摘要
合成了一系列自负载吡啶双亚胺酸酯钒(Ⅲ)催化剂(V(Ⅲ)),并通过傅里叶变换红外光谱仪(FTIR)、元素分析及核磁共振波谱仪(NMR)等技术手段对配合物进行了表征。在倍半乙基氯化铝(EASC)活化下,V(Ⅲ)催化剂对乙烯聚合表现出很高的催化活性(7. 2~12. 1 g/(mol·h·Pa)),且自负载基团的链长对催化剂的活性及所得聚合物的性质影响较小。同时,该类V催化剂催化乙烯与1-己烯共聚合性能良好,得到高相对分子质量(高达68. 1×10~3)的聚合物。所得聚合物经扫描电子显微镜(SEM)表征,其微观结构为片层叠加结构。
A series of alkenyl-functionalized bis( imidate) pyridine vanadium V( Ⅲ) complexes was synthesized and used for olefin polymerization in a self-immobilization mode. All the complexes were wellcharacterized by Fourier transform infrared spectrometer( FTIR),elemental analysis and nuclear magnetic resonance spectroscopy( NMR). Being activated by ethylaluminum sesquichloride( EASC),the V( Ⅲ)complexes displayeded high activity in ethylene polymerization( 7. 2 ~ 12. 1 g/( mol·h·Pa)). Additionally,the length of self-immobilized alkenyl chains showed a little influence on the catalytic activity of the precatalysts. These V( Ⅲ) complexes also exhibited high activity in initiating ethylene/1-hexene copolymerization,affordiong copolymer products with high molecular weight( up to 68. 1 × 10~3). Scanning electron microscope( SEM) studies showed that the polymer products formed platelet clusters.
引文
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