Thermally induced interconversions of metal−pyrimidine-4,6-dicarboxylate polymers: a structural, spectroscopic, and magnetic study
Articolo
Data di Pubblicazione:
2009
Citazione:
Thermally induced interconversions of metal−pyrimidine-4,6-dicarboxylate polymers: a structural, spectroscopic, and magnetic study / N. Masciocchi, S. Galli, G. Tagliabue, A. Sironi, O. Castillo, A. Luque, G. Beobide, W. Wang, M. A. Romero, E. Barea, J. A. R. Navarro. - In: INORGANIC CHEMISTRY. - ISSN 0020-1669. - 48:7(2009), pp. 3087-3094.
Abstract:
Continuing our work on the structural and magnetic aspects of the one-dimensional (1-D) coordination polymers of
the [M(pmdc)(H2O)2] · H2O kind (M ) Fe, Co, Ni, Cu, Zn; pmdc ) pyrimidine-4,6-dicarboxylate), we have combined
ab initio X-ray powder diffraction methods with in situ thermodiffractometry and thermal analyses to characterize
the selective and reversible transformation of the [M(pmdc)(H2O)2] · H2O compounds (M ) Fe, Co, Ni, Cu) into the
bis-hydrated [M(pmdc)(H2O)2] counterparts by moderate heating, which is followed by an irreversible transformation
into two-dimensional (2-D) anhydrous species. The structural features of the transient bis-hydrated species and of
the completely dehydrated one are described for M ) Cu. Remarkably, the first dehydration process does not alter
the 1-D nature of the [M(pmdc)(H2O)2] chains; on the contrary, the second dehydration gives rise to the loss of the
axially coordinated water molecules with a concomitant condensation of the 1-D chains into 2-D layers through
ancillary carboxylate bridging groups. The magnetic properties of the anhydrous [M(pmdc)] species (M ) Co, Ni,
Cu) have been investigated, showing that these phases behave as 1-D antiferromagnets with interchain interactions.
Notably, in the case of the [Ni(pmdc)] system, a weak ferromagnetic ordering, arising from a spin canting phenomenon
with a blocking temperature of 13 K, is observed.
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
N. Masciocchi, S. Galli, G. Tagliabue, A. Sironi, O. Castillo, A. Luque, G. Beobide, W. Wang, M. A. Romero, E. Barea, J. A. R. Navarro
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