The influence of solvent polarity on the electronic transition of four different
N-hexadecyl styrylpyridinium dyes has been investigated in 15 solvents. The
ET(30) scale has been used to propose a quantitative approach towards the relative stability of the electronic ground and excited state species. The extents of contribution of dipolar aprotic solvents towards the solvation of the excited species have been determined to be 42–48%for some of the dyes. Instead of a steady
solvatochromism, all the dyes suffer a reversal in
solvatochromism. The transitions of the
solvatochromism, referred to as solvatochromic switches, are found to be at
ET(30) values of
![not, vert, similar](http://www.sciencedirect.com/scidirimg/entities/223c.gif)
50 for methyl and
N,
N-dimethylamino substituted dyes while at 37.6 for hydroxyl substituted dye and
![not, vert, similar](http://www.sciencedirect.com/scidirimg/entities/223c.gif)
45 for 4-(1-methyl-2-phenylethenyl) pyridinium dye. A reversal in the trend of solvent effect in the later dye corresponding to 4-(4-methyl styryl)pyridinium dye has been attributed to an analogy of series and parallel electron flow.