The hydrothermal reactions of Na2MoO4. 2H(2)O and 2,2 ' :6 ' ,2 " -terpyridine with appropriate salts of Fe(II), Cu(II), and Zn(II) yield a variety of mixed metal oxide phases. The Cu(II) system affords the molecular cluster [Cu(terpy)MoO4]. 3H(2)O(MOXI-40 . 3H(2)O), as well as a one-dimensional material [Cu(terpy)Mo2O7](MOXI-41) which is constructed from {Mo4O14}(4-) clusters linked through {Cu(terpy}(2+) units. In constrast, the Zn(II) phase of stoichiometry identical to that of MOXI-41, [Zn(terpy)Mo2O7](MOXI-42), exhibits a one-dimensional structure characterized by a {Mo2O7}(n)(2n-) chain decorated with peripheral {Zn(terpy)}(2+) subunits. The iron species [{Fe-(terpy)}(2)Mo4O12](MOXI-43) is also one-dimensional but exhibits [{Fe(terpy)}(2){MoO4}(2)](2+) rings linked through {MoO4}(2-) tetrahedra. A persistent structural motif which appears in MOXI-40, MOXI-41, and MOXI-43 is the [{M(terpy)}(2){MoO4}(2)](n) cluster with a cyclic {M2Mo2O4) core. In general, the secondary metal sites M(II, III) are effective bridging groups between molybdate subunits of varying degrees of aggregation. Furthermore, the ligands passivate the bimetallic oxide from spatial extension in two or three dimensions and provide a routine entree into low-dimensional structural types of the molybdenum oxide family of materials.