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
相关论文
共 37 条
[1]  
Addison A.W., 2003, DALTON T, P1349
[2]   LIVING AND IMMORTAL POLYMERIZATIONS [J].
AIDA, T .
PROGRESS IN POLYMER SCIENCE, 1994, 19 (03) :469-528
[3]   Metalloporphyrins as initiators for living and immortal polymerizations [J].
Aida, T ;
Inoue, S .
ACCOUNTS OF CHEMICAL RESEARCH, 1996, 29 (01) :39-48
[4]   Electronic influence of ligand substituents on the rate of polymerization of ε-caprolactone by single-site aluminium alkoxide catalysts [J].
Alcazar-Roman, LM ;
O'Keefe, BJ ;
Hillmyer, MA ;
Tolman, WB .
DALTON TRANSACTIONS, 2003, (15) :3082-3087
[5]   Phenolate Substituent Effects on Ring-Opening Polymerization of ε-Caprolactone by Aluminum Complexes Bearing 2-(Phenyl-2-olate)-6-(1-amidoalkyl)pyridine Pincers [J].
Alkarekshi, Wafaa ;
Armitage, Andrew P. ;
Boyron, Olivier ;
Davies, Christopher J. ;
Govere, Matifadza ;
Gregory, Andrew ;
Singh, Kuldip ;
Solan, Gregory A. .
ORGANOMETALLICS, 2013, 32 (01) :249-259
[6]  
Biela T, 2002, MACROMOL SYMP, V183, P1, DOI 10.1002/1521-3900(200207)183:1<1::AID-MASY1>3.0.CO
[7]  
2-Q
[8]   Aluminum Complexes of Fluorinated Dialkoxy-Diimino Salen-like Ligands: Syntheses, Structures, and Use in Ring-Opening Polymerization of Cyclic Esters [J].
Bouyahyi, Miloud ;
Grunova, Ekaterina ;
Marquet, Nicolas ;
Kirillov, Evgueni ;
Thomas, Christophe M. ;
Roisnel, Thierry ;
Carpentier, Jean-Francois .
ORGANOMETALLICS, 2008, 27 (22) :5815-5825
[9]   Aluminum Complexes of Bidentate Fluorinated Alkoxy-lmino Ligands: Syntheses, Structures, and Use in Ring-Opening Polymerization of Cyclic Esters [J].
Bouyahyi, Miloud ;
Roisnel, Thierry ;
Carpentier, Jean-Francois .
ORGANOMETALLICS, 2012, 31 (04) :1458-1466
[10]   Ancillary ligand effect on single-site styrene polymerization:: Isospecificity of group 4 metal bis(phenolate) catalysts [J].
Capacchione, C ;
Proto, A ;
Ebeling, H ;
Mülhaupt, R ;
Möller, K ;
Spaniol, TP ;
Okuda, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (17) :4964-4965