The formation of a metastable supercooled alkyl-π molecular liquid was prohibited by subtle alteration of the molecular structure.

No abstract

Novel pyridine-substituted subphthalocyanines were prepared for an additional harvesting of a green spectral region of the solar light spectrum for zinc phthalocyanine-based dye-sensitized solar cells. These compounds can bind with the central metal of zinc phthalocyanines to form the corresponding supramolecular complexes as monitored by the absorption and fluorescence spectral changes. The stability constants of these complexes were altered by the number and position of pyridine units in the pyridine-substituted subphthalocyanines. On the basis of fluorescence titration study, the complexes efficiently transfer energy from the subphthalocyanine to zinc phthalocyanine. The solar cells using TiO electrodes stained with the supramolecular complexes, composed of zinc phthalocyanine sensitizer and pyridine-substituted subphthalocyanines, showed panchromatic responses, and the photocurrent generation in the range of 500-600 nm is attributed to the efficient Förster resonance energy transfer from subphthalocyanine to zinc phthalocyanine on the TiO surface.