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Under the solvothermal condition, the reaction of 4,4′′-(1,3-phenylene)-bis[2,3′-bipyridine]-6-carboxylic acid (H2L1) with Mn(NO3)2·4H2O in dimethylacetamide (DMA) afforded a novel zero-dimensional (0D) metallomacrocycle, [Mn4(L1)4(H2O)8]·20H2O (1). However, in a similar solvothermal condition to 1, the reaction of H2L1 with Mn(OAc)2·4H2O in dimethylsulfoxide (DMSO) yielded one new three-dimensional (3D) metal–organic framework, [Mn(L1)]·4H2O·DMSO (2). Furthermore, other three 3D metal–organic frameworks, [M(L1)]·4H2O·DMSO (M = Cd (3), Cu (4) and Zn (5)), were obtained under the same solvothermal condition as 2, which are isostructural with 2. Interestingly, a novel two-dimensional (2D) metallomacrocycle network, [Zn2(L2)(H2O)3]·3H2O·DMA (6), was solvothermally synthesized through the reaction between 4,4′-(6,6′-([1,1′-biphenyl]-4,4′-diyl)bis(2-(4-carboxyphenyl)pyridine-6,4-diyl))dibenzoic acid (H4L2) and Zn(NO3)2·6H2O in DMA. 1–6 were fully characterized by infrared spectra, elemental analyses, thermogravimetric analyses, powder X-ray diffraction patterns, or single-crystal X-ray diffractions. The changes from 0D metallomacrocycle (1) to 3D isostructural metal–organic frameworks (2–5) are mediated by increasing solvent polarity (from DMA to relatively high polar DMSO) because the more polar DMSO solvent helps the coordination sites of L12− ligand to take part in coordination. More interestingly, 3, 5, and 6 achieve close to white-light emission upon excitation at 365 nm. The gas adsorption properties of 2–5 have also been investigated, and the results indicate that the CO2 adsorption capacities are relative to the framework stability of MOFs 2–5. The present work provides a promising approach to constructing novel metal–organic frameworks or metallomacrocycles and may open new perspectives for developing single-component white-light-emitting materials. [ABSTRACT FROM AUTHOR]