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Tetra- and hexanuclear coordination cages were obtained in reactions of [Pd(CH 3 CN) 4 ](BF 4 ) 2 with low-symmetry dipyridyl ligands. In both cases, only one structurally defined complex was formed out of a vast pool of potential isomers.

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Orientational self-sorting: formation of structurally defined Pd4L8 and Pd6L12 cages from low-symmetry dipyridyl ligands