Reaction of carbon monoxide with tri-tert-butylgallium: The first example of CO insertion into a gallium-carbon bond

Inorganica Chimica Acta

Volumn 361, Issue 11, 2008, Pages 3332-3337

  Mason, Mark R ^a   Song, Bingxu ^a   Han, Yaohua ^a   Hu, Xiche ^a  

^a UNIVERSITY OF TOLEDO   (United States)

Author keywords

CO insertion; DFT calculations; Organogallium compounds; X ray crystal structure

Indexed keywords

ALUMINUM COMPOUNDS; ATMOSPHERIC PRESSURE; CARBON MONOXIDE; CRYSTAL STRUCTURE; DENSITY FUNCTIONAL THEORY; GALLIUM; X RAY CRYSTALLOGRAPHY; X RAYS;

CARBON BOND; DFT CALCULATION; ENTROPY CHANGES; ISOTOPIC LABELING; ORGANOGALLIUM; REACTION CONDITIONS; X RAY CRYSTAL STRUCTURES;

GALLIUM COMPOUNDS;

EID: 46749142896     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2007.11.021     Document Type: Article

References (39)

1. Local density functional calculations suggest that the monocarbonyl complexes of the Group 13 elements are more stable than their isocarbonyl isomers. See:. Bridgeman A.J. J. Chem. Soc., Dalton Trans. (1997) 1323
2. Howard J.A., Sutcliffe R., Hampson C.A., and Mile B. J. Phys. Chem. 90 (1986) 4268
3. Kasai P.H., and Jones P.M. J. Phys. Chem. 89 (1985) 2019
4. Hatton W.G., Hacker N.P., and Kasai P.H. J. Phys. Chem. 93 (1989) 1328
5. Himmel H.-J., Downs A.J., Green J.C., and Greene T.M. J. Phys. Chem. A 104 (2000) 3642
6. Downs A.J., Himmel H.-J., and Manceron L. Polyhedron 21 (2002) 473
7. Burg A.B., and Schlesinger H.I. J. Am. Chem. Soc. 59 (1937) 780
8. Bethke G.W., and Wilson M.K. J. Chem. Phys. 26 (1957) 1118
9. Taylor R.C. J. Chem. Phys. 26 (1957) 1131
10. Jeffery J.C., Norman N.C., Pardoe J.A.J., and Timms P.L. Chem. Commun. (2000) 2367
11. Finze M., Bernhardt E., Terheiden A., Berkei M., Willner H., Christen D., Oberhammer H., and Aubke F. J. Am. Chem. Soc. 124 (2002) 15385
12. Mackie I.D., Hinchley S.L., Robertson H.E., Rankin D.W.H., Pardoe J.A.J., and Timms P.L. J. Chem. Soc., Dalton Trans. (2002) 4162
13. Zhou M., Xu Q., Wang Z.-X., and Schleyer P.v.R. J. Am. Chem. Soc. 124 (2002) 14854
14. Sanchez R., Arrington C., and Arrington Jr. C. J. Am. Chem. Soc. 111 (1989) 9110
15. Mason M.R., Song B., and Kirschbaum K. J. Am. Chem. Soc. 126 (2004) 11812
16. Li X., Ni C., Song H., and Cui C. Chem. Commun. (2006) 1763
17. Gao Y., Cheng X., Song H., Zhang J., and Cui C. Organometallics 26 (2007) 1308
18. For examples, see:. Seyferth D., and Weinstein R.M. J. Am. Chem. Soc. 104 (1982) 5534
19. Seyferth D., Weinstein R.M., Hui R.C., Wang W.-L., and Archer C.M. J. Org. Chem. 56 (1991) 5768
20. For examples see:. Sprangers W.J.J.M., Van Swieten A.P., and Louw R. Chimia 30 (1976) 199
21. Sprangers W.J.J.M., and Louw R. J. Chem. Soc., Perkin Trans. II (1976) 1895
22. Brown H.C. Acc. Chem. Res. 2 (1969) 65
23. Kovar R.A., Derr H., Brandau D., and Callaway J.O. Inorg. Chem. 14 (1975) 2809
24. Kohn W., and Sham L.J. Phys. Rev. 140 (1965) A1133
25. Becke A.D. J. Chem. Phys. 98 (1993) 1372
26. Perdew J.P., Chevary J.A., Vosko S.H., Jackson K.A., Pederson M.R., Singh D.J., and Fiolhais C. Phys. Rev. B 46 (1992) 6671
27. M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, J.A. Montgomery, T. Vreven, K.N. Kudin, J.C. Burant, J.M. Millam, S.S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G.A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J.E. Knox, H.P. Hratchian, J.B. Cross, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, P.Y. Ayala, K. Morokuma, G.A. Voth, P. Salvador, J.J. Dannenberg, V.G. Zakrzewski, S. Dapprich, A.D. Daniels, M.C. Strain, O. Farkas, D.K. Malick, A.D. Rabuck, K. Raghavachari, J.B. Foresman, J.V. Ortiz, Q. Cui, A.G. Baboul, S. Clifford, J. Cioslowski, B.B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R.L. Martin, D.J. Fox, T. Keith, M.A. Al-Laham, C.Y. Peng, A. Nanayakkara, M. Challacombe, P.M.W. Gill, B. Johnson, W. Chen, M.W. Wong, C. Gonzalez, J.A. Pople, Gaussian 03, Revision B.04, Gaussian, Pittsburgh, PA, 2003.
28. smart, Software for the CCD Detector System; Siemens Analytical Instruments Division: Madison, WI, 1995.
29. saint plus 6.22, Software for the CCD Detector System; Bruker Analytical Instruments Division: Madison, WI, 2001.
30. Sheldrick G.M. sadabs: Absorption Correction Program (1996), University of Göttingen, Göttingen, Germany
31. shelxtl, Version 5.10/NT; Bruker AXS Inc., Madison, WI, 1998.
32. Cowley A.R., Downs A.J., Marchant S., Macrae V.A., Taylor R.A., and Parsons S. Organometallics 24 (2005) 5702
33. Woski M., and Mitzel N.W. Z. Naturforsch. 59b (2004) 269
34. Timoshkin A.Y., and Schaefer III H.F. J. Am. Chem. Soc. 125 (2003) 9998
35. Stimson R.E., and Shriver D.F. Inorg. Chem. 19 (1980) 1141
36. Karabatsos G.J., Graham J.D., and Vane F. J. Am. Chem. Soc. 83 (1961) 2778
37. Karabatsos G.J. J. Am. Chem. Soc. 83 (1961) 1230
38. See for example:. Keys A., Barbarich T.J., Bott S.G., and Barron A.R. J. Chem. Soc., Dalton Trans. (2000) 577
39. Power M.B., Cleaver W.M., Apblett A.W., Barron A.R., and Ziller J.W. Polyhedron 11 (1992) 477