Five unique Keggin-type polyoxometalate (POM)-based metal-organic frameworks (POMFs), namely [CH(2)L1](2)[(CuL1(2))((PMo9Mo3O40)-Mo-VI-O-V)] (1), [Zn-0.5(H2O)(L1)][Zn(L1)(1.5)Cl][H(2)L1](0.5)[PMo12O40]center dot 1.25H(2)O (2), (TBA)[Cu(H2O)(2)L1(2)][PMo12O40] (3), [Cu-2(H2O)(2)(L1)(3)][(PM11MoO40)-Mo-VI-O-V] (4), (H(2)L2)(0.5)[(Cu(I)L2)(2)(PMo12O40)]center dot H2O (5), L1 = 4,4'-bis((1H-1,2,4-triazol-1-yl)methyl)-biphenyl, L2 = 1,4-bis((1H-1,2,4-triazol-1-yl)methyl)-benzene, have been synthesized under ionothermal conditions. According to single-crystal data, 1 exhibits a novel mechanically interlocked molecular architecture (MIMA) constructed by two-dimensional (2D) interpenetrating polyrotaxane layers with unique cyclophanes (tetra-cationic viologen macrocycle cyclobis(paraquat-p-phenylene) (CBPQT(4+) system)), resulting in an H-bonded 3D supermolecule, and is the first synthesis of self-assembled cyclophane-PMOFs under ionothermal conditions. 2 shows a novel 2D three-fold interpenetrating polyrotaxane host and guest network. 1 and 2 are presented as the first MIMA polyrotaxane structures to have been synthesized under ionothermal conditions. Electrochemical impedance spectroscopy (EIS) reveals that 2, 4, and 5 show high proton conductivity owing to their unique structural properties. Solid-state diffuse reflection UV-vis-NIR measurements show the title compounds are potentially semiconductor materials. Photocatalytic investigations indicate that 1-5 possess high and stable photocatalytic H-2 evolution and rhodamine B (RhB) degradation under visible-light irradiation.