NOVEL MULTIFUNCTIONAL AZO INITIATORS FOR FREE RADICAL POLYMERIZATIONS: METHODS OF PREPARATION
The invention provides compositions of matter, methods of their synthesis, and methods of their use in polymerization reactions. The compositions include polyfunctional initiators used to make star polymers when polymerized with monomers. The polyfunctional initiators are synthesized out of a multifunctional core with at least two functional groups and two or more initiator units bonded to the functional groups. The initiator units have two electron-withdrawing groups bonded to a central carbon atom and an azo group between the central carbon atom and the functional group. The polyfunctional initiators are particularly effective because when they decompose to form the radical core of a star polymer, the electron-withdrawing groups prevent the corresponding radical from forming any linear polymer contamination and only desired star polymers result.
1 . A polyfunctional initiator comprising a multifunctional core bonded to at least two initiator units wherein each initiator unit comprises at least one radical stabilizing group bonded to a central atom and an azo group between the central atom and the multifunctional core.
2 . The polyfunctional initiator of claim 1 wherein the at least one radical stabilizing group is one selected from the list consisting of: an electron-withdrawing group, a steric hindrance group, and any combination thereof.
3 . The polyfunctional initiator of claim 1 wherein the central atom is selected from the list consisting of: carbon, oxygen, and silicon.
4 . The polyfunctional initiator of claim 1 wherein the multifunctional core comprises at least two end atoms;
each end atom is bonded to an initiator unit, the atom of each end atom is selected from the list consisting of carbon, oxygen, nitrogen, primary amine nitrogen, secondary amine nitrogen, tertiary amine nitrogen, sulfur, silicon, and siloxane silicon;
the multifunctional core spans at least one string with a string length of between 1 and 200 atoms between each end atom not including the end atoms;
the atoms within the string comprise at least one item selected from the list consisting of saturated carbon, unsaturated carbon, carbonyl carbon, saturated nitrogen, unsaturated nitrogen, and oxygen.
5 . The polyfunctional initiator of claim 3 further comprising between 1 and 4 branching atoms, each branching atom is an atom within at least three different strings, and is selected from the list consisting of carbon, nitrogen, and silicon.
6 . The polyfunctional initiator of claim 1 according to formula I:
wherein:
R is a multifunctional core with at least two functional groups,
R 1 is a linker group selected from the list consisting of: one or more carbons, an amide, an ester, an amine, a silane, sulfur, silicon, a thiol, an ether, and any combination thereof
R 2 is a hydrocarbon having between 4 and 100 carbon atoms having a structure selected from the list consisting of linear, branched, aromatic, and aliphatic,
at least one of R 3 and R4 are radical stabilizing groups,
R 5 is hydrocarbon having between 1 and 50 carbon(s) or a radical stabilizing group, and X is greater than 1.
7 . The polyfunctional initiator of claim 1 wherein the multifunctional core is one selected from the list consisting of: 2,2′,2″-Nitrilotriethylamine, triethanol amine, pentaerythritol and its derivatives, dendritic molecules, multifunctional amines, multifunctional acid chlorides, multifunctional esters, multifunctional acids, and multifunctional alcohols.
8 . The polyfunctional initiator of claim 6 wherein R 2 is selected from the list consisting of a linear substituted alkyl group, a non-linear substituted alkyl group, a linear unsubstituted alkyl group, a non-linear unsubstituted alkyl group, a linear substituted aryl group, a non-linear substituted aryl group, a linear unsubstituted aryl group, a non-linear unsubstituted aryl group, a linear substituted cyclo alkyl group, a non-linear substituted cyclo alkyl group, a linear unsubstituted cyclo alkyl group, and a non-linear unsubstituted cyclo alkyl group.
9 . The polyfunctional initiator of claim 6 wherein R 5 is selected from the list consisting of: a linear alkyl group, a non-linear alkyl group, an aryl group, an electron withdrawing group, and any combination thereof.
10 . The polyfunctional initiator of claim 5 wherein at least one of the electron withdrawing groups are selected from the list consisting of CN, CONR 6 R 7 , COOR 8 , COOH, NO 2 , CF 3 , and —C 6 H 4 ,R 9 wherein:
R 6 , R 7 , and R 8 are each one selected from the list consisting of hydrogen, a linear alkyl group, a linear aryl group, a linear alkoxy group, a linear amino group, a linear alkylamino group, a linear hydroxyl group, a branched alkyl group, a branched aryl group, a branched alkoxy group, a branched amino group, a branched alkylamino group, and a branched hydroxyl group and R 9 is selected from the group consisting of CN, CONR 6 R 7 , COOR 8 , COOH, NO 2 , and CF 3 .
11 . The polyfunctional initiator of claim 1 constructed and arranged for use in a free radical polymerization reaction selected from the list consisting of: solution, suspension, bulk, emulsion, inverse emulsion, precipitation/dispersion, inverse suspension, and any combination thereof.
12 . A method of synthesizing a star polymer comprising the steps of:
providing at least one 4-functional peroxide initiator having a multifunctional core and 4 initiator units,
providing a plurality of monomers,
decomposing at least two initiator units to form at least one initiator radical, and
initiating a polymerization reaction between each of the at least one initiator radicals and the plurality of monomers.
13 . The polyfunctional initiator of claim 12 constructed and arranged for use in a free radical polymerization reaction selected from the list consisting of: solution, suspension, bulk, emulsion, inverse emulsion, precipitation/dispersion, inverse suspension, and any combination thereof.