Preparation of benzophenone imine complexes of transition metals

Inorganica Chimica Acta

Volumn 361, Issue 6, 2008, Pages 1744-1753

  Albertin, Gabriele ^a   Antoniutti, Stefano ^a   Magaton, Alberto ^a  

^a CA' FOSCARI UNIVERSITY OF VENICE   (Italy)

Author keywords

Benzophenone imine complexes; Iridium; Manganese and rhenium; Phosphite ligands; Ruthenium and osmium; Synthesis

Indexed keywords

ARSENIC COMPOUNDS; CHELATION; CHLORINE COMPOUNDS; HYDRIDES; IRIDIUM; SYNTHESIS (CHEMICAL); TRANSITION METALS;

13C NMR; BENZOPHENONE IMINE COMPLEXES; DIHYDRIDES; DOUBLE BONDS; N-COMPOUNDS; PHOSPHITE LIGANDS; TRIFLATES;

IRIDIUM COMPOUNDS;

EID: 39649117123     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2006.12.001     Document Type: Article

References (38)

1. In: Wilkinson G., Gillard R.D., and McCleverty J.A. (Eds). Comprehensive Coordination Chemistry (1987), Pergamon Press, Oxford, UK
2. In: McCleverty J.A., and Meyer T.J. (Eds). Comprehensive Coordination Chemistry II (2003), Elsevier, Pergamon, Oxford, UK
3. Harman W.D., and Taube H. Inorg. Chem. 27 (1988) 3261
4. McGilligan B.S., Wright T.C., Wilkinson G., Motevalli M., and Hursthouse M.B. J. Chem. Soc., Dalton Trans. (1988) 1737
5. Michelin R.A., Bertani R., Mozzon M., Bombieri G., Benetollo F., and Angelici R. Organometallics 10 (1991) 1751
6. Feng S.G., and Templeton J.L. Organometallics 11 (1992) 1295
7. Knight D.A., Dewey M.A., Stark G.A., Bennett B.K., Arif A.M., and Gladysz J.A. Organometallics 12 (1993) 4523
8. Esteruelas M.A., Lahoz F.J., Lopez A.M., Oñate E., and Oro L.A. Organometallics 14 (1995) 2496
9. Bustelo F., Jimenez-Tenorio M., Puerta M.C., and Valerga P. J. Chem. Soc., Dalton Trans. (1999) 2399
10. Albertin G., Antoniutti S., Bacchi A., Bordignon E., Busatto F., and Pelizzi G. Inorg. Chem. 36 (1997) 1296
11. Albertin G., Antoniutti S., Bacchi A., Ballico G.B., Bordignon E., Pelizzi G., Ranieri M., and Ugo P. Inorg. Chem. 39 (2000) 3265
12. Albertin G., Antoniutti S., Bacchi A., Bordignon E., Miani F., and Pelizzi G. Inorg. Chem. 39 (2000) 3283
13. Albertin G., Antoniutti S., Bordignon E., and Perinello G. J. Organomet. Chem. 625 (2001) 217
14. Albertin G., Antoniutti S., and Giorgi M.T. Eur. J. Inorg. Chem. (2003) 2855
15. Albertin G., Antoniutti S., and Bredariol F. J. Organomet. Chem. 679 (2003) 208
16. Albertin G., Antoniutti S., Bacchi A., Fregolent B., and Pelizzi G. Eur. J. Inorg. Chem. (2004) 1922
17. Albertin G., Antoniutti S., Lanfranchi M., Pelizzi G., and Bordignon E. Inorg. Chem. 25 (1986) 950
18. Albertin G., Antoniutti S., Pelizzi G., Vitali F., and Bordignon E. J. Am. Chem. Soc. 108 (1986) 6627
19. Albertin G., Antoniutti S., Pelizzi G., Vitali F., and Bordignon E. Inorg. Chem. 27 (1988) 829
20. Albertin G., Antoniutti S., and Bordignon E. J. Chem. Soc., Dalton Trans. (1989) 2353
21. Albertin G., Antoniutti S., Bacchi A., Barbera D., Bordignon E., Pelizzi G., and Ugo P. Inorg. Chem. 37 (1998) 5602
22. Albertin G., Antoniutti S., and Boato M. Inorg. Chim. Acta 357 (2004) 1119
23. Albertin G., Antoniutti S., Bordignon E., and Menegazzo F. J. Chem. Soc., Dalton Trans. (2000) 1181
24. Albertin G., Antoniutti S., Bordignon E., and Tasin A. J. Organomet. Chem. 627 (2001) 99
25. Rabinowitz R., and Pellon J. J. Org. Chem. 26 (1961) 4623
26. Balacco G. J. Chem. Inf. Comput. Sci. 34 (1994) 1235
27. Albertin G., Antoniutti S., Bettiol M., Bordignon E., and Busatto F. Organometallics 16 (1997) 4959
28. Albertin G., Antoniutti S., García-Fontán S., Carballo R., and Padoan F. J. Chem. Soc., Dalton Trans. (1998) 2071
29. Peet W.G., and Gerlach D.H. Inorg. Synth. 15 (1974) 38
30. Gerlach D.H., Peet W.G., and Muetterties E.L. J. Am. Chem. Soc. 94 (1972) 4545
31. 4 with an equimolar amount of triflic acid. See:. Albertin G., Antoniutti S., Bacchi A., Bordignon E., Dolcetti P.M., and Pelizzi G. J. Chem. Soc., Dalton Trans. (1997) 4435
32. Albertin G., Antoniutti S., Bacchi A., Bergamo M., Bordignon E., and Pelizzi G. Inorg. Chem. 37 (1998) 479
33. 4 is often used as an oxidant in coordination chemistry, and its ability to oxidize coordinate hydrazine to diazene selectively is largely documented. See:. Albertin G., Antoniutti S., Bortoluzzi M., Castro-Fojo J., and García-Fontán S. Inorg. Chem. 43 (2004) 4511
34. Sutton D. Chem. Rev. 93 (1993) 995
35. Albertin G., Antoniutti S., Bacchi A., De Marchi F., and Pelizzi G. Inorg. Chem. 44 (2005) 8947 and references therein
36. Geary W.J. Coord. Chem. Rev. 7 (1971) 81
37. Adams D.M. Metal-Ligand and Related Vibrations (1968), St. Martin's Press, New York
38. Albertin G., Antoniutti S., Bacchi A., Bordignon E., Giorgi M.T., and Pelizzi G. Angew. Chem., Int. Ed. 41 (2002) 2192