Syntheses, crystal structures and luminescence properties of lanthanide coordination polymers involving in situ C–S bond cleavage of (4-pyridylthio)acetic acid

Lanthanide coordination polymers with the formula [Ln2(C2O4)3(H2O)6]n (1) (Ln = Nd, 1) and [Ln2(C2O4)3(pythioH)2(H2O)2]n (Ln = Eu 2; Dy 3; Er 4) pythio = 4-pyridinethiolate) were synthesized by treating LnIII nitrates with (4-pyridylthio)acetic acid under hydrothermal conditions. Single-crystal X-ray diffraction studies indicate that these lanthanide coordination polymers consist of extended oxalate-bridged two-dimensional layer structure. Interestingly, in situ C–S bond cleavage occurred and (4-pyridylthio)acetic acid was transformed into 4-pyridinethiolate and oxalate. The complexes 2 and 3 display strong fluorescent emission in the solid state at room temperature.

The treatment of the (4-pyridylthio) acetic acid and lanthanide nitrates under hydrothermal conditions leads to generate the two-dimensional lanthanide coordination polymers involving in situ C–S bond cleavage and (4-pyridylthio) acetic acid was transformed into 4-pyridinethiolate and oxalate.Figure optionsDownload as PowerPoint slide