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Catalysts based on hyperbranched pyridylphenylene polymers and palladium nanoparticles for the Suzuki—Miyaura cross-coupling reaction

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Abstract

Synthesis of catalysts based on hyperbranched pyridylphenylene polymer and palladium nanoparticles (РРР-Рd) is described. Catalytic activity in the Suzuki—Miyaura cross-coupling reaction is studied for the interaction of bromobenzene with phenylboronic acid. Optimal reaction conditions providing maximum conversion (100%) of the initial compounds are established.

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References

  1. B. Karimi, H. Behzadnia, E. Farhangi, E. Jafari, A. Zamani, Current Organic Synthesis, 2010, 7: 543.

    Article  CAS  Google Scholar 

  2. A. Balanta, C. Godard, C. Claver, Chem. Soc. Rev., 2011, 40: 4973.

    Article  CAS  PubMed  Google Scholar 

  3. P. W. Zheng, W. Q. Zhang, J. Catalysis, 2007, 250: 324.

    Article  CAS  Google Scholar 

  4. Nanoparticles and Catalysi s, Ed. D. Astruc, Wiley-VCH, Weinheim, Germany, 2007, 622.

  5. T. J. Dickerson, N. N. Reed, K. D. Janda, Chem. Rev., 2002, 102: 3325.

    Article  CAS  PubMed  Google Scholar 

  6. A. Modak, M. Pramanik, S. Inagaki, A. Bhaumik, J. Mater. Chem. A, 2014, 2: 11642.

    Article  CAS  Google Scholar 

  7. Palladium-Catalyzed Coupling Reactions: Practical Aspects and Future Developments, Ed. A. Molnar, Willey, 2013.

  8. R. van de Coevering, R. J. M. K. Gebbink, G. van Koten, Progress in Polymer Science, 2005, 30: 474.

    Article  CAS  Google Scholar 

  9. P. W. Liu, Z. B. Ye, W. J. Wang, B. G. Li, Macromolecules, 2013, 46: 72.

    Article  CAS  Google Scholar 

  10. H. Mahda vi, R. Sahraei, Catal. Lett., 2016, 146: 977.

    Article  CAS  Google Scholar 

  11. Z. B. Shifrina, M. S. Raja durai, N. V. Firsova, L. M. Bronstein, X. Huang, A. L. Rus anov, K. Muellen, Macromolecules, 2005, 38: 9920.

    Article  CAS  Google Scholar 

  12. N. V. Kuchkina, E. Y. Yuzik-Klimova, S. A. Sorokina, A. S. Peregudov, D. Y. Antonov, S. H. Gage, B. S. Boris, L. Z. Nikoshvili, E. M. Sulman, D. G. Morgan, W. E. Mahmoud, A. A. Al-Ghamdi, L. M. Bronstein, Z. B. Shifrina, Macromolecules, 2013, 46: 5890.

    Article  CAS  Google Scholar 

  13. K. Alibegovic, D. G. Morgan, Y. Losovyj, M. Pink, B. D. Stein, N. V. Kuchkina, E. S. Serkova, K. E. Salnikova, Z. B. Shifrina, V. G. Matveeva, E. M. Sulman, L. M. Bronstein, Chemistry Select, 2017, 2: 5485.

    CAS  Google Scholar 

  14. N. Baird, J. W. Dittmar, Y. B. Losovyj, D. G. Morgan, B. D. Stein, M. Pink, N. V. Ku chkina, E. S. Serkova, O. L. Lependina, M. E. Grigoriev, A. I. Sidorov, M. G. Sulman, Z. B. Shifrina, L. M. Bronstein, ACS Applied Materials & Interfaces, 2017, 9: 2285.

    Article  CAS  Google Scholar 

  15. N. V. Kuchkina, M. S. Zinatullina, E. S. Serkova, P. S. Vlasov, A. S. Peregudov, Z. B. Shifrina, RSC Advances, 2015, 5: 99510.

    Article  CAS  Google Scholar 

  16. W. C. Shieh, J. A. Carlson, J. Org. Chem., 1992, 57: 379.

    Article  CAS  Google Scholar 

  17. G. Budroni, A. Corma, H. García, A. Primo, J. Catalysis, 2007, 251: 345.

    Article  CAS  Google Scholar 

  18. C. R. LeBlond, K. M. Butler, M. W. Ferrington, M. A. Browe, Synth. Commun., 2009, 39: 636.

    Article  CAS  Google Scholar 

  19. N. Miyaura, T. Yanagi, A. Suzuki, Synth. Commun., 1981, 11: 513.

    Article  CAS  Google Scholar 

  20. M. T. Reetz, R. Breinbauer, K. Wanninger, Tetrahedron Lett., 1996, 37: 4499.

    Article  CAS  Google Scholar 

  21. R. G. Heidenreich, K. Köhler, J. G. E. Krauter, J. Pietsch, Synlett, 2002, 2002: 1118.

    Article  Google Scholar 

  22. M. T. Reetz, E. Westermann, Angew. Chem. Int. Ed. Engl., 2000, 39: 165.

    Article  CAS  PubMed  Google Scholar 

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Authors and Affiliations

  1. A. N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences Russia, 28 ul. Vavilova, 119991, Moscow, Russian Federation

    N. V. Kuchkina, S. A. Sorokina, I. Yu. Krasnova, E. S. Serkova & Z. B. Shifrina

  2. Organic and Medicinal Chemistry, Dr. Reddy’s Institute of Life Sciences, University of Hyderabad Campus, Gachibowli, Hyderabad (AP), 500046, India

    M. Rajadurai, M. Pal & S. Basaveni

Authors
  1. N. V. Kuchkina
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  2. M. Rajadurai
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  3. M. Pal
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  4. S. Basaveni
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  5. S. A. Sorokina
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  6. I. Yu. Krasnova
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  7. E. S. Serkova
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  8. Z. B. Shifrina
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Corresponding author

Correspondence to N. V. Kuchkina.

Additional information

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1035–1040, June, 2018.

Proceedings of International Conference «Modern Trends in Dendrimer Chemistry and Applications» (October 1–4, 2017, Moscow).

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Kuchkina, N.V., Rajadurai, M., Pal, M. et al. Catalysts based on hyperbranched pyridylphenylene polymers and palladium nanoparticles for the Suzuki—Miyaura cross-coupling reaction. Russ Chem Bull 67, 1035–1040 (2018). https://doi.org/10.1007/s11172-018-2176-6

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  • DOI: https://doi.org/10.1007/s11172-018-2176-6

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