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

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

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Poly(macromonomers), Homo- and Copolymerization 141<br />

3.5<br />

Some Other New Macromonomers<br />

<strong>Polymer</strong>ization of hexamethylcyclotrisiloxane with 3-butadienyllithium afforded<br />

butadienyl-ended polysiloxane macromonomer, 20 [27]. Polycondensation of<br />

a chiral methyl b-hydroxyisobutyrate at a temperature higher than 150 ˚C with<br />

Ti(O-nBu) 4 afforded directly a biodegradable polyester macromonomer, 21 [28].<br />

(20)<br />

(21)<br />

Glycopeptide macromonomers, 22, were prepared from p-v<strong>in</strong>ylbenzylam<strong>in</strong>e<strong>in</strong>itiated<br />

r<strong>in</strong>g-open<strong>in</strong>g polymerization of sugar-substituted a-am<strong>in</strong>o acid N-carboxyanhydrides<br />

[29]. They have been copolymerized with acrylamide to afford<br />

the correspond<strong>in</strong>g sugar-grafts with molecular recognition ability.<br />

4<br />

Homopolymerization and Copolymerization of Macromonomers<br />

(22)<br />

S<strong>in</strong>ce macromonomers are already polymers with MW between 10 3 and 10 4 ,<br />

their polymerization and copolymerization <strong>in</strong>volves polymer-polymer reactions.<br />

Thus a question of cont<strong>in</strong>u<strong>in</strong>g concern has been how and why a macromonomer<br />

is different <strong>in</strong> its reactivity from a correspond<strong>in</strong>g conventional monomer<br />

of low MW.

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