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Kinetics of Dicyclopentadiene Polymerization in the Presence of the Second Generation Hoveyda-Grubbs Catalyst with N-Chelating Ligand

机译:第二代Hoveyda-Grubbs催化剂与N螯合配体存在下二环戊二烯聚合的动力学

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摘要

This article considers the thermodynamic aspects, thermo- and rheokinetics of endo-dicyclopentadiene polymerization in the presence of the original metathesis second Hoveyda-Grubbs catalyst with an N-chelating ligand. The activation energy of endo-dicyclopentadiene polymerization was determined as 88.9-89.2 kJ/mol. The thermal effect of the ring-opening metathesis endo-dicyclopentadiene polymerization reaction reaches 52.7 kJ/mol. This is lower than the values for molybdenum- and tungsten-containing catalysts reported in the literature, which can be explained by a different microstructure of the polymer produced in the presence of ruthenium-based metathesis catalysts.
机译:本文考虑了在原始复分解型第二Hoveyda-Grubbs催化剂存在下具有N-螯合配体的原始复分解率的热力学方面,热和流管学。 内钴 - 二环戊二烯聚合的活化能测定为88.9-89.2kJ / mol。 开环复分解的热效应外荷 - 二环戊二烯聚合反应达到52.7kJ / mol。 这低于文献中报道的含钼和含钨的催化剂的值,这可以通过在钌基复分解催化剂存在下产生的聚合物的不同微观结构来解释。

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