Abstract
We report a family of hybrid [2]rotaxanes based on inorganic [Cr(7)NiF(8)(O(2)C(t)Bu)(16)](-) ("{Cr(7)Ni}") rings templated about organic threads that are terminated at one end with pyridyl groups. These rotaxanes can be coordinated to [Cu(hfac)(2)] (where Hhfac = 1,1,1,5,5,5-hexafluoroacetylacetone), to give 1:1 or 1:2 Cu:{Cr(7)Ni} adducts: {[Cu(hfac)(2)](py-CH(2)NH(2)CH(2)CH(2)Ph)[Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}, {[Cu(hfac)(2)][py-CH(2)NH(2)CH(2)CH(3)][Cr(7)NiF(8)(O(2)C(t)Bu)(16)]}, {[Cu(hfac)(2)]([py-CH(2)CH(2)NH(2)CH(2)C(6)H(4)SCH(3)][Cr(7)NiF(8)(O(2)C(t)Bu)(16)])(2)}, {[Cu(hfac)(2)]([py-C(6)H(4)-CH(2)NH(2)(CH(2))(4)Ph][Cr(7)NiF(8)(O(2)C(t)Bu)(16)])(2)}, and {[Cu(hfac)(2)]([3-py-CH(2)CH(2)NH(2)(CH(2))(3)SCH(3)][Cr(7)NiF(8)(O(2)C(t)Bu)(16)])(2)}, the structures of which have been determined by X-ray diffraction. The {Cr(7)Ni} rings and Cu(II) ions both have electronic spin S = 1/2, but with very different g-values. Continuous-wave EPR spectroscopy reveals the exchange interactions between these dissimilar spins, and hence the communication between the different molecular components that comprise these supramolecular systems. The interactions are weak such that we observe AX or AX(2) type spectra. The connectivity between the {Cr(7)Ni} ring and thread terminus is varied such that the magnitude of the exchange interaction J can be tuned. The coupling is shown to be dominated by through-bond rather than through-space mechanisms.