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İki çekirdekli rutenyum II aren komplekslerinin ketonların transfer hidrojenasyonuna uygulanması

Year 2013, Volume: 2 Issue: 1, 1 - 8, 01.06.2013

Abstract

Geçifl metal katalizörlerinin transfer hidrojenasyon reaksiyonuyla organik substratlara hidrojen katılmasıveya çıkarılması önemli bir sentetik araçtır. Bu amaçla, N3,N3'-di-2-hidroksibenziliden-[2,2']bipiridinil3,3'-diamin bilefliğinden elde edilen bir P-O ligandı olan N3,N3'-di-2- difenilfosfino benziliden-[2,2']bipiridinil3,3'-diaminin bir dizi metal kompleksi sentezlendi. N3,N3'-di-2- difenilfosfino benziliden-[2,2']bipiridinil3,3'-diaminin [Ru η-benzen µ-Cl Cl] yada [Ru η-p-simen µ-Cl Cl]2 ile reaksiyonu köprülü ve ikiçekirdekli [CH16N4{OPPh2-Ru η6-benzen Cl2}2] 1 ve [Ckomplekslerini vermektedir. Ru II -bisfosfinit kompleksleri ayrıca basit birçok alkil ve aril alkil ketonuntransfer hidrojenasyonunda katalizör olarak kullanıldı ve iyi düzeyde % 99'a kadar dönüflümler eldeedildi

References

  • 1. S. Gladiali, E. Alberico, in Transition Metals for Organic Synthesis, ed. M. Beller and C. Bolm, WileyVCH, Weinheim, 2004, vol. 2, pp. 145.
  • 2. S. E. Clapham, A. Hadzovic, R. H. Morris, Coord. Chem. Rev. 248 (2004) 2201-2237.
  • 3. J. E. Backvall, J. Organomet. Chem. 652 (2002) 105- 111.
  • 4. J. S. M. Samec, Jan-E. Backvall, P. G. Andersson, P. Brandt, Chem. Soc. Rev. 35 (2006) 237-248.
  • 5. J. S. M. Samec, Jan-E. Backvall, Chem. Eur. J. 8 (2002) 2955-2961.
  • 6. (a) D. A. Alonso, S. J. M. Nordin; P. Roth, T. Tarnai, P. G. Andersson, J. Org. Chem. 65 (2000) 3116-3122. (b) D. Totev, A. Salzer, D. Carmona, L. A. Oro, F. J. Lahoz, I. T. Dobrinovitch, Inorg. Chim. Acta 357 (2004) 2889-2898.
  • 7. R. V. Wisman, J. G. de Vries, B.-J. Deelman, H. J. Heeres, Organic Process Res. & Develop. 10 (2006) 423-429.
  • 8. J. Bayardon, D. Sinou, O. Holczknecht, L. Mercs, G. Pozzi, Tetrahedron: Asymmetry 16 (2005) 2319- 2327.
  • 9. (a) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 345 (2003) 67-77; (b) K. Aboulaala, C. Goux-Henry, D. Sinou, M. Safi, M. Soufiaoui, J. Mol. Catal. A.: Chem. 237 (2005) 259-266; (c) M. Pasto, A. Riera, M. Pericas, Eur. J. Org. Chem. (2002) 2337-2341.
  • 10. M. Leautey, P. Jubault, X. Pannexoucke, J.-C. Quirion, Eur. J. Org. Chem. (2003) 3761-3765.
  • 11. (a) A. Bogevig, I. M. Pastor, H. Adolfsson, Chem. Eur. J. 10 (2004) 294-302; (b) D. Carmona, M. P. Lamata, F. Viguri, I. T. Dobrinovich, F. J. Lahoz, L. A. Oro, Adv. Chem. Catal. 344 (2002) 499-502; (c) I. M. Pastor, P. Vastila, H. Adolfsson, Chem. Eur. J. 9 (2003) 4031-4045.
  • 12. (a) Y. Nishibayashi, J. D. Singh, Y. Arikawa, S. Uemura, M. Hidai, J. Organomet. Chem. 531 (1997) 13-18; (b) A. Patti, S. Pedotti, Tetrahedron: Asymmetry 14 (2003) 597-602.
  • 13. M. Aydemir, A. Baysal, S. Özkar, L. T. Y›ld›r›m, Polyhedron 30 (2011) 796-804.
  • 14. M. Aydemir, A. Baysal, Polyhedron 29 (2010) 1219- 1224.
  • 15. M. Aydemir, N. Meriç, A. Baysal, B. Gümgüm, M. Toğrul, Y. Turgut, Tetrahedron: Asymmetry 21 (2010) 703-710.
  • 16. D. Cuervo, M. P. Gamasa, J. Gimeno, Chem. Eur. J. 10 (2004) 425-432.
  • 17. M. Aydemir, A. Baysal, B. Gümgüm, Appl. Organometal. Chem. 26 (2012) 1-8.
  • 18. E. Encarnacion, J. Pons, R. Yanez, J. Ros, Inorg. Chim. Acta 358 (11) (2005) 3272-3276.
  • 19. R. Noyori, M. Yamakawa, S. Hashiguchi, J. Org. Chem. 66 (24) (2001) 7931 7944.
  • 20. M. Aydemir, F. Durap, A. Baysal, N. Meriç, A. Bulda, B. Gümgüm, S. Özkar, L. T. Yıldırım, J. Molecular Catal. A: Chemical 326 (2010) 75 81.
  • 21. A. D. Burrows, M. F. Mahon, M. T. Palmer, J. Chem. Soc., Dalton Trans. (2000) 1669-1677.
  • 22. M. Aydemir, N. Meric, A. Baysal, J. Organomet. Chem. 720 (2012) 38-45.
  • 23. M. Aydemir, A. Baysal, N. Meric, B. Gumgum J. Organomet. Chem. 694 (2009) 2488 2492.
  • 24. R. Le Lagadec, L. Rubio, L. Alexandrova, R. Toscano, E. V. Ivanova, R. Meskys, V. Laurinavicius, M. Pfeffer, A. D. Ryabov, J. Organomet. Chem. 689 (2004) 4820-4832.
  • 25. A. D. Ryabov, V. S. Kurova, V. Ekaterina, R. Ivanova, R. Le Lagadec, L. Alexandrova, Anal. Chem. 77 (2005) 1132-1139.
  • 26. M. Aydemir, A. Baysal, N. Meric, C. Kayan, B. Gümgüm, S. Özkar, E. Sahin J. Organomet. Chem. 696 (2011) 2584-2588.
  • 27. A. M. Maj, K. M. Pietrusiewicz, I. Suisse, F. Agbossou, A. Mortreux, J. Organomet. Chem. 626 (2001) 157- 160.
  • 28. J. X. Gao, X. D. Yi, P. P. Xu, C. -L. Tang, H. L. Wan, T. Ikariya, J. Organometal. Chem. 592 (1999) 290-295.
  • 29. J. X. Gao, H. Zhang, X. D. Yi, P. P. Xu, C. L. Tang, H. L. Wan, K. R. Tsai, T. Ikariya, Chirality 12 (2000) 383-388.
  • 30. R. Noyori, T. Ohkuma, Angew. Chem. Int. Ed. Engl. 40 (2001) 40-73.
  • 31. J. Canivet, G. Labat, H. Stockli-Evans, G. Süss-Fink, Eur. J. Inorg. Chem. (2005) 4493-4500.
  • 32. P. Stepnicka, J. Ludvíc, J. Canivet, G. Süss-Fink, Inorg. Chim. Acta 359 (2006) 2369-2374.
  • 33. P. Dani, T. Karlen, R. A. Gossage, S. Gladialli, F. G. Koten, Angew. Chem. Int. Ed. Engl. 39 (2000) 743-745.
  • 34. Z. Fei, R. Scopelliti, P.J. Dyson, Inorg. Chem. 42 (2003) 2125-2130.
  • 35. Z. Fei, R. Scopelliti, P.J. Dyson, Eur. J. Inorg. Chem. (2004) 530-537.
  • 36. S. Berger, S. Braun, H. O. Kolinowski, NMRSpektroskopie von Nichtmetallen Band 3, 31P NMR Spektroskopie, Georg Theime Verlag, Stuttgart, New York, (1993).
  • 37. R. A. Zelonka, M.C. Baird, J. Organomet. Chem. 35 (1972) C43-C46.
  • 38. M. A. Bennet, A. K. Smith, J. Chem. Soc. Dalton Trans. (1974) 233-241.
  • 39. M. A. Bennet, T. N. Huang, T. W. Matheson, A. K. Smith, Inorg. Synth. 7 (1982) 74-78.

Application of dinuclear ruthenium II arene complexes in transfer hydrogenation of ketones

Year 2013, Volume: 2 Issue: 1, 1 - 8, 01.06.2013

Abstract

The ability of transition metal catalysts to add or remove hydrogen from organic substrates by transferhydrogenation process is a valuable synthetic tool. For this aim, a series of metal complexes with a P-Oligand, N3,N3'-di-2- diphenylphosphino benzylidene-[2,2']bipyridinyl-3,3'-diamine derived from N3,N3'di-2-hydroxybenzylidene-[2,2']bipyridinyl-3,3'-diamine were synthesized. Reaction of N3,N3'-di-2 diphenylphosphino benzylidene-[2,2']bipyridinyl-3,3'-diamine with [Ru η6-benzene µ-Cl Cl]2 or [Ru η6p-cymene µ-Cl Cl]2 gave bridged dinuclear complexes [C24H16N4{OPPh2-Ru η6-benzene Cl2}2] 1 and[C24H16N4{OPPh2-Ru η6-p-cymene Cl}2] 2, respectively. Ru II -bisphosphinite complexes have also beenused as catalysts for the transfer hydrogenation of a variety of simple alkyl and aryl alkyl ketones and goodconversions up to 99 % were obtained

References

  • 1. S. Gladiali, E. Alberico, in Transition Metals for Organic Synthesis, ed. M. Beller and C. Bolm, WileyVCH, Weinheim, 2004, vol. 2, pp. 145.
  • 2. S. E. Clapham, A. Hadzovic, R. H. Morris, Coord. Chem. Rev. 248 (2004) 2201-2237.
  • 3. J. E. Backvall, J. Organomet. Chem. 652 (2002) 105- 111.
  • 4. J. S. M. Samec, Jan-E. Backvall, P. G. Andersson, P. Brandt, Chem. Soc. Rev. 35 (2006) 237-248.
  • 5. J. S. M. Samec, Jan-E. Backvall, Chem. Eur. J. 8 (2002) 2955-2961.
  • 6. (a) D. A. Alonso, S. J. M. Nordin; P. Roth, T. Tarnai, P. G. Andersson, J. Org. Chem. 65 (2000) 3116-3122. (b) D. Totev, A. Salzer, D. Carmona, L. A. Oro, F. J. Lahoz, I. T. Dobrinovitch, Inorg. Chim. Acta 357 (2004) 2889-2898.
  • 7. R. V. Wisman, J. G. de Vries, B.-J. Deelman, H. J. Heeres, Organic Process Res. & Develop. 10 (2006) 423-429.
  • 8. J. Bayardon, D. Sinou, O. Holczknecht, L. Mercs, G. Pozzi, Tetrahedron: Asymmetry 16 (2005) 2319- 2327.
  • 9. (a) K. Everaere, A. Mortreux, J.-F. Carpentier, Adv. Synth. Catal. 345 (2003) 67-77; (b) K. Aboulaala, C. Goux-Henry, D. Sinou, M. Safi, M. Soufiaoui, J. Mol. Catal. A.: Chem. 237 (2005) 259-266; (c) M. Pasto, A. Riera, M. Pericas, Eur. J. Org. Chem. (2002) 2337-2341.
  • 10. M. Leautey, P. Jubault, X. Pannexoucke, J.-C. Quirion, Eur. J. Org. Chem. (2003) 3761-3765.
  • 11. (a) A. Bogevig, I. M. Pastor, H. Adolfsson, Chem. Eur. J. 10 (2004) 294-302; (b) D. Carmona, M. P. Lamata, F. Viguri, I. T. Dobrinovich, F. J. Lahoz, L. A. Oro, Adv. Chem. Catal. 344 (2002) 499-502; (c) I. M. Pastor, P. Vastila, H. Adolfsson, Chem. Eur. J. 9 (2003) 4031-4045.
  • 12. (a) Y. Nishibayashi, J. D. Singh, Y. Arikawa, S. Uemura, M. Hidai, J. Organomet. Chem. 531 (1997) 13-18; (b) A. Patti, S. Pedotti, Tetrahedron: Asymmetry 14 (2003) 597-602.
  • 13. M. Aydemir, A. Baysal, S. Özkar, L. T. Y›ld›r›m, Polyhedron 30 (2011) 796-804.
  • 14. M. Aydemir, A. Baysal, Polyhedron 29 (2010) 1219- 1224.
  • 15. M. Aydemir, N. Meriç, A. Baysal, B. Gümgüm, M. Toğrul, Y. Turgut, Tetrahedron: Asymmetry 21 (2010) 703-710.
  • 16. D. Cuervo, M. P. Gamasa, J. Gimeno, Chem. Eur. J. 10 (2004) 425-432.
  • 17. M. Aydemir, A. Baysal, B. Gümgüm, Appl. Organometal. Chem. 26 (2012) 1-8.
  • 18. E. Encarnacion, J. Pons, R. Yanez, J. Ros, Inorg. Chim. Acta 358 (11) (2005) 3272-3276.
  • 19. R. Noyori, M. Yamakawa, S. Hashiguchi, J. Org. Chem. 66 (24) (2001) 7931 7944.
  • 20. M. Aydemir, F. Durap, A. Baysal, N. Meriç, A. Bulda, B. Gümgüm, S. Özkar, L. T. Yıldırım, J. Molecular Catal. A: Chemical 326 (2010) 75 81.
  • 21. A. D. Burrows, M. F. Mahon, M. T. Palmer, J. Chem. Soc., Dalton Trans. (2000) 1669-1677.
  • 22. M. Aydemir, N. Meric, A. Baysal, J. Organomet. Chem. 720 (2012) 38-45.
  • 23. M. Aydemir, A. Baysal, N. Meric, B. Gumgum J. Organomet. Chem. 694 (2009) 2488 2492.
  • 24. R. Le Lagadec, L. Rubio, L. Alexandrova, R. Toscano, E. V. Ivanova, R. Meskys, V. Laurinavicius, M. Pfeffer, A. D. Ryabov, J. Organomet. Chem. 689 (2004) 4820-4832.
  • 25. A. D. Ryabov, V. S. Kurova, V. Ekaterina, R. Ivanova, R. Le Lagadec, L. Alexandrova, Anal. Chem. 77 (2005) 1132-1139.
  • 26. M. Aydemir, A. Baysal, N. Meric, C. Kayan, B. Gümgüm, S. Özkar, E. Sahin J. Organomet. Chem. 696 (2011) 2584-2588.
  • 27. A. M. Maj, K. M. Pietrusiewicz, I. Suisse, F. Agbossou, A. Mortreux, J. Organomet. Chem. 626 (2001) 157- 160.
  • 28. J. X. Gao, X. D. Yi, P. P. Xu, C. -L. Tang, H. L. Wan, T. Ikariya, J. Organometal. Chem. 592 (1999) 290-295.
  • 29. J. X. Gao, H. Zhang, X. D. Yi, P. P. Xu, C. L. Tang, H. L. Wan, K. R. Tsai, T. Ikariya, Chirality 12 (2000) 383-388.
  • 30. R. Noyori, T. Ohkuma, Angew. Chem. Int. Ed. Engl. 40 (2001) 40-73.
  • 31. J. Canivet, G. Labat, H. Stockli-Evans, G. Süss-Fink, Eur. J. Inorg. Chem. (2005) 4493-4500.
  • 32. P. Stepnicka, J. Ludvíc, J. Canivet, G. Süss-Fink, Inorg. Chim. Acta 359 (2006) 2369-2374.
  • 33. P. Dani, T. Karlen, R. A. Gossage, S. Gladialli, F. G. Koten, Angew. Chem. Int. Ed. Engl. 39 (2000) 743-745.
  • 34. Z. Fei, R. Scopelliti, P.J. Dyson, Inorg. Chem. 42 (2003) 2125-2130.
  • 35. Z. Fei, R. Scopelliti, P.J. Dyson, Eur. J. Inorg. Chem. (2004) 530-537.
  • 36. S. Berger, S. Braun, H. O. Kolinowski, NMRSpektroskopie von Nichtmetallen Band 3, 31P NMR Spektroskopie, Georg Theime Verlag, Stuttgart, New York, (1993).
  • 37. R. A. Zelonka, M.C. Baird, J. Organomet. Chem. 35 (1972) C43-C46.
  • 38. M. A. Bennet, A. K. Smith, J. Chem. Soc. Dalton Trans. (1974) 233-241.
  • 39. M. A. Bennet, T. N. Huang, T. W. Matheson, A. K. Smith, Inorg. Synth. 7 (1982) 74-78.
There are 39 citations in total.

Details

Primary Language Turkish
Journal Section Research Article
Authors

Nermin Meriç This is me

Cezmi Kayan This is me

Murat Aydemir This is me

Yusuf Selim Ocak This is me

Akın Baysal This is me

Hamdi Temel This is me

Publication Date June 1, 2013
Published in Issue Year 2013 Volume: 2 Issue: 1

Cite

IEEE N. Meriç, C. Kayan, M. Aydemir, Y. S. Ocak, A. Baysal, and H. Temel, “İki çekirdekli rutenyum II aren komplekslerinin ketonların transfer hidrojenasyonuna uygulanması”, DUFED, vol. 2, no. 1, pp. 1–8, 2013.


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