One-dimensional coordination polymers of praseodymium(III)–vanadium(V) complexes with pyridine-2,6-dicarboxylic acid

This paper represents the hydrothermal synthesis of new isomorphous lanthanide–vanadium complexes with one-dimensional coordination polymers: [Pr2(VO2)2(dipic)4(H2O)9] · nH2O with dipic = pyridine-2,6-dicarboxylic acid and n = 7.75. The structure determination shows a unique one-dimensional structure in which three types of chains run along the c-axis: the chain of positively charged praseodymium complexes bridged by a dipic ligand ([Pr(dipic)(H2O)5]+), the chain of negatively charged, stacked vanadium complexes ([VO2(dipic)]−), and the chain of neutral praseodymium complexes with a bridged dipic ligand and a coordinating dipic ligand ([Pr(dipic)[VO2(dipic)](H2O)4]). Such one-dimensional chains provide open channels which can accommodate water molecules. Not only accommodated water molecules but also ones coordinated to praseodymium ions were easily removed and absorbed upon heating at 200 °C and exposure of humidity at room temperature, respectively.

Graphical abstractNew isomorphous lanthanide–vanadium complexes with one-dimensional coordination polymers, [Ln2(VO2)2(dipic)4(H2O)9] · nH2O. Three types of chains in the complex provide open channels which can accommodate water molecules. Water molecules were easily removed and absorbed upon heating at 200 °C and exposure of humidity at room temperature, respectively.Figure optionsDownload full-size imageDownload as PowerPoint slide