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İki çekirdekli rutenyum II aren komplekslerinin ketonların transfer hidrojenasyonuna uygulanması

Yıl 2013, Cilt: 2 Sayı: 1, 1 - 8, 01.06.2013

Nermin Meriç Cezmi Kayan Murat Aydemir Yusuf Selim Ocak Akın Baysal Hamdi Temel

Öz

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

Anahtar Kelimeler

Bis fosfinit Transfer hidrojenasyon Rutenyum Kataliz Keton

Kaynakça

  • 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

Yıl 2013, Cilt: 2 Sayı: 1, 1 - 8, 01.06.2013

Nermin Meriç Cezmi Kayan Murat Aydemir Yusuf Selim Ocak Akın Baysal Hamdi Temel

Öz

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

Anahtar Kelimeler

Bis phosphinite Transfer hydrogenation Ruthenium Catalysis Ketone

Kaynakça

  • 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.
Toplam 39 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Research Article
Yazarlar

Nermin Meriç Bu kişi benim

Cezmi Kayan Bu kişi benim

Murat Aydemir Bu kişi benim

Yusuf Selim Ocak Bu kişi benim

Akın Baysal Bu kişi benim

Hamdi Temel Bu kişi benim

Yayımlanma Tarihi 1 Haziran 2013
Yayımlandığı Sayı Yıl 2013 Cilt: 2 Sayı: 1

Kaynak Göster

IEEE N. Meriç, C. Kayan, M. Aydemir, Y. S. Ocak, A. Baysal, ve H. Temel, “İki çekirdekli rutenyum II aren komplekslerinin ketonların transfer hidrojenasyonuna uygulanması”, DÜFED, c. 2, sy. 1, ss. 1–8, 2013.


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