Services on Demand
Journal
Article
Indicators
Related links
- Cited by Google
- Similars in Google
Share
South African Journal of Chemistry
On-line version ISSN 1996-840XPrint version ISSN 0379-4350
S.Afr.j.chem. (Online) vol.64 Durban 2011
RESEARCH ARTICLE
Coordination of tridentate Schiff base derivatives of 4-aminoantipyrine to rhenium (V)
Kim C. PotgieterI; Thomas I.A. GerberI, *; Peter MayerII
IDepartment of Chemistry, Nelson Mandela Metropolitan University, 6031 Port Elizabeth, South Africa
IIDepartment of Chemistry, Ludwig-Maximilians University, D-81377, München, Germany
ABSTRACT
The potentially tridentate Schiff base derivatives H2nap and Hoap were synthesized by the condensation reaction of 4-amino-2,3-dimethyl-1-phenyl-5-pyrazoline (4-aminoantipyrine)with 2-aminobenzaldehyde and salicylaldehyde, respectively. The reaction of H2nap with [ReOBr3(PPh3)2] and cis-[ReO2I(PPh3)2](1) gives rise to the products [Re(nap)Br2(PPh3)]Br (2) and [ReO(OEt)(Hnap)(PPh3)]I (3), respectively. In 2 the ligand nap is coordinated as a tridentate imido-imino-ketone, while in 3 Hnap is bonded as an amido-imino-ketone. The reaction of Hoap with [ReO2I(PPh3)2] affords the product [ReO(OMe)(oap)(PPh3)]I (4). Spectroscopic data and the X-ray crystal structures of compounds 2-4 are reported.
Keywords: Tridentate, rhenium(V), imido, crystal structures
Full text available only in pdf format.
References
1 A.P. Mishra, J. Indian. Chem. Soc., 1999, 76, 35-40; V Cechiral Filho, R. Correa, Z. Vaz, J.B. Calixto, R.J. Nunes, T.R. Pinheiro, A.D. Andricopulo and R.A. Yunes, Farmaco, 1998, 53, 55-57; R. Bose, D.S.R. Murty, G. Chakrapani, J. Radioanal. Nucl. Chem., 2005, 265, 115-122. [ Links ]
2 F. Bao, X. Lu, B. Kang and Q. Wu, Eur. Polym. J, 2006, 42, 928-934. [ Links ]
3 S.M. Sondhi, N. Shinghal, R.P. Verma, S.K. Arora and S.G. Dastidar, Indian J. Chem, 2001, B40, 113-119. [ Links ]
4 T. Ito, C. Goto and K. Noguchi, Anal. Chim. Acta, 2001, 443,41-51. [ Links ]
5 R.A. Bailey and T.R. Peterson, Can. J. Chem.,1969, 47,1681-1687. [ Links ]
6 N.P. Johnson, C.J.L. Lock and G. Wilkinson, Inorg. Synth.,1967, 9,145-146; G.F. Ciani, G. D'Alfonso, P. Romiti, A. Sironi and M. Freni, Inorg. Chim. Acta, 1983, 72, 29-37. [ Links ]
7 A. Altomare, M.C. Burla, M. Camalli, G.L. Gascarano, C. Giacavazco, A. Guagliardi, A.G. Moliterni, G. Polidori and R. Spagna, J. Appl. Crystallogr.,1999, 32,115-117. [ Links ]
8 G.M. Sheldrick, SHELXL-97, Program for Structure Solutions and Refinement, University of Göttingen, Germany, 1997. [ Links ]
9 Xred, rev. 1.09, STOE, Darmstadt, Germany, 2005. [ Links ]
10 XShape, rev. 1.02, STOE, Darmstadt, Germany, 2005. [ Links ]
11 T.I.A. Gerber, D. Luzipo and P. Mayer, J. Coord. Chem, 2004, 57, 1419-1423. [ Links ]
12 T.I.A. Gerber, D. Luzipo and P. Mayer, J. Coord. Chem.,2005, 58, 637-641 (and references therein). [ Links ]
13 V.W.W. Yam, K.K. Tam, M.C. Cheng, S.M. Peng and Y. Wang, J. Chem. Soc. Dalton Trans., 1992, 1717-1723; J.R. Winkler and H.B. Gray, Inorg. Chem. 1985, 24, 346-355; V.W.W. Lam, Y.L. Pui, K.M.C. Wong and K.K. Cheung, Inorg. Chim. Acta, 2000, 300, 721-732. [ Links ]
14 J.M. Mayer, Inorg. Chem, 1988, 27, 3899-3903. [ Links ]
15 T.I.A. Gerber and A. Abrahams, C. Imrie, P. Mayer, J. Coord. Chem., 2004, 57, 1339-1343. [ Links ]
16 I. Booysen, T.I.A. Gerber, E. Hosten, D. Luzipo and P. Mayer, J. Coord. Chem., 2007, 60, 635-640; I. Booysen, T.I.A. Gerber, E. Hosten and P. Mayer, Bull. Chem. Soc. Eth, 2008, 22, 101-105; P. Mayer, E. Hosten, T.I.A. Gerber and I. Booysen, J. Iran. Chem. Soc., 2010, 7, 775-780. [ Links ]
17 A. Abrahams, G. Bandoli, S. Gatto, T.I.A. Gerber and J.G.H. Du Preez, J. Coord. Chem., 1998, 43, 297-307; T.I.A. Gerber, P. Mayer and Z.R. Tshentu J. Coord. Chem, 2005, 58, 1589-1595. [ Links ]
Received 16 May 2011
Revised 20 July 2011
Accepted 11 November 2011
Submitted by invitation to celebrate 2011 the 'International Year of Chemistry'.
* To whom correspondence should be addressed. E-mail: thomas.gerber@nmmu.ac.za