Synthesis, characterization, redox behavior and hydrogenation catalytic activity of bis(N-aryl-3,5-Bu2t-salicylaldiminato) palladium(II) complexes

Polyhedron

Volumn 24, Issue 2, 2005, Pages 319-325

  Kasumov, Veli T ^a   Taş, Eşref ^a   Koksal F ^b   Özalp Yaman, Şeniz ^c  

^a HARRAN UNIVERSITY   (Turkey)

^b ONDOKUZ MAYIS UNIVERSITY   (Turkey)

^c ATILIM UNIVERSITY   (Turkey)

Author keywords

Catalytic hydrogenation; Electrochemistry; N Aryl ,5 Bu2t salicylaldiminepalladium(II) complexes; Nitroxide radicals; Pd(II) phenoxyl radicals; Spectroscopy

Indexed keywords

ANILINE; ANODIC OXIDATION; CYCLIC VOLTAMMETRY; FREE RADICAL REACTIONS; HYDROGENATION; PALLADIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

CATALYTIC HYDROGENATION; CATALYTIC REACTIVITY; ELECTRON TRANSFER; HYDROGENATION CATALYTIC; N-ARYL-,5-BU2T-SALICYLALDIMINEPALLADIUM(II) COMPLEX; NITROXIDE RADICALS; PD(II)-PHENOXYL RADICAL; PHENOXYL RADICAL; REDOX BEHAVIOR; TRANSFER PROPERTIES;

CATALYST ACTIVITY;

ANILINE; BROMINE; CERIUM; CHLORIDE; FLUORINE; HYDROGEN; IMINE; N,N DIMETHYLFORMAMIDE; NITROBENZENE; NITROXIDE; OXIDE; PALLADIUM COMPLEX; PHENOL DERIVATIVE; RADICAL; SALICYLALDEHYDE;

ARTICLE; CATALYSIS; CYCLIC POTENTIOMETRY; ELECTRON TRANSPORT; HYDROGENATION; INFRARED SPECTROSCOPY; OXIDATION; OXIDATION REDUCTION REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 12344257065     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2004.11.020     Document Type: Article

References (42)

1. P.C. Wikins, and J.M. Berg Inorganic Chemistry in Biology 1997 Oxford University Press Oxford
2. J.W. Wittaker K.D. Karlin Z. Tyeklar Bioinorganic Chemistry of Copper 1993 Chapman and Hall New York
3. R.H. Holm, and M.J. O'Connor Prog. Inorg. Chem. 14 1971 325
4. J. Vargas, J. Costamagna, R. Latorre, A. Alvardo, and G. Mena Coord. Chem. Rev. 119 1992 67
5. S. Yamada Coord. Chem. Rev. 190-192 1999 537
6. V. Casellato, P.A. Vigato, D.E. Fenton, and M. Vidali Chem. Soc. Rev. 8 1979 199
7. D.E. Fenton Chem. Soc. Rev. 28 1999 159
8. L. Canali, and D.C. Sherrington Chem. Soc. Rev. 28 1999 85
9. Y.N. Ito, and T. Katsuki Bull. Chem. Soc. Jpn. 72 1999 603
10. Y. Suzuki, H. Herao, and T. Fujta Bull. Chem. Soc. Jpn. 75 2003 1493
11. J. Stubbe, and van der Donk Chem. Rev. 98 1998 705
12. A.A. Medjidov, V.T. Kasumov, and H.S. Mamedov Koord. Khim. 7 1981 66
13. M.K. Guseyinova, A.A. Medjidov, and V.T. Kasumov Rus. J. Struct. Chem. 23 1982 114
14. V.T. Kasumov, and A.A. Medjidov Koord. Khim. 15 1989 1404
15. V.T. Kasumov, S.N. Lyubchenko, A.A. Medjidov, and V.A. Kogan Koord. Khim. 16 1990 1633
16. V.T. Kasumov, and A.A. Medjidov Koord. Khim. 16 1990 1355
17. V.T. Kasumov, A.A. Medjidov, R.Z. Rzaev, and R.D. Kasumov Koord. Khim. 21 1995 209
18. A.A. Rzaev, V.T. Kasumov, and A.A. Medjidov Kinet. Catal. 32 1991 594
19. V.T. Kasumov, A.A. Medjidov, I.A. Golubeva, O.V. Shubina, and R.Z. Rzaev Rus. J. Coord. Chem. 17 1991 1698
20. W. Zhang, J.L. Loebach, S.R. Wilson, and E.N. Jacobsen JACS 112 1990 2801
21. D.A. Atwood Coord. Chem. Rev. 176 1998 407
22. B.A. Jazdzewski, and W.B. Tolman Coord. Chem. Rev. 200-202 2000 633
23. V.T. Kasumov, A.A. Medjidov, R.Z. Rzaev, and I.A. Golubeva Rus. J. Coord. Chem. 19 1993 933
24. S. Matsui, Y. Tohi, J. Saito, H. Makio, H. Tanaka, M. Nitabaru, T. Nakana, and T. Fujita Chem. Lett. 1999 1065
25. P.A. Cameron, C.C. Gibson, J.A. Segal, C. Redshaw, G. Solan, A.J.P. White, and D.J. Williams J. Chem. Soc., Dalton Trans. 2001
26. V.T. Kasumov, F. Köksal, and R. Köşeoǧlu J. Coord. Chem. 57 2004 591
27. J.F. Larrow, E.N. Jacobsen, Y. Gao, Y. Hong, X. Nie, and C.M. Zeppe J. Org. Chem. 59 1994 1939
28. L.A. Safronova, A.D. Shebaldova, and M.L. Khidekel Zh. Obsh. Khim. 52 1984 385
29. K. Ueno, and A.E. Martell J. Am. Chem. Soc. 60 1956 1270
30. S.J. Gruber, C.M. Harris, and E. Sinn J. Inorg. Nucl. Chem. 30 1968 1805
31. A.B.P. Lever Inorganic Electronic Spectroscopy 1984 Elsevier Amsterdam
32. G.K. Rauth, J. Dinda, S. Jasimuddin, and S. Sinha Trans. Met. Chem. 27 2003 88
33. M.A. Malcrow, L.M.L. Chia, X. Liu, E.R.J.L. McInnes, L.J. Yellowlees, F.E. Mabs, and J.E. Devies Chem. Commun. 1998 2465
34. M.L. Glashen, D.D. Eads, T.G. Spiro, and J.W. Wittaker J. Phys. Chem. 99 1995 4918
35. G. Schetty, and E. Steiner Helv. Chim. Acta 57 1974 2149
36. R.L. Lintvedt, K.A. Rupp, and M.J. Heeg Inorg. Chem. 27 1988 331
37. B. Crociani, M. Sala, A. Polo, and G. Bombieri Organometallics 5 1986 1369
38. V.T. Kasumov, B. Karabulut, I. Kartal, and F. Köksal Trans. Met. Chem. 26 2001 64
39. V.T. Kasumov Spectrochim. Acta A 57 2001 2337
40. R.S. Nichelson, and I. Shain Anal. Chem. 36 1964 706
41. Y. Wang, J.L. DuBois, B. Hedman, K.O. Hodgson, and T.D.P. Stack Science 279 1998
42. M.A. Wasserman, V.A. Kasaikin, and V.P. Timofeev Spectrochim. Acta A 54 1998