Synthesis of amphiphilic triblock copolymer of polystyrene and poly(4[hyphen]vinylbenzyl glucoside) via TEMPO[hyphen]mediated living radical polymerization

4[hyphen]Vinylbenzyl glucoside peracetate 1 was polymerized with α,α′[hyphen]bis(2′,2′,6′,6′[hyphen]tetramethyl[hyphen]1′[hyphen]piperidinyloxy)[hyphen]1,4[hyphen]diethylbenzene 2 in chlorobenzene using (1S)[hyphen]([plus ])[hyphen]10[hyphen]camphorsulfonic acid anhydrous (CSA) as an accelerator ([1][equals]0.4 M,[1]/[2]/[CSA][equals]75/1/1.3) at 125 °C for 5 h. The polymerization afforded poly(4[hyphen]vinylbenzyl glucoside peracetate) having TEMPO moieties on both sides of the chain ends, 3, with a molecular weight (Mw,SLS) of 8500, a polydispersity index (Mw/Mn) of 1.09, and an average degree of polymerization of the 1 unit (x) of 17. Styrene (St) was polymerized with 3 in chlorobenzene at 125 °C (St/chlorobenzene[equals]1/2, w/w). The polymerization successfully afforded polystyrene–poly(4[hyphen]vinyl glucoside peracetate)–polystyrene, 4, when the polymerization time was below about 2 h. Polymer 4 with the Mw,SLS of 12,500, 17,900, and 29,400, the compositions (y–x–y) of 20–17–20, 45–17–45, and 100–17–100, and the Mw/Mn of 1.12, 1.14 and 1.17 were modified by deacetylation using sodium methoxide in dry[hyphen]THF into polystyrene–poly(4[hyphen]vinyl glucoside peracetate)–polystyrene, 5. The solubility of polymer 5 was examined using a good solvent for polystyrene such as toluene and for the saccharide such as H2O. [Copyright &y& Elsevier]