Controllable bulk solvent-free melt ring-opening polymerization (ROP) of L-lactide catalyzed by Ni(II) and Ni(II)-Ln(III) complexes based on the Salen-type Schiff-base ligand

被引:20
|
作者
Jin, Wen-Juan [1 ]
Ding, Li-Qin [1 ,2 ]
Chu, Zeng [1 ]
Chen, Lei-Lei [1 ]
Lue, Xing-Qiang [1 ,3 ]
Zheng, Xiao-Yan [1 ]
Song, Ji-Rong [1 ]
Fan, Dai-Di [1 ]
机构
[1] NW Univ Xian, Shaanxi Key Lab Degradable Med Mat, Shaanxi Key Lab Phys Inorgan Chem, Xian 710069, Shaanxi, Peoples R China
[2] Xian Shiyou Univ, Sch Chem & Chem Engn, Xian 710065, Shaanxi, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Salen-type Schiff base transition metal or mixed metal complex; Bulk solvent-free melt ring-opening polymerization; L-Lactide; METAL-COMPLEXES; BIOMEDICAL APPLICATIONS; ALIPHATIC POLYESTERS; INITIATORS; ALKOXIDES; POLYLACTIDE; POLYMERS; LACTONES;
D O I
10.1016/j.molcata.2011.01.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A monometallic (Ni2+, 1) and a series of bimetallic (Ni2+-Ln(3+), Ln = Ce (2); Ln = Nd (3); Ln = Sm (4); Ln = Eu (5); Ln = Tb (6); Ln = Ho (7); Ln = Tm (8)) complexes based on the Salen-type Schiff-base ligand H2L (H2L=N,N'-bis(3-methoxysalicylidene)ethylene-1,2-diamine) were synthesized and characterized by EA, FT-IR, ESI-MS and X-ray crystallography. The catalysis results showed that the two kinds of complexes with different active species, could efficiently catalyze the bulk solvent-free melt ring-opening polymerization (ROP) of L-lactide with moderate molecular weights and narrow molecular weight distributions. Especially for the series of bimetallic complexes 2-8, the involvement of rare ions effectively passivated the catalytic behaviors on the ROP of L-lactide, while was in favor of the increase of polymeric molecular weights (M-w, or M-n) and the polymerization controllability, and the type of rare ions was important and influential factor contributing to the catalytic behaviors. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 32
页数:8
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