Gas-phase Lewis acidity of perfluoroaryl derivatives of group 13 elements

Alexey Y. Timoshkin, Gernot Frenking

科研成果: 期刊稿件文章同行评审

107 引用 (Scopus)

摘要

The gas-phase Lewis acidity of group 13 element aryl and perfluorinated aryl derivatives E(C6H5)3, E(C 6H4F)3, and E(C5F5) 3 (E = B, Al, Ga) toward different donor molecules (NH3, H2O, PH3, H-, CH3-, F-) has been theoretically studied at the RI-BP86/def2-TZVPP level of theory. The following order of the acceptor ability has been established: E(C6H5)3 ≈ E(C6H 4F)3 < E(C6F5)3 ≈ ECl3. The acceptor strengths of E(C6H5) 3 and E(C6H4F)3 are comparable to each other but much weaker compared to E(C6H5) 3, which has a similar acceptor strength to those of the corresponding trihalides ECl3. The acceptor ability of ER3 decreases in the order Al > Ga > B. In the gas phase, Al(C 6F5)3 is found to be a stronger Lewis acid than B(C6F5)3 toward all electron donors but H -. In contrast to AlCl3, which forms stable dimers, Al(C6F3)3 is monomelic and tiierefore has a much higher Lewis acid reactivity . The reactivity of perfluorinated derivatives E(C5F5)3 (E = B, Al, Ga) toward ammonolysis and hydrolysis processes and L2ZrMe2 (L = Cl, Cp, Cp*) as cocatalysts in olefin polymerization is also discussed.

源语言英语
页(从-至)371-380
页数10
期刊Organometallics
27
3
DOI
出版状态已出版 - 11 2月 2008
已对外发布

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