698370-06-8Relevant academic research and scientific papers
Stabilization of hypophosphite in the binding pocket of a dinuclear macrocyclic complex: Synthesis, structure, and properties of [Ni 2L(μ-O2PH2)]BPh4 (L = N 6S2 Donor Ligand)
Lach, Jochen,Jeremies, Alexander,Lozan, Vasile,Loose, Claudia,Hahn, Torsten,Kortus, Jens,Kersting, Berthold
, p. 12380 - 12388 (2012)
The dinickel(II) complex [Ni2L(ClO4)]ClO4 (1), where L2- represents a 24-membered macrocyclic hexaamine-dithiophenolate ligand, reacts with [nBu4N]H 2PO2 to form the hypophosphito-bridged complex [Ni 2L(μ-O2PH2)]+, which can be isolated as an air-stable perchlorate [Ni2L(μ-O2PH 2)]ClO4 (2) or tetraphenylborate [Ni2L(μ- O2PH2)]BPh4 (3) salt. 3·MeCN crystallizes in the triclinic space group P1. The bisoctahedral [Ni 2L(μ-O2PH2)]+ cation has a N 3Ni(μ1,3-O2PH2)(μ-S) 2NiN3 core structure with the hypophosphito ligand attached to the two NiII ions in a μ1,3-bridging mode. The hypophosphito ligand is readily replaced by carboxylates, in agreement with a higher affinity of the [Ni2L]2+ dication for more basic oxoanions. Treatment of [Ni2L(μ-O2PH 2)]ClO4 with H2O2 or MCPBA results in the oxidation of the bridging thiolato to sulfonato groups. The hypophosphito group is not oxidized under these conditions due to the steric protection offered by the supporting ligand. An analysis of the temperature-dependent magnetic susceptibility data for 3 reveals the presence of ferromagnetic exchange interactions between the NiII (S = 1) ions with a value for the magnetic exchange coupling constant J of +22 cm-1 (H = -2JS 1S2). These results are additionally supported by DFT (density functional theory) calculations.
