Polymers containing polyunsaturated acid radicals, process for their preparation and use thereof

Claim 2

A non-toxic polymer having a molecular weight between 1,000 and 1,500,000 characterized in that it contains the radical of a polyunsaturated acid selected from the group consisting of 8,11,14-eicosatrienoic acid; 5,8,11,14-eicosatetraenoic acid; and 5,8,11,14,17-eicosapentenoic acid, bound to a macromolecular backbone of polyacrylic or polymethacrylic units through oxyalkylenic, aminoalkylenic, or oxyaminoalkylenic chains, said polymer containing units of the formula ##STR1## wherein R is H or CH 3 , A represents an alkylene radical terminated at its ends with an --NH-- group or an --O-- group, and B represents a radical of such polyunsaturated acid sans a carboxyl group.

Claim 3

The non-toxic polymer of claim 1 wherein said alkylene radical is derived from compounds selected from the group consisting of N,N-dihydroxy ethyl-1,3-propanediamine, ethanolamine, ethylene diamine, and ethyleneglycol.

Claim 4

A process for preparing the non-toxic polymers of claim 1 comprising polymerizing a monomer selected from the group consisting of 1-acryloylbenzotriazole, 1-acryloylmethoxybenzotriazole, 1-acryloylmethylbenzotriazole, 1-acryloylimidazole, N-acryloylsuccimide, and N-(2,4,5-trichlorophenyl) acrylamide, reacting the resulting polymer with an alkylenediamine, an hydroxyalkylamine, or a glycol and then reacting the resulting polymer with said polyunsaturated acid in an inert anhydrous organic solvent under an inert atmosphere at a temperature between about 10 and 80° C. for a period of time from about 5 to about 72 hours.

Claim 5

A process for preparing the non-toxic polymers of claim 1 comprising polymerizing acrylic acid or methacrylic acid, reacting the resulting polymer with carbonyldiimidazole to introduce reactive acetylimidazole groups along the chain of the polymer, reacting the obtained activated polymer with an alkylenediamine, an hydroxyalkylamine, or a glycol and then reacting the resulting polymer with said polyunsaturated acid in an inert anhydrous solvent under an inert atmosphere at a temperature between about 10° and 80° C. for a period of time from about 5 to about 72 hours.

Claim 6

A non-toxic copolymer having a molecular weight between 1,000 and 1,500,000 characterized in that it contains the radical of a polyunsaturated acid selected from the group consisting of 8,11,14-eicosatrienoic acid; 5,8,11,14-eicosatetraenoic acid; and 5,8,11,14,17-eicosapentenoic acid, bound to a macromolecular backbone of polyacrylic or polymethacrylic units through oxyalkylenic, aminoalkylenic, or oxyaminoalkylenic chains, said polymer containing units of the formula ##STR2## wherein R is H or CH 3 , A represents an alkylene radical terminated at its end with an --NH-- group or an --O-- group, B represents a radical of such polyunsaturated acid sans a carboxyl group, and D represents a divalent radical supplied by a comonomer selected from the group consisting of 1-acryloyl-4-methyl piperazine, N-acryloyl morpholine, N-vinyl pyrrolidone, divinylbenzene, methylene bis-acrylamide, N,N'-bisacryloyl piperazine, and N,N'-bisacryloyl N,N'-dimethylethylene diamine.

Claim 7

A non-toxic copolymer having a molecular weight between 1,000 and 1,500,000 characterized in that it contains the radical of a polyunsaturated acid selected from the group consisting of 8,11,14-eicosatrienoic acid; 5,8,11,14-eicosatetraenoic acid; and 5,8,11,14,17-eicosapentenoic acid, bound to a macromolecular backbone of polyacrylic or polymethacrylic units through oxyalkylenic, aminoalkylenic, or oxyaminoalkylenic chains, said polymer containing units of the formula ##STR2## wherein R is H or CH 3 , A represents an alkylene radical terminated at its end with an --NH-- group or an --O-- group, B represents a radical of such polyunsaturated acid sans a carboxyl group, and D represents a divalent radical supplied by a comonomer selected from the group consisting of 1-acryloyl-4-methyl piperazine, N-acryloyl morpholine, N-vinyl pyrrolidone, divinylbenzene, methylene bis-acrylamide, N,N'-bisacryloyl piperazine, and N,N'-bisacryloyl N,N'-dimethylethylene diamine.

Claim 8

The non-toxic copolymer of claim 5 wherein said alkylene radical is derived from compounds selected from the group consisting of N,N-dihydroxy ethyl-1,3-propanediamine, ethanolamine, ethylene diamine, and ethyleneglycol.

Claim 9

A process for preparing the non-toxic copolymers of claim 5 comprising polymerizing a monomer selected from the group consisting of 1-acryloylbenzotriazole, 1-acryloylmethoxybenzotriazole, 1-acryloylmethylbenzotriazole, 1-acryloylimidazole, N-acryloylsuccimide, and N-(2,4,5-trichlorophenyl)acrylamide with a comonomer selected from the group consisting of 1-acryloyl-4-methyl piperazine, N-acryloyl morpholine, N-vinyl pyrrolidone, divinylbenzene, methylene bisacrylamide, N,N'-bisacryloyl piperazine, and N,N'-bisacryloyl N,N'-dimethylethylene diamine, reacting the resulting polymer with an alkylenediamine, an hydroxyalkylamine, or a glycol and then reacting the resulting polymer with said polyunsaturated acid in an inert anhydrous organic solvent under an inert atmosphere at a temperature between about 10° and 80° C. for a period of time from about 5 to about 72 hours.

Claim 10

A process for preparing the non-toxic copolymers of claim 5 comprising polymerizing acrylic acid or methacrylic acid with a comonomer selected from the group consisting of 1-acryloyl-4-methyl piperazine, N-acryloyl morpholine, N-vinyl pyrrolidone, divinylbenzene, methylene bisacrylamide, N,N'-bisacryloyl piperazine, and N,N'-bisacryloyl N,N'-dimethylethylene diamine, reacting the resulting polymer with carbonyldiimidazole to introduce reactive acetylimidazole groups along the chain of the polymer, reacting the obtained activated polymer with an alkylenediamine, an hydroxyalkylamine, or a glycol and then reacting the resulting polymer with said polyunsaturated acid in an inert anhydrous solvent under an inert atmosphere at a temperature between about 10° and 80° C. for a period of time from about 5 to about 72 hours.

Claim 11

The process of claim 3 wherein the side-chain forming compound is selected from the group consisting of N,N-dihydroxy ethyl-1,3-propanediamine, ethanolamine, ethylenediamine and ethyleneglycol.

Claim 12

The process of claim 4 wherein the side-chain forming compound is selected from the group consisting of N,N-dihydroxy ethyl-1,3-propanediamine, ethanolamine, ethylenediamine and ethyleneglycol.