Some bimetallic half sandwich iron complexes with metal carbene substitution at the cyclopentadienyl ligand: synthesis, characterization, structure, and cyclic voltammetry

1999 ◽  
Vol 23 (8) ◽  
pp. 891-895 ◽  
Author(s):  
Uwe Behrendt ◽  
Robert-Michael Pfeifer ◽  
Rudolf Wartchow ◽  
Holger Butenschön
2017 ◽  
Vol 1149 ◽  
pp. 162-170 ◽  
Author(s):  
Basava Punna Rao Aradhyula ◽  
Werner Kaminsky ◽  
Mohan Rao Kollipara

2014 ◽  
Vol 67 (3) ◽  
pp. 398 ◽  
Author(s):  
Peter Comba ◽  
Hubert Wadepohl ◽  
Arkadius Waleska

The solution coordination chemistry of iron complexes with the pentadentate bispidine ligands L1, L2, and L3 (dimethyl 9-oxo-2,4-di(pyridin-2-yl)-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarboxylate derivatives) was examined. While in acetonitrile, (L1,2)FeII/III species have a preference for Cl– as co-ligand. The corresponding aqua and hydroxido complexes also prevail in the presence of Cl– in aqueous solution. The observed FeII/III potentials in water (cyclic voltammetry) and potentials of (L1–3)FeIV=O (buffered and unbuffered aqueous solutions) are strikingly similar, i.e. the latter are assigned to (L1–3)FeII/III potentials, and published potentials of FeIV=O complexes with other ligands with uncharged amine-pyridine donors, obtained by cyclic voltammetry, have to be considered with caution.


2005 ◽  
Vol 690 (9) ◽  
pp. 2263-2271 ◽  
Author(s):  
Markus Schwarz ◽  
Marc Vollmann ◽  
Rudolf Wartchow ◽  
Holger Butenschön

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