Abstract
Porphyrin macrocycles and their supramolecular nanoassemblies are being widely explored in energy harvesting, sensor development, catalysis, and medicine because of a good tunability of their light-induced charge separation and electron/energy transfer properties. In the present work, we prepared and studied photoresponsive porphyrin nanotubes formed by the self-assembly of meso-tetrakis(4-sulfonatophenyl)porphyrin and Sn(IV) meso-tetra(4-pyridyl)porphyrin. Scanning electron microscopy and transmission electron microscopy showed that these tubular nanostructures were hollow with open ends and their length was 0.4-0.8 μm, the inner diameter was 7-15 nm, and the outer diameter was 30-70 nm. Porphyrin tectons, H(4) TPPS42- : Sn(IV)TPyP(4+), self-assemble into the nanotubes in a ratio of 2:1, respectively, as determined by the elemental analysis. The photoconductivity of the porphyrin nanotubes was determined to be as high as 3.1 × 10(-4) S m(-1), and the dependence of the photoconductance on distance and temperature was investigated. Excitation of the Q-band region with a Q-band of SnTPyP(4+) (550-552 nm) and the band at 714 nm, which is associated with J-aggregation, was responsible for about 34 % of the photoconductive activity of the H(4) TPPS42- -Sn(IV)TPyP(4+) porphyrin nanotubes. The sensor properties of the H(4) TPPS42- - Sn(IV)TPyP(4+) nanotubes in the presence of iodine vapor and salicylate anions down to millimolar range were examined in a chemiresistor sensing mode. We have shown that the porphyrin nanotubes advantageously combine the characteristics of a sensor and a transducer, thus demonstrating their great potential as efficient functional layers for sensing devices and biomimetic nanoarchitectures.