首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Group 4 metal complexes of Trost's semi-crown ligand: synthesis, structural characterization and studies on the ring-opening polymerization of lactides and epsilon-caprolactone
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Group 4 metal complexes of Trost's semi-crown ligand: synthesis, structural characterization and studies on the ring-opening polymerization of lactides and epsilon-caprolactone

机译:Trost半冠配体的第4组金属配合物:丙交酯和ε-己内酯的合成,结构表征和开环聚合研究

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摘要

The synthesis of titanium(IV), zirconium(IV) and hafnium(IV) complexes of Trost's semi-crown ligand is described. All complexes were fully characterized by H-1 and C-13 NMR and mass spectroscopy. The molecular structures of the representative complexes 2, 3 and 4 were determined by single-crystal X-ray diffraction studies. The X-ray diffraction studies reveal that complexes 2, 3 and 4 crystallized in an orthorhombic crystal system. Complexes 2 and 3 have a monomeric structure in the solid state with distorted octahedral geometry around the metal center, whereas complex 4 was found to crystallize in a trimeric structure bridging with an oxygen atom, where the geometry around the titanium is distorted trigonal bipyramidal. The activities and stereoselectivities of these complexes toward the ring-opening polymerization (ROP) of lactides (L-LA and rac-LA) and epsilon-caprolactone (CL) have been investigated. Complexes 1-4 were found to be efficient single-component initiators for the ring-opening polymerization of cyclic esters and yielded high molecular weight polymers (M-n) with narrow molecular weight distributions (MWD). The microstructure of the resultant polylactides (PLAs) from rac-LA was determined. Complexes 2 and 3 afforded isotactic-enriched PLA (P-m = 0.78-0.71) with narrow MWD (1.07-1.04), on the other hand complexes 1 and 4 produced atactic PLA. Kinetic and post polymerization studies confirm that the polymerization proceeds through the coordination-insertion mechanism.
机译:描述了Trost半冠配体的钛(IV),锆(IV)和ha(IV)配合物的合成。所有配合物均通过H-1和C-13 NMR和质谱进行了充分表征。通过单晶X射线衍射研究确定代表性的配合物2、3和4的分子结构。 X射线衍射研究表明,复合物2、3和4在正交晶体系统中结晶。配合物2和3具有固态的单体结构,在金属中心周围具有扭曲的八面体几何形状,而发现配合物4在与氧原子桥连的三聚体结构中结晶,其中钛周围的几何形状是扭曲的三角双锥体。研究了这些配合物对丙交酯(L-LA和rac-LA)和ε-己内酯(CL)的开环聚合(ROP)的活性和立体选择性。发现配合物1-4是有效的单组分引发剂,用于环状酯的开环聚合并产生具有窄分子量分布(MWD)的高分子量聚合物(M-n)。测定了由rac-LA得到的聚丙交酯(PLA)的微观结构。配合物2和3提供了具有等宽MWD(1.07-1.04)的等规富集PLA(P-m = 0.78-0.71),另一方面,配合物1和4产生了无规PLA。动力学和后聚合研究证实,聚合是通过配位插入机理进行的。

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