ISOMERIZATION POLYMERIZATIONS OF 4-SUBSTITUTED STYRENES - SYNTHESIS OF MACROMONOMERS WITH AMINO AND OR SILYL GROUPS/

Citation
Y. Nagasaki et al., ISOMERIZATION POLYMERIZATIONS OF 4-SUBSTITUTED STYRENES - SYNTHESIS OF MACROMONOMERS WITH AMINO AND OR SILYL GROUPS/, Macromolecules, 27(25), 1994, pp. 7236-7239
Citations number
14
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00249297
Volume
27
Issue
25
Year of publication
1994
Pages
7236 - 7239
Database
ISI
SICI code
0024-9297(1994)27:25<7236:IPO4S->2.0.ZU;2-B
Abstract
Lithium diisopropylamide (LDA) induced metalation reaction of styrenes with para substituents such as 4-methylstyrene (MST), 4-[(trimethylsi lyl)methyl]styrene (SMS), and 4-[(dimethylamino)methyl]styrene (AMS) t o form vinylbenzyllithium (VBL) derivatives. VBL derivatives initiated isomerization polymerizations to form oligomers with a polymerizable vinyl end and with functional groups such as amino groups and trimethy lsilyl groups in the side chain. Cooligomerization of the 4-substitute d styrenes gave macromonomers with a predicted extent of functional gr oups in the side chain.