Use of a cyclo-P4 building block - a way to networks of host-guest assemblies.

Abstract

Despite the proven ability to form supramolecular assemblies via coordination to copper halides, organometallic building blocks based on four-membered cyclo-P4 ligands find only very rare application in supramolecular chemistry. To date, only three types of supramolecular aggregates were obtained based on the polyphosphorus end-deck complexes CpRTa(CO)2(η4-P4) (1a: CpR = Cp′′; 1b: CpR = Cp′′′), with none of them, however, possessing a guest-accessible void. To achieve this target, the use of silver salts of the weakly coordinating anion SbF6− was investigated as to their self-assembly in the absence and in the presence of the template molecule P3Se4. The two-component self-assembly of the building block 1a and the coinage-metal salt AgSbF6 leads to the formation of 1D or 3D coordination polymers. However, when the template-driven self-assembly was attempted in the presence of an aliphatic dinitrile, the unprecedented barrel-like supramolecular host–guest assembly P3Se4@[{(Cp′′Ta(CO)2(η4-P4))Ag}8]8+ of 2.49 nm in size was formed. Moreover, cyclo-P4-based supramolecules are connected in a 2D coordination network by dinitrile linkers. The obtained compounds were characterised by mass-spectrometry, 1H and 31P NMR spectroscopy and X-ray structure analysis.