DEGRADATIVE ROUTES TO TELECHELIC OLIGOMERS AND MACROMONOMERS

Citation
Jr. Ebdon et al., DEGRADATIVE ROUTES TO TELECHELIC OLIGOMERS AND MACROMONOMERS, Pure and applied chemistry, A32, 1995, pp. 603-611
Citations number
19
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00334545
Volume
A32
Year of publication
1995
Supplement
5-6
Pages
603 - 611
Database
ISI
SICI code
0033-4545(1995)A32:<603:DRTTOA>2.0.ZU;2-N
Abstract
A variety of telechelic oligomers with terminal aldehyde, hydroxyl, ke tone or carboxylic acid end groups can be synthesized by ozonolyses of suitable free radical copolymers containing small amounts of randomly distributed C=C bonds. These bonds can be introduced using either a d iene or an acetylene as comonomer. The average molecular weights of th e oligomers are controlled by the C=C content, and the nature of the e nd groups by the choice of diene or acetylene and by the procedures us ed to work up the ozonides. Potentially macromonomeric oligomers can b e synthesized by the photolysis of copolymers containing small amounts of alkyl vinyl or aryl vinyl ketone units. Telechelic oligomers can b e chain-extended by a variety of means, including by Michael additions , depending on the nature of the end groups.