6533b7d2fe1ef96bd125edb7

RESEARCH PRODUCT

Templated synthesis of a rotaxane with a [Ru(diimine)3]2+ core.

Damien JouvenotDidier PomerancDidier PomerancValérie HeitzJean-claude ChambronJean-claude ChambronJean-paul CollinJean-pierre Sauvage

subject

Rotaxane010405 organic chemistryStereochemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesCatalysis0104 chemical sciencesRutheniumBipyridinechemistry.chemical_compoundCrystallographychemistryOctahedron[ CHIM.ORGA ] Chemical Sciences/Organic chemistryProton NMR[CHIM.COOR]Chemical Sciences/Coordination chemistryDiimineComputingMilieux_MISCELLANEOUS

description

A rotaxane containing a ruthenium bisphenanthroline complex, acting as an axis, and a macrocycle incorporating a 2,2'-bipyridine (bpy) unit, threaded by the axis, has been synthesized. The bisphenanthroline ligand is such that its ruthenium(II) complexes possess a clearly identified axis, making such compounds ideal components of rotaxanes constructed around an octahedral ruthenium(II) center, which serves as a template. The ring is threaded by the axial ruthenium(II) precursor complex, to afford the corresponding pseudorotaxane in moderate yield. The X-ray structure analysis of this compound reveals the threaded nature of the complex. The length of the threaded ring (35 atoms in the periphery) is too short to allow easy threading of the axis through the macrocycle. As a consequence, an isomer is also obtained for which the axial ruthenium complex is attached in an exo fashion. (1)H NMR studies have been carried out, which reveal various conformational equilibria for the pseudorotaxane. Light-induced decoordination of the bpy-containing cyclic fragment was shown to be quantitative and to lead to the free ring and the axial ruthenium(II) complex, regardless of the starting compound (pseudorotaxane or exo isomer). Finally, the real rotaxane could be prepared, although it could not be separated from its exo isomer.

10.1002/chem.200304716https://pubmed.ncbi.nlm.nih.gov/12953210