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Cyclodextrin-based supramolecular assemblies of iridium(III) metallocene complexes.
A series of metallocene (MC,M) complexes of the general formula [MC(Cn n H(2) n )](+)(PF(6)(-))(-) (Cn=secondary, tertiary and quaternary alpha-cyclodextrin) were prepared and characterized. The MCs are a derivative of the well known [Cp(1)Ir(COD)(2) ]PF(6)(-), where Cp(1) =[Cp(C(5)H(5))(2)](+) (Cp(1)=symmetrical cyclopentadienyl; COD = 2,2′-bipyridyl-6,6′-dicarboxylic acid), and C(n) is the cavity of alpha-cyclodextrin with the cavity diameter (cavity diameter) ranging from 4.4 to 6.8 A. The six-coordinate MCs were prepared in three steps, (i) precatalytic reaction of Cp(1)Ir(COD)(2) with alpha-cyclodextrin to form a MC precursor and (ii) methylation at the Ir-Cp’ positions to form the MCs, and (iii) removal of the trifluoromethanesulfonate counterion. C(2), C(3) and C(4) cyclodextrin derivatives were obtained through C(2), C(3) – and C(4) -selective metalations and subsequent methylation, respectively. MC isomers of C(3) and C(4), referred to as Me(n) MC, were also prepared, where n is the number of methyl groups of the cavity of the host. The C(3) MC compound [Cp(1)Ir(COD)(C(3) H(2) OCH(3))](+)[PF(6)(-)](-) was characterized by single crystal X-ray diffraction, showing a C(3) cavity with the cavity diameter ranging from 6.35 to 6.86 A. In addition, the C(3) and C(4) MCs showed considerably improved air and moisture stability in comparison to the precursor. The C(3) and C
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