We report the photochemistry of (OCS)(n)(-) cluster ions following 395 nm (n=2-28) and 790 nm (n=2-4) excitation. In marked contrast to (CO2)(n)(-) extensive bond breaking and rearrangement is observed. Three types of ionic products are identified : S-2(-)(OCS)(k), S-(OCS)(k) /OCS2-(OCS)(k-1), and (OCS)(k)(-). For n<16, 395 nm dissociation is dominated by St-based fragments, supporting the theoretical prediction of a cluster core with a C-2 nu (OCS)(2)(-) dimer structure and covalent C-C and S-S bonds. A shift in the branching ratio in favor of S--based products is observed near n = 16, consistent with an opening of the photodissociation pathway of OCS- core-based clusters. These monomer-based cluster ions may coexist with the dimer-based clusters over a range of n, but electron detachment completely dominates photodissociation as long as their vertical electron detachment energy, increasing with addition of each solvent molecule, is less then the photon energy. An (OCS)(2)(-) conformer of C-2 symmetry With a covalent C-C bond is believed to be responsible for 790 nm dissociation of (OCS)(2)(-) yielding primarily OCS- products. The yield of OCS-, and thus the importance of the C-2 form of (OCS)(2)(-) cluster core, decreases with ncreasing n, perhaps due to more favorable solvation of the C-2 nu form of (OCS)(2)(-) and/or a solvent-induced increase in the rate of interconversion of conformers. The (OCS)(k)(-) products observed in 395 nm photodissociation of the larger (n greater than or equal to 7) clusters are attributed to photofragment caging. Formation and dissociation mechanisms of clusters with different core types are discussed. The photochemical properties of (OCS)(n)(-) are compared to those of the isovalent (CO2)(n)(-) and (CS2)(n)(-) species.