Yttrium(III) complex as a highly active catalyst for lactide polymerization

被引:34
作者
Hodgson, Linda M. [1 ]
White, Andrew J. P. [1 ]
Williams, Charlotte K. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
catalysts; kinetics (polym.); living polymerization;
D O I
10.1002/pola.21743
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The application of Yttrium(III) complex as a S-N-N-S donor ligand for lactide polymerization catalysis was analyzed. The complex was prepared in situ in a quantitative yield, as determined by NMR spectrometry, by the stirring of 1,3-bis(P,P-di-i-propyl thiophosphinic amine)-2,2-dimethylpropane and [Y{N(TMS)2}3] in THF until the ligand signal disappeared from the NMR spectrum. Initial polymerizations were conducted in toluene at 70 °C and at a catalyst concentration of 5mM and showed complete conversion in 10 s. and thus polymerization was rapid to monitor with the conventional aliquot technique. The catalyst used a softer S-N-N-S donor ligand, and the complex showed very fast polymerization rates. The end-group analysis indicated that polymerization proceeds via a coordination insertion mechanism, which leads to a polymer chain terminated with the bis(trimethylsilyl)amide group.
引用
收藏
页码:6646 / 6651
页数:6
相关论文
共 20 条
[1]   SYNTHESIS, STRUCTURE, AND SPECTROSCOPIC PROPERTIES OF COPPER(II) COMPOUNDS CONTAINING NITROGEN SULFUR DONOR LIGANDS - THE CRYSTAL AND MOLECULAR-STRUCTURE OF AQUA[1,7-BIS(N-METHYLBENZIMIDAZOL-2'-YL)-2,6-DITHIAHEPTANE]COPPER(II) PERCHLORATE [J].
ADDISON, AW ;
RAO, TN ;
REEDIJK, J ;
VANRIJN, J ;
VERSCHOOR, GC .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1984, (07) :1349-1356
[2]  
Amass W, 1998, POLYM INT, V47, P89, DOI 10.1002/(SICI)1097-0126(1998100)47:2<89::AID-PI86>3.0.CO
[3]  
2-F
[4]  
[Anonymous], 1992, Polym. Prepr. (Am. Chem Soc. Div. Polym Chem.)
[5]  
Aubrecht KB, 2001, J POLYM SCI POL CHEM, V39, P284, DOI 10.1002/1099-0518(20010115)39:2<284::AID-POLA40>3.0.CO
[6]  
2-C
[7]   Stereoselective ring-opening polymerization of racemic lactide using alkoxy-amino-bis(phenolate) group 3 metal complexes [J].
Cai, CX ;
Amgoune, A ;
Lehmann, CW ;
Carpentier, JF .
CHEMICAL COMMUNICATIONS, 2004, (03) :330-331
[8]   Controlled polymerization of DL-lactide and ε-caprolactone by structurally well-defined alkoxo-bridged di- and triyttrium(III) complexes [J].
Chamberlain, BM ;
Jazdzewski, BA ;
Pink, M ;
Hillmyer, MA ;
Tolman, WB .
MACROMOLECULES, 2000, 33 (11) :3970-3977
[9]  
Drumright RE, 2000, ADV MATER, V12, P1841, DOI 10.1002/1521-4095(200012)12:23<1841::AID-ADMA1841>3.0.CO
[10]  
2-E