Abstract
This article discusses a facile and inexpensive reaction process for preparing polypropylene-based graft copolymers containing an isotactic polypropylene (i-PP) main chain and several functional polymer side chains. The chemistry involves an i-PP polymer precursor containing several pendant vinylbenzene groups, which is prepared through the Ziegler-Natta copolymerization of propylene and 1,4-divinylbenzene mediated by an isospecific MgCl 2$-supported TiCl 4 catalyst. The selective monoenchainment of 1,4-divinylbenzene comonomers results in pendant vinylbenzene groups quantitatively transformed into benzyl halides by hydrochlorination. In the presence of CuCl/pentamethyldiethylenetriamine, the in situ formed, multifunctional, polymeric atom transfer radical polymerization initiators carry out graft-from polymerization through controlled radical polymerization. Some i-PP-based graft copolymers, including poly(propylene-g-methyl methacrylate) and poly(propylene-g-styrene), have been prepared with controlled compositions.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 429-437 |
| Number of pages | 9 |
| Journal | Journal of Polymer Science, Part A: Polymer Chemistry |
| Volume | 43 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 15 2005 |
All Science Journal Classification (ASJC) codes
- Polymers and Plastics
- Organic Chemistry
- Materials Chemistry
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