Lanthanide Metal-Organic Frameworks as Ziegler-Natta Catalysts for the Selective Polymerization of Isoprene

被引:72
|
作者
Vitorino, Marta J. [1 ]
Devic, Thomas [2 ]
Tromp, Moniek [3 ]
Ferey, Gerard [2 ]
Visseaux, Marc [1 ]
机构
[1] ENSCL, CNRS, Unite Catalyse & Chim Solide, UMR 8181, F-59652 Villeneuve Dascq, France
[2] Univ Versailles, CNRS, Inst Lavoisier Versailles, UMR 8180, F-78035 Versailles, France
[3] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会;
关键词
lanthanides; matrix; metal-organic frameworks; polyisoprene; ziegler-natta polymerization; RADICAL POLYMERIZATION; COORDINATION POLYMERS; HYDROGEN STORAGE; XYLENE ISOMERS; SEPARATION; CARBOXYLATE; ADSORPTION; MONOMERS; MIL-100; SOLIDS;
D O I
10.1002/macp.200900354
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 unprecedented ability of neodymium-based metal organic frameworks (MOFs) as polymerisation pre-catalysts towards isoprene is reported. Combined with methylaluminoxane (MAO) or modified MAO (MMAO), they afford mainly cis-selective polyisoprene, up to 90.7%. Both the activity and the selectivity are tentatively ascribed to the intrinsic microstructure of the starting materials. Compared to conventional carboxylates, MOFs associated to an Al co-catalyst are less active but the selectivity is found to be higher, and it may be modified by controlling the access to the pores, which would be favored at higher temperatures. Some residual crystalline MOF remains disseminated within polymer matrix, as shown by X-ray diffraction and X-ray absorption spectroscopy studies.
引用
收藏
页码:1923 / 1932
页数:10
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