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A simple self-assembled [Pd 2 L 4 ] coordination cage consisting of four carbazole-based ligands was found to dimerize into the interpenetrated double cage [3 X@Pd 4 L 8 ] upon the addition of 1.5 equivalents of halide anions (X = Cl À , Br À ). [5] Furthermore, the temporal and spatial control of structural rearrangements and encapsulation processes by the addition of external triggers, [6] a change in pH [7] or electrochemical potential, [8] and irradiation with light [9] is of high current interest.With regard to self-assembled coordination cages, [10] we and others have provided first examples implementing controllable elements such as light-switchable ligands [11] and redox-active functionalities [12] within the last couple of years. The subsequent addition of larger amounts of the same halide triggers another structural conversion, now yielding a triply catenated link structure in which each Pd II node is trans-coordinated by two pyridine donors and two halide ligands.