Abstract

A reversible solid state structural transformation of a new 1D lead(II) coordination polymer [Pb(MPOAc)2(H2O)]n (1), (MPOAc−: mono phenyl acetate) involving in situ ligand synthesis with O7Pb⋯C6 coordination sphere to a 2D supramolecular network [Pb(MPOAc)2]n (2) with O6Pb⋯C4 coordination environment has been observed upon heating and dehydration. This change in coordination-mode was confirmed by single-crystal X-ray diffraction analyses of compounds 1 and 2. Thermogravimetric (TG) and differential thermal analyses (DTA) were employed to study the thermal stabilities of compounds 1 and 2. Powder X-ray diffraction experiments showed that the structural transformation occurs in the batch powder samples and lead to monophasic products. Nanoplates of compound 1 were synthesized by a microwave-assisted process and characterized by scanning electron microscopy (SEM), powder X-ray diffraction, IR spectroscopy and elemental analyses. The SEM images showed that no morphology change occurs during this solid state structural transformation.

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