Synthesis of basic molecular brushes: ATRP of 4-vinylpyridine in organic media

Abstract

A poly(2-(2-bromopropionyloxy)ethyl methacrylate) (PBPEM) was used as macroinitiator in the synthesis of molecular brushes with poly(4-vinylpyridine) side chains, (P(BPEM- g-4VP). Atom transfer radical polymerization (ATRP) was employed as the polymerization technique. The polymerizations were carried out in DMF at 30 °C using a copper–chloride-based ATRP catalyst, which converted all the dormant polymer chain ends to alkyl chloride groups, thus minimizing branching and crosslinking, which occurred when a copper bromide-based catalyst was employed. Tris(2-pyridylmethyl)amine was selected as the ligand due to the high activity of its Cu I complex in ATRP as well as its strong binding to both Cu I and Cu II, which prevented competitive complexation of the monomer or polymer to the metal center. In order to prevent crosslinking via radical coupling, the monomer conversion was kept low (under 3%) and the alkyl chloride end groups of P4VP side chains were converted to alkoxyamines upon activation followed by a reaction with TEMPO radical. Dynamic light scattering measurements showed the hydrodynamic diameter ( D H) of the brushes was pH-dependent. Aggregation of single P(BPEM-g-4VP) brushes in water was very pronounced at high pH values but was observed even when the amount of added HCl was enough to completely protonate the pyridine units ( D H = 278 nm).