Pd12MnL24 (for n=6, 8, 12) nanospheres by post-assembly modification of Pd12L24 spheres

In this contribution, we describe a post-assembly modification approach to selectively coordinate transition metals in Pd12L24 cuboctahedra. The herein reported approach involves the preparation of Pd12L24 nanospheres with protonated nitrogen donor ligands that are covalently linked at the interior. The so obtained Pd-12(LH+)(24) nanospheres are shown to be suitable for coordinative post-modification after deprotection by deprotonation. Selective formation of tetra-coordinated M-B in (Pd12M6L24)-L-B, tri-coordinated M-B in (Pd12M8L24)-L-B nanospheres and two-coordinated M-B in (Pd12M12L24)-L-B nanospheres is achieved as a result of different nitrogen donor ligands. A combination of pulsed EPR spectroscopy (DEER) to measure Cu-Cu distances in the different spheres, NMR studies and computational investigations, support the presence of the complexes at precise locations of the (Pd12M6L24)-L-B nanosphere. The general post-assembly modification methodology can be extended using other transition metal precursors or supramolecular systems and can guide precise formation and investigation of novel transition metal-complex containing nanospheres with well-defined composition.

Automated summary

In this study, a post-assembly modification approach is described to selectively coordinate transition metals in Pd12L24 cuboctahedra. The method involves the preparation of Pd12L24 nanospheres with protonated nitrogen donor ligands that are covalently linked at the interior. Selective formation of different coordination forms of the transition metals is achieved by using different nitrogen donor ligands. Experimental and computational investigations support the presence of complexes at precise locations in the nanospheres.