4.7 Article

(Ferrocenylthienyl)phosphines for the Suzuki-Miyaura C,C coupling

Journal

INORGANIC CHEMISTRY COMMUNICATIONS
Volume 54, Issue -, Pages 96-99

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.inoche.2015.02.018

Keywords

Suzuki-Miyaura; C,C coupling; Phosphine thiophenes; Homogenous catalysis; Solid state structure

Funding

  1. Fonds der Chemischen Industrie (FCI)

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2-(3-Ferrocenylthienyl)phosphines of type 2-PR2-3-Fc-(C4H2S)-C-c (R = Bu-t (2); R = Ph (3); Fc = Fe(eta(5)-C5H4)(eta(5)-C5H5)) were synthesized and the structures of 2 and 3 in the solid state were determined by single X-ray structure analysis. Inter- and intra-molecular T-shaped pi center dot center dot center dot pi stackings involving cyclopentadienyl and phenyl rings are characteristic for 3. The application of 2 and 3 as ligands in the Pd-catalyzed Suzuki-Miyaura C,C cross-coupling of aryl halides with boronic acids to give the respective biaryls is reported. Electron-rich, electron-poor and sterically hindered substrates could be coupled with high yields at Pd-loadings as low as 0.1 mol%. (C) 2015 Elsevier B.V. All rights reserved.

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