To create new types of organic ligands covalently grafted onto polyoxometalates and identify the reaction mechanism, we selected Cu-II as the central heteroatom for the synthesis of a series of disklike Anderson-Evans clusters bearing different triol derivatives on both their faces via one-pot and/or step-by-step routes. By using a [(n-C4H9)(4)N](4)[Mo8O26] precursor cluster and copper acetate as the starting materials, several organically modified ? isomers with Cu-II heteroatom centers were obtained. Starting from a [(n-C4H9)(4)N](2)[Mo2O7] subcluster, however, a half-malposition coordination fashion of triol ligands with a d isomer on one face and a ? isomer on the other face of the Anderson-Evans cluster was obtained. By changing the reaction solvent from acetonitrile to methanol, we realized a secondary organic modification of the triol-grafted clusters and obtained a triol ligand/methanol codecoration on the Anderson-Evans polyoxometalate. In addition, by changing the reaction environment, we succeeded in modulating the transformation of triol ligands from one site to another on the polyoxometalate cluster. Importantly, by control of the reaction condition, the methanol molecules were also taken off from the cluster.