Controlled Synthesis of Multi‐Arm Star Polyether–Polycarbonate Polyols Based on Propylene Oxide and CO 2
Multi‐arm star copolymers based on a hyperbranched poly(propylene oxide) polyether–polyol ( hb PPO) as a core and poly(propylene carbonate) (PPC) arms are synthesized in two steps from propylene oxide (PO), a small amount of glycidol and CO 2 . The PPC arms are prepared via carbon dioxide (CO 2 )/PO...
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Published in: | Macromolecular rapid communications. Vol. 35; no. 2; pp. 198 - 203 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-01-2014
|
Online Access: | Get full text |
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Summary: | Multi‐arm star copolymers based on a hyperbranched poly(propylene oxide) polyether–polyol (
hb
PPO) as a core and poly(propylene carbonate) (PPC) arms are synthesized in two steps from propylene oxide (PO), a small amount of glycidol and CO
2
. The PPC arms are prepared via carbon dioxide (CO
2
)/PO copolymerization, using
hb
PPO as a multifunctional macroinitiator and the (R,R)‐(salcy)CoOBzF
5
catalyst. Star copolymers with 14 and 28 PPC arms, respectively, and controlled molecular weights in the range of 2700–8800 g mol
−1
are prepared (
M
w
/
M
n
= 1.23–1.61). Thermal analysis reveals lowered glass transition temperatures in the range of −8 to 10 °C for the PPC star polymers compared with linear PPC, which is due to the influence of the flexible polyether core. Successful conversion of the terminal hydroxyl groups with phenylisocyanate demonstrates the potential of the polycarbonate polyols for polyurethane synthesis.
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ISSN: | 1022-1336 1521-3927 |
DOI: | 10.1002/marc.201300663 |