Two pairs of supramolecular isomers based on ternary zinc(II)/triazolate/X (triazolate = 3,5-dimethyl-1,2,4-triazolate (Hdmtz), X = HCOO-, F-) metal azolate frameworks, namely, [Zn(dmtz)(HCOO)]center dot H2O (MAF-X3, 1a), [Zn(dmtz)(HCOO)]center dot(1/6Me(2)NH)(1/4H(2)O) (MAF-X4, 1b), [Zn(dmtz)F] (MAF-X5, 2a), and [Zn(dmtz)F] (MAF-X6, 2b), have been synthesized via variations of the reaction conditions. The 3-connected Zn(dmtz) networks in la, 1b, 2a, and 2b can be described as rarely observed 4.8(2), 4.12(2), (8,3)-b, and 8(2).10-a, respectively, Besides the mu(3)-dmtz, tetrahedral and trigonal-bipyramidal/square-pyramidal coordination of the Zn ions are accomplished by monodentate formate and mu-F, respectively. While la and 2b are nonporous structures, 1b and 2a exhibits 1D nanotubular hydrophilic (d 3.2 angstrom) and hydrophobic (d 3.6 angstrom) channels, respectively. Thermogravimetric analysis shows that the stabilities of 2a and 2b are much better than those of la and 1b, which may be ascribed to different coordination numbers of zinc atoms. Moreover, 1b and 2a with different pore properties show selective sorption behavior.