𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of block copolymers by nitroxyl-controlled radical polymerization

✍ Scribed by M. Steenbock; M. Klapper; K. Müllen; N. Pinhal; M. Hubrich


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
427 KB
Volume
47
Category
Article
ISSN
0323-7648

No coin nor oath required. For personal study only.

✦ Synopsis


The homopolymerization of methyl methacrylate (MMA) in the presence of 2,2,6,6-tetramethyl-l-piperidinyloxy (TEMPO) is described and compared to the TEMPO-mediated polymerization of styrene. Furthermore, the formation of block copolymers between MMA and styrene from polystyrene chains with TEMPO fragments as end groups is examined. The degree ofblock formation is estimated by GPC analyses. ESRexperiments are performed on the polystyrene chains to study the scission behavior of the TEMPO fragments.


📜 SIMILAR VOLUMES


Synthesis of block copolymers by radical
✍ Xiao-Min Yang; Kun-Yuan Qiu 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 1 views

End-functional polystyrenes with an N,N-diethyldithiocarbamyl group were prepared by the photopolymerization of styrene with novel diethyldithiocarbamate derivatives as photoiniferters. Under ultraviolet light, the end-functional polymers could initiate a second monomer to polymerize and form block

Diblock and triblock functional copolyme
✍ M. Mariani; M. Lelli; K. Sparnacci; M. Laus 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 213 KB

Controlled polystyrenes with different molar mass values were synthesized starting from benzoyl peroxide and TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxy). The polystyrene homopolymers served as initiators for the block copolymerization of phthalimide methylstyrene (PIMS) to synthesize polystyrene-b-