The synthesis of copper(II) salicylaldiminato complexes and their catalytic activity in the hydroxylation of phenol

Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

Volumn 62, Issue 3, 2007, Pages 331-338

  Van Wyk, Juanita L ^a   Mapolie, Selwyn ^a   Lennartson, Anders ^b   Håkansson, Mikael ^b   Jagner, Susan ^c  

^a UNIVERSITY OF THE WESTERN CAPE   (South Africa)

^b UNIVERSITY OF GOTHENBURG   (Sweden)

^c CHALMERS UNIVERSITY OF TECHNOLOGY   (Sweden)

Author keywords

Hydroxylation; Phenol; Salicylaldimine; Tetracoordinated copper(II) complexes

Indexed keywords

CATALYST ACTIVITY; HYDROXYLATION; LIGANDS; MOLAR RATIO; PH; PHENOLS; SYNTHESIS (CHEMICAL); VOLATILE FATTY ACIDS;

AQUEOUS MEDIA; CATALYTIC HYDROXYLATION OF PHENOLS; COPPER ACETATES; COPPER COMPLEXES; DINUCLEAR COMPLEX; HYDROXYLATION OF PHENOL; SALICYLALDIMINES; X RAY CRYSTAL STRUCTURES;

COPPER COMPOUNDS;

EID: 35648969967     PISSN: 09320776     EISSN: None     Source Type: Journal    
DOI: 10.1515/znb-2007-0305     Document Type: Article

References (23)

1. J. Zhang, Y. Tang, J.-Q. Xie, J.-Z. Li, W. Zeng, C.-W. Hu, J. Serb. Chem. Soc. 2005, 70, 1137.
2. J. Zhang, Y. Tang, J.-Q. Xie, Z.-R. Song, L. Wing, C.-W. Hu, React. Kinet. Catal. Lett. 2005, 85, 269.
3. J. Q. Xie, J.-Z. Li, X.-G. Meng, C.-W. Hu, X.-C. Zeng, Trans. Met. Chem. 2004, 29, 388.
4. H. Liu, G. Lu, T. Guo, Y. Guo, Appl. Catal. A. Gen. 2005, 293, 153.
5. H. Liu, G. Lu, Y. Guo, Y. Guo, J. Wang, Chem. Eng. J. 2006, 116, 179.
6. J. A. Martens, Ph. Buksen, P. A. Jacobs, A. vander Pol, J. H. C. van Hooff, C. Ferrini, H. W. Kouwenhoven, P. J. Kooyman, H. van Bekkum, Appl. Catal. A. Gen. 1993, 99, 71.
7. C. Wang, S. Friedrich, T.R. Youkin, R. T. Li, R. H. Grubbs, D. A. Bansleben, M. W. Day, Organometallics 1998, 17, 3149.
8. R.B. Coles, C.M. Harris, E. Sinn, Inorg. Chem. 1969, 8, 2607.
9. W.-H. Chen, H.-H. Wei, G.-H. Lee, Y. Hung, Polyhedron 2001, 20, 515.
10. E. Schön, D. A. Plattner, P. Chen, Inorg. Chem. 2004, 43, 3164.
11. E. Tas, M. Asloanoglu, M. Ulusoy, H. Temel, J. Coord. Chem. 2004, 57, 677.
12. E. Tas, M. Aslanoglu, M. Guler, M. Ulusoy, J. Coord. Chem. 2004, 57, 583.
13. S. F. Mapolie, J. L. Van Wyk, unpublished results.
14. A. Dubey, V Rives, S. Kannan, J. Mol. Catal. A 2002, 181, 151.
15. Y. H. Hue, A. Gedeon, J. L. Bonardet, N. Melush, J. B. D'Espinose, J. Fraissard, Chem. Commun. 1999, 1967.
16. C. Liu, Y. Shan, X. Yang, X. Ye, Y. Wu, J. Catal. 1997, 168, 35.
17. L. Wang, A. Kong, B. Chen, H. Ding, Y. Shan, M. He, J. Mol. Catal. A 2005, 230, 143.
18. J. N. Parrk, J. Wang, K. Y. Choi, W.-Y. Dong, S.-J. Hong, C. W. Lee, J. Mol. Catal. 2006, 247, 73.
19. SIR92: A. Altomare, G. Cascarano, C. Giacovazzo, A. Guagliardi, J. Appl. Crystallogr. 1993, 26, 343.
20. G. M. Sheldrick, SHELX97 (Release 97-2), Programs for the Determination of Crystal Structures, University of Göttingen, Göttingen (Germany) 1998.
21. L.J. Farrugia, J. Appl. Crystallogr. 1999, 32, 837.
22. L.J. Farrugia, J. Appl. Crystallogr. 1997, 30, 565.
23. CCDC 622393 - 622395 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac. uk/data_request/cif.