

FOLLOWUS
a.Key Laboratory of Biobased Polymer Materials, Shandong Provincial Education Department; School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China
b.State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620, China
E-mail shaofengliu@qust.edu.cn (S.F.L.)
E-mail zbli@qust.edu.cn (Z.B.L.)
Received:10 August 2017,
Accepted:08 September 2017,
Online First:01 November 2017,
Published:05 February 2018
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Tong Shi, Quan-De Zheng, Wei-Wei Zuo, et al. Bimetallic Aluminum Complexes Supported by Bis(salicylaldimine) Ligand: Synthesis, Characterization and Ring-opening Polymerization of Lactide[J]. Chinese Journal of Polymer Science, 2018, 36(2): 149-156.
Tong Shi, Quan-De Zheng, Wei-Wei Zuo, et al. Bimetallic Aluminum Complexes Supported by Bis(salicylaldimine) Ligand: Synthesis, Characterization and Ring-opening Polymerization of Lactide[J]. Chinese Journal of Polymer Science, 2018, 36(2): 149-156. DOI: 10.1007/s10118-018-2039-5.
Two types of bifunctional bis(salicylaldimine) ligands (
syn
-L
and
anti
-L
) were designed and synthesized to support bimetallic aluminum complexes. Owing to the rigid anthracene skeleton
syn
-L
and
anti
-L
successfully locked two Al centers in close proximity (
syn
-Al
2
) and far apart (
anti
-Al
2
)
respectively. The distance between two Al centers in
syn
-Al
2
was defined by X-ray diffraction as 6.665 Å
which is far shorter than that in
anti
-Al
2
. In the presence of stoichiometrical BnOH
syn
-Al
2
and
anti
-Al
2
were both efficient for ring-opening polymerization (ROP) of
rac
-LA with the former being more active. In the presence of excess BnOH
syn
-Al
2
showed an efficient and immortal feature
consistent with high conversions
matched
M
n
s
narrow molecular weight distributions and end group fidelity
while
anti
-Al
2
had a much lower activity or even became entirely inactive due to rapid decomposition
indicated by
in situ
1
H-NMR experiments of Al complexes with BnOH.
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