In situ FTIR spectroscopy during addition of trimethylaluminium (TMA) to methylaluminoxane (MAO) shows no formation of MAO-TMA compounds

被引:39
作者
Eilertsen, JL
Rytter, E
Ystenes, M [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Chem, N-7491 Trondheim, Norway
[2] Statoil Res Ctr, N-7005 Trondheim, Norway
[3] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
关键词
methylaluminoxane; trimethylaluminium; metallocene catalyst; infrared spectroscopy;
D O I
10.1016/S0924-2031(00)00093-X
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Commercial methylaluminoxane (MAO) solutions were dried under reduced pressure to remove trimethylaluminium (TMA) and solvent. TMA has been added to a solution of such dried MAO, and the response was followed by a special in situ FTIR spectroscopic technique. No reaction was seen between TMA and MAO in toluene solution at room temperature within a time span of up to 4h TMA and MAO remained in the solution as separate components, as verified by the spectra of the mixtures being superpositions of the spectra of the two components, linear dependence of the main TMA dimer peaks to the added amount, and appearance of isosbestic points. Experiments at 80 degreesC gave the same results. A further important observation is the identification of bridging methyl groups in the TMA-depleted MAO, clearly seen as an IR band at 1257 cm(-1). This, in addition to the documented lack of reaction between MAO and TMA, forces a rethinking of the hitherto proposed models of the MAO structure. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:257 / 264
页数:8
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