The bromine addition at the polydiene block double bonds of a radial s
tyrene-butadiene (SBS) and a linear styrene-isoprene (SIS) block copol
ymer (thermoplastic elastomers), in tetrahydrofurane solution at 0 deg
rees C, has been investigated by IR spectroscopy. In both cases the br
omine reacts exclusively with the polydiene middle block double bonds;
the polystyrene blocks are unaffected. The bromine reacts preferentia
lly with the 1,4-type (cis and trans) double bonds of the polybutadien
e block of SBS. At low bromination level (below 5%) the bromine reacts
mainly with the 1,4-cis type double bonds of polyisoprene block of SI
S, while at higher bromination level the bromine presents the same rea
ctivity towards the 1,4-type (cis and trans) and vinylic (3,4-type) do
uble bonds. (C) 1997 Elsevier Science Ltd.