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
相关论文
共 42 条
[1]  
Agarwal S, 2000, MACROMOL RAPID COMM, V21, P195, DOI 10.1002/(SICI)1521-3927(20000301)21:5<195::AID-MARC195>3.0.CO
[2]  
2-4
[3]   Recent developments in ring opening polymerization of lactones for biomedical applications [J].
Albertsson, AC ;
Varma, IK .
BIOMACROMOLECULES, 2003, 4 (06) :1466-1486
[4]   Ring-opening polymerization of lactide with group 3 metal complexes supported by dianionic alkoxy-amino-bisphenolate ligands: Combining high activity, productivity, and selectivity [J].
Amgoune, A ;
Thomas, CM ;
Roisnel, T ;
Carpentier, JF .
CHEMISTRY-A EUROPEAN JOURNAL, 2006, 12 (01) :169-179
[5]   Lanthanide compounds as environmentally-friendly corrosion inhibitors of aluminium alloys:: A review [J].
Bethencourt, M ;
Botana, FJ ;
Calvino, JJ ;
Marcos, M ;
Rodríguez-Chacón, MA .
CORROSION SCIENCE, 1998, 40 (11) :1803-1819
[6]   Coordination of substitutionally inert phenolate ligands to lanthanide(II) and (III) compounds-catalysts for ring-opening polymerization of cyclic esters [J].
Binda, Pascal I. ;
Delbridge, Ewan E. ;
Abrahamson, Harmon B. ;
Skelton, Brian W. .
DALTON TRANSACTIONS, 2009, (15) :2777-2787
[7]  
Browning E., 1969, TOXICITY IND METALS, P383
[8]   Iminophosphorane Neodymium(III) Complexes As Efficient Initiators for Lactide Polymerization [J].
Buchard, Antoine ;
Platel, Rachel H. ;
Auffrant, Audrey ;
Le Goff, Xavier F. ;
Le Floch, Pascal ;
Williams, Charlotte K. .
ORGANOMETALLICS, 2010, 29 (13) :2892-2900
[9]   Synthesis and characterization of dinuclear rare-earth complexes supported by amine-bridged bis(phenolate) ligands and their catalytic activity for the ring-opening polymerization of L-lactide [J].
Duan, Yu-Lai ;
He, Jia-Xuan ;
Wang, Wei ;
Zhou, Jing-Jing ;
Huang, Yong ;
Yang, Ying .
DALTON TRANSACTIONS, 2016, 45 (26) :10807-10820
[10]   THE RARE-EARTH INDUSTRY - A WORLD OF RAPID CHANGE [J].
FALCONNET, P .
JOURNAL OF ALLOYS AND COMPOUNDS, 1993, 192 (1-2) :114-117