Radical Chain End Chemical Transformation of SG1-Based Polystyrenes

Yohann Guillaneuf (1) , Pierre-Emmanuel Dufils (2) , Laurent Autissier , Marion Rollet (3) , Didier Gigmes (3) , Denis Bertin (3)

1 LCP - Laboratoire Chimie Provence
2 Solvay
3 ICR - Institut de Chimie Radicalaire

Radical chain end functionalization of polystyrene previously prepared by NMP using the SG1 nitroxide was investigated. Hydroxy-functional polystyrenes were easily prepared by two different pathways: via an exchange with TEMPO nitroxide followed by a Zn/AcOH reduction or via a radical hydroxylation using the in situ preparation/reduction of the corresponding hydroperoxide. The introduction of a bromine end group was performed by radical bromination under mild conditions using ethyl 2-bromoisobutyrate as bromine transfer agent. The latter polymer was further reacted with NaN3 and also used as a macroinitiator to prepare PS-b-PMMA by ATRP to confirm the chemical post-transformation. Azide-functional polystyrenes were also prepared by a one-step radical azidation reaction using ethanesulfonyl azide. In all cases, the chemical transformations were followed by both liquid chromatography at the critical condition in pure eluent and Maldi-Tof MS.

Domaines: Chimie

Yohann Guillaneuf, Pierre-Emmanuel Dufils, Laurent Autissier, Marion Rollet, Didier Gigmes, et al.. Radical Chain End Chemical Transformation of SG1-Based Polystyrenes. Macromolecules, 2010, 43 (1), pp.91--100. ⟨10.1021/ma901838m⟩. ⟨hal-01460226⟩