化学
甲基铝氧烷
电喷雾电离
齿合度
加合物
光化学
金属有机化学
接受者
高分子化学
聚合
催化作用
离子
茂金属
金属
有机化学
聚合物
物理
凝聚态物理
作者
Harmen S. Zijlstra,Anuj Joshi,Mikko Linnolahti,Scott Collins,J. Scott McIndoe
标识
DOI:10.1002/ejic.201900153
摘要
Methylaluminoxane (MAO) is a key activator for olefin polymerization catalysts, making its chemistry of ongoing interest. Strong and bidentate neutral donors such as 2,2′‐bipyridine are effective abstractors of the dimethylaluminum cation, [Me 2 Al] + , from methylaluminoxane (MAO), while monodentate, weaker donors such as THF appear most prone to adduct formation with both free and bound trimethylaluminum. The ionization process can be readily investigated using electrospray ionization mass spectrometry (ESI‐MS) in fluorobenzene (PhF) solution. Complementary studies employing 1D and 2D 1 H NMR spectroscopic studies in [D 5 ]bromobenzene solution provide details on the extent of ionization vs. donor‐acceptor complex formation for the different donors studied. DFT studies employing different neutral model precursors and mono‐ vs. didentate donors shed light on possible mechanisms for ion‐pair formation.
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