a.Key Laboratory of Marine Materials and Related Technologies, Key Laboratory of Marine Materials and Protective Technologies of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China
b.University of Chinese Academy of Sciences, Beijing 100049, China
c.State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China
Miao Hong, miaohong@sioc.ac.cn
收稿:2017-09-26,
录用:2017-10-21,
网络首发:2017-11-27,
纸质出版:2018-02-05
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Hui Li, Bai-Ru Ai, Miao Hong. Stereoselective Ring-opening Polymerization of
Hui Li, Bai-Ru Ai, Miao Hong. Stereoselective Ring-opening Polymerization of
Hui Li, Bai-Ru Ai, Miao Hong. Stereoselective Ring-opening Polymerization of
Hui Li, Bai-Ru Ai, Miao Hong. Stereoselective Ring-opening Polymerization of
Despite the extraordinary success has been achieved in metal catalyst-promoted stereoselective ring-opening polymerization (ROP) of
rac
-lactide (
rac
-LA)
well-controlled stereoselective
rac
-LA ROP by organic catalyst still remains a scientific challenge. Here we report our investigations into organocatalytic stereoselective ROP of
rac
-LA by utilizing novel bulky chiral and achiral
N
-heterocyclic carbenes (NHC)
1
3-bis-(1'-naphthylethyl)imidazolin-2-ylidene. The effect of polymerization conditions (
e
.
g
. solvent
temperature
alcohol initiator) on ROP behavior by these bulky NHCs has been fully studied
leading to the formation of isotactic-rich stereoblock polylactide (
P
i
=0.81) under optimized conditions with high activity (Conv.=98% in 30 min) and narrow molecular weight dispersity (
Đ
=1.05).
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