Structurally well-defined group 4 metal complexes as initiators for the ring-opening polymerization of lactide monomers

被引:251
|
作者
Sauer, Andreas [1 ]
Kapelski, Andreas [1 ]
Fliedel, Christophe [2 ,3 ]
Dagorne, Samuel [2 ]
Kol, Moshe [4 ]
Okuda, Jun [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Inorgan Chem, D-52056 Aachen, Germany
[2] Univ Strasbourg, CNRS, Inst Chim Strasbourg, F-67000 Strasbourg, France
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE, P-2829516 Caparica, Portugal
[4] Tel Aviv Univ, Raymond & Beverly Sackler Fac Exact Sci, Sch Chem, IL-69978 Tel Aviv, Israel
关键词
STEREOSELECTIVE POLYMERIZATION; RAC-LACTIDE; SINGLE-SITE; TITANIUM COMPLEXES; RACEMIC LACTIDE; ZIRCONIUM COMPLEXES; CONTROLLED ROP; ALKOXIDE INITIATORS; ALUMINUM CATALYSTS; SALEN-ALUMINUM;
D O I
10.1039/c3dt00010a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Polylactide (PLA) is an attractive polymeric material due to its origin from annually renewable resources and its biodegradability. The ring-opening polymerization (ROP) of lactide initiated by Lewis acidic and oxophilic metal-based catalysts constitutes the method of choice to access PLA in a controlled and stereoselective manner. The design and synthesis of ligand-supported metal complexes to act as effective ROP initiators of lactide monomers have been the subject of numerous investigations over the past decades. In view of their oxophilic nature, well-defined group 4 metal complexes supported by polydentate supporting ligands have appeared as active initiators for lactide ROP. This perspective summarizes various classes of structurally well-defined group 4 metal initiators developed for lactide ROP. It also provides observed trends regarding their catalytic performance. Whenever appropriate and possible, catalyst structure-ROP performance (i.e. activity, control and stereoselectivity) relationships are rationalized.
引用
收藏
页码:9007 / 9023
页数:17
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