A series of microporous lanthanide metal-organic frameworks [Ln(BTC)(DMF)(2)(H2O)-H-., Ln = Tb (1), Dy (2), Ho (3), Er (4), Tm (5), Yb (6); DMF = N,N'-dimethylformamide] with 4(.)4(.)4(.)6(.)6(.)8 topology, which is very common in the zeolite topologies, have been synthesized under mild conditions. The single-crystal X-ray diffraction analysis reveals that they exhibit the same three-dimensional (3D) architecture and crystallize in monoclinic symmetry space group C2/c. Organic and inorganic four-connected nodes link each other to form a 3D open framework. The framework contains approximate 13 angstrom x 7 angstrom rectangle channels along the [1,1,0] and [1,-1,0] directions, respectively. The luminescent properties of these complexes have been studied, and complex 1 shows a Tb3+ characteristic emission in the range of 450-650 nm at room temperature. Complexes 1-5 exhibit antiferromagnetic interaction between Ln(3+) ions. The water sorption isotherm shows that about 15 water molecules per unit cell can be adsorbed into the micropores of dehydrated complex 4.