Facile synthetic route to polymerizable hindered amine light stabilizers for transition-metal-catalyzed olefin copolymerization

Markku Auer, R. Nicolas, A. Vesterinen, H. Luttikhedde, Carl Wilen (Corresponding Author)

Research output: Contribution to journalArticleScientificpeer-review

10 Citations (Scopus)

Abstract

This work describes a facile method by which a polymerizable hindered amine light stabilizer, 4‐(10‐undecylidene)‐2,2,6,6‐tetramethylpiperidine, was prepared in a single‐step procedure by means of a Wittig reaction. The monomer was successfully copolymerized with ethylene with a rac‐[dimethylsilylenebis(4,5,6,7‐tetrahydro‐1‐indenyl)]zirconium dichloride/methylalumoxane catalyst system.
Original languageEnglish
Pages (from-to)1350-1355
JournalJournal of Polymer Science, Part A: Polymer Chemistry
Volume42
Issue number6
DOIs
Publication statusPublished - 2004
MoE publication typeA1 Journal article-refereed

Fingerprint

Dive into the research topics of 'Facile synthetic route to polymerizable hindered amine light stabilizers for transition-metal-catalyzed olefin copolymerization'. Together they form a unique fingerprint.

Cite this