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取代茚基二价稀土配合物催化己内酯开环聚合反应 被引量:2

Ring-open Polymerization of ε-Caprolactone Catalyzed by Substituted Indenyl Complexes
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摘要 研究了1-环戊烷基茚基二价镱配合物(1-C5H9C9H6)2Yb(THF)2作为单组分催化剂催化己内酯开环聚合反应,考察了催化剂用量、聚合反应时间、聚合反应温度对己内酯聚合反应的影响.结果表明,配合物(1-C5H9C9H6)2Yb(THF)2对己内酯聚合有较高的催化活性;温度升高,聚合反应的转化率增加,但产物的数均分子量及分子量分布无明显变化;所得聚合物分子量分布较窄.其它几种取代茚基稀土配合物也显示出较高的催化活性,其活性有下列次序:(1-C2H5C9H6)2Sm(THF)2>(1-C5H9C9H6)2Sm(THF)>KSm(1-C5H9C9H6)3(THF)3>(1-PhCH2C9H6)2Sm(THF)2>(1-C5H9C9H6)2Yb(THF)2,二价钐配合物较二价镱配合物具有较高的催化活性.通过凝胶渗透色谱法测定了聚合产物的数均分子量及其分布. Abstract The substituted indenyl lanthanide ( Ⅱ ) complex ( C5H9 C9H6 ) 2Yb (THF) 2 applied to catalyzing the polymerization of ^-caprolactone was investigated. The results indicate that the complex (C5H9C9H6)2 Yb(THF)2 as single component catalyst showed a high activity, the conversion of the polymerization and the number-average molecular weight of the polymers were affected by temperature and time of polymerization, and using dose of the catalyst in polymerization process. The number-average molecular weight and molecular weight distribution of the polymer were not sensitive to temperature. But the conversion increased to increasing the polymerization temperature; molecular weight distribution of PCL gained was narrow. Other modified substituted indenyl lanthanide ( Ⅱ ) complexes also showed a good catalytic activity. The order of catalytic activity of the substituted indenyl lanthanide ( Ⅱ ) complexes was as follows: (1-C2H5C9H6)2Sm(THF)2〉(1-C5H9C9H6)2Sm(THF)〉KSm(1-C5H9C9H6)3(THF)3〉(1-PhCH2C9H6)2Sm(THF)2〉(1-C5H9C9H6)2Yb(THF)2, The number-average molecular weight and molecular weight distribution of PCL was measured by GPC.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2007年第12期2418-2421,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20072027)资助
关键词 取代茚基 稀土配合物 己内酯 开环聚合 Substituted indenyl Lanthanide complex ε-Caprolactone Ring-opening polymerization
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