S-(α, α′-disubstituted-α″-acetic acid) substituted dithiocarbonate derivatives for controlled radical polymerization, process and polymers made therefrom
View Patent ↗Dithiocarbonate derivatives are disclosed, along with a process for preparing the same. The dithiocarbonate compounds can be utilized as initators, chain transfer agents and/or terminators in controlled free radical polymerizations. The dithiocarbonates can be used to produce polymers having narrow molecular weight distribution. Advantageously, the compounds of the present invention can also introduce functional groups into the resulting polymers. The dithiocarbonate compounds have low odor and are substantially colorless.
1. A method for forming a O-alkyl-S-(α,α′-disubstituted-α″ acetic acid) xanthate compound, comprising the steps of:
reacting a alkoxylate salt of a xanthate compound, carbon disulfide, a haloform, and a ketone in the presence of a base, and optionally a solvent and a catalyst selected from quaternary amines and salts thereof, and a polyether to form a reaction product; and
acidifying said reaction product to form a O-alkyl-S-(α,α′-disubstituted-α″ acetic acid) xanthate compound represented by the formula:
wherein R 12 and R 13 , independently, can be the same or different, can optionally be substituted, and are selected from a linear or branched alkyl having from 1 to about 12 carbon atoms; an aryl group having from 6 to about 18 carbon atoms; R 12 and R 13 can form and be part of a substituted or unsubstituted cyclic ring having from 3 to about 12 carbon atoms; wherein when R 12 and R 13 are substituted said substituents are selected from alkyl having from 1 to 6 carbon atoms, aryl, halogen, cyano, an ether having a total of 2 to 20 carbon atoms, nitro, and combinations thereof; wherein R 14 is optionally substituted, and is selected from linear or branched alkyl having from 1 to about 12 carbon atoms, an aryl group optionally saturated or unsaturated; an arylalkyl having from about 7 to about 18 carbon atoms; an acyl group; an alkene group; an alkenealkyl having from 3 to about 18 carbon atoms; an alkylene group; an alkoxyalkyl; a polyalkylene glycol residue; a polyalkylene glycol monoalkyl ether residue having from about 3 to about 200 carbon atoms; a polyalkylene glycol monoaryl ether residue having from about 3 to about 200 carbon atoms, 2-trifluoroethyl; alkyl substituted with phosphorous; wherein said “a” is 1 to about 4; and wherein when R 14 is substituted said substituents are selected from alkyl having from 1 to 6 carbon atoms, aryl, halogen, cyano, amino, alkene, alkoxycarbonyl, aryloxycarbonyl, carboxy, acyloxy, carbamoyl, alkylcarbonyl, alkylarylcarbonyl, arylcarbonyl, arylalkylcarbonyl, phthalimido, maleimido, succinimido, amidino, guanidimo, allyl, epoxy, alkoxy, quaternary ammonium salt, hydroxyl, an ether having a total of from 2 to about 20 carbon atoms, nitro, sulfur, phosphorous, carboalkoxy, and combinations thereof.
2. A method according to claim 1 , wherein said reaction is conducted at a temperature from about minus 15° C. to about 80° C.
3. A method according to claim 2 , wherein said haloform is chloroform or bromoform, or a blend thereof, and wherein said ketone has the formula:
wherein R 12 and R 13 are as previously defined.
4. A method according to claim 3 , wherein said haloform is utilized in an amount from 0 percent to about 500 percent molar excess and said ketone is used in an amount from 0 percent to about 300 percent molar excess, based on the molar amount of said metal salt of said dithiocarbamate.
5. A method according to claim 4 , wherein R 12 and R 13 , independently, are a phenyl group or an alkyl group having 1 to about 10 carbon atoms, or wherein R 12 and R 13 are part of a cyclic ring, and wherein R 14 is an alkyl having from 1 to about 8 carbon atoms.
6. A method for forming an O-alkyl-S-(α,α′-disubstituted-α″ acetic acid) xanthate polymer or copolymer, comprising the steps of:
providing a O-alkyl-S-(α,α′-disubstituted-α″-acetic acid) xanthate compound having the formula:
wherein R 12 and R 13 , independently, can be the same or different, can optionally be substituted, and are selected from a linear or branched alkyl having from 1 to about 12 carbon atoms; an aryl group having from 6 to about 18 carbon atoms; R 12 and R 13 can form and be part of a substituted or unsubstituted cyclic ring having from 3 to about 12 carbon atoms; wherein when R 12 and R 13 are substituted said substituents are selected from alkyl having from 1 to 6 carbon atoms, aryl, halogen, cyano, an ether having a total of 2 to 20 carbon atoms, nitro, and combinations thereof; wherein R 14 is optionally substituted, and is selected from linear or branched alkyl having from 1 to about 12 carbon atoms, an aryl group optionally saturated or unsaturated; an arylalkyl having from about 7 to about 18 carbon atoms; an acyl group; an alkene group; an alkenealkyl having from 3 to about 18 carbon atoms; an alkylene group; an alkoxyalkyl; a polyalkylene glycol residue; a polyalkylene glycol monoalkyl ether residue having from about 3 to about 200 carbon atoms; a polyalkylene glycol monoaryl ether residue having from about 3 to about 200 carbon atoms, 2-trifluoroethyl; alkyl substituted with phosphorous; and wherein when R 14 is substituted said substituents are selected from alkyl having from 1 to 6 carbon atoms, aryl, halogen, cyano, amino, alkene, alkoxycarbonyl, aryloxycarbonyl, carboxy, acyloxy, carbamoyl, alkylcarbonyl, alkylarylcarbonyl, arylcarbonyl, arylalkylcarbonyl, phthalimido, maleimido, succinimido, amidino, guanidimo, allyl, epoxy, alkoxy, quaternary ammonium salt, hydroxyl, an ether having a total of from 2 to about 20 carbon atoms, nitro, sulfur, phosphorous, carboalkoxy, and combinations thereof,
wherein said “a” is 1 to about 4; and reacting at least one vinyl monomer, or at least one conjugated diene monomer with said O-alkyl-S-(α,α′-disubstituted-α″-acetic acid) xanthate compound.
7. A method according to claim 6 , wherein said conjugated diene monomer has from 4 to 12 carbon atoms, and wherein said vinyl monomer has the formula:
wherein R 3 is selected from hydrogen, halogen, C 1 -C 4 alkyl, or substituted C 1 -C 4 alkyl wherein said substituents, independently, are selected from one or more hydroxy, alkoxy, aryloxy(OR 5 ), carboxy, acyloxy, aroyloxy(O 2 CR 5 ), alkoxy-carbonyl(CO 2 R 5 ), or aryloxy-carbonyl; N-pyrrolidonyl;
wherein R 4 is selected from hydrogen, R 5 , CO 2 H, CO 2 R 5 , COR 5 , CN, CONH 2 , CONHR 5 , O 2 CR 5 , OR 5 and halogen; and
wherein R 5 is selected from C 1 -C 18 alkyl, substituted C 1 -C 18 alkyl, C 2 -C 18 alkenyl, aryl, heterocyclyl, aralkyl, or alkaryl, and wherein said substituents, independently, are selected from one or more epoxy, hydroxy, alkoxy, acyl, acyloxy, carboxy, (and salts), sulfonic acid (and salts), alkoxy- or aryloxy-carbonyl, dicyanato, cyano, silyl, halo and dialkylamino.
8. A method according to claim 7 , wherein said vinyl monomer is selected from alkyl acrylate, vinyl acetate, acrylic acid, styrene, N-vinyl pyrrolidone, and combinations thereof.
9. A method according to claim 8 , wherein R 12 and R 13 , independently, are a phenyl group or an alkyl group having 1 to about 10 carbon atoms, or wherein R 12 and R 13 are part of a cyclic ring.
10. A method according to claim 9 , wherein a is 2, and wherein R 12 and R 13 , independently, are a phenyl group or alkyl group having 1 to about 10 carbon atoms, or R 12 and R 13 are part of a cyclic ring, and wherein R 14 an alkyl having from 1 to about 8 carbon atoms.
11. A method according to claim 1 , wherein said alkoxylate salt of said xanthate compound is represented by the formula:
R 14 O − Na +
wherein R 14 is as previously described.