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Porphyrin Nanotubes Based on Self-Assembly of Mo(V)−Dodecaphenylporphyrin Complexes and Inclusion of Mo−Oxo Clusters: Synthesis and Characterization by X-ray Crystallography and Transmission Electron Microscopy

2006; American Chemical Society; Volume: 19; Issue: 1 Linguagem: Inglês

10.1021/cm062031k

1520-5002

Takahiko Kojima, Ryosuke Harada, Tatsuaki Nakanishi, Kenji Kaneko, Shunichi Fukuzumi,

Supramolecular Self-Assembly in Materials

A saddle-distorted molybdenum(V)−dodecaphenylporphyrin (H2DPP) complex, [Mo(DPP)(O)(OMe)] (1), was converted to [Mo(DPP)(O)(H2O)]+ (2) in the course of recrystallization from toluene with vapor diffusion of methanol. The complex 2 was organized via self-assembly to form a porphyrin nanotube having a diameter of 1 nm, concomitant with size-selective inclusion of three kinds of novel tetranuclear Mo(VI)−oxo clusters in the nanotube. This porphyrin nanotube exhibits amphiphilic characteristics, that is, a hydrophobic porphyrin surface and a hydrophilic inner-sphere made of aquo ligands to include ionic and hydrophilic entities. Each nanotube has no direct interaction; however, the toluene molecules of crystallization linked the nanotubes together with intermolecular π−π and CH/π interactions. Transmission electron microscopy measurements and energy-dispersive X-ray analysis revealed that the diameters of porphyrin nanotubes could be altered by the size of the Mo−oxo clusters included and also a porphyrin nanoring could be obtained. These results indicate that a variety of porphyrin nanotubular structures can be fabricated by using DPP complexes via cooperatively template-assisted self-assembly.