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

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

2.2.1.1.5<br />

Other Methods<br />

Individual methods have also been devised for the preparation of miktoarm<br />

stars. One of these approaches <strong>in</strong>volves the preparation of macromonomers possess<strong>in</strong>g<br />

either central or end v<strong>in</strong>yl groups which can be used to produce miktoarm<br />

stars either by copolymerization of the double bonds or by react<strong>in</strong>g the<br />

double bonds with liv<strong>in</strong>g polymer cha<strong>in</strong>s, thus creat<strong>in</strong>g active centers able to <strong>in</strong>itiate<br />

the polymerization of another monomer. All these methods are limited to<br />

specific synthetic problems and cannot be used for the preparation of a wide<br />

range of different structures.<br />

2.2.1.2<br />

Synthesis of A 2B Miktoarm Star Copolymers<br />

One miktoarm star copolymer of the A 2B type was prepared by Mays us<strong>in</strong>g a<br />

method similar to the one adopted by Pennisi and Fetters for the synthesis of<br />

asymmetric stars [21]. Accord<strong>in</strong>g to this method liv<strong>in</strong>g PS cha<strong>in</strong>s were reacted<br />

with excess CH 3SiCl 3 to produce the monosubstituted l<strong>in</strong>k<strong>in</strong>g agent, followed by<br />

the removal of the excess silane by the addition of a slight excess of liv<strong>in</strong>g PI<br />

cha<strong>in</strong>s. Fractionation was performed to remove the excess PI after the l<strong>in</strong>k<strong>in</strong>g<br />

Scheme 5<br />

Scheme 6

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