The Reaction of Rhenium(V) Cores with a Tetradentate Schiff Base. The Isolation of ‘3+3’ and ‘4+0’ Complexes of Rhenium(V)
Kim C. Potgieter A , Peter Mayer B and Thomas I. A. Gerber A CA Department of Chemistry, Nelson Mandela Metropolitan University, 6031 Port Elizabeth, South Africa.
B Department of Chemistry, Ludwig-Maximilians University, D-81377 München, Germany.
C Corresponding author. Email: thomas.gerber@nmmu.ac.za
Australian Journal of Chemistry 63(9) 1382-1388 https://doi.org/10.1071/CH09660
Submitted: 17 December 2009 Accepted: 21 April 2010 Published: 9 September 2010
Abstract
The reaction of the potentially tetradentate N 4-donor ligand N,N′-bis[(2-aminophenyl)methylidene]ethane-1,2-diamine (H2ane) with various rhenium(V) precursors led to the formation of different rhenium(V) complexes. With trans-[ReOBr3(PPh3)2], the unusual ‘3+3’ complex cation [Re(tnn)(Htnn)]2+ (H2tnn = N-(2-aminophenylmethylidene)ethane-1,2-diamine) was isolated. With trans-[ReO2(py)4]Cl, the complex [ReO(dne)] was found (H3dne = N 1-2-aminobenzyl-N 2-2-aminobenzylideneethane-1,2-diamine), and the cationic complex [ReO(ane)]+ was formed from cis-[ReO2I(PPh3)2]. These products were characterized by 1H NMR and IR spectroscopy, and by X-ray diffraction.
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