Han, YiChilton, Nicholas F.Li, MingHuang, ChaoXu, HongHou, HongweiMoubaraki, BoujemaaLangley, Stuart K.Batten, Stuart R.Fan, YaotingMurray, Keith S.2026-01-012026-01-010947-6539Bibtex:han_postsynthetic_2013https://hdl.handle.net/1885/733799631From a predesigned grid, [CuII5CuI4L6]⋅(I)2⋅13 H2O (1), in which LH2 was a pyrazinyl-triazolyl-2,6-substituted pyridine, we successfully synthesized an extended 3D complex, 1∞[{CuII5CuI8L6}{μ-[CuI3(CN)6]}2⋅2 CH3- CN] (2), that displayed unprecedented coexistence of all the five known coordination geometries of copper. Grid 1 displayed monovalent central metal exchange (CME) of CuI for AgI for the first time, as well as the formation of tri-iodide in the crystalline state. These systems were investigated for their magnetic properties. Remarkably, grid 1 showed much higher catalytic activity than the Ag-exchanged product for synthesis of a substituted triazole, 1-benzyl-4-phenyl-1H-1,2,3-triazole.8enPost-Synthetic Monovalent Central-Metal Exchange, Specific I2 Sensing, and Polymerization of a Catalytic [3×3] Grid of [CuII5CuI4L6]⋅(I)2⋅13 H2O2013-03-2010.1002/chem.20120411584877301892