TWI468439B - Photosensitive polyimides - Google Patents

Description

Photosensitive polyimine

The present invention relates to an isocyanate-modified photosensitive polyimine. The photosensitive polyimide of the present invention has excellent heat resistance, chemical resistance and flexibility, and can be applied to liquid photoresist or dry film photoresist, or used for solder resist, cover film or printed wiring board.

Nowadays, electronic products have become lighter and shorter, and the size of various electronic components has also been reduced. Due to the flexibility and weight advantages of flexible printed circuit boards, their demand has increased.

At present, the materials of the coverlay film can be classified into three categories, the first type is a photosensitive coverlay film, and the second type is a non-photosensitive coverlay film. The third type is a thermal plastic coverlay film. For the first type of photosensitive cover film, it can be divided into a polyimide-based cover film (PI based coverlay film) and a non-polyimine-based cover film (non-PI based coverlay). Film), wherein the non-polyimine-based cover film is more limited in application due to factors such as poor heat resistance and high coefficient of thermal expansion ("CTE"). The second type of non-photosensitive cover film is inferior in practicality to the photosensitive cover film because the process is more complicated than the photosensitive cover film. As for the thermoplastic type cover film, it is required to be processed after the hole is formed, and therefore it is also inferior in convenience to the photosensitive cover film.

A photosensitive polyimine modified with an epoxy is disclosed in U.S. Patent No. 6,605,353. However, since this polymer reacts with an epoxide and an acid, its reactivity is poor, and the OH functional group after ring opening reacts with an epoxy, and thus faces stability and thermal stability. .

In order to improve the heat resistance of the cover film and the process convenience, it is still required in the art to find a photosensitive polyimide which can solve the above problems.

The present invention provides an isocyanate-modified photosensitive polyimine which has better reactivity, excellent stability, thermal stability, and can be hardened at a low temperature.

The present invention further provides a photosensitive composition comprising the above-mentioned photosensitive polyimine, which can be used as a protective film material or a photoresist, and the photosensitive composition of the present invention has excellent electrical properties and heat resistance after film formation. Flexibility and chemical resistance. Therefore, the photosensitive composition of the present invention can be applied as a solder resist, a cover film material, and a printed circuit board as a protective film material.

The photosensitive polyimine polymer of the present invention has the structure of the following formula (I): Wherein, B and D may be the same or different, each independently being a divalent organic group; A is a tetravalent organic group containing at least one modifying group R', and J is a tetravalent organic group containing no modifying group R' A group, n is equal to 0 or an integer greater than 0, and m is an integer greater than zero. R' is selected from the following groups: Wherein R represents an unsaturated group containing a vinyl group or a group selected from the group consisting of: Wherein R1 is a substituted or unsubstituted C1-C20 saturated or unsaturated organic group; and R2 is a vinyl-containing unsaturated group.

Preferably, the above vinyl group-containing unsaturated group is selected from the group consisting of: Wherein R 4 and R 5 are each H or a substituted or unsubstituted alkyl group having C 1 -C 5 , and R 6 is a covalent bond or a substituted or unsubstituted organic group having C 1 -C 20 .

More preferably, the above vinyl group-containing unsaturated group is selected from the group consisting of the following groups: Wherein z represents an integer from 0-6.

More preferably, the above vinyl group-containing unsaturated group is selected from the group consisting of the following groups: Wherein z represents an integer from 0-6.

The above R1 group is preferably selected from the group consisting of: Wherein o, p, q and r are each an integer of 0 or greater than 0; R4, R5 and R6 are as defined above; R7 is H or is substituted or unsubstituted organic group having C1-C12 And R8 is a covalent bond or an organic group selected from the group consisting of:

More preferably, the above R1 group is selected from the group consisting of the following groups:

The divalent organic groups B and D contained in the photosensitive polyimine polymer of the formula (I) of the present invention are not particularly limited, and are, for example, a divalent aromatic group, a divalent aliphatic group or a divalent group containing oxygen. Preferably, the B and D lines are each selected from the group consisting of the following groups: Wherein, R "is -H, C1-C4 alkyl, C1-C4 perfluoroalkyl group, methoxy, ethoxy, halogen, OH, COOH, NH ₂ or SH; R9 is H, methyl or ethyl c is an integer from 0 to 4; d is an integer from 0 to 4; a is an integer greater than 0; b is an integer greater than 0; and R11 each represents a covalent bond or a group selected from the group consisting of: Wherein w and x are each an integer greater than 0; and R12 is -S(O) ₂ -, -C(O)-, a covalent bond or a substituted or unsubstituted organic group having a C1-C18 group .

More preferably, B and D in the above formula (I) are each selected from the group consisting of the following groups: Wherein y is an integer from 1 to 12, more preferably an integer from 1 to 6.

The A-form contained in the photosensitive polyimine polymer of the formula (I) of the present invention is derived from an acid anhydride having a reactive functional group including OH, COOH or NH ₂ . Preferably, the A lines are each selected from the group consisting of the following groups: Wherein R' is an organic group selected from the group consisting of Wherein R is as defined above; R ₁₃ :-CH ₂ -, -O-, -S-, -CO-, -SO ₂ -, -C(CH ₃ ) ₂ -, -C(CF ₃ ) ₂ -; R ₁₄ :-H, -CH ₃ -; X: -O-, -NH-, -S-.

A in the above formula (I) is more preferably selected from the group consisting of the following groups: Wherein R' has the definitions described above.

The J group contained in the photosensitive polyimine of the formula (I) of the present invention is derived from an acid anhydride monomer which may or may not have a reactive functional group. Preferably, the J series is selected from the group consisting of the following groups: Wherein R ₁₅ : OH, COOH, NH ₂ ; R ₁₃ : -CH ₂ -, -O-, -S-, -CO-, -SO ₂ -, -C(CH ₃ ) ₂ -, -C(CF ₃ ) ₂ -; R ₁₄ : -H, -CH ₃ -; X: -O-, -NH-, -S-.

The J in the formula (I) is more preferably selected from the group consisting of the following groups:

The photosensitive polyimine polymer of the present invention can be obtained by a polymerization method known to those skilled in the art to which the present invention is known, for example, by a method comprising the following steps:

(a) making a diamine monomer of the formula H ₂ NP-NH ₂ with a formula Di-anhydride monomer and another formula The dianhydride monomer is reacted to form a compound of the following formula (1): Wherein G is a reactive functional group such as an OH group, a COOH group or an NH ₂ group.

If COOH is taken as an example, the next reaction step is:

(b) adding an isocyanate compound of the formula O=C=NR to the product of step (a) to form a compound of formula (2) Where f+g=i.

In the above method for producing a photosensitive polyimine polymer, the reactive functional anhydride monomer of the present invention may be selected from the group consisting of the following compounds: Wherein R ₁₅ : OH, COOH, NH ₂ ; R ₁₃ : -CH ₂ -, -O-, -S-, -CO-, -SO ₂ -, -C(CH ₃ ) ₂ -, -C(CF ₃ ) ₂ -; R ₁₄ : -H, -CH ₃ -; X: -O-, -NH-, -S-.

Preferably, the reactive functional anhydride monomer used in the present invention may be selected from the group consisting of the following compounds:

In the above method for producing a photosensitive polyimine polymer, another acid anhydride monomer to be used is not particularly limited and may or may not have a reactive functional group. Anhydride monomers which are useful in the present invention having no reactive functional groups are well known to those skilled in the art and are, for example, but not limited to: Wherein E, F and H each represent a covalent bond or a substituted or unsubstituted organic group having a C1-C20 saturated or unsaturated, cyclic or acyclic group; R3 is a covalent bond or is selected from The following groups:

Preferably, another anhydride monomer useful in the present invention may be selected from the group consisting of the following compounds:

In the above method for preparing a photosensitive polyimine polymer, the diamine monomer used may generally be an aliphatic, aromatic or a halogen-containing divalent group, and preferred examples include, but are not limited to, having The following diamine monomer: Wherein, R "is -H, C1-C4 alkyl, C1-C4 perfluoroalkyl group, methoxy, ethoxy, halogen, OH, COOH, NH ₂ or SH; R9 is H, methyl or ethyl c is an integer from 0 to 4; d is an integer from 0 to 4; a is an integer greater than 0; b is an integer greater than 0; and R11 each represents a covalent bond or a group selected from the group consisting of: Wherein w and x are each an integer greater than 0; and R12 is -S(O) ₂ -, -C(O)-, a covalent bond or a substituted or unsubstituted organic group having a C1-C18 group .

Preferably, the above diamine monomer may be selected from the group consisting of the following compounds: Wherein y is an integer from 1 to 12, more preferably an integer from 1 to 6.

In order to make the polyimine polymer have a photosensitive group for the photocuring mechanism of the polymer, the present invention uses a photoreceptor-containing isocyanate to modify the polyimine polymer to be photosensitive after modification. The group, for example, has a C=C double bond. The above isocyanate may be a monoisocyanate or a diisocyanate, preferably a monoisocyanate. The isocyanate used in the present invention can be reacted with a reactive group such as a hydroxyl group (-OH), a carboxyl group (-COOH) or an amine group (-NH ₂ ) in the polyiminoimine polymer, thereby further imparting the polyimine polymer. Upgraded. The isocyanate used in the present invention has the structure: O = C = NR, wherein R is R ^* or a group having the following structure: Wherein R ^* and R2 each represent a photosensitive group containing a vinyl group-unsaturated group; and R1 is a substituted or unsubstituted organic group having a C1-C20 saturated or unsaturated group.

According to a particular embodiment of the invention, the vinyl group-containing unsaturated group is selected from the group consisting of: Wherein R4 and R5 are each H or a substituted or unsubstituted alkyl group having C1-C5, and R6 is a covalent bond or a substituted or unsubstituted organic group having C1-C20; R1 is selected from the following groups: Wherein, o, p, q and r are each an integer of 0 or greater than 0; R4, R5 and R6 are as defined above; R7 is H or is substituted or unsubstituted organic having C1-C12 a group; and R8 is a covalent bond or is selected from the group consisting of:

The present invention further provides a photosensitive composition comprising at least 1% by weight of a photosensitive polyimine polymer having the structure of the above formula (I), a photoinitiator, and a solvent. The photosensitive composition of the present invention can be used for liquid photoresist or dry film photoresist, or for solder resist, cover film or printed wiring board. In the above photosensitive composition, the weight percentage of each component can be adjusted according to the product requirements. Generally, the content of the photosensitive polyimine polymer of the formula (I) is at least 1% by weight based on the total weight of the whole composition. Preferably, it is between 10 and 50% by weight; the photoinitiator is present in an amount of at least 0.001% by weight, preferably from 0.01% to 1% by weight, based on the total weight of the total composition.

According to the present invention, the photoinitiator suitable for use in the above composition is not particularly limited and may be selected from the group consisting of benzophenone, benzoin, 2-hydroxyl 2-hydroxy-2-methyl-1-phenyl-propan-1-one, 2,2-dimethoxy-1,2-diphenylethyl-1- Ketone (2,2-dimethoxy-1,2-diphenylethan-1-one), 1-hydroxy cyclohexyl phenyl ketone, 2,4,6-trimethylbenzhydryl 2,4,6-trimethylbenzoyl diphenyl phosphine oxide, N-phenylglycine, 9-phenylacridine , benzyldimethylketal, 4,4'-bis(diethylamine)benzophenone, 2,4,5-triarylimidazole dimer (2,4,5-triarylimidazole dimers And mixtures thereof; preferred photoinitiators are 2,4,6-trimethylbenzimidyldiphenylphosphine oxide.

The solvent to be used in the above composition is not particularly limited according to the present invention, and is, for example, but not limited to, selected from the group consisting of N-methylpyrrolidone (NMP), dimethylacetamide (DMAC). ), dimethylformamide (DMF), dimethyl hydrazine (DMSO), toluene, xylene, and mixtures thereof.

In order to increase the degree of photocrosslinking, the photosensitive composition of the present invention may be added with a certain amount of a reactive monomer or a short-chain oligomer as needed to form an erosslinking between the molecule and the molecule. According to the present invention, the reactive monomer or oligomer suitable for use in the above composition is not particularly limited, and it may, for example, be selected from the group consisting of 1,6-hexanediol diacrylate (1,6). -hexanediol diacrylate), neopentyl glycol diacrylate, ethylene glycol diacrylate, pentaerythritol diacrylate, trimethylolpropane Triacrylate), pentaerythritol triacrylate, dipentaerythritol hexaacrylate, tetramethylolpropane tetraacrylate, tetraethylene glycol diacrylate, 1, 1,6-hexanediol dimethacrylate, neopentyl glycol dimethacrylate, ethylene glycol dimethacrylate, pentaerythritol II Pentaerythritol dimethacrylate, trimethylolpropane trimethyl propyl Trimethylolpropane trimethacrylate, pentaerythritol trimethacrylate, dipentaerythritol hexamethacrylate, tetramethylolpropane tetramethacrylate, tetraethylene glycol Tetraethylene glycol dimethacrylate, rnethoxydiethylene glycol methacrylate, methoxypolyethylene glycol methacrylate, β-methacryl oxime --methacryloyloxyethylhydrodiene phthalate, β-methacryloyloxyethylhydrodiene succinate, 3-chloro-2-hydroxy methacrylate 3-chloro-2-hydroxypropyl methacrylate, stearyl methacrylate, phenoxyethyl acrylate, phenoxydiethylene glycol acrylate, Phenoxypolyethyle Ne glycol acrylate), β-acryloyloxyethylhydrodiene succinate, lauryl acrylate, ethylene glycol dimethacrylate, Diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, polyethylene glycol dimethacrylate, 1,3-butyl 1,3-butylene glycol dimethacrylate, polypropylene glycol dimethacrylate, 2-hydroxy-1,3-dimethylpropenyloxypropane (2-hydroxy-) 1,3-dimethacryloxypropane), 2,2-bis[4-(methacryloxyethoxy)phenyl]propane, 2,2 -2[2-(methacryloxydiethoxy)phenyl]propane), 2,2-bis[4-(methacryl) 2,2-bis[4-(methacryloxypolyethoxy)phenyl]propane), polyethylene glycol II Polyethylene glycol diacrylate, tripropylene glycol diacrylate, polypropylene glycol diacrylate, 2,2-bis[4-(propyleneoxydiethoxy)benzene 2,2-bis[4-(acryloxydiethoxy)phenyl]propane), 2,2-bis[4-(acryloxypolyethoxy)phenyl]propane (2,2-bis[4] -(acryloxypolyethoxy)phenyl]propane), 2-hydroxy-1-acryloxy-3-methacryloxypropane, trimethylolpropane trimethyl Trimethylolpropane trimethacrylate, tetramethylolmethane triacrylate, tetramethylolmethane tetraacrylate, methoxydipropylene glycol methacrylate, A Methoxytriethylene glycol acrylate, nonylphenoxypolyethylene glycol acrylate, nonylphenoxypolypropylene acrylate Lycol acrylate), 1-acryloyloxypropyl-2-phthalate, isostearyl acrylate, polyoxyethylene alkyl ether Acrylate), nonylphenoxyethylene glycol acrylate, polypropylene glycol dimethacrylate, 1,4-butanediol dimethacrylate (1,4-butanediol) Dimethacrylate), 3-methyl-1,5-pentanediol dimethacrylate, 1,6-hexanediol methacrylate (1,6-hexanediol) Methacrylate), 1,9-nonanediol methacrylate, 2,4-diethyl-1,5-pentanediol dimethacrylate (2,4-diethyl- 1,5-pentanediol dimethacrylate), 1,4-cyclohexanedimethanol dimethacrylate, dipropylene glycol diacrylate, tricyclodecane dimethanol diacrylate Tricyclodecanedimethanol diacrylate, 2,2-dihydrobis[4-propenyloxypolyethylene 2,2-hydrogenated bis[4-acryloxypolyethoxy]phenylpropane), 2,2-bis[4-propenyloxypolypropoxy]phenyl]propane (2,2-bis[ 4-acryloxypolypropoxy]phenyl)propane), 2,4-diethyl-1,5-pentanediol diacrylate, ethoxylated trimethylolpropane Ethoxylated trimethylolpropane triacrylate, propoxylated trimethylolpropane triacrylate, isocyanuric acid tri(ethaneacrylate), pentaerythritol tetraacrylate (pentaerythritol) Tetraacrylate), ethoxylated pentaerythritol tetraacrylate, propoxylated pentaerythritol tetraacrylate, ditrimethylolpropane tetraacrylate, dipentaerythritol polyacrylate ,triallyl isocyanurate, glycidyl methacrylate, allylic Allyl glycidyl ether, 1,3,5-triacryloylhexahydro-s-triazine, 1,3,5-benzoic acid triene Trial (triallyl 1,3,5-benzenecarboxylate), triallylamine, triallyl citrate, triallyl phosphate, allobarbital , diallylamine, diallyldimethylsilane, diallyl disulfide, diallyl ether, diphenyl cyanurate Diallyl cyanurate, diallyl isophthalate, diallyl terephthalate, 1,3-diallyloxy-2-propanol (1,3-diallyloxy) -2-propanol), diallyl sulfide, diallyl maleate, 4,4 ' -isopropylidene biphenol dimethacrylate (4,4 ' -isopropylidenediphenol dimethacrylate) and 4,4 '- isopropylidene diphenol diacrylate (4,4' -isopropylidenediphenol diacrylate). The reactive monomer or oligomer used in the photosensitive composition of the present invention, when present, is used in an amount of at least 0.1% by weight, preferably 0.1% to 30% by weight based on the total weight of the total composition.

The invention is further illustrated by the following examples, which are not intended to limit the scope of the present invention, and any modifications and variations which are obtained without departing from the spirit of the invention are intended to be The scope.

In the examples, the abbreviations used are defined as follows:

6FDA: 4,4'-hexafluoroisopropylidene-2,2-bis-(phthalic acid anhydride)

DMDB: 2,2'-dimethylbiphenyl-4,4'-diamine (2,2'-dimethylbiphenyl-4,4'-diamine)

ODA: 4,4'-oxydibenzenamine

2-IEA: 2-isocyanatoethyl acrylate

1-MI: 1-methylimidazole

PTZ: phenothiazine

DMAC: dimethyl acetamide

NMP: N-methylpyrrolidone

Example 1: Synthesis of Isocyanate Modified Polyimine (P1)

64.85 g (0.2 mol) of DA1 and 42.46 g (0.2 mol) of DMDB were weighed, and 300 mL of NMP was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P1.

Example 2: Synthesis of Isocyanate Modified Polyimine (P2)

73.256 g (0.2 mol) of DA2 and 42.46 g (0.2 mol) of DMDB were weighed, and 350 mL of NMP was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, add 50 mL of toluene, at Water was removed at 130 ° C with a dean-stark unit. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P2.

Example 3: Synthesis of Isocyanate Modified Polyimine (P3)

100.074 g (0.2 mol) of DA3 and 42.46 g (0.2 mol) of DMDB were weighed, 450 mL of NMP was added, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P3.

Example 4: Synthesis of Isocyanate Modified Polyimine (P4)

124.1 g (0.2 mol) of DA4 and 42.46 g (0.2 mol) of DMDB were weighed, and 550 mL of NMP was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 14 g (0.1 mol) of 2-IEA, 0.1 g of 1-MI and 0.12 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P4.

Example 5: Synthesis of Isocyanate Modified Polyimine (P5)

126.9 g (0.2 mol) of DA5 and 42.46 g (0.2 mol) of DMDB were weighed, and 550 mL of NMP was added, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 14 g (0.1 mol) of 2-IEA, 0.1 g of 1-MI and 0.12 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P5.

Example 6: Synthesis of Isocyanate Modified Polyimine (P6)

115.7 g (0.2 mol) of DA6 and 42.46 g (0.2 mol) of DMDB were weighed, 500 mL of NMP was added, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P6.

Example 7: Synthesis of Isocyanate Modified Polyimine (P7)

64.85 g (0.2 mol) of DA1 and 40.05 g (0.2 mol) of ODA were weighed, and 300 mL of DMAC was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P7.

Example 8: Synthesis of Isocyanate Modified Polyimine (P8)

73.26 g (0.2 mol) of DA2 and 40.05 g (0.2 mol) of ODA were weighed, added to 350 mL of DMAC, stirred at room temperature for 1 hour, and then warmed to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P8.

Example 9: Synthesis of Isocyanate Modified Polyimine (P9)

100.074 (0.2 mol) of DA3 and 40.05 g (0.2 mol) of ODA were weighed, added to 450 mL of DMAC, stirred at room temperature for 1 hour, and then warmed to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P9.

Example 10: Synthesis of Isocyanate Modified Polyimine (P10)

124.1 g (0.2 mol) of DA4 and 40.05 g (0.2 mol) of ODA were weighed, added to 550 mL of DMAC, stirred at room temperature for 1 hour, and then warmed to 50 ° C and stirred for 4 hours. After 4 hours, add 50 mL of toluene, at Water was removed at 130 ° C with a dean-stark unit. After the water was completely removed, the solution was cooled to room temperature, and 14 g (0.1 mol) of 2-IEA, 0.1 g of 1-MI and 0.12 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P10.

Example 11: Synthesis of Isocyanate Modified Polyimine (P11)

126.9 g (0.2 mol) of DA4 and 40.05 g (0.2 mol) of ODA were weighed, and 550 mL of DMAC was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 14 g (0.1 mol) of 2-IEA, 0.1 g of 1-MI and 0.12 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P11.

Example 12: Synthesis of Isocyanate Modified Polyimine (P12)

115.7 g (0.2 mol) of DA4 and 40.05 g (0.2 mol) of ODA were weighed, and 550 mL of DMAC was added thereto, and the mixture was stirred at room temperature for 1 hour, and then heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P12.

Example 13: Synthesis of Isocyanate Modified Polyimine (P13)

57.85 g (0.1 mol) of DA4, 44.42 g (0.1 mol) of 6FDA and 40.05 g (0.2 mol) of ODA were weighed, and 500 mL of DMAC was added thereto, and the mixture was stirred at room temperature for 1 hour, and further heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were further added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P13.

Example 14: Synthesis of Isocyanate Modified Polyimine (P14)

63.45 g (0.1 mol) of DA5, 44.42 g (0.1 mol) of 6FDA and 40.05 g (0.2 mol) of ODA were weighed, and 500 mL of DMAC was added thereto, and the mixture was stirred at room temperature for 1 hour, and further heated to 50 ° C and stirred for 4 hours. After 4 hours, 50 mL of toluene was added and the water was removed at 130 ° C with a dean-stark apparatus. After the water was completely removed, the solution was cooled to room temperature, and 7 g (0.05 mol) of 2-IEA, 0.05 g of 1-MI and 0.06 g of PTZ were further added. After the addition was completed, the solution was warmed to 80 ° C and stirred for 8 hours. You can get P14.

Claims (14)

A photosensitive polyimine polymer having the structure of the following formula (I), Wherein: B and D may be the same or different, each independently being a divalent organic group; A is a tetravalent organic group containing at least one modifying group R', and J is a tetravalent organic having no modifying group R' a group, n is equal to 0 or an integer greater than 0, and m is an integer greater than 0, R' Wherein R represents an ethylenically unsaturated group selected from the group consisting of: Or a group selected from the group consisting of: Wherein R1 is a substituted or unsubstituted C1-C20 saturated or unsaturated organic group; R2 is a vinyl-containing unsaturated group; and R4 and R5 are each H or substituted or unsubstituted An alkyl group of C1-C5, and R6 is a covalent bond or a substituted or unsubstituted organic group having C1-C20. The photosensitive polyimine polymer of claim 1, wherein the R2 is selected from the group consisting of: Wherein R4 and R5 are each H or a substituted or unsubstituted alkyl group having a C1-C5 group, and R6 is a covalent bond or a substituted or unsubstituted organic group having a C1-C20 group. The photosensitive polyimine polymer of claim 1, wherein the R2 is selected from the group consisting of: Wherein z represents an integer from 0-6. The photosensitive polyimine polymer of claim 1, wherein R1 is selected from the group consisting of: Wherein, o, p, q and r are each 0 or an integer greater than 0; R4, R5 and R6 are as defined in the scope of claim 2; R7 is H or is substituted or unsubstituted organic having C1-C12 a group; and R8 is a covalent bond or an organic group selected from the group consisting of: A photosensitive polyimine polymer according to claim 4, wherein R1 is selected from the group consisting of: The photosensitive polyimine polymer of claim 1, wherein the A is selected from the group consisting of the following groups: Wherein R' has the definition as defined in claim 1; R ₁₃ :-CH ₂ -, -O-, -S-, -CO-, -SO ₂ -, -C(CH ₃ ) ₂ -, -C(CF ₃ ) ₂ -; R ₁₄ :-H, -CH ₃ -; X: -O-, -NH-, -S-. The photosensitive polyimine polymer of claim 1, wherein the A is selected from the group consisting of the following groups: Wherein R' has the definition as in item 1 of the scope of the patent application. The photosensitive polyimine polymer of claim 1, wherein the J series is selected from the group consisting of the following groups: Wherein R ₁₃ , R ₁₄ , X are as defined in claim 6; R ₁₅ is OH, COOH, NH ₂ . The photosensitive polyimine polymer of claim 1, wherein the J series is selected from the group consisting of the following groups: The photosensitive polyimine polymer according to claim 1, wherein the divalent organic groups of B and D are each selected from the group consisting of the following groups: Wherein: R "is -H, C1-C4 alkyl, C1-C4 perfluoroalkyl group, methoxy, ethoxy, halogen, OH, COOH, NH ₂ or SH, R9 is H, methyl or ethyl c is an integer from 0 to 4; d is an integer from 0 to 4; a is an integer greater than 0; b is an integer greater than 0; and R11 each represents a covalent bond or a group selected from the group consisting of: O-, -S-, -CH ₂ -, -S(O) ₂ -, , -C(CF ₃ ) ₂ -, -C(O)-, -C(CH ₃ ) ₂ -, , Wherein w and x are each an integer greater than 0; and R12 is -S(O) ₂ -, -C(O)-, a covalent bond or a substituted or unsubstituted organic group having a C1-C18 group . The photosensitive polyimine polymer according to claim 1, wherein the divalent organic groups of B and D are selected from the group consisting of the following groups: Where y is an integer from 1 to 12. A photosensitive composition comprising at least 1% by weight, based on the total weight of the composition, of a photosensitive polyimine polymer as in claim 1 of the patent application, and at least one photoinitiator. The photosensitive composition of claim 12, further comprising a reactive monomer or oligomer. The photosensitive composition of claim 12 or 13, which is for use in liquid photoresist or dry film photoresist.