Structures and Spectral and Magnetic Properties of a Series of Carbacylamidophosphate Pentanuclear Lanthanide(III) Hydroxo Complexes.
Nataliia S KariakaSergey V KolotilovPaula GawryszewskaEwa KasprzyckaMarek WeselskiViktoriya V DyakonenkoSvetlana V ShiskinaVictor A TrushVladimir M AmirkhanovPublished in: Inorganic chemistry (2019)
A series of pentanuclear lanthanide complexes Ln5L6(μ-L)4(μ3-OH)4(μ4-OH) (LnIII = Nd, Dy, Ho, Er, Yb; L- = dimethyl N-benzoylamidophosphate ion, [C6H5C(O)-N-P(O)(OCH3)2]-) was obtained by the reaction of sodium dimethyl N-benzoylamidophosphate with the corresponding lanthanide nitrates. The pentanuclear cores formed as a result of self-arrangement and their composition did not depend on the lanthanide ion. The complexes and sodium dimethyl N-benzoylamidophosphate have been characterized by single-crystal X-ray diffraction. The absorption spectra of the complexes were measured at 300 and 4 K. The dysprosium and ytterbium complexes exhibited weak emission in the visible and IR regions, respectively. Temperature dependences of magnetic susceptibility (χM) of the dysprosium, holmium, and erbium compounds were studied. It was found that χM vs T dependences were governed by the crystal field splitting effects with the Δ parameter being in the range 5-17 cm-1. Slow magnetic relaxation was found for the dysprosium complex by ac magnetic measurements, while no significant out-of-phase signals were detected for holmium and erbium complexes.