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Polycationic Ligands in Gold Catalysis: Synthesis and Applications of Extremely π-Acidic Catalysts

MPG-Autoren
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Carreras,  Javier
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Gopakumar,  Gopinadhanpillai
Research Department Thiel, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Gu,  Lianghu
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Gimeno,  Ana
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Linowski,  Pawel
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Petuškova,  Jekaterina
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Thiel,  Walter
Research Department Thiel, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Alcarazo,  Manuel
Research Group Alcarazo, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Zitation

Carreras, J., Gopakumar, G., Gu, L., Gimeno, A., Linowski, P., Petuškova, J., et al. (2013). Polycationic Ligands in Gold Catalysis: Synthesis and Applications of Extremely π-Acidic Catalysts. Journal of the American Chemical Society, 135(50), 18815-18823. doi:10.1021/ja411146x.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0014-CB0D-4
Zusammenfassung
Very often ligands are anionic or neutral species. Cationic ones are rare, and, when used, the positively charged groups are normally appended to the periphery of the ligand. Here, we describe a dicationic phosphine with no spacer between the phosphorus atom and the two positively charged groups. This structural feature makes its donor ability poorer than that of phosphites and only comparable to extremely toxic or pyrophoric compounds such as PF3 or P(CF3)3. By exploiting these properties, a new Au catalyst has been developed displaying a dramatically enhanced capacity to activate π-systems. This has been used to synthesize very sterically hindered and naturally occurring 4,5-disubstituted phenanthrenes. The present approach is expected to be applicable to the development and improvement of many other transition metal catalyzed transformations that benefit from extremely strong π-acceptor ligands. The mechanism of selected catalytic transformations has been explored by density functional calculations.