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  • 1 Duesbergweg 10–14 Johannes Gutenberg University Mainz D-55128 Mainz Germany
  • 2 Carl-Zeiss-Str. 18–20 Fraunhofer ICT-IMM 55129 Mainz Germany
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The method of combining the concept of fluorous biphasic catalysis (FCB) with micro multiple emulsions benefits from the advantages of homogeneous as well as from heterogeneous catalysis in continuous micro flow. In this particular case, three immiscible fluid phases in continuous micro segmented flow were used to perform palladium-catalyzed Heck cross-coupling reactions of styrene with aryl halides. A capillary tube-in-tube coaxial flow setup in combination with a glass micro reactor was used to produce monodisperse aqueous phase/organic phase/perfluorinated phase double emulsions. The resulting emulsions had a core–shell droplet structure composed of a perfluorcarbon fluid in which a palladium catalyst with fluorinated phosphine ligands was dissolved, an organic phase consisting of a solvent and two reagents, and an alkaline aqueous solution. The fluorous and organic phases of the double emulsion form a thermomorphous system which can be converted into one phase by an increase of temperature above 150 °C, and the catalytic reaction is performed temporarily. By decreasing the temperature, a phase separation takes place; after that, the organic phase contains the product and the catalyst is located in the fluorous phase. The separated catalyst solution was reused several times without a noticeable loss of activity. The main advantage of this method is to use temporarily very high catalyst concentrations in each droplet, while employing only small amounts of the catalyst for the overall reaction volume.

  • Heck, R. F.; Nolley, J. P. J. Org. Chem. 1972, 37, 2320–2322.

  • Beletskaya, I. P.; Cheprakov, A. V. Chem. Rev. 2000, 100, 3009–3066.

  • de Meijere, A.; Meyer, F. E. Angew. Chem., Int. Ed. 1995, 33, 2379–2411.

  • Danishefsky, S. J.; Masters, J. J.; Young, W. B.; Link, J. T.; Snyder, L. B.; Magee, T. V.; Jung, D. K.; Isaacs, R. C. A.; Bornmann, W. G.; Alaimo, C. A.; Coburn, C. A.; Di Grandi, M. J. J. Am. Chem. Soc. 1996, 12, 2843–2859.

  • Ramchandani, R. K.; Vinod, M. P.; Wakharkar, R. D.; Choudhary, V. R.; Sudalai, A. Chem. Comm. 1997, 1997, 2071–2072.

  • Djakovitch, L.; Koehler, K. J. Am. Chem. Soc. 2001, 123, 5990–5999.

  • Molnar, A.; Papp, A.; Miklos, K.; Forgo, P. Chem. Comm. 2003, 49, 2626–2627.

  • Horvath, I. T.; Rabai, J. Science 1994, 266, 72–75.

  • Behr, A.; Henze, G.; Johnen, L.; Awungacha, C. J. Mol. Catal. 2008, 285, 20–28.

  • Schneider, S.; Bannwarth, W. Angew. Chem. 2000, 39, 4142–4145.

  • Lu, N.; Lin, Y.-C.; Chen, J.-Y.; Fan, C.-W.; Liu, L.-K. Tetrahedron 2007, 63, 2019–2023.

  • Lu, N.; Lin, Y.-C.; Chen, J.-Y.; Fan, C.-W.; Liu, L.-K. Tetrahedron Lett. 2008, 49, 371–375.

  • Li, C.-K.; Ghalwadkar, A.; Lu, N. J. Organomet. Chem. 2011, 696, 3637–3642.

  • Rocaboy, C.; Gladysz, J. A. New J. Chem. 2003, 27, 39–49.

  • Song, H.; Tice, J. D.; Ismagilov, R. F. Angew. Chem., Int. Ed. 2003, 42, 768–772.

  • Seemann, R.; Brinkmann, M.; Pfohl, T.; Herminghaus, S. Rep. Prog. Phys. 2012, 75, 016601.

  • Song, H.; Chen, D. L.; Ismagilov, R. F. Angew. Chem., Int. Ed. 2006, 45, 7336–7356.

  • Beletskaya, I. P.; Cheprakov, A. V. J. Organomet. Chem. 2004, 689, 4055–4082.