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Paul J Lusby

Publications and source records attributed to Paul J Lusby.

6 recordsLinked to original sources
PubMed2006

Catalytic "click" rotaxanes: a substoichiometric metal-template pathway to mechanically interlocked architectures.

A route to mechanically interlocked architectures that requires only a catalytic quantity of template is described. The strategy utilizes the Cu(I)-catalyzed 1,3-cycloaddition of azides with terminal alkynes. Chelating the Cu(I) to an endotopic-binding macrocycle means that the metal atom binds to the alkyne and azide in such a way that the metal-mediated bond-forming reaction occurs through the cavity of the macrocycle, forming a rotaxane. Addition of pyridine to the reaction mixture enables the Cu(I) to turn over during the reaction, permitting substoichiometric amounts of the metal to be used. The yields are very high for a rotaxane-forming reaction (up to 94% with stoichiometric Cu(I); 82% with 20 mol % of Cu(I)), and the procedure is practically simple to do (no requirement for an inert atmosphere nor dried or distilled solvents).

Journal Article↗
PubMed2005

Selecting topology and connectivity through metal-directed macrocyclization reactions: a square planar palladium [2]catenate and two noninterlocked isomers.

We report the synthesis of a [2]catenate using a square planar palladium(II) template, together with two isomers of the interlocked structure: a single tetradentate macrocycle that adopts a "figure of eight" conformation to encapsulate the metal and a complex in which the two macrocycles of the catenane are not interlocked. The three isomers can each be selectively formed depending on how the building blocks are assembled and cyclized. Olefin metathesis of both building blocks while they are attached to the metal gives the single large macrocycle in 77% yield. Cyclizing the monodentate unit prior to attaching both ligands to the metal gives the [2]catenate in 78% yield. Preforming the tridentate macrocycle produces a complex in two atropisomeric forms-threaded and nonthreaded-in a 2:3 ratio, which do not interconvert in dichloromethane at room temperature over 7 days. RCM of the nonthreaded atropisomer affords the complex with two noninterlocked macrocyclic ligands; RCM of the threaded atropisomer generates the topologically isomeric [2]catenate. Heating the acyclic atropisomers in acetonitrile provides a mechanism for their interconversion via ligand exchange, allowing the threaded:nonthreaded ratio to be varied from 2:3 to 8:1. All three fully ring-closed complexes were characterized unambiguously by 1H NMR spectroscopy and X-ray crystallography. As far as we are aware, this is the first time such a set of three formal topological and constitutional isomers has been described.

Catenanes↗