Synthesis, characterization of aluminum complexes supported by multidentate aminophenol ligands and application in the ring-opening polymerization of ε-caprolactone

被引:11
作者
Liu, Xianyu [1 ]
Jian, Chunli [1 ]
Yu, Dawei [1 ]
Zhang, Jinfeng [1 ]
Tang, Ning [1 ]
Wang, Cheng [2 ]
Wu, Jincai [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Key Lab Nonferrous Met Chem & Resources Utilizat, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Affiliated Hosp 2, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Aluminum complex; epsilon-Caprolactone; Initiator; Ring-opening polymerization; LIVING POLYMERIZATION; IMMORTAL POLYMERIZATION; RANDOM COPOLYMERIZATION; EFFICIENT CATALYSTS; TITANIUM COMPLEXES; L-LACTIDE; INITIATORS; ZIRCONIUM; LITHIUM; ZINC;
D O I
10.1016/j.inoche.2013.09.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactions of H4L1 (L-1 = N-1,N-1,N-2,N-2-tetra((2-hydroxy-3,5-dibutyl)benzyl)-1, 2-ethanediamine) and H4L2 (L-2 = N-1,N-1,N-2,N-2-tetra((2-hydroxy-3,5-dimethyl)benzyl)-1,2-ethanediamine) with AlMe3 in toluene give [Al-2(CH3)(2)L-1(THF)(2)] (1) and[Al-2(CH3)(2)L-2] (3) respectively. Treatment of complex 1 with 2-methoxyethanol affords [Al-2(OCH2CH2OCH3)(2) L-1] (2). The experimental results indicate that complexes 1 and 2 can efficiently initiate the ring-opening polymerization of epsilon-caprolactone under a controlled manner, yielding polymers with relatively narrow molecular weight distribution and desirable molecular weights, while the performance of dinuclear complex 3 is not good due to the side reactions between the two neighboring active groups in the propagation progress. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 211
页数:6
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