Stereoselective cyclopalladation of [{(N-methyl-N-aryl)amino}methyl]ferrocenes: Crystal structure of σ-Pd[ClPPh3(η5-C5 H5)Fe(η5-C5H3CH2 N(CH3)C6H4OCH3-4)] · H2O

Inorganic Chemistry Communications

Volumn 9, Issue 6, 2006, Pages 658-661

  Wang, Hong Xing ^a   Li, Ying Jie ^a   Gao, Ren Qing ^a   Wu, Hong Fei ^a   Geng, Feng Ying ^a   Jin, Rong ^b  

^a TIANJIN UNIVERSITY   (China)

^b TIANJIN FIRST CENTRAL HOSPITAL   (China)

Author keywords

Crystal; Cyclopalladation; Ferrocenylamines; Stereoselectivity

Indexed keywords

EID: 33746231543     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2006.03.024     Document Type: Article

References (32)

1. Dupont J., Consorti C.S., and Spencer J. Chem. Rev. 105 (2005) 2527
2. Vicente J., and Arcas A. Coord. Chem. Rev. 249 (2005) 1135
3. Beletskaya I.P., and Cheprakov A.V. J. Organomet. Chem. 689 (2004) 4055
4. Wu Y.J., Huo S.Q., Gong J.F., Cui X.L., Ding L., Ding K.L., Du C.X., Liu Y.H., and Song M.P. J. Organomet. Chem. 637-639 (2001) 27
5. Togni A., and Venanzi L.M. Angew. Chem., Int. Ed. Engl. 33 (1994) 497
6. Omae I. Coord. Chem. Rev. 83 (1988) 137
7. Iyer S., and Ramesh C. Tetrahedron Lett. 41 (2000) 8981
8. Weissmann H., and Milstein D. Chem. Commun. (1999) 1901
9. Lopez C., Bosque R., Solans X., Font-Bardia M., Silver J., and Fern G. J. Chem. Soc., Dalton Trans. (1995) 1839
10. Bosque R., Lopez C., and Sales J. J. Organomet. Chem. 498 (1995) 147
11. Bosque R., Lopez C., Sales J., Solans X., and Font-Bardia M. J. Chem. Soc., Dalton Trans. (1994) 735
12. Huo S.Q., Wu Y.J., Du C.X., Zhu Y., Yuan H.Z., and Mao X.A. J. Organomet. Chem. 483 (1994) 139
13. Wu Y.J., Liu Y.H., Ding K.L., Yuan H.Z., and Mao X.A. J. Organomet. Chem. 505 (1995) 37
14. Wang H.X., Ding L., and Wu Y.J. J. Organomet. Chem. 679 (2003) 130
15. Wang H.X., Li Y.J., Jin R., Niu J.R., Wu H.F., Zhou H.C., Xu J., Gao R.Q., and Geng F.Y. J. Organomet. Chem. 691 (2006) 987
16. H.X. Wang, H.F. Wu, H.C. Zhou, R. Jin, R.Q. Gao, F.Y. Geng, J. Xu, Y.J. Li, W.Q. Zhang, Polyhedron (2006), in press.
17. Benito A., Cano J., Martinez-Manez R., Sato J., Paya J., Lioret J., Julve M., and Faus J. Inorg. Chem. 32 (1993) 1197
18. Bracci M., Ercolani C., Floris B., Bassetti M., Chiesi-Vila A., and Guastini C. J. Chem. Soc., Dalton Trans. (1990) 1357
19. Louati A., Gross M., Douce L., and Matt D. J. Organomet. Chem. 438 (1992) 167
20. Hamamura K., Kita M., Nonoyama N., and Fujita J. J. Organomet. Chem. 463 (1993) 169
21. 2PPd: C 57.40, H 4.28, N 3.72; Found C 57.12, H 4.25, N 3.70.
22. Rosenblum M., and Woodward R.B. J. Am. Chem. Soc. 80 (1958) 5443
23. Wang H.X., Li Y.J., and Hou J.F. Acta Cryst. E61 (2005) m1785
24. Wang H.X., Li Y.J., Wu H.F., Zhou H.C., Gao R.Q., and Geng F.Y. Acta Cryst. E61 (2005) m1871
25. Li Y.J., Wang H.X., and Wu H.F. Acta Cryst. E61 (2005) m1579
26. Wang H.X., Li Y.J., Wu H.F., Zhou H.C., Geng F.Y., and Gao R.Q. Acta Cryst. E61 (2005) m2322
27. Cahn R.S., Ingold C., and Prelog V. Angew. Chem., Int. Ed. Engl. 4 (1966) 385 and references therein
28. 3, F(0 0 0) = 772, R = 0.0441.
29. Dunina V.V., Gorunova O.N., Averina E.B., Grishin Y.K., Kuz'mina L.G., and Howard J.A.K. J. Organomet. Chem. 603 (2000) 138
30. Lopez C., Bosque R., Solans X., and Font-Bardia M. New J. Chem. (1998) 977
31. Allen T.H., and Kennard O. Chem. Des. Auto. News 8 (1993) 146
32. Sheldrick G.M. SHELXS-97 and SHELXL-97, Programs for Crystal Structure Solution and Refinement (1997), University of Göttingen