Abstract
A multiply interlocked catenane with a novel molecular topology was synthesized; a phthalocyanine bearing four peripheral crown ethers was quadruply interlocked with a cofacial porphyrin dimer bridged with four alkylammonium chains. The supramolecular conjugate has two nanospaces surrounded by a porphyrin, a phthalocyanine, and four alkyl chains to accommodate guest molecules. Because the phthalocyanine can move along the alkyl chains, it acts as an adjustable wall, thus permitting the invasion of large molecules into the nanospaces without spoiling the affinity of the association. The dynamic molecular invasion allowed the intercalation of dianionic porphyrins into both nanospaces with high affinity. A photometric titration experiment revealed the two-step inclusion phenomenon. The multiply interlocked catenane complexed with three Cu2+ ions, and the spin–spin interaction was switched off by the intercalation of dianionic porphyrins.
An elevator for guests: A phthalocyanine molecule bearing four peripheral crown ethers was quadruply interlocked with a cofacial porphyrin dimer bridged by four alkylammonium chains to create a catenane with a novel topology. The phthalocyanine unit moved along the threads to enable the invasion of large guest molecules without affecting the affinity of the association (see picture).
