Inversion Symmetry Breaking in Order-Disorder Transitions of Globular Ligands Coordinating to Cobalt(II) and Nickel(II) Bisacetylacetonato Complexes During Heating.

Chemistry : a European Journal
Norihisa Hoshino, Tomoyuki Akutagawa

Abstract

Unexpected inversion-symmetry breaking was observed in the order-disorder phase transitions of [M(acac)2 (abco)2 ] (1; M=Co2+ , 2; Ni2+ , acac- =2,4-pentanedionato, abco=1-azabicyclo-[2.2.2]-octane=quinuclidine) during heating. The isostructural, transition-free complexes [M(acac)2 (cabco)2 ] (3; M=Co2+ , 4; Ni2+ , cabco=3-chloro-1-azabicyclo-[2.2.2]-octane=3-chloroquinuclidine) were also studied for comparison. Complexes 1 and 2 crystallized in ordered phases in the centrosymmetric I2/m space group at 100 K, whereas they crystallized in disordered phases in the non-symmetric I2 space group at 300 K. The 60° step rotation disordering of the abco ligands was observed in the electron density maps of 1 and 2, which was consistent with the transition enthalpies estimated by differential scanning calorimetry (DSC). Gradual phase transitions were observed for 1 and 2 by DSC and powder X-ray diffraction (PXRD) at approximately 225 K. The inversion-symmetry disordering was likely induced by the local pseudo-symmetry of the abco ligands, increasing from trigonal to hexagonal and the increased steric repulsion pathways among them.

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