the core layer is in the range of 35 to 73% of the total thickness of the multilayer film; and, The minimum peel strength of at least one of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B. Multilayer film. 2. The first thermoplastic polyimide is Aromatic dianhydrides selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, and mixtures thereof; Aromatic diamines selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, 2,2-bis-(4-[4-aminophenoxy]phenyl)propane, and mixtures thereof, A multilayer film according to claim 1, including the above. 3. The aromatic dianhydride includes pyromellitic dianhydride and 4,4'-oxydiphthalic dianhydride; The aforementioned aromatic diamine contains 1,3-bis(4-aminophenoxy)benzene, The multilayer film described in item 2 above. 4. The second thermoplastic polyimide is Aromatic dianhydrides selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, and mixtures thereof; Aromatic diamines selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, hexamethylenediamine and mixtures thereof, A multilayer film according to claim 1, including the above. 5. The aromatic dianhydride includes pyromellitic dianhydride and 4,4'-oxydiphthalic dianhydride; The aforementioned aromatic diamine contains 1,3-bis(4-aminophenoxy)benzene, The multilayer film described in item 4 above. 6. The multilayer film according to claim 1, wherein the first thermoplastic polyimide and the second thermoplastic polyimide are the same. 7. The multilayer film according to claim 1, wherein the core layer further comprises a second aromatic dianhydride. 8. The multilayer film according to 7, wherein the second aromatic dianhydride is selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, bisphenol A dianhydride, 1,2,5,6-naphthalenetetracarboxylic acid dianhydride, 1,4,5,8-naphthalenetetracarboxylic acid dianhydride, and 2,3,6,7-naphthalenetetracarboxylic acid dianhydride. 9. The multilayer film according to claim 1, wherein the core layer further comprises a second aromatic diamine. 10. The multilayer film according to 9, wherein the second aromatic diamine is selected from the group consisting of 4,4'-diaminodiphenyl ether, 3,4'-diaminodiphenyl ether, 2,2'-bis(trifluoromethyl)benzidine, m-phenylenediamine, and 4,4'-diaminodiphenylmethane. 11. The multilayer film according to claim 1, wherein the core layer further comprises both a second aromatic dianhydride and a second aromatic diamine. 12. The multilayer film according to claim 1, wherein the polyimide of the core layer contains at least 80 mole percent of 3,3',4,4'-biphenyltetracarboxylic dianhydride based on the total dianhydride content of the polyimide, and at least 80 mole percent of p-phenylenediamine based on the total diamine content of the polyimide. 13. The multilayer film according to claim 1, wherein the multilayer film has a coefficient of thermal expansion of less than 25 μm / (meter-°C) over a temperature range of 50 to 400°C. 14. The first thermoplastic polyimide and the second thermoplastic polyimide each have a temperature range of 150 to 320°C. g A multilayer film according to claim 1, having the following characteristics. 15. The multilayer film according to claim 1, wherein the multilayer film has a transmittance of at least 50% and a degree of cloudiness of less than 30%. 16. The multilayer film according to claim 1, wherein the multilayer film has a total thickness in the range of 5 to 75 μm. 17. The multilayer film according to claim 1, wherein the minimum peel strength of each of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm). 18. The multilayer film according to claim 1, wherein the thickness of the core layer is in the range of 55 to 73% of the total thickness of the multilayer film. 19. A metal-clad laminate comprising the multilayer film described in 1 above and a first metal layer adhered to the outer surface of the first outer layer of the multilayer film. 20. The metal-clad laminate according to 19, further comprising a second metal layer adhered to the outer surface of the second outer layer of the multilayer film.

Claims

1. A first outer layer comprising a first thermoplastic polyimide; A core layer comprising a polyimide, wherein the polyimide comprises a first aromatic dianhydride containing 3,3',4,4'-biphenyltetracarboxylic acid dianhydride and a first aromatic diamine containing p-phenylenediamine; A second outer layer containing a second thermoplastic polyimide and A multilayer film comprising, The core layer further comprises a second aromatic dianhydride, The multilayer film has a total thickness in the range of 5 to 150 μm; the thickness of the core layer is in the range of 35 to 73% of the total thickness of the multilayer film; The minimum peel strength of at least one of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B; and, The multilayer film has a thermal expansion coefficient of less than 25 μm / (meter-°C), a transmittance of at least 50%, and a cloudiness of less than 30% over a temperature range of 50 to 400°C. The copper foil is a rolled and annealed copper foil, or a copper foil that has been chemically or mechanically treated. Multilayer film.

2. The first thermoplastic polyimide is Aromatic dianhydrides selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, and mixtures thereof; Aromatic diamines selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, 2,2-bis-(4-[4-aminophenoxy]phenyl)propane, and mixtures thereof, A multilayer film according to claim 1, comprising:

3. The aromatic dianhydride includes pyromellitic dianhydride and 4,4'-oxydiphthalic dianhydride; The aromatic diamine includes 1,3-bis(4-aminophenoxy)benzene, The multilayer film according to claim 2.

4. The second thermoplastic polyimide is Aromatic dianhydrides selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-biphenyltetracarboxylic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, and mixtures thereof; Aromatic diamines selected from the group consisting of 1,3-bis(4-aminophenoxy)benzene, hexamethylenediamine, and mixtures thereof, A multilayer film according to claim 1, comprising:

5. The aromatic dianhydride includes pyromellitic dianhydride and 4,4'-oxydiphthalic dianhydride; The aromatic diamine includes 1,3-bis(4-aminophenoxy)benzene, The multilayer film according to claim 4.

6. The multilayer film according to claim 1, wherein the first thermoplastic polyimide and the second thermoplastic polyimide are the same.

7. The multilayer film according to claim 1, wherein the second aromatic dianhydride is selected from the group consisting of 4,4'-oxydiphthalic acid dianhydride, pyromellitic acid dianhydride, 3,3',4,4'-benzophenonetetracarboxylic acid dianhydride, bisphenol A dianhydride, 1,2,5,6-naphthalenetetracarboxylic acid dianhydride, 1,4,5,8-naphthalenetetracarboxylic acid dianhydride, and 2,3,6,7-naphthalenetetracarboxylic acid dianhydride.

8. The multilayer film according to claim 1, wherein the core layer further comprises a second aromatic diamine.

9. The multilayer film according to claim 1, wherein the core layer further comprises both a second aromatic dianhydride and a second aromatic diamine.

10. The multilayer film according to claim 1, wherein the polyimide of the core layer contains at least 80 mole percent of 3,3',4,4'-biphenyltetracarboxylic dianhydride and at least 80 mole percent of p-phenylenediamine based on the total diamine content of the polyimide.

11. The first thermoplastic polyimide and the second thermoplastic polyimide each have a temperature range of 150 to 320°C. g A multilayer film according to claim 1, having the following characteristics.

12. The multilayer film according to claim 1, wherein the multilayer film has a total thickness in the range of 5 to 75 μm.

13. The multilayer film according to claim 1, wherein the minimum peel strength of each of the first and second outer layers is greater than 0.9 kgf / cm (0.88 N / mm) when bonded to a copper foil and tested according to ASTM Method IPC-TM-650, Method No. 2.4.9B.

14. The multilayer film according to claim 1, wherein the thickness of the core layer is in the range of 55 to 73% of the total thickness of the multilayer film.

15. A metal-clad laminate comprising a multilayer film according to claim 1 and a first metal layer bonded to the outer surface of the first outer layer of the multilayer film.

16. The metal-clad laminate according to claim 15, further comprising a second metal layer adhered to the outer surface of the second outer layer of the multilayer film.

Images