6533b7d9fe1ef96bd126ceab
RESEARCH PRODUCT
Cyclic [2]Pseudorotaxane Tetramers Consisting of Two Rigid Rods Threaded through Two Bis-Macrocycles: Copper(I)-Templated Synthesis and X-ray Structure Studies
V. HeitzJean-pierre SauvageJulien FreyKari RissanenJ.-p. CollinChristian Tocksubject
Models MolecularMacrocyclic CompoundsMolecular StructureRotaxanesChemistryX-raychemistry.chemical_elementStereoisomerismStereoisomerismGeneral ChemistryCrystallography X-RayBiochemistryCopperCatalysisRodCrystallographyColloid and Surface ChemistryYield (chemistry)Organometallic CompoundsThreading (manufacturing)MoleculeCopperPhenanthrolinesGroup 2 organometallic chemistrydescription
Variously substituted coordinating rigid rods have been synthesized which incorporate a central 4,7-phenanthroline nucleus attached to two 2-pyridyl groups via its 3 and 8 positions, so as to yield bis-bidentate chelates, the two-coordinating axes of the chelates being parallel to one another. Regardless of the nature of the substituents borne by the rods, the copper(I)-induced threading reaction of two such rods through the rings of two bis-macrocycles affords in a quantitative yield the 4-copper(I) threaded assembly. The [2]pseudorotaxane tetramers thus obtained have been fully characterized in solution and, for one of them, an X-ray structure could be obtained, confirming the threaded nature of the complex and providing important structural information.
year | journal | country | edition | language |
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2008-07-25 | Journal of the American Chemical Society |