Modification of polymers having aromatic groups through formation of boronic ester groups
View Patent ↗The C—H bond of pendant aromatic groups such as commercial polystyrenes with three types of tacticities (syndiotactic, isotactic, atactic) undergo catalyzed functionalization with boron reagents. A boronic ester group formed on the polymer in the polystyrene was further converted to hydroxy and arene via oxidation and coupling reactions, respectively. These functionalizations proceeded without significantly affecting the molecular weight of starting polymer and the functional concentrations could be easily controlled by changing the ratio of boron reagent to monomer unit.
1. A method of modifying properties of a polymer comprising:
providing a polymer in a solvent environment, the polymer having aromatic groups on a polymer chain;
providing a boronic ester in the solvent environment; and
catalytically attaching a boron-containing group derived from the boronic ester onto a carbon atom on at least some aromatic groups of the polymer chain.
2. The method of claim 1 wherein the boron-containing group on the carbon atom on at least some aromatic groups is selected from the group consisting of boronic ester, boronic acid or trifluoroboronate.
3. The method of claim 2 wherein the boron-containing group is subsequently reacted to form hydroxyl or phenoxy groups and boron removed from at least some links to the aromatic groups.
4. The method of claim 1 wherein the polymer comprises linkages derived from functionalized arene compounds.
5. The method of claim 1 wherein the polymer comprises linkages derived from styrene.
6. A method of modifying properties of a polymer comprising:
providing a polymer in a solvent environment, the polymer having aromatic groups on a polymer chain; and
catalytically attaching a boron-containing group on a carbon atom on at least some aromatic groups of the polymer chain
wherein the boron-containing group is attached by catalyzed reaction of at least one pinacolborane or bis(pinacolato)diboron compound with at least one aromatic group on the polymer.
7. The method of claim 6 wherein the aromatic group is selected from the group comprising phenyl groups and naphthyl groups as main chain aromatic groups, side chain aromatic groups or pendant aromatic groups.
8. The method of claim 7 wherein the aromatic group is selected from the group consisting of pendant phenyl groups and pendant naphthyl groups.
9. A method of modifying properties of a polymer comprising:
providing a polymer in a solvent environment, the polymer having aromatic groups on a polymer chain; and
catalytically attaching a boron-containing group on a carbon atom on at least some aromatic groups of the polymer chain
wherein the catalyst for attaching the boron group has a formula:
IrABn
wherein Ir is an iridium cation, A is an anion and B is an alkene.
10. The method of claim 9 wherein the catalyst for attaching the boron group has a formula:
IrABn
wherein Ir is an iridium cation, A is an anion and B is an alkene,
wherein the polymer comprises linkages derived from functionalized arene compounds.
11. The method of claim 9 wherein the catalyst for attaching the boron group has a formula:
IrABn
wherein Ir is an iridium cation, A is an anion and B is an alkene and a borane is used as a source of the boron groups,
wherein the polymer comprises linkages derived from styrene.
12. The method of claim 10 wherein the aromatic groups of the polymer chain are selected from the group consisting of pendant aromatic groups, main chain aromatic groups and side chain aromatic groups.
13. A polymer having aromatic groups thereon, at least some of the aromatic groups having a boronic ester or boronic acid group bound to a carbon atom of the aromatic group, the boronic ester or boronic acid group containing a derivative of a boron compound having a formula:
IrABn
wherein Ir is an iridium cation, A is an anion and B is an alkene.
14. The method of claim 6 wherein the boronic ester has the formula:
(—B(OR)) 2 ,
wherein R=alkyl.
15. The method of claim 4 wherein the arene group has a functional group selected from the group consisting of silane, siloxy, halide, hydroxy, amine, carbonyl, nitrile, sulfonyl, phosphine, alkyl, alkenyl, alkynyl, aryl, ethylenically unsaturated groups, acryloyl and epoxy.