Abstract
The aggregation of the basic dye is explained adequately in terms of van der Waals force and the hydrophobic bond. It is difficult, however, to estimate the contribution of the hydrophobic bond to the aggregation. The interaction between the dye and tetraalkylammonium chloride (R4 NCl) was studied spectrophotometrically to estimate the contribution of the hydrophobic bond. Results obtained were as follows:
1) R4NCl causes the aggregation or disaggregation of C. I. Basic Blue 9, C. I. Basic Violet 10, and C. I. Basic Red 1 depending on the given conditions. The effect of tetraalkylammonium cation is greater than that of the Cl anion.
2) C. I. Basic Blue 9 and Basic Red 1 aggregate in the dilute solution of R4NCl, i.e. Me4NCl, Et4NCl, and n-Bu4NCl. These dyes disaggregate in concentrated solution of R4NCl. C. I. Basic Violet 10 disaggregate in the presence of R4NCl. The effect was in the order; n-Bu4NCl>Et4NCl>Me4NCl.
3) The effect of NH4Cl on the aggregation of C. I. Basic Violet 10 becomes larger at lower temperatures. The effect of Me4NCl, Et4NCl, and n-Bu4NCl on the disaggregation becomes larger at higher temperatures.
4) The intensity of the interaction between the dye and R4N+ was in the order; C. I. Basic Violet 10>C. I. Basic Red 1>C. I. Basic Blue 9.
Results described above revealed facts that the aggregation of the dye cation is caused by the formation of the ionic atmosphere of the dye cation, and that the disaggregation is caused by the formation of the hydrophobic bond between the dye cation and R4N+.