TY - JOUR
TI - Magnetostructural correlations in S = 1 trans-[Ni{(OPPh2)(EPPh2)N}2(dmso)2], E = S, Se, and related complexes
AU - Ferentinos, E.
AU - Raptopoulou, C.P.
AU - Psycharis, V.
AU - Terzis, A.
AU - Krzystek, J.
AU - Kyritsis, P.
JO - Polyhedron
PY - 2018
VL - 151
TODO - null
SP - 177-184
PB - Elsevier Ireland Ltd
SN - 0277-5387
TODO - 10.1016/j.poly.2018.05.032
TODO - null
TODO - In this work, the structural and spectroscopic characterization of trans-[Ni(OPPh2)(EPPh2)N)2(dmso)2], E = S, Se, complexes is described. These Ni(II) complexes contain two chelating (O,E) = [(OPPh2)(EPPh2)N)]− ligands, as well as two dimethyl sulfoxide (dmso) molecules coordinated via their O atoms. X-ray crystallography studies revealed a highly anisotropic pseudo-octahedral trans-NiO4E2 coordination environment, extending the literature dataset of their trans-[Ni(O,E)2(sol)2], sol = dmf, thf, counterparts. Collectively considered, these six complexes contain similar coordination spheres, exhibiting, however, subtle structural differences due to the nature of the donor atom (E) and solvent molecule (sol) coordinated to Ni(II). The spin Hamiltonian parameters of S = 1 trans-[Ni(O,Se)2(dmso)2], E = S, Se, were accurately determined by high-frequency and -field EPR spectroscopy, applying a methodology already used for trans-[Ni(O,E)2(sol)2], sol = dmf, thf. Magnetostructural correlations are explored between all members of this sub-family of Ni(II) complexes. © 2018 Elsevier Ltd
ER -