Controlled Synthesis of Poly(neopentyl p-styrene sulfonate) via Reversible Addition-Fragmentation Chain Transfer Polymerisation. - Archive ouverte HAL Access content directly
Journal Articles Polymer international Year : 2015

Controlled Synthesis of Poly(neopentyl p-styrene sulfonate) via Reversible Addition-Fragmentation Chain Transfer Polymerisation.

Abstract

The controlled synthesis of poly(neopentyl p-styrene sulfonate) (PNSS) using reversible addition-fragmentation chain transfer polymerisation has been studied under a wide range of experimental conditions. PNSS can be used as an organic-soluble, thermally labile precursor for industrially valuable poly(p-styrene sulfonate), widely employed in technologies such as ionic exchange membranes and organic electronics. The suitability of two different chain transfer agents, three solvents, three different monomer concentrations and two different temperatures for the polymerisation of neopentyl p-styrene sulfonate is discussed in terms of the kinetics of the process and characteristics of the final polymer. Production of PNSS with systematically variable molecular weights and low dispersities (Đ ≤ 1.50 in all cases) has been achieved using 2-azidoethyl 2-(dodecylthiocarbonothioylthio)-2-methylpropionate in anisole at 75 °C, with an initial monomer concentration of 4.0 mol L−1. Finally, a poly(neopentyl p-styrene sulfonate)-b-polybutadiene-b-poly(neopentyl p-styrene sulfonate) (PNSS-b-PBD-b-PNSS) triblock copolymer has been synthesised via azide-alkyne click chemistry. Moreover, subsequent thermolysis of the PNSS moieties generated poly(p-styrene sulfonate) end blocks. This strategy allows the fabrication of amphiphilic copolymer films from single organic solvents without the need for post-deposition chemical treatment. © 2014 Society of Chemical Industry

Dates and versions

hal-01205573 , version 1 (25-09-2015)

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Isabel Fraga Domínguez, Joanna Kolomanska, Priscilla Johnston, Agnès Rivaton, Paul D Topham. Controlled Synthesis of Poly(neopentyl p-styrene sulfonate) via Reversible Addition-Fragmentation Chain Transfer Polymerisation.. Polymer international, 2015, 64, pp.621-630. ⟨10.1002/pi.4840⟩. ⟨hal-01205573⟩
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