Soluble imide oligomer and a method for producing the same

Claim 2

A soluble imide oligomer having an inherent viscosity (n inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU4## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR13## wherein R 1 and R 6 are tetravalent and trivalent carbocyclic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups; are ##STR14## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; R is hydrogen or alkyl or acetyl group; m and n each are an integer of 1, 2 or 3, and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(m+n)-1 and r≦q<2r-1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU5##

Claim 3

A soluble imide oligomer as claimed in claim 1, wherein x and y are values satisfying the following equation: ##EQU6##

Claim 4

A soluble imide oligomer as claimed in claim 1, wherein R 1 is ##STR15##

Claim 5

A soluble imide oligomer as claimed in claim 1, wherein R 6 is ##STR16##

Claim 6

A soluble imide oligomer as claimed in claim 1, wherein R 2 , R 3 and R 8 each are ##STR17##

Claim 7

A soluble imide oligomer as claimed in claim 1 wherein R 4 , R 5 and R 7 each are --CH 3 , --C 2 H 5 , or ##STR18##

Claim 8

A process for preparing a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU7## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidine at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR19## which process comprises reacting an amic acid compound represented by a general formula (II) mentioned below, or a mixture thereof with 10% by mole or less of an amic acid compound represented by a general formula (III) mentioned below, in the presence of 70% by weight or more, based on a solution, of a solvent, at a temperature of 60°-200° C. for 0.2˜6 hours, ##STR20## wherein R 1 and R 6 are tetravalent and trivalent carbocyclic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups are ##STR21## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; X is an alkoxyl group, an acetoxyl group, a halogen atom, or a hydroxyl group; R is hydrogen or alkyl or acetyl group derived from X; m and n each are an integer of 1, 2 or 3; and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(m+n)-1 and r≦q<2r-1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU8##

Claim 9

A process for preparing a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU7## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidine at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR19## which process comprises reacting an amic acid compound represented by a general formula (II) mentioned below, or a mixture thereof with 10% by mole or less of an amic acid compound represented by a general formula (III) mentioned below, in the presence of 70% by weight or more, based on a solution, of a solvent, at a temperature of 60°-200° C. for 0.2˜6 hours, ##STR20## wherein R 1 and R 6 are tetravalent and trivalent carbocyclic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups are ##STR21## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; X is an alkoxyl group, an acetoxyl group, a halogen atom, or a hydroxyl group; R is hydrogen or alkyl or acetyl group derived from X; m and n each are an integer of 1, 2 or 3; and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(m+n)-1 and r≦q<2r-1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU8##

Claim 10

A process for preparing a soluble imide oligomer as claimed in claim 7, wherein R 1 is ##STR22##

Claim 11

A process for preparing an soluble imide oligomer as claimed in claim 7, wherein R 6 is ##STR23##

Claim 12

A process for preparing a soluble imide oligomer as claimed in claim 7, wherein R 2 , R 3 and R 8 each are ##STR24##

Claim 13

A process for preparing a solution imide oligomer as claimed in claim 7, wherein R 4 , R 5 and R 7 each are --CH 3 , --C 2 H 5 , or ##STR25##

Claim 14

A process for preparing a soluble imide oligomer as claimed in claim 7, wherein said solvent includes 30 to 100% by weight of at least one member selected from the group consisting of N-methyl-2-pyrrolidone, dimethylacetamide, dimethylformamide, toluene, xylene, ethylene glycolmonomethyl ether, and dimethyl sulfoxide.

Claim 15

A process for preparing a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU9## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR26## which process comprises reacting an amic acid compound represented by a general formula (II) mentioned below, or a mixture thereof with 10% by mole or less of an amic acid compound represented by a general formula (III) mentioned below, in the presence of 70% by weight or more, based on a solution, of a solvent, at a temperature of 60°˜200° C. for 0.2˜6 hours, and, in the additional presence of {(m+n-2)x+(r-1)y} mole or less per mole of said amic acid compound of water at a temperature of 60° to 200° C. for 0.2 to 6 hours; ##STR27## wherein R 1 and R 6 are tetravalent and trivalent carbocylic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups, are ##STR28## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; X is an alkoxy group, an acetoxyl group, a halogen atom, or a hydroxyl group; m and n each are an integer of 1, 2 or 3, and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(m+1)-1 and r≦q<2r-1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU10##

Claim 16

A process for preparing a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU9## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR26## which process comprises reacting an amic acid compound represented by a general formula (II) mentioned below, or a mixture thereof with 10% by mole or less of an amic acid compound represented by a general formula (III) mentioned below, in the presence of 70% by weight or more, based on a solution, of a solvent, at a temperature of 60°˜200° C. for 0.2˜6 hours, and, in the additional presence of {(m+n-2)x+(r-1)y} mole or less per mole of said amic acid compound of water at a temperature of 60° to 200° C. for 0.2 to 6 hours; ##STR27## wherein R 1 and R 6 are tetravalent and trivalent carbocylic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups, are ##STR28## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; X is an alkoxy group, an acetoxyl group, a halogen atom, or a hydroxyl group; m and n each are an integer of 1, 2 or 3, and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(m+1)-1 and r≦q<2r-1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU10##

Claim 17

A process for preparing a soluble imide oligomer as claimed in claim 13, wherein R 1 is ##STR29##

Claim 18

A process for preparing a soluble imide oligomer as claimed in claim 13, wherein R 6 is ##STR30##

Claim 19

A process for preparing a soluble imide oligomer as claimed in claim 13, wherein R 2 , R 3 and R 8 each are ##STR31##

Claim 20

A process for preparing a soluble imide oligomer as claimed in claim 13, wherein R 4 , R 5 and R 7 each are --CH 3 , --C 2 H 5 , or ##STR32##

Claim 21

A process for preparing a soluble imide oligomer as claimed in claim 13, wherein said solvent includes 30 to 100% by weight of at least one member selected from the group consisting of N-methyl-2-pyrrolidone, dimethylacetamide, dimethylformamide, toluene, xylene, ethylene glycolmonomethyl ether, and dimethyl sulfoxide.

Claim 22

A coating solution for electronic materials comprising a solvent, and 30% by weight or less (based on the total of said solvent and the following soluble imide oligomer), a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU11## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR33## wherein R 1 and R 6 are tetravelent and trivalent carbocyclic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups, are ##STR34## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; R is hydrogen or alkyl or acetyl group; m and n each are an integer of 1, 2 or 3, and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(n+1) and r≦q<2r+1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU12##

Claim 23

A coating solution for electronic materials comprising a solvent, and 30% by weight or less (based on the total of said solvent and the following soluble imide oligomer), a soluble imide oligomer having an inherent viscosity (η inh) of 0.05 to 0.5 dl/g as determined by the following equation: ##EQU11## wherein η is a value as measured using an Ubbellohde viscometer at an oligomer concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at a temperature of 30±0.01° C., η 0 is a value for N-methyl-2-pyrrolidone as measured using the same viscometer as described above at the same temperature as described above, and C represents said oligomer concentration of 0.5 g/dl; and represented by the following general formula (I): ##STR33## wherein R 1 and R 6 are tetravelent and trivalent carbocyclic aromatic groups, respectively, carbonyl groups being bonded to said carbocyclic aromatic groups at the mutually different ring-forming carbon atoms thereof, every pair of imide ring-forming carbonyl groups being bonded to a carbocyclic ring of said carbocyclic aromatic groups in the mutual ortho positions thereof; R 2 , R 3 and R 8 , which are the same or different groups, are ##STR34## wherein s is an integer of 1 to 4; R 4 , R 5 and R 7 , which are the same or different groups, are an alkyl group having 1 to 6 carbon atoms, a phenyl group, or an alkyl-substituted phenyl group having 7 to 12 carbon atoms; R is hydrogen or alkyl or acetyl group; m and n each are an integer of 1, 2 or 3, and satisfy an equation: m+n≧3; r is 2 or 3; p and q are integers and satisfy the relation of m+n≦p<2(n+1) and r≦q<2r+1; t is 0 or 2; and x and y are values satisfying the following equation: ##EQU12##

Claim 24

A coating solution for electronic materials as claimed in claim 19, wherein x and y satisfy the following equation: ##EQU13##

Claim 25

A coating solution for electronic materials as claimed in claim 19, wherein R 1 is ##STR35##

Claim 26

A coating solution for electronic materials as claimed in claim 19, wherein R 6 is ##STR36##

Claim 27

A coating solution for electronic materials as claimed in claim 19, wherein R 2 , R 3 and R 8 each are ##STR37##

Claim 28

A coating solution for electronic materials as claimed in claim 19, wherein R 4 , R 5 and R 7 each are --CH 3 , --C 2 H 5 or ##STR38##

Claim 29

A coating solution for electronic materials as claimed in claim 19, wherein said solvent includes 30 to 100% by weight of at least one member selected from the group consisting of N-methyl-2-pyrrolidone, dimethylacetamide, dimethylformamide, toluene, xylene, ethylene glycolmonomethyl ether, ethylene glycolmonoethyl ether, and dimethyl sulfoxide.