Maleated siloxane derivatives

Claim 2

A compound having the formula: ##STR17## wherein R is independently selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and phenyl; R' is ##STR18## and n=1 to 6.

Claim 3

The compound of claim 1, wherein R is methyl, and n is 2 or 3.

Claim 4

The compound of claim 1, wherein the compound is 1,3-bis(4-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-maleamic acid; 1,3-bis(4-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-maleimide; or 1,3-bis(4-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-isomaleimide.

Claim 5

The compound of claim 1, wherein the compound is 1,3-bis(3-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-maleamic acid; 1,3-bis(3-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-maleimide; or 1,3-bis(3-aminophenoxy)-1,1,3,3-tetramethyldisiloxane bis-isomaleimide.

Claim 6

The compound of claim 1, wherein the compound is 1,5-bis(3-aminophenoxy)-1,1,3,3,5,5-hexamethyltrisiloxane bis-maleamic acid; 1,5-bis(3-aminophenoxy)-1,1,3,3,5,5-hexamethyltrisiloxane bis-maleimide; or 1,5-bis(3-aminophenoxy)-1,1,3,3,5,5-hexamethyltrisiloxane bis-isomaleimide.

Claim 7

A process for the preparation of the bis-maleamic acid siloxane of claim 1, wherein R' is ##STR19## which comprises reacting a diaminodiphenoxysiloxane of the formula ##STR20## wherein R and n are as defined in claim 1, with maleic anhydride in at least a 1:2 molar ratio in an inert organic solvent at a temperature of 0°-60° C. and recovering the bis-maleamic acid siloxane.

Claim 8

The process of claim 6, wherein the inert organic solvent is acetone.

Claim 9

A process for the preparation of a bis-maleimide siloxane having the formula ##STR21## wherein R is independently selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and phenyl; n=1 to 6; and R' is ##STR22## which comprises reacting a diaminodiphenoxysiloxane of the formula ##STR23## wherein R and n are already defined, with maleic anhydride in at least a 1:2 molar ratio in an inert organic solvent at a temperature of 0°-60° C.; cyclizing the maleated siloxane employing a dehydrating agent at a temperature of 0°-20° C., in the presence of a nucleophilic catalyst which is present as a by-product of the maleation or which has been additionally added; and recovering the bis-maleimide siloxane.

Claim 10

A process for the preparation of a bis-maleimide siloxane having the formula ##STR21## wherein R is independently selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and phenyl; n=1 to 6; and R' is ##STR22## which comprises reacting a diaminodiphenoxysiloxane of the formula ##STR23## wherein R and n are already defined, with maleic anhydride in at least a 1:2 molar ratio in an inert organic solvent at a temperature of 0°-60° C.; cyclizing the maleated siloxane employing a dehydrating agent at a temperature of 0°-20° C., in the presence of a nucleophilic catalyst which is present as a by-product of the maleation or which has been additionally added; and recovering the bis-maleimide siloxane.

Claim 11

The process of claim 8 wherein the dehydrating agent is N,N'-dicyclohexylcarbodiimide.

Claim 12

The process of claim 8 wherein the maleation reaction is conducted in acetone, the maleated siloxane is recovered from said acetone and the cyclization reaction is conducted in dichloromethane.

Claim 13

The process of claim 8 wherein the nucleophilic catalyst is additionally added in an amount of 40 to 200 weight percent based on the maleated siloxane.

Claim 14

A process for the preparation of a bis-isomaleimide siloxane having the formula ##STR24## wherein R is independently selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and phenyl; n=1 to 6; and R' is ##STR25## which comprises reacting a diaminodiphenoxysiloxane of the formula ##STR26## wherein R and n are already defined, with maleic anhydride in at least a 1:2 molar ratio in an inert organic solvent at a temperature of 0°-20° C.; cyclizing the maleated siloxane employing a dehydrating agent at a temperature of 0°-20° C.; and recovering the bis-isomaleimide siloxane.

Claim 15

A process for the preparation of a bis-isomaleimide siloxane having the formula ##STR24## wherein R is independently selected from the group consisting of hydrogen, alkyl of 1 to 3 carbon atoms and phenyl; n=1 to 6; and R' is ##STR25## which comprises reacting a diaminodiphenoxysiloxane of the formula ##STR26## wherein R and n are already defined, with maleic anhydride in at least a 1:2 molar ratio in an inert organic solvent at a temperature of 0°-20° C.; cyclizing the maleated siloxane employing a dehydrating agent at a temperature of 0°-20° C.; and recovering the bis-isomaleimide siloxane.

Claim 16

The process of claim 12, wherein the dehydrating agent is N,N'-dicyclohexylcarbodiimide.

Claim 17

The process of claim 12, wherein the maleation reaction is conducted in acetone, the maleated siloxane is recovered from said acetone, and the cyclization reaction is conducted in dichloromethane.

Claim 18

A process for the isomerization of the bis-isomaleimide siloxane of claim 12 to the corresponding bis-maleimide which comprises isomerizing the bis-isomaleimide in the presence of a nucleophilic catalyst in an inert organic solvent at a temperature of 0°-30° C. and recovering the bis-maleimide siloxane.