Solvent-induced aggregation and cation-controlled self-assembly of tripodal squaraine dyes: optical, chiroptical and morphological properties.

The synthesis, characterisation, optical, chiroptical, aggregation, and alkaline earth metal cation assisted self-assembly properties of tripodal squaraine dyes have been described. In the tripodal geometry, these dyes exhibit three absorption bands around 650, 620 and 580 nm in contrast to the single, sharp absorption of a simple dye (SQ) at 640 nm. The fluorescence quantum yield of the squaraine dyes are 25-30 times lower when compared to that of SQ, which indicates intramolecular exciton interaction as a result of the confinement of the dyes. The evaporation of an acetonitrile solution of the dye resulted in the formation of vesicular objects as confirmed by AFM and TEM analyses. However, evaporation of an acetonitrile solution containing 10-12 % water gave short fibrous aggregates. In the presence of Ca(2+) or Mg(2+) ions, the dyes exhibit an intense and sharp absorption band at 547 nm with a concomitant decrease of the native absorption. Interestingly, the dye with chiral groups failed to give a circular dichroic signal during aggregation in solvent mixtures, whereas strong signals were observed in the presence of Ca(2+) and Mg(2+) ions. AFM and TEM analyses of the corresponding cation complexes revealed the formation of worm like nanohelices. However, addition of EDTA to the Ca(2+) or Mg(2+) complex exhibited a reversal of the absorption, emission, and circular dichroic spectra to that of the native dye, indicating decomplexation. AFM analyses revealed the transformation of the helices to particles. These observations reveal the difference in the nature and properties of the simple aggregates formed in solvent mixtures and those formed in the presence of cations. In the present study, we were able to establish the importance of specific cation binding in controlling the size, shape, and properties of the hierarchical assemblies of tripodal squaraines.