2015
DOI: 10.1080/00958972.2015.1079627
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A comparison of solution and solid state coordination environments for calcium(II), zirconium(IV), cadmium(II) and mercury(II) complexes with dipicolinic acid and methylimidazole derivatives

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Cited by 12 publications
(2 citation statements)
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“…In the crystal structure, a complex 3D network of H-bonds is found (Table S8). Several metal complexes with the ligand 2,6-pyridinedicarboxylat have been reported, which exhibit the same coordination environments as observed in 1 . …”
Section: Resultsmentioning
confidence: 73%
“…In the crystal structure, a complex 3D network of H-bonds is found (Table S8). Several metal complexes with the ligand 2,6-pyridinedicarboxylat have been reported, which exhibit the same coordination environments as observed in 1 . …”
Section: Resultsmentioning
confidence: 73%
“…In particular, the presence of electron donating heteroatom (-N-) at the center of two COO – groups enables DPA to act as a tridentate ligand, enhancing its binding efficiency with heavy metal ions. Thus, DPA is usually used as a strong chelator for Zr 4+ ions , accompanied by the formation of a Zr 4+ -DPA complex of a high stability constant. The observed reversal of the Zr 4+ -induced AIEE effect and disassembly of the Zr 4+ -CoA@GNCs aggregates could indicate that the binding affinity of DPA as a tridentate ligand for Zr 4+ could be higher than that of the ligands of the CoA@GNCs.…”
Section: Resultsmentioning
confidence: 99%