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

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84 N. Hadjichristidis, S. Pispas, M. Pitsikalis, H. Iatrou, C. Vlahos<br />

Scheme 8<br />

Scheme 9<br />

Liv<strong>in</strong>g polymer cha<strong>in</strong>s were reacted with bromomethyl naphthalene but a<br />

fairly large amount of the coupled byproduct was formed. The byproduct was<br />

m<strong>in</strong>imized to 5–10% by us<strong>in</strong>g the Grignard reagent, lead<strong>in</strong>g to the formation of<br />

A 2 B stars. The f<strong>in</strong>al polymer was contam<strong>in</strong>ated by the start<strong>in</strong>g homopolymers<br />

and traces of PEO homopolymer. Polydispersity <strong>in</strong>dices as high as 1.2–1.3 were<br />

obta<strong>in</strong>ed with this procedure.<br />

A special technique was employed by Naka et al. for the preparation of A 2 B<br />

stars, A be<strong>in</strong>g PEO and B polyoxazol<strong>in</strong>e (POX) [26] accord<strong>in</strong>g to Scheme 8. Ru(III)<br />

complexes with bipyridyl term<strong>in</strong>ated polymers were utilized <strong>in</strong> this method.<br />

Characterization data were not provided for these miktoarm star copolymers.<br />

The chlorosilane method was adopted for the synthesis of miktoarm stars of<br />

the type B(A-b-B) 2 where A is PI and B is PS [27]. The synthetic procedure was<br />

similar to that used for the preparation of A 2B stars except that two of the arms<br />

are diblock copolymers, as shown <strong>in</strong> Scheme 9. Extensive characterization data<br />

were given to confirm the synthesis of well def<strong>in</strong>ed copolymers.

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