TY - JOUR T1 - İki çekirdekli rutenyum II aren komplekslerinin ketonların transfer hidrojenasyonuna uygulanması TT - Application of dinuclear ruthenium II arene complexes in transfer hydrogenation of ketones AU - Meriç, Nermin AU - Kayan, Cezmi AU - Aydemir, Murat AU - Ocak, Yusuf Selim AU - Baysal, Akın AU - Temel, Hamdi PY - 2013 DA - June JF - Dicle Üniversitesi Fen Bilimleri Enstitüsü Dergisi JO - DUFED PB - Dicle Üniversitesi WT - DergiPark SN - 2146-4693 SP - 1 EP - 8 VL - 2 IS - 1 LA - tr AB - 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 KW - Bis fosfinit KW - Transfer hidrojenasyon KW - Rutenyum KW - Kataliz KW - Keton N2 - 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 CR - 1. S. Gladiali, E. Alberico, in Transition Metals for Organic Synthesis, ed. M. Beller and C. Bolm, WileyVCH, Weinheim, 2004, vol. 2, pp. 145. CR - 2. S. E. Clapham, A. Hadzovic, R. H. Morris, Coord. Chem. Rev. 248 (2004) 2201-2237. CR - 3. J. E. Backvall, J. Organomet. Chem. 652 (2002) 105- 111. CR - 4. J. S. M. Samec, Jan-E. Backvall, P. G. Andersson, P. Brandt, Chem. Soc. Rev. 35 (2006) 237-248. CR - 5. J. S. M. Samec, Jan-E. Backvall, Chem. Eur. J. 8 (2002) 2955-2961. CR - 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. CR - 7. R. V. Wisman, J. G. de Vries, B.-J. Deelman, H. J. Heeres, Organic Process Res. & Develop. 10 (2006) 423-429. CR - 8. J. Bayardon, D. Sinou, O. Holczknecht, L. Mercs, G. Pozzi, Tetrahedron: Asymmetry 16 (2005) 2319- 2327. CR - 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. CR - 10. M. Leautey, P. Jubault, X. Pannexoucke, J.-C. Quirion, Eur. J. Org. Chem. (2003) 3761-3765. CR - 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. CR - 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. CR - 13. M. Aydemir, A. Baysal, S. Özkar, L. T. Y›ld›r›m, Polyhedron 30 (2011) 796-804. CR - 14. M. Aydemir, A. Baysal, Polyhedron 29 (2010) 1219- 1224. CR - 15. M. Aydemir, N. Meriç, A. Baysal, B. Gümgüm, M. Toğrul, Y. Turgut, Tetrahedron: Asymmetry 21 (2010) 703-710. CR - 16. D. Cuervo, M. P. Gamasa, J. Gimeno, Chem. Eur. J. 10 (2004) 425-432. CR - 17. M. Aydemir, A. Baysal, B. Gümgüm, Appl. Organometal. Chem. 26 (2012) 1-8. CR - 18. E. Encarnacion, J. Pons, R. Yanez, J. Ros, Inorg. Chim. Acta 358 (11) (2005) 3272-3276. CR - 19. R. Noyori, M. Yamakawa, S. Hashiguchi, J. Org. Chem. 66 (24) (2001) 7931 7944. CR - 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. CR - 21. A. D. Burrows, M. F. Mahon, M. T. Palmer, J. Chem. Soc., Dalton Trans. (2000) 1669-1677. CR - 22. M. Aydemir, N. Meric, A. Baysal, J. Organomet. Chem. 720 (2012) 38-45. CR - 23. M. Aydemir, A. Baysal, N. Meric, B. Gumgum J. Organomet. Chem. 694 (2009) 2488 2492. CR - 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. CR - 25. A. D. Ryabov, V. S. Kurova, V. Ekaterina, R. Ivanova, R. Le Lagadec, L. Alexandrova, Anal. Chem. 77 (2005) 1132-1139. CR - 26. M. Aydemir, A. Baysal, N. Meric, C. Kayan, B. Gümgüm, S. Özkar, E. Sahin J. Organomet. Chem. 696 (2011) 2584-2588. CR - 27. A. M. Maj, K. M. Pietrusiewicz, I. Suisse, F. Agbossou, A. Mortreux, J. Organomet. Chem. 626 (2001) 157- 160. CR - 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. CR - 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. CR - 30. R. Noyori, T. Ohkuma, Angew. Chem. Int. Ed. Engl. 40 (2001) 40-73. CR - 31. J. Canivet, G. Labat, H. Stockli-Evans, G. Süss-Fink, Eur. J. Inorg. Chem. (2005) 4493-4500. CR - 32. P. Stepnicka, J. Ludvíc, J. Canivet, G. Süss-Fink, Inorg. Chim. Acta 359 (2006) 2369-2374. CR - 33. P. Dani, T. Karlen, R. A. Gossage, S. Gladialli, F. G. Koten, Angew. Chem. Int. Ed. Engl. 39 (2000) 743-745. CR - 34. Z. Fei, R. Scopelliti, P.J. Dyson, Inorg. Chem. 42 (2003) 2125-2130. CR - 35. Z. Fei, R. Scopelliti, P.J. Dyson, Eur. J. Inorg. Chem. (2004) 530-537. CR - 36. S. Berger, S. Braun, H. O. Kolinowski, NMRSpektroskopie von Nichtmetallen Band 3, 31P NMR Spektroskopie, Georg Theime Verlag, Stuttgart, New York, (1993). CR - 37. R. A. Zelonka, M.C. Baird, J. Organomet. Chem. 35 (1972) C43-C46. CR - 38. M. A. Bennet, A. K. Smith, J. Chem. Soc. Dalton Trans. (1974) 233-241. CR - 39. M. A. Bennet, T. N. Huang, T. W. Matheson, A. K. Smith, Inorg. Synth. 7 (1982) 74-78. UR - https://dergipark.org.tr/tr/pub/dufed/issue//698248 L1 - https://dergipark.org.tr/tr/download/article-file/992015 ER -