Controlled formation of isocyanate-terminated star polyethers avoiding chain extension

Citation
Cf. Bartelink et al., Controlled formation of isocyanate-terminated star polyethers avoiding chain extension, J POL SC PC, 38(14), 2000, pp. 2555-2565
Citations number
28
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
ISSN journal
0887624X → ACNP
Volume
38
Issue
14
Year of publication
2000
Pages
2555 - 2565
Database
ISI
SICI code
0887-624X(20000715)38:14<2555:CFOISP>2.0.ZU;2-E
Abstract
Star polymers with reactive isocyanate end groups were prepared via the end capping of hydroxy-terminated star polyether polyols with toluene diisocya nate (TDI; 80% = 2,4 TDI, 20% = 2,6 TDI). The multifunctional polyols and T DI were reacted in bulk without a catalyst. This procedure was optimal in r egard to the product yield, minimizing unfavorable coupling side reactions and avoiding crosslinking reactions. The experimental results were based on theoretical studies of the reaction kinetics. (C) 2000 John Wiley & Sons, Inc.