Trispyrazolylmethane piano stool complexes of iron(II) and cobalt(II)

Abstract

A series of cationic trispyrazolylmethane complexes of the general form [Tm RM(CH 3CN) 3] 2+ (Tm = tris(pyrazolyl)methane, 1, R = 3,5-Me 2, M = Fe(II); 2, R = 3-Ph, M = Fe(II); 3, R = 3,5-Me 2, M = Co(II); 4, R = 3-Ph, M = Co(II)) with ‘piano-stool’ structures was prepared by the reaction of the N 3tripodal ligands (Tm R)with [(CH 3CN) 6M](BF 4) 2 in a 1:1 stoichiometric ratio. Magnetic susceptibility measurements indicate that all four complexes with BF 4 − counter anions are paramagnetic, high-spin systems in the solid state with μ eff at high temperatures of 5.2 ( 1, S = 2), 5.4 ( 2, S = 2), 4.9 ( 3, S = 3/2) and 4.6 ( 4, S = 3/2) BM, respectively. Comparisons of bond lengths from the metal centre to the Tm R nitrogen donors, and from the metal centre to the acetonitrile nitrogen donors indicate that the neutral tripodal ligands appear to be more weakly coordinated to the metal centre than are the acetonitrile ligands. Reactions of these tripodal complexes with bidentate phosphine ligands, such as 1,2-diphosphinoethane or 1,2-bis(diallylphosphino)ethane leads to displacement of the tripodal ligand, or to the formation of more thermally stable bis-ligand complexes M(Tm R) 2 (R = 3,5-dimethyl).