Solvent-controlled synthesis of various Anderson-type polyoxometalate-based metal-organic complexes with excellent capacity for the chromatographic separation of dyes

By changing solvent systems, five new Anderson-type polyoxometalates (POMs)-based metal-organic complexes, namely,{(H(2)PCAP')(2)[CrMo6(OH)(5)O-19]}center dot H2O (1), {Cu-3(PCAP)(2)[CrMo6(OH)(5)O-19](H2O)(3)(DMF)(2)}center dot 4H(2)O center dot 2HCHO (2), {Cu-3(PCAP)(2)[CrMo6(OH)(6)O-18]Cl(H2O)(5)}center dot 10H(2)O (3),{Co-3(PCAP)(2)[CrMo6(OH)(5)O-19](H2O)(6)}center dot 9H(2)O center dot HCHO (4) and {Co-3(HPCAP)(2)[CrMo6(OH)(6)O-18](2)(H2O)(10)}center dot 7H(2)O center dot 2CH(3)CH(2)OH (5) (HPCAP = 3-(2-pyridinecarboxylic acid amido)pyridine, PCAP' = 3-(pyridinecarboxylic acid)amido pyridine), were successfully synthesized and structurally characterized by single-crystal X-ray diffraction, IR spectra, powder X-ray diffraction (PXRD) and thermogravimetric analyses (TGA). Complex 1 was obtained with H2O as the solvent and exhibited a 3D supramolecular network based on CrMo6 anions and protonated H(2)PCAP' molecules via hydrogen bonds. It should be noted that the PCAP' was in situ transformed from HPCAP. Complexes 25 were synthesized with different mixed solvents. In complex 2, the CrMo6 anions acted as an inorganic bridging ligand to link the 1D [Cu-3(PCAP)(2)](n)(4n+) chains to construct a 2D layer. Complexes 3 and 4 showed similar 3D frameworks. Two orientations of metalorganic loops [M-2(PCAP)(2)] (M = Cu for 3, Co for 4) could be observed, which directly extended the 1D M-CrMo6 chains into 3D networks with a 3,3,4,4-connected {4(2).12(3).14}{4(2).6}(2) topology. In 5, the 1D Co-CrMo6 inorganic chain, [Co-2(PCAP)(2)] binuclear loop unit and discrete CrMo6 polyanion were connected with each other by hydrogen-bonding interactions to form a 1D ladder-like supramolecular dual chain. The structural diversities showed that the solvents play key roles in the construction of various architectures and in the in situ transformation of HPCAP. The adsorption behaviours of the title complexes for organic dyes were investigated in detail. All of the title complexes showed an efficient adsorption capacity for the cationic dyes gentian violet (GV) and methylene blue (MB). In particular, complex 4 could selectively separate GV from the mixture of GV&RhB and GV&MO within 510 min, which can be used as a chromatography column for dye removal. In addition, the electrochemical properties of the title complexes were also studied.