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142 Advances in Polymer Science Editorial Board: A. Abe. A.-C ...

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62 B. Charleux, R. Faust<br />

Scheme 16<br />

correspond<strong>in</strong>g primary ester which may affect the copolymerization behavior of<br />

the macromonomer.<br />

The third route for the synthesis of PIB macromonomer was based on the addition<br />

of p-hydroxy-thiophenol onto the PIB double bonds followed by esterification<br />

with methacryloyl chloride (Scheme 14).<br />

High conversion of double bonds was found only with Glissopal, but it was<br />

necessary, even <strong>in</strong> this case, to separate from non-functional PIB before esterification.<br />

While the feasibility to synthesize methacrylate functional PIBs by all<br />

three methods was demonstrated, due to the necessary column chromatography<br />

step to obta<strong>in</strong> high functionality PIB macromonomers, the utility of the method<br />

is questionable.

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