Polymerization of ε-Caprolactone Using Bis(phenoxy)-amine Aluminum Complex: Deactivation by Lactide

被引:13
作者
Chumsaeng, Phongnarin [1 ]
Haesuwannakij, Setsiri [2 ]
Bureekaew, Sareeya [3 ]
Ervithayasuporn, Vuthichai [1 ]
Namuangruk, Supawadee [4 ]
Phomphrai, Khamphee [2 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
[2] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Mol Sci & Engn, Dept Mat Sci & Engn, Wangchan 21210, Rayong, Thailand
[3] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Energy Sci & Engn, Dept Chem & Biomol Engn, Wangchan 21210, Rayong, Thailand
[4] Natl Sci & Technol Dev Agcy, Natl Nanotechnol Ctr, Klongluang 12120, Pathumthani, Thailand
关键词
RING-OPENING POLYMERIZATION; ZIRCONIUM COMPLEXES; TITANIUM COMPLEXES; COORDINATION POLYMERIZATION; ISOSPECIFIC POLYMERIZATION; 1-HEXENE POLYMERIZATION; OLEFIN POLYMERIZATION; LIVING POLYMERIZATION; PHENOLATE LIGANDS; CYCLIC ESTERS;
D O I
10.1021/acs.inorgchem.8b01364
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Polymerizations of biodegradable lactide and lactones have been the subjects of intense research during the past decade. They can be polymerized/copolymerized effectively by several catalyst systems. With bis(phenolate)-amine aluminum complex, we have shown for the first time that lactide monomer can deactivate the aluminum complex during the ongoing polymerization of epsilon-caprolactone to a complete stop. After hours of dormant state, the aluminum complex can be reactivated again by heating at 100 degrees C without the addition of any external chemicals still giving polymer with narrow dispersity. Studies using NMR, in situ FTIR, and single-crystal X-ray crystallography indicated that the coordination of the carbonyl group in lactyl unit was responsible for the unusual behavior of lactide. In addition, the unusual methyl-migration from methyl lactate ligand to the amine side chain of the aluminum complex was observed through intermolecular nucleophilic-attack mechanism.
引用
收藏
页码:10170 / 10179
页数:10
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