The synthesis and guest recognition properties of a neutral Pd-cubic cage, [{Pd(NPr)PO}(μ-Cl)] 1 are reported. The formation of the cubical assembly takes place by an exclusive one-pot ligand-assisted pathway directed by an oximido linker. The initial coordination of the oximido ligand pre-organizes the [Pd(NPr)PO] polyhedral building units into a tetrameric intermediate, which then transforms into an oximido-tethered tetrahedral assembly and to the cubical cage 1 in the presence of chloride ions. In the absence of the directing oximido linker, no cage formation was observed, and the Pd-precursor was found to undergo self-condensation, giving rise to a new pentameric polyhedral cluster, [Pd{(NPr)PO}(OAc)(OH)] 2. The central cavity of the cube has been probed for guest encapsulation studies, which shows a high binding with phenolic guest molecules with association constants of the order of 10-10 M. The favorable formation of host-guest complexes was attributed to the strong hydrogen bonding interactions between the host and guest functional groups.

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http://dx.doi.org/10.1002/anie.202406358DOI Listing

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The synthesis and guest recognition properties of a neutral Pd-cubic cage, [{Pd(NPr)PO}(μ-Cl)] 1 are reported. The formation of the cubical assembly takes place by an exclusive one-pot ligand-assisted pathway directed by an oximido linker. The initial coordination of the oximido ligand pre-organizes the [Pd(NPr)PO] polyhedral building units into a tetrameric intermediate, which then transforms into an oximido-tethered tetrahedral assembly and to the cubical cage 1 in the presence of chloride ions.

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A primary criterion for the design of polyhedral metal-organic cages is the requirement of geometrically matched pairs of metal ions and ligand moieties. However, understanding the pathway it takes to reach the final polyhedral structure can provide more insights into the self-assembly process and improved design strategies. In this regard, we report two neutral tetrahedral cages with the formulas {[Pd(NPr)PO](L)} () and {[Pd(NPr)PO](L)} () starting from the acetate-bridged cluster {[Pd(NPr)PO](OAc)(OH)}·2(CH)SO () and the respective oxamide precursors (LH: [C(NH)O]) and (LH: (C(NHMe)O]).

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