Neodymium-based catalysts bearing phosphate ligands for ring-opening polymerization of -caprolactone

被引:10
|
作者
Ren, Yixin [1 ,2 ]
Kularatne, Ruvanthi N. [1 ,2 ]
Miller, Justin T. [1 ,2 ]
Polderman, Stefanie T. [1 ,2 ]
Vo, Trinh D. [1 ,2 ]
Biewer, Michael C. [1 ,2 ]
Stefan, Mihaela C. [1 ,2 ]
机构
[1] Univ Texas Dallas, Dept Chem & Biochem, Richardson, TX 75080 USA
[2] Univ Texas Dallas, Dept Bioengn, Richardson, TX 75083 USA
基金
美国国家科学基金会;
关键词
coordination insertion mechanism; -caprolactone; NdCl3 center dot 3TEP; TEHP; ring-opening polymerization; CYCLIC ESTERS POLYMERIZATION; EPSILON-CAPROLACTONE; L-LACTIDE; LANTHANIDE COMPLEXES; IN-SITU; INITIATORS; MECHANISM; EFFICIENT; LACTONES; KINETICS;
D O I
10.1002/pola.29010
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Neodymium-based catalysts coordinated with phosphate ligands (NdCl3<bold></bold>3L), where L=triethyl phosphate (TEP) or tris(2-ethylhexyl) phosphate (TEHP), were synthesized. The ring-opening polymerizations (ROP) of -caprolactone (-CL) with these catalysts in the presence of benzyl alcohol initiator were performed, yielding polymers with well-defined molecular weights and relatively narrow polydispersity index (PDI=1.22-1.65). In situ NMR analysis of the reaction between NdCl3<bold></bold>3TEP and benzyl alcohol indicated that ROP proceeds through a coordination-insertion mechanism. The end groups of the resultant polymers were determined using MALDI-ToF mass spectrometry and NMR spectroscopy. The quasi-living nature of this catalytic system was demonstrated by kinetic studies and the successful synthesis of the block copolymer poly(-caprolactone)-block-poly(l-lactide) by sequential monomer addition. Kinetic studies revealed that the catalyst with the bulkier TEHP ligand increased the rate of ROP of -CL as compared to the TEP ligand. (c) 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 1289-1296
引用
收藏
页码:1289 / 1296
页数:8
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