Multifunctional crosslinking agent, crosslinked polymer, and method of making same

Abstract

A multifunctional crosslinking agent, a crosslinked polymer, and a method of making the same are disclosed. The multifunctional crosslinking agent, which may be used to crosslink amine-terminated polyamides, polyimides, or poly(amide-imide)s, includes three or four anhydride functional groups. The multifunctional crosslinking agent may be defined by a general chemical formula (I): (ZAr).sub.nW, wherein W represents an anhydride functional group that is directly or indirectly bonded to Ar; Ar represents an aryl group that is directly bonded to W; and n is equal to 3 when W is PO or N, or n is equal to 4 when W is Si or a carbon moiety.

Claims

1. A multifunctional crosslinking agent comprising a plurality of anhydride functional groups, and defined by a chemical formula (I):
(ZAr).sub.nW(I) wherein Z represents an anhydride functional group that is directly bonded to Ar; Ar represents an aryl-ether group that is directly bonded to W; and n is equal to 3 when W is PO or N, or n is equal to 4 when W is Si or a carbon moiety.

2. The multifunctional crosslinking agent of claim 1, wherein W is PO.

3. The multifunctional crosslinking agent of claim 1, wherein W is N.

4. The multifunctional crosslinking agent of claim 1, wherein W is the carbon moiety.

5. The multifunctional crosslinking agent of claim 1, wherein W is Si.

6. The multifunctional crosslinking agent of claim 1, wherein Ar is an oxyphenylene group (OPh-) that is para- or meta-substituted with respect to oxygen, and the agent is further defined by a formula (II):
(ZOPh).sub.n-W.

7. The multifunctional crosslinking agent of claim 1, wherein Z is an aromatic anhydride.

8. The multifunctional crosslinking agent of claim 7, wherein the aromatic anhydride is a phthalic anhydride or a naphthalic anhydride.

9. The multifunctional crosslinking agent of claim 1, wherein Ar is an oxyphenylene group (OPh-) that is para- or meta-substituted with respect to oxygen, and wherein Z is a phthalic anhydride group that is connected to the oxyphenylene group through an ether bond.

10. The multifunctional crosslinking agent of claim 1, wherein W is PO, wherein Ar is an oxyphenylene group (OPh-) that is para- or meta-substituted with respect to oxygen, and wherein the agent is further defined by a formula (III):
(ZOPh).sub.3-PO.

11. The multifunctional crosslinking agent of claim 10, wherein Z is a phthalic anhydride group that is connected to the oxyphenylene group through the ether bond, and wherein the agent is further defined by a formula (IV): ##STR00013## wherein R.sup.1 through R.sup.8 are independently selected from H or C1-C4 alkyl.

12. The multifunctional crosslinking agent of claim 11, wherein the agent is selected from tris[3-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide trianhydride or tris[4-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide trianhydride.

13. The multifunctional crosslinking agent of claim 1, wherein W is N, wherein Ar is an oxyphenylene group (OPh-) that is para- or meta-substituted with respect to oxygen, and wherein the agent is further defined by a general formula (V):
(ZOPh).sub.3-N.

14. The multifunctional crosslinking agent of claim 13, wherein Z is a phthalic anhydride group that is connected to the oxyphenylene group through the ether bond, and wherein the agent is further defined by a general formula (VI): ##STR00014## wherein R.sup.1 through R.sup.8 are independently selected from H or C1-C4 alkyl.

15. The multifunctional crosslinking agent of claim 14, wherein the agent is selected from tris[3-(3,4-dicarboxyphenoxy)phenyl]amine trianhydride or tris[4-(3,4-dicarboxyphenoxy)phenyl]amine trianhydride.

16. A crosslinked polymer composition comprising an amino-terminated polymer selected from a polyamide, a polyimide, a poly(amide-imide), or mixtures thereof, which is cross-linked by the multifunctional cross-linking agent of claim 1.

17. The crosslinked polymer composition of claim 16, wherein the polyamide is a polymerization reaction product of a diamine with a dicarboxylic acid, a diacid halide, or a combination thereof; and wherein the diamine is reacted in a stoichiometric excess relative to the dicarboxylic acid, the diacid halide, or a sum total of the combination thereof.

18. The crosslinked polymer composition of claim 16, wherein the polyimide is a polymerization reaction product of a diamine with a dianhydride; and wherein the diamine is reacted in a stoichiometric excess relative to the dianhydride.

19. The crosslinked polymer composition of claim 16, wherein the polyimide is a polymerization reaction product of a diamine with 1) a trimellitic anhydride, a diacid derivative of trimellitic acid, or trimellitic acid, or 2) a dianhydride, and a dicarboxylic acid, a diacid halide, or a combination thereof; and wherein the diamine is reacted in a stoichiometric excess relative to a sum total of 1) or 2).

20. The crosslinked polymer composition of claim 16, wherein the poly(amide-imide) is a polymerization reaction product of a diamine with 1) diimide-dicarboxylic acid monomer, and/or 2) a diamide-dianhydride monomer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and, together with the summary given above, and the detailed description given below, serve to explain the invention.

(2) FIG. 1 illustrates an exemplary synthetic scheme toward producing phosphine oxide-based tri-anhydride crosslinking agent 1a,b and amine-based tri-anhydride crosslinking agent 2a,b;

(3) FIG. 2 illustrates an exemplary synthetic scheme for producing amine-based tri-anhydride crosslinking agent 3;

(4) FIG. 3 illustrates an exemplary synthetic scheme toward producing carbon-based tetra-anhydride crosslinking agent 4a,b;

(5) FIG. 4 illustrates an exemplary synthetic scheme toward producing silicon-based and sp.sup.3 hybridized carbon-based tetra-anhydride crosslinking agents, 5a and 5c, respectively;

(6) FIG. 5 illustrates exemplary synthetic schemes toward producing diimide-dicarboxylic acid monomers and diamide-dianhydride monomers useful for synthesizing poly(amide-imide)s; and

(7) FIG. 6 illustrates an exemplary synthetic scheme toward producing crosslinked polyimides using an exemplary phosphine oxide-based tri-anhydride crosslinking agent 1a.

DETAILED DESCRIPTION OF THE INVENTION

(8) Embodiments of the present invention overcome an existing need in the prior art by providing a multi-anhydride crosslinking agent, which is suitable to crosslink polyimide, polyamide, and poly(amide-imide) polymers. Accordingly, the composition and synthesis of a new family of multi-anhydride containing crosslinking agents, as well as the corresponding crosslinked polymers, are described herein. The disclosed crosslinking agents are useful toward imparting shape-memory effects to heat-resistant polymers, (e.g., polyimides, polyamides and poly(amide-imides). More specifically, embodiments of the present invention relate to multi-anhydride compounds that may be used to crosslink polyimides, polyamides, and poly(amide-imides) to create covalent network structure that results in shape memory effects at elevated temperatures.

(9) Multi-Anhydride Crosslinking Agents

(10) In accordance with embodiments of the present invention, a multifunctional crosslinking agent is provided that has three or four anhydride functional groups (i.e., tri-anhydride crosslinking agents or tetra-anhydride crosslinking agents, respectively). The multifunctional crosslinking agents may be defined by the general chemical formula (I): Z(Ar).sub.nW, wherein Z represents an anhydride functional group that is directly or indirectly bonded to Ar; wherein Ar represents an aryl group that is directly bonded to W; and wherein n is equal to 3 when W is N or PO, or n is equal to 4 when W is Si or an sp.sup.3 hybridized carbon moiety. Accordingly, the tri-anhydride crosslinking agents may be Z(Ar).sub.3N or Z(Ar).sub.3PO; and the tetra-anhydride crosslinking agents may be Z(Ar).sub.4Si or Z(Ar).sub.4R, where R represents the carbon moiety (e.g., fluorenyl).

(11) In accordance with an aspect of the invention, the aryl group (Ar), which is directly bonded to W through a carbon atom, may be a phenyleneoxy group (OPh-) that is para- or meta-substituted with respect to oxygen, and thus the agent may be further defined by the general chemical formula (II): Z(OPh-).sub.nW. In one embodiment, the phenyleneoxy group represents that the benzene ring portion may unsubstituted (i.e., OC.sub.6H.sub.4); alternatively, the phenyleneoxy group may have substituents (e.g., C1-C4 alkyl groups) around the benzene ring. In one example, where W is PO, the agent may be further defined by the general chemical formula (III): Z(OPh-).sub.3-PO.

(12) In accordance with another aspect, the aryl group (Ar) may be a phenyleneoxy group (OPh-) that is para- or meta-substituted with respect to oxygen, and Z may be a phthalic anhydride group that is connected to the phenyleneoxy group through an ether bond. Accordingly, the agent may be further defined by the general chemical formula (IVa):

(13) ##STR00001##
wherein W and n are as defined above, and R.sup.1 through R.sup.8 are independently selected from H or C1-C4 alkyl. Where W is PO, these phosphine oxide-based crosslinking agents may be defined by the general chemical formula (IV):

(14) ##STR00002##
As shown in Table 1 (below), where R.sup.1 to R.sup.3 and R.sup.5 to R.sup.8 are H, an exemplary phosphine oxide-based crosslinking agent is tris[4-(3,4-dicarboxyphenoxy)phenyl] phosphine oxide tri-anhydride (1a). An isomeric phosphine oxide-based crosslinking agent to (1a) is its meta-isomer, which is tris[3-(3,4-dicarboxyphenoxy)phenyl] phosphine oxide tri-anhydride (i.e., R.sup.1 to R.sup.4 and R.sup.6 to R.sup.8 are H, see FIG. 1, agent 1b).

(15) The synthesis of the para- and meta-isomers of (1a,b) are depicted in FIG. 1. The synthesis of the para-isomer of triphenylphosphine oxide tri-anhydride (i.e., 1a) has been accomplished in 5-steps starting from commercially available tris(4-methoxyphenyl)phosphine oxide and experimental details are provided in the Examples. Briefly and with reference to FIG. 1, tris(4-methoxyphenyl)phosphine (12) was oxidized to tris(4-methoxyphenyl)phosphine oxide (13). While BBr.sub.3 may be used to de-methylate compound (13), demethylation with pyridine hydrochloride above its melting point was observed to be more effective and cleaner. Nucleophilic substitution reaction of the resulting tris(4-hydroxyphenyl)phosphine oxide (14) with 4-nitro-phthalonitrile (15) after deprotonation in situ by potassium carbonate) in DMF afforded the corresponding tris(ether di-nitrile) compound, namely tris[4-(3,4-dicyanophenoxy)phenyl]phosphine oxide (16). Upon subsequent alkaline hydrolysis, (16) was converted to the corresponding tris(ether diacid) (17), which was then cyclo-dehydrated to produce the desired tri-anhydride monomer (1a). The meta,meta,meta-isomer (1b) of crosslinker (1a) can be prepared following the same synthetic sequence starting from tris(3-methoxyphenyl)phosphine (12b).

(16) In accordance with yet another aspect, where W is N, and where the aryl group (Ar) is the phenyleneoxy group (OPh-), which is para- or meta-substituted with respect to oxygen, a tertiary amine-based crosslinking agent may be defined by the general chemical formula (V): Z(OPh-).sub.3N. In another embodiment, where Z is the phthalic anhydride group that is connected to the phenyleneoxy group through an ether bond, exemplary tertiary amine-based crosslinking agents may be defined by the general chemical formula (VI):

(17) ##STR00003##
As shown in Table 1 (below), where R.sup.1 to R.sup.3 and R.sup.5 to R.sup.8 are H, an exemplary tertiary amine-based crosslinking agent is tris[4-(3,4-dicarboxyphenoxy)phenyl]amine tri-anhydride (2a). An isomeric tertiary amine-based crosslinking agent to compound (2a) is its meta-isomer, which is tris[3-(3,4-dicarboxyphenoxy)phenyl]amine tri-anhydride (i.e., R.sup.1 to R.sup.4 and R.sup.6 to R.sup.8 are H, see FIG. 1, agent (2b)).

(18) An amenable synthesis for the para- and meta-isomers of (2a,b) is also depicted in FIG. 1. Starting from tris(4-methoxyphenyl)amine or tris(3-methoxyphenyl)amine, the desired tri-anhydride tertiary amine-based crosslinking agents (2a,b) may be realized.

(19) In accordance with yet another aspect where W is nitrogen (N), and where Z and Ar from Formula (I) in combination form a phthalic anhydride moiety that is directly bonded to nitrogen, this tertiary amine-based crosslinking agent may be defined by the general formula (VII):

(20) ##STR00004##
wherein R.sup.9 to R.sup.11 are independently selected from H or C1-C4 alkyl. As shown in Table 1 (below), where R.sup.9 through R.sup.11 are H, an exemplary tertiary amine-based crosslinking agent is tris(phthalic anhydride)amine (3) (see also FIG. 2).

(21) As shown in FIG. 2, an amenable synthetic sequence toward making tris(phthalic anhydride)amine (3) starts with a two-step imidization reaction of commercially available 4-halophthalic anhydride (18, XCl or Br) and/or 4-nitrophthalic anhydride (18, XNO.sub.2) with aniline in a polar solvent, followed by addition of acetic anhydride and trimethylamine, which would afford the 4-substituted N-phenylphthalimide compound (19). For compound (19), (with XNO.sub.2), the nitro group can be reduced under standard hydrogenation conditions to afford N-phenyl 4-aminophthalimide (20). Following a method derived from Wenmu Li et al. (Macromolecules 2007, 40, 8205-8211), 4-aminophthalimide (20) can be twice N-arylated with two equivalents of N-phenyl-4-halophthalimide (19, XCl or Br) with an in situ-generated catalyst from palladium acetate, and a phosphine ligand. For N-phenyl-4-bromo-phthalimide, a preferred phosphine ligand is BINAP=2,2-bis(diphenylphosphino)-1,1-binaphthyl, and for N-phenyl-4-chlorophthalimide, a preferred phosphine ligand is tert-butyldiphenylphosphine (.sup.tBuPh.sub.2P). The resulting tris(phthalimide)amine intermediate (21) can be readily hydrolyzed under alkaline conditions to generate the corresponding tris(phthalic acid)amine intermediate (22), which upon treatment with acetic anhydride/acetic/heat will lead to the desired tri-anhydride crosslinking agent (3).

(22) TABLE-US-00001 TABLE 1 Exemplary Multi-Anhydride Crosslinking Agents Tri-anhydride crosslinkers Tetra-anhydride crosslinkers

(23) In accordance with another embodiment, complementary tetra-anhydride crosslinking agents include where W (in Formulas (I), (II), and (IVa)) is a carbon moiety, and thus n is 4. Further, exemplary carbon-based tetra-anhydride crosslinking agents (4a), (4b), and 5(c) are also shown in Table 1. The carbon moiety may include a centralized sp.sup.3 hybridized carbon to provide a generally tetrahedral geometry to the agent. For example, agents 4a and 4b include a fluorenyl group, where the C9 carbon of the fluorenyl group is sp.sup.3 hybridized.

(24) Amenable synthetic sequences toward making crosslinking agents 4a, 4b are provided in FIG. 3. For tetra-anhydride (4a), the synthesis can start with the Ullmann reaction between 2,7-dibromofluorene (23) and excess sodium methoxide and CuI catalyst, preferably in neat mixture form and with high temperature heating (200 C.) to generate the corresponding dimethoxylated fluorene (24). Following a method based on the work of Xiao Cao et al. (Organic Letters (2013), 15(12), 3102-3105), 2,7-dimethoxyfluorene (25) is subsequently doubly arylated via sp.sup.3C-sp.sup.2C cross-coupling reaction at the C-9 position of fluorene with 4-bromoanisole and the aid of a palladium catalyst in the presence of potassium t-butoxide to afford the corresponding methoxylated spiro-9,9-bifluorene compound 26a (n=0). Then, the tetra-phenol intermediate (27a) can be readily obtained by demethylation with aqueous HBr or pyridinium hydrochloride and heat. A subsequent aromatic nitro-displacement reaction of 4-nitrophthalonitrile (4 equivalents) with the corresponding potassium salt of the tetra-phenol intermediate (27a) leads to the formation of the tetrakis(4-oxyphthalonitrile) compound (28a), which upon hydrolysis is converted to the corresponding tetrakis(4-oxyphthalic acid) precursor (29a). The latter compound, upon treatment with acetic anhydride/acetic acid, leads to the desired carbon-based tetra-anhydride crosslinking agent (4a).

(25) Tetra-anhydride (4b) can be prepared similarly from 2,7-dibromofluorene (23) by following the same synthetic sequence, except for the first (Ullmann reaction) step, which is replaced by a Suzuki cross-coupling reaction with 4-methoxphenylboronic acid or its pinacol boronate ester, a suitable Pd-catalyst, and a base to generate the corresponding 2,7-bis(4-methoxyphenyl)fluorene compound (25).

(26) As also shown in Table 1, the complementary tetra-anhydride crosslinking agents include where W (in Formulas (I), (II), and (IVa)) is silicon or an sp.sup.3 hybridized carbon, and thus n is 4. Further, exemplary silicon-based (5a and 5b, E=Si) or sp.sup.3 hybridized carbon-based (5c and 5d, E=C) tetra-anhydride crosslinking agents are also shown in Table 1.

(27) With respect to the silicon-based tetra-anhydride crosslinking agents with four para-phenyleneoxy linkages (5a), an amenable synthetic sequence toward making these agents is shown in FIG. 4. The synthesis of tetra-anhydride (5a) starts with a reaction between tetrachlorosilane (30) and either a Grignard reagent generated from Mg metal and 4-bromoanisole or a lithiated anisole from n-butyllithium and 4-bromoanisole (31) (4 equivalents), following the method of Hao Yu, et al. (Macromolecules, 2012, 45(12), 5140-5150). Then, the intermediate (33) (E=Si), i.e. tetrakis(4-hydroxyphenyl)silicon, can be readily obtained by demethylation of tetrakis(4-hydroxyphenyl)silicon (32) with aqueous HBr or pyridinium hydrochloride and heat, or preferably with BBr.sub.3 in a chlorinated solvent at room or colder temperature. A subsequent aromatic nitro-displacement reaction of 4-nitrophthalonitrile (4 equivalents) with the corresponding potassium salt of the tetrakis(4-hydroxyphenyl) intermediate (33) leads to the formation of the tetrakis(4-oxyphthalonitrile) compound (34), which upon hydrolysis is converted to the corresponding tetrakis(4-oxyphthalic acid) precursor (35). The latter compound, upon treatment with acetic anhydride/acetic acid leads to the desired silicon-based tetra-anhydride crosslinking agent (5a).

(28) The isomeric (5b) (E=Si, with four meta-phenyleneoxy linkages) can be synthesized following a similar synthetic path except with the substitution of para-phenyleneoxy reagent with the meta-phenyleneoxy reagent in the first of the synthetic scheme shown in FIG. 4. Accordingly, 3-bromoanisole, instead of 4-bromoanisole, is used in the generation of Grignard or aryllithium reagent, which is subsequently reacted with tetrachlorosilane (30).

(29) As shown in FIG. 4, the latter part of the synthetic route from the requisite intermediate (33) (E=C, tetrakis(4-hydroxyphenyl)methane) onward to the carbon-based tetra-anhydride, (5c) (E=C), is similar to that for the silicon-based counterparts, (5a) and (5b). Thus, following the method of J. Lu and J. Zhang (Journal of Materials Chemistry A: Materials for Energy and Sustainability (2014), 2(34), 13831-13834), the synthesis of tetrakis(4-hydroxyphenyl)methane starts with the conversion of readily available 4-aminophenyltriphenylmethane (36) to tetraphenylmethane (37) via sequential diazotization reaction with isopentyl nitrile/H.sub.2SO.sub.4 in ethanol, followed by reduction with the aid of hypophosphorous acid. Nitration of tetraphenylmethane, followed by catalytic hydrogenation of the resultant tetrakis(4-nitrophenyl)methane (38) by Raney nickel and hydrazine monohydrate leads to tetrakis(4-aminophenyl)methane (39). Finally, following the method of E. Diez-Barra et al. (Tetrahedron 60 (2004) 1563-1569), diazotization of all the amino groups of 39, followed by acid hydrolysis would provide tetrakis(4-hydroxyphenyl)methane.

(30) Crosslinked Polymers

(31) Because of the similar polymerization chemistry to generate polyimides, polyamides, and poly(amide-imides), the multi-anhydride compounds disclosed herein may be used to crosslink these classes of polymers to create covalent network structures capable of showing shape memory effects at elevated temperatures.

(32) Synthesis of a polyimide is typically accomplished by polymerization of a diamine and a dianhydride in a 1:1 molar ratio to generate a poly(amic acid) precursor, which is then converted to the corresponding polyimide typically by either thermal cure (e.g., by heating to >200 C. in solution or solid state) or chemical imidization using a dehydrating agent or promoter such as acetic anhydride/triethylamine or acetic anhydride/pyridine. To generate a polyimide having the desired amount of crosslinking, an amine-terminated poly(amic acid) precursor is first generated by off-setting the dianhydride:diamine ratio so that the amount of diamine is in excess to cap both ends of the poly(amic acid) precursor. An appropriate amount of a multi-anhydride crosslinking agent is then added to the precursor solution so that all or substantially all of the terminal amine groups will be consumed. Crosslinked polyimides may then be created using appropriate imidization conditions.

(33) In accordance with an aspect of the polymer, the diamine monomer comprises an aromatic diamine, which includes, but is not limited to, 1,3-bis(3-aminophenoxy)benzene (APB); 1,4-bis(3-aminophenoxy)benzene; 1,2-bis(3-aminophenoxy)benzene; 1,2-bis(4-aminophenoxy)benzene; 1,3-bis(4-aminophenoxy)benzene; 1,4-bis(4-aminophenoxy)benzene; 3,4-oxydianiline; 4,4-oxydianiline; 1,3-diamino-4-methylbenzene; 1,3-diamino-4-(trifluoromethyl)benzene; 2,4-diaminobiphenyl; 2,2-bis(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropane; 2,2-bis(4-aminophenyl)propane; 2,2-bis[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane; 2,2-bis[4-(4-aminophenoxy)phenyl]propane; or a mixture of thereof.

(34) In accordance with another aspect, the dianhydride monomer includes, but is not limited to 2,2-[bis(4-phthalic anhydrido)]-1,1,1,3,3,3-hexafluoroisopropane (6FDA); 4,4-oxybis(phthalic anhydride); 3,3,4,4-diphenylsulfone tetracarboxylic dianhydride; 3,3,4,4-benzophenone tetracarboxylic dianhydride; 4,4-(2,2,2-trifluoro-1-phenylethylidene)bis[phthalic anhydride]; 2,2-bis[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride; 4,4-(p-phenylenedioxy)bis[phthalic anhydride]; 4,4-(m-phenylenedioxy)bis[phthalic anhydride]; 4,4-(o-phenylenedioxy)bis[phthalic anhydride]; or mixtures thereof.

(35) In accordance with an embodiment, the cross-linked polyimides of the present invention may be defined by the following general chemical formula (VIII):

(36) ##STR00010##
where W may be PO, N, Si, or a carbon moiety (e.g., fluorenyl); wherein L denotes either a direct covalent bond to W or a linking group (e.g., a phenyleneoxy group) for indirect bonding to W; n,m,l denote the degree of polymerization (DP) of each branch of polyimide, which may be of the same or different values, with the DP range of about 3 to about 30. For example, in an embodiment, DP is in a range of about 5 to about 25, or about 10 to about 20. The overall network structure is denoted by the infinity symbol (Do). The linking group Y is one of the following moieties: C(CF.sub.3).sub.2, O, SO.sub.2, C(O), -(Ph)C(CF.sub.3), OPh-C(CF.sub.3).sub.2OPh-, OPh-C(CH.sub.3).sub.2OPh-. In another embodiment, Y is C(CF.sub.3).sub.2.

(37) In accordance with another embodiment, the cross-linked polyimides may be defined by the following general chemical formula (IX):

(38) ##STR00011##
where W may be N or PO; L, n, m, l, and Y are as defined above.

(39) In accordance with yet another embodiment, the cross-linked polyimides may be defined by the following general chemical formula (X):

(40) ##STR00012##
where W is N or benzene-1,3,5-trioxy (1,3,5-C.sub.6H.sub.3O.sub.3); and n, m, l, and Y are as defined above.

(41) Synthesis of a polyamide is typically accomplished by two general methods. A first method involves polymerization of a diamine and a diacid halide (e.g., chloride) in a 1:1 molar ratio in an amide solvent such as N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAc), N-methylpyrrolidone (NMP), etc. However, to generate a polyamide having the desired amount of crosslinking, an amino-terminated polymer is first generated by off-setting the diacid halide:diamine ratio so that the amount of diamine is in excess to cap both ends of the polymer. Subsequent addition of a multi-anhydride crosslinking agent in appropriate amounts to the amino-terminated polymer so that all or substantially all of the terminal amine groups are consumed, immediately followed by casting and thermal curing under reduced pressure, leads to the crosslinked polyamide films.

(42) A second method of synthesizing a polyamide involves polymerization of a diamine and a dicarboxylic acid with the aid of a promoter/catalyst combination such as triethylphosphite/pyridine (via Yamazaki-Higashi reaction) in an amide solvent such as N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAc), N-methylpyrrolidone (NMP), etc. However, to generate a polyamide having the desired amount of crosslinking, an amino-terminated polymer is first generated by off-setting the diacid:diamine ratio so that the amount of diamine monomer is in excess to cap both ends of the polymer. After the amino-terminated polyamide has been isolated by precipitation in water and filtration, it is washed (e.g. water and/or methanol) and dried. It is then dissolved in an amide solvent and mixed with an amide solution of a multi-anhydride crosslinking agent in an appropriate amount so that all or substantially all of the terminal amine groups are consumed, which is subsequently followed by casting and thermal curing under reduced pressure to create crosslinked polyamide films.

(43) Similar to the polyimides, the diamine of the polyamides may include, but not limited to, an aromatic diamine, such as 1,3-bis(3-aminophenoxy)benzene (APB); 1,4-bis(3-aminophenoxy)benzene; 1,2-bis(3-aminophenoxy)benzene; 1,2-bis(4-aminophenoxy)benzene; 1,3-bis(4-aminophenoxy)benzene; 1,4-bis(4-aminophenoxy)benzene; 3,4-oxydianiline; 4,4-oxydianiline; 1,3-diamino-4-methylbenzene; 1,3-diamino-4-(trifluoromethyl)benzene; 2,4-diaminobiphenyl; 2,2-bis(4-aminophenyl)-1,1,1,3,3,3-hexafluoropropane; 2,2-bis(4-aminophenyl)propane; 2,2-bis[4-(4-aminophenoxy)phenyl]-1,1,1,3,3,3-hexafluoropropane; 2,2-bis[4-(4-aminophenoxy)phenyl]propane; or a mixture of thereof. Exemplary diacid halide monomers include, but are not limited to, isophthaloyl chloride; terephthaloyl acid; 4,4-oxydibenzoyl chloride; 3,4-oxydibenzoyl chloride; 3,3-oxydibenzoyl chloride; 4,4-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis(benzoyl chloride); 4,4-(1-methylethylidene) bis(benzoyl chloride); 4,4-(9H-fluoren-9-ylidene)bis(benzoyl chloride); or a mixture thereof.

(44) Exemplary dicarboxylic acid monomers include, but are not limited to, isophthalic acid, terephthaloyl acid; 4,4-oxydibenzoic acid; 3,4-oxydibenzoic acid; 3,3-oxydibenzoic acid; 4,4-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis(benzoic acid); 4, 4-(1-methylethylidene)bis-benzoic acid; 4,4-(9H-fluoren-9-ylidene)bis(benzoic acid); or a mixture thereof.

(45) The synthesis of a poly(amide-imide) is typically accomplished by polymerization of i) a diamine and a trimellitic anhydride (TMA) or trimellitic anhydride acid chloride (TMAC); or ii) a diamine and a diimide-dicarboxylic acid monomer derived from a selective condensation of TMA and an aromatic diamine (e.g., H.sub.2NArNH.sub.2) (see FIG. 5). When acid monomers are used, the polymerization process is aided by triethylphosphite/pyridine (Yamazaki-Higashi reagent) in a 1:1 molar ratio in an amide solvent such as N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAc), N-methylpyrrolidone (NMP), etc.

(46) Persons having ordinary skill in the art will appreciate that these polymerization methods may be applied to other dianhydride monomers containing preformed aromatic amide moieties. For example, bis(phthalic anhydride) monomers with preformed amide as part of the linking group, which are also known as diamide-dianhydrides, can be prepared from trimellitic anhydride acid chloride (TMAC) and an aromatic diamine (e.g., H.sub.2NArNH.sub.2) in refluxing acetone with pyridine as HCl scavenger (see FIG. 5).

(47) However, to generate a poly(amide-imide) having the desired amount of crosslinking, it is more suitable that an amino-terminated poly (amide-imide) is first generated via Yamazaki-Higashi reaction by off-setting TMA:diamine ratio so that the amount of diamine is in excess to cap both ends of the polymer. After the amino-terminated polyamide has been isolated by precipitation in methanol and filtration, it is washed with methanol and dried (e.g., in vacuo at 200 C. overnight). The amino-terminated polyamide is then dissolved in an amide solvent and mixed with an amide solution of a multi-anhydride crosslinking agent in an appropriate amount so that all or substantially all of the terminal amine groups are consumed, which is immediately followed by casting and thermal curing under reduced pressure to create crosslinked poly(amide-imide) films.

(48) The following examples and methods are presented as illustrative of the present invention or methods of carrying out the invention, and are not restrictive or limiting of the scope of the invention in any manner.

EXAMPLES

Example 1

Tris(4-methoxyphenyl)phosphine Oxide (13a)

(49) Into a 100 mL three-necked flask equipped with a magnetic stir bar and nitrogen inlet and outlet were placed commercially available tris(4-methoxyphenyl)phosphine ((12a), 3.0 g, 8.5 mmol) and acetone (30 mL). A mixture of water (2 mL) and H.sub.2O.sub.2 (35%, 1 mL, 9 mmol) was added slowly. After the mixture was stirred at room temperature for 1 h, acetone was evaporated and methylene chloride (50 mL) was added. The organic phase was washed with a saturated NaCl solution (35 mL) three times. The organic layer was dried over sodium sulfate. The solvent was removed under vacuum to afford 3.0 g (95%) of a white solid, m.p. 144.7-145.4 C. (lit. 143-144 C.). MS (m/e): 368 (M.sup.+). Anal. Calcd. for C.sub.21H.sub.21O.sub.4P: C, 68.47%; H, 5.75%; P, 8.41%. Found: C, 68.42%; H, 5.72%; P, 8.11%. FT-IR (KBr, cm.sup.1): 3068, 3026, 2959, 2837, 1597, 1569, 1503, 1468, 1289, 1254, 1179, 1121, 1019, 803, 671, 543. .sup.1H-NMR (CDCl.sub.3, 8 in ppm): 3.84 (s, 6H, CH.sub.3), 6.94-6.97 (dd, 6H, ArH), 7.54-7.60 (dd, 6H, ArH). .sup.13C-NMR (DMSO-d.sub.6, in ppm): 55.29, 114.08, 114.21, 124.19, 125.28, 133.21, 133.32, 161.79, 161.822

Example 2

Tris(4-hydroxyphenyl)phosphine Oxide (14a)

(50) Into a 500 mL 3-neck round bottom flask equipped with stir bar, nitrogen inlet and condenser was charged tris(4-methoxyphenyl)phosphine oxide ((13a), 25.0 g, 67.9 mmol) followed by pyridine hydrochloride (250 g). The mixture was heated to 210 C. for 2 hours and allowed to cool to about 100 C. It was poured into water to afford 21.0 g (95.0%) of white crystals. m.p.: 274.8-276.8 C. (lit. 275-276 C.). The product was used without further purification. Anal. Calcd. for C.sub.18H.sub.15O.sub.4P: C, 66.26%; H, 4.63%; P, 9.49%; Found: C, 65.72%; H, 4.68%; P, 9.59%. .sup.1H-NMR (DMSO-d.sub.6, in ppm): 6.84-6.86 (dd, 6H, ArH), 7.30-7.45 (dd, 6H, ArH), 10.07 (s, 3H, ArOH). .sup.13C-NMR (DMSO-d.sub.6, 8 in ppm): 115.32, 115.45, 122.59, 123.69, 133.29, 133.40, 160.28, 160.30.

Example 3

Tris[4-(3,4-dicyanophenoxy)phenyl]phosphine Oxide (16a)

(51) Into a 500 mL 3-neck round bottom flask equipped with stir bar, condenser, and nitrogen inlet were charged tris(4-hydroxyphenyl)phosphine oxide ((14a) 8.13 g, 25.0 mmol), 4-nitrophthalonitrile ((15), 13.0 g, 75.0 mmol), K.sub.2CO.sub.3 (11.5 g, 85.5 mmol), and DMF (150 mL). The mixture was heated at 50 C. for 24 h. Then it was poured into distilled water. The organic layer was extracted with ethyl acetate 3 times and dried over magnesium sulfate. The mixture was filtered and the filtrate was dried on a rotary evaporator afford 15.8 g (81%) of a yellow powder. m.p. 205.0-206.6 C. m.p. 127.6-132.8 C. The yellow powder was further purified by slurrying in ethyl acetate. m.p. 138.1-139.4 C. Anal. Calcd. for C.sub.42H.sub.21N.sub.6O.sub.4P: C, 71.59%; H, 3.00%; N, 11.93%. Found: C, 71.41%; H, 2.99%; N, 11.59%. .sup.1H-NMR (DMSO-d.sub.6, in ppm): 7.33-7.35 (dd, 6H, ArH), 7.54-7.57 (dd, 3H, ArH), 7.73-7.78 (dd, 6H, ArH), 7.95-7.96 (d, 3H, ArH) 8.14-8.16 (d, 3H, ArH). .sup.13C-NMR (DMSO-d.sub.6, in ppm): 109.40, 115.28, 115.77, 116.87, 119.78, 119.90, 128.47, 129.53, 134.19, 134.30, 136.30, 136.40, 157.41, 157.44, 159.59.

Example 4

Tris[4-(3,4-dicarboxyphenoxy)phenyl]phosphine Oxide (17a)

(52) Into a 250 mL 3-neck round bottom flask equipped with stir bar, condenser, and nitrogen inlet were charged tris[4-(3,4-dicyanophenoxy)phenyl]phosphine oxide ((16a), 2.5 g, 3.2 mmol), KOH (2.7 g, 48 mmol), and ethanol/water (1:1, 60 mL). The mixture was heated under reflux for 12 h until it formed a clear solution. The solution was allowed to cool to room temperature and neutralized with conc. HCl solution to pH 1-3. The white precipitate was collected and dried in oven to afford 2.60 g (99%) of white crystals. m.p.>300 C. .sup.1H-NMR (DMSO-d.sub.6, in ppm): 7.22-7.27 (m, 12H, ArH), 7.67-7.72 (dd, 6H, ArH), 7.76-7.78 (d, 3H, ArH). .sup.13C-NMR (DMSO-d.sub.6, in ppm): 118.35, 118.90, 119.02, 120.51, 127.35, 127.40, 128.46, 131.40, 134.02, 134.13, 136.46, 157.46, 158.83, 158.86, 167.52, 168.21.

Example 5

Tris[4-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide tri-anhydride (1a)

(53) Into a 100 mL 3-neck round bottom flask equipped with stir bar, condenser, and nitrogen inlet were charged tris[4-(3,4-dicarboxyphenoxy)phenyl]phosphine oxide ((17a), 2.0 g, 2.44 mmol), acetic acid (7 mL), and acetic anhydride (15 mL). The mixture was refluxed for 4 h until it formed a clear solution, which was then filtered while hot to remove insoluble impurities. After cooling to room temperature, the crystallized solid was collected, washed with dry toluene, and dried under vacuum to afford 1.4 g (75%) of golden yellow crystals. m.p. 151.8-152.1 C. Anal. Calcd. for C.sub.42H.sub.21O.sub.13P: C, 65.98%; H, 2.77%; N, 0%; P, 4.05%. Found: C, 65.34%; H, 2.91%; N, <0.1%; P, 3.94. .sup.1H-NMR (DMSO-d.sub.6, in ppm): 7.34-7.36 (dd, 6H, ArH), 7.62-7.65 (dd, 3H, ArH), 7.66-7.68 (dd, 3H, ArH), 7.77-7.82 (dd, 6H, ArH), 8.01-8.12 (d, 3H, ArH). .sup.13C-NMR (DMSO-d.sub.6, in ppm): 114.48, 119.75, 119.88, 125.95, 125.98, 127.94, 128.39, 129.44, 134.18, 134.26, 134.37, 157.92, 157.95, 162.29, 162.40, 162.47.

Example 6

(54) Representative procedure for the synthesis of trianhydride-crosslinked polyimides (2 mol % tri-anhydride, PAn-CP2-2). 1,3-bis(3-aminophenoxy)benzene ((APB), 1.169 g, 4.000 mmol) and DMAc (15 mL) were added to a 50 mL 3-necked flask equipped with a magnetic stirrer, nitrogen inlet and outlet, and stirred under dry nitrogen at room temperature for 30 min. 2,2-[bis(4-phthalic anhydride)]-1,1,1,3,3,3-hexafluoroisopropane ((6FDA), 1.724, 3.880 mmol) was then charged. The light yellow solution was agitated at room temperature for about 24 hr to afford a poly(amic acid) solution. Then the tri-anhydride crosslinking agent ((1a), 0.0612 g, 0.080 mmol) was added to this solution. After the tri-anhydride crosslinking agent was totally dissolved in DMAc, the mixture was poured into a glass dish, followed by vacuum evaporation of DMAc at 50 C., and heat-treated sequentially at: 100 C./1 h, 150 C./1 h, 175 C./1 h, 200 C./1 h, 250 C./1 h, and 300 C./1 h to form crosslinked polyimide films. The film thickness of the crosslinked polyimide film was in a range of approximately 20 to approximately 100 m. This general procedure was followed to prepare other PAn-CP2-x (x stands for mole percentage of tri-anhydride crosslinking agent.

Example 9

(55) TABLE-US-00002 TABLE 2 Composition and properties of polyimide films 6FDA APB Trianhydride T.sub.d5%.sup.c (mol (mol (1a) Tg E.sup.b ( C.) Gel Swelling Sample %) %) (mol %) ( C.) (GPa) in air M.sub.c.sup.d Content.sup.e,g Ratio.sup.f,g Linear CP2.sup.d 100 100 0 219 1.90 0.15 526 PAn-CP2-0.5 99.75 100 0.5 219 2.03 0.32 514 140,150 62.1 17.2 PAn-CP2-1 98.5 100 1 220 2.18 0.27 519 46,800 91.9 5.5 PAn-CP2-2 97.0 100 2 222 2.54 0.19 518 23,460 94.4 4.7 PAn-CP2-5 92.5 100 5 232 2.84 0.32 518 9,460 97.7 3.1 (a) Tg measured from the peak of tan delta (DMA) as an average value taken from 4 measurements; (b) Modulus determined in tension at 25 C. as average from 5 specimens per sample; (c) Temperature at which 5 wt % loss as determined by TGA at a heating rate of 10 C./min; (d) M.sub.c is the theoretical molecular weight of chains between crosslinks; (e) Gel Content = Wi/Wx 100%; (f) Swelling Ratio = Wg/Wx 100%. (g) Test procedure for (e) and (f): Films weighed at room temp (Wi). Films immersed in DMAc (2 days). Gel rinsed in fresh DMAc (2X) to remove soluble fractions, wiped with tissue paper and weighed (Wg). Gel heat-treated in an oven at 300 C. Crosslinked CP2 weighed at room temperature (Wx).

(56) While the present invention has been illustrated by the description of one or more embodiments thereof, and while the embodiments have been described in considerable detail, they are not intended to restrict or in any way limit the scope of the appended claim to such detail. Additional advantages and modification will be readily apparent to those skilled in the art. The invention in its broader aspects is therefore not limited to the specific details, representative apparatus and methods and illustrative examples shown and described. Accordingly, departures may be made from such details without departing from the scope or the spirit of the general inventive concept exemplified herein.