Self-assembly of novel macrocyclic aminomethylphosphines with hydrophobic intramolecular cavities

Dalton Transactions Pub Date: 2004-01-06 DOI: 10.1039/B311592E

Abstract

Novel macroheterocyclic tetraphosphines, namely, 1,1′,5,5′-bis(arylene)-bis(1,5-diaza-3,7-diphosphacyclooctanes) 2–6, were obtained without the use of high-dilution techniques or any matrix by the reaction of bis(hydroxymethyl)organylphosphines with primary aromatic diamines containing two p-phenylene fragments linked by various one-atom bridges in a molecular self-assembly process. The structures of 4, 5 and 6 were investigated by X-ray crystal structure analyses. The macrocyclic cavities can be described as a truncated rhombohedral prism with side faces formed by phenylene rings and 1,5-diaza-3,7-diphosphacyclooctanes in the truncated acute angles. In the crystals of these macrocycles, solvating DMF molecules are present, and a methyl group from each of two DMF molecules penetrates the macrocyclic cavities of 4 and 5 from either side, whereas only one disordered molecule of DMF penetrates the cavity of macrocycle 6. Different types of crystal packing are observed for the P-benzyl-substituted compounds 4 and 5 and for the P-mesityl-substituted compound 6: for 4 and 5 the formation of alternating layers containing the macrocycles and the DMF molecules is observed, in which the cavities of the macrocyclic molecules form channels and the DMF molecules are located in the centers of the channels; in the crystal of 6, six molecules are arranged around the [3 with combining macron] axis in the fashion of a six-bladed propeller.

Graphical abstract: Self-assembly of novel macrocyclic aminomethylphosphines with hydrophobic intramolecular cavities
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