Ethynyl and substituted ethynyl-terminated polysulfones

Claim 2

The class of ethynyl or substituted ethynyl-terminated polysulfones of the general formula: ##STR6## where PS is a polysulfone with a molecular weight between 1000 and 50,000 g/mole, and X is selected from the group consisting of: Si(CH 3 ) 3 ; H; straight or branched organic radials having 4 to 10 carbon atoms; substituted aromatic groups of the formula: ##STR7## where R is selected from the group consisting of: straight or branched organic radicals having from 1 to 12 carbon atoms, H, and ##STR8## and halogenated derivatives of all of the above.

Claim 3

The cross-linked polymer recovered by thermally treating a polysulfone of claim 1.

Claim 4

The polymer of claim 2 wherein the thermal treatment consists of heating to temperatures from 150°-400° C. for times ranging from 5 minutes to 4 hours.

Claim 5

A process for preparing ethynyl and substituted ethynyl-terminated polysulfones comprised of: disolving a polysulfone, having a molecular weight between 1000 and 50,000 g/mole, in a mixture of chlorinated organic solvent and an organic base, adding dropwise with stirring a solution of 4-bromobenzoyl chloride in a chlorinated organic solvent at temperatures ranging from 10°-50° C., and allowing this mixture to stir 3 hours, precipitating the 4-bromobenzoyl-terminated polymer with a non-solvent, drying the precipitate, and dissolving it in a highly polar solvent, adding an organic base, dichlorobis(triphenylphosphine)palladium, and a substituted acetylene under an inert atmosphere, stirring the mixture for 0.5 to 4 hours at 50°-100° C., and precipitating the resulting substituted ethynyl-terminated polymer with cold dilute aqueous acid.

Claim 6

A process for preparing ethynyl and substituted ethynyl-terminated polysulfones comprised of: disolving a polysulfone, having a molecular weight between 1000 and 50,000 g/mole, in a mixture of chlorinated organic solvent and an organic base, adding dropwise with stirring a solution of 4-bromobenzoyl chloride in a chlorinated organic solvent at temperatures ranging from 10°-50° C., and allowing this mixture to stir 3 hours, precipitating the 4-bromobenzoyl-terminated polymer with a non-solvent, drying the precipitate, and dissolving it in a highly polar solvent, adding an organic base, dichlorobis(triphenylphosphine)palladium, and a substituted acetylene under an inert atmosphere, stirring the mixture for 0.5 to 4 hours at 50°-100° C., and precipitating the resulting substituted ethynyl-terminated polymer with cold dilute aqueous acid.

Claim 7

The process of claim 4 wherein the substituted acetylene is of the formula HC.tbd.C--X, where X is selected from the group consisting of: Si(CH 3 ) 3 ; straight or branched organic radical having 4 to 10 carbon atoms; substituted aromatic groups of the formula: ##STR9## where R is selected from the group consisting of: straight or branched organic radicals having from 1 to 12 carbon atoms, H, and ##STR10## and halogenated derivatives of all of the above.

Claim 8

A process for preparing ethynyl and substituted ethynyl-terminated polysulfones comprising dissolving a polysulfone, having a molecular weight between 1000 and 50,000 g/mole, in a mixture of a chlorinated organic solvent and an organic base, adding a substituted 4-ethynylbenzoyl chloride of the formula: ##STR11## stirring for 0.5 to 4 hours and quenching in a non-solvent to precipitate the resulting substituted ethynyl-terminated polysulfone; where Z is selected from the group consisting of: Si(CH 3 ) 3 ; H; straight or branched organic radicals having from 1 to 10 carbon atoms; substituted aromatic groups of the formula: ##STR12## where R is selected from the group including: straight or branched organic radicals having from 1 to 12 carbon atoms, H, and ##STR13## and halogenated derivatives of all of the above.

Claim 9

A process for preparing ethynyl and substituted ethynyl-terminated polysulfones comprising dissolving a polysulfone, having a molecular weight between 1000 and 50,000 g/mole, in a mixture of a chlorinated organic solvent and an organic base, adding a substituted 4-ethynylbenzoyl chloride of the formula: ##STR11## stirring for 0.5 to 4 hours and quenching in a non-solvent to precipitate the resulting substituted ethynyl-terminated polysulfone; where Z is selected from the group consisting of: Si(CH 3 ) 3 ; H; straight or branched organic radicals having from 1 to 10 carbon atoms; substituted aromatic groups of the formula: ##STR12## where R is selected from the group including: straight or branched organic radicals having from 1 to 12 carbon atoms, H, and ##STR13## and halogenated derivatives of all of the above.