Molecular Borromean rings

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Schematic of a molecular borromean ring
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Schematic of a molecular borromean ring

Molecular Borromean rings are the molecular pendants of Borromean rings. The study of Borromean links is part of mechanically-interlocked molecular architectures. One Borromean ring system reported in 2004 is made up of macrocycles formed from 2,6-diformylpyridine and diamine compounds complexed with zinc. 1.

This compound was synthesized from two building blocks: 2,6-diformylpyridine and a diamine containing a 2,2'-bipyridine group. Zinc acetate is added as the template for the reaction, resulting in one zinc in each of a total of 6 pentacoordinate complexation sites. Trifluoroacetic acid (TFA) is added to catalyse the imine bond-forming reactions. The preparation of the tri-ring Borromeate involves a total 18 precursor molecules and is only possible because the building blocks self-assemble through 12 aromatic pi-pi interactions and 30 zinc to nitrogen dative bonds. Because of these interactions, the Borromeate is thermodynamically the most stable reaction product out of potentially many others, and because all the reactions that take place are equilibria, the Borromeate is the predominant reaction product.

Synthesis of one ring in Borromean ring system from 2,6-diformylpyridine and a diamine in presence of zinc acetate and TFA. The ring-system consists of three such interlocked rings

Reduction with sodium borohydride in ethanol affords the neutral Borromeand 2. True to a Borromean system, cleavage of just one imine bond (to an amine and an orthoester) in this structure breaks the mechanical bond between the three constituent macrocycles, releasing the other two individual rings.

From left to right: Zinc complex with pyridine group and orthogonal bipyridine groups in Borromeate. Reduction to Borromeand with removal of zinc coordination. Bond cleavage of imine to orthoether by action of ethanol
From left to right: Zinc complex with pyridine group and orthogonal bipyridine groups in Borromeate. Reduction to Borromeand with removal of zinc coordination. Bond cleavage of imine to orthoether by action of ethanol

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