Efficient microwave syntheses of the compounds Os3(CO)11L, L = NCMe, py, PPh3

Journal of Organometallic Chemistry

Volumn 694, Issue 21, 2009, Pages 3526-3528

  Jung, Jade Y ^a   Newton, Brittney S ^a   Tonkin, Michelle L ^a   Powell, Cynthia B ^a   Powell, Gregory L ^a  

^a ABILENE CHRISTIAN UNIVERSITY   (United States)

Author keywords

Acetonitrile ligand; Activated osmium carbonyl cluster; Microwave synthesis; Monosubstituted triosmium cluster; Pyridine; Triphenylphosphine

Indexed keywords

ACTIVATED OSMIUM CARBONYL CLUSTER; CLUSTER COMPLEXES; DECARBONYLATIONS; HIGH YIELD; LABILE COMPLEXES; LIGAND SUBSTITUTION REACTIONS; MICROWAVE SYNTHESIS; MICROWAVE-ASSISTED; MONOSUBSTITUTED TRIOSMIUM CLUSTER; ONE-POT SYNTHESIS; SHORT PERIODS; TRIMETHYLAMINE OXIDE; TRIPHENYLPHOSPHINE;

ACETONITRILE; BIOACTIVITY; CARBONYLATION; CHELATION; COMPLEXATION; DYES; LIGANDS; MICROWAVE IRRADIATION; PYRIDINE; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

OSMIUM;

EID: 68949207075     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2009.06.041     Document Type: Short Survey

References (26)

1. Johnson B.F.G., Lewis J., and Pippard D. J. Organomet. Chem. 160 (1978) 263
2. Bruce M.I., Liddell M.J., Hughes C.A., Skelton B.W., and White A.H. J. Organomet. Chem. 347 (1988) 157
3. Roberto D., Lucenti E., Roveda C., and Ugo R. Organometallics 16 (1997) 5974
4. Poe J.A., and Sekhar V.C. J. Am. Chem. Soc. 108 (1986) 3673
5. Leadbeater N.E. J. Organomet. Chem. 573 (1999) 211
6. Johnson B.F.G., Lewis J., and Pippard D.A. J. Chem. Soc., Dalton Trans. (1981) 407
7. Nicholls J.N., and Vargas M.D. Inorg. Synth. 28 (1990) 232
8. In: Kingston H.M., and Haswell S.J. (Eds). Microwave-Enhanced Chemistry: Fundamentals, Sample Preparation, and Applications (1997), American Chemical Society, Washington, DC
9. In: Loupy A. (Ed). Microwaves in Organic Synthesis. second ed. (2006), Wiley-VCH, Weinheim
10. In: Kappe C.O., Dallinger D., and Murphree S.S. (Eds). Practical Microwave Synthesis for Organic Chemists: Strategies, Instruments, and Protocols (2009), Wiley-VCH, Weinheim
11. Baghurst D.R., Mingos D.M.P., and Watson M.J. J. Organomet. Chem. 368 (1989) C43
12. Mingos D.M.P., and Baghurst D.R. Chem. Soc. Rev. 20 (1991) 1
13. Dabirmanesh Q., and Roberts R.M.G. J. Organomet. Chem. 542 (1997) 99
14. Roberts R.M.G. J. Organomet. Chem. 691 (2006) 2641
15. Roberts R.M.G. J. Organomet. Chem. 691 (2006) 4926
16. Harcourt E.M., Yonis S.R., Lynch D.E., and Hamilton D.G. Organometallics 27 (2008) 1653
17. Lee Y.T., Choi S.Y., Lee S.T., Chung Y.K., and Kang T.J. Tetrahedron Lett. 47 (2006) 6569
18. Pedotti S., and Patti A. J. Organomet. Chem. 693 (2008) 1375
19. VanAtta S.L., Duclos B.A., and Green D.B. Organometallics 19 (2000) 2397
20. Ardon M., Hogarth G., and Oscroft D.T.W. J. Organomet. Chem. 689 (2004) 2429
21. Barnard T.M., and Leadbeater N.E. Chem. Commun. (2006) 3615
22. Leadbeater N.E., and Shoemaker K.M. Organometallics 27 (2008) 1254
23. Johnson K.D., and Powell G.L. J. Organomet. Chem. 693 (2008) 1712
24. Bradford C.W., Van Bronswijk W., Clark R.J.H., and Nyholm R.S. J. Chem. Soc. A (1970) 2889
25. Leadbeater N.E., Lewis J., Raithby P.R., and Ward G.N. J. Chem. Soc., Dalton Trans. (1997) 2511
26. Castiglioni M., Giordano R., and Sappa E. J. Organomet. Chem. 342 (1988) 97