Influence of molecular structure on the aggregating properties of thiacarbocyanine dyes adsorbed to Langmuir films at the air-water interface

The influence of substituents on the adsorption and aggregation of the anio nic 3,3'-disulfopropyl-5,5'dichloro -9-ethylthiacarbocyanine (THIATS) and i ts cationic analogue 3,3'-diethyl-5,5'-dichloro-9-ethylthiacarbocyanine (TD C) was investigated in Langmuir films at the air-water interface. Dioctadec yldimethylammonium bromide (DODAB) and octadecylammonium chloride (ODAC1) w ere used to adsorb THIATS. Arachidic acid (AA) and dihexadecyl phosphate (D HP) were used to adsorb TDC. J-aggregate formation has been observed for th e four different combinations of dyes and surfactants. The absorption and e mission spectra of THIATS at the air-water interface revealed one narrow in tense J-band which was not influenced by the chemical structure of the amph iphiles or by the concentration of THIATS in the subphase. Fluorescence mic roscopy experiments suggest that, depending on the subphase dye concentrati on, aggregation of dye molecules leads either to a layer of J-aggregates di stributed homogeneously on the scale of a few micrometers or to the observa tion of individual domains of J-aggregates. For TDC adsorbed to an AA film, the absorption and emission spectra revealed the formation of two J-bands that coexist at the interface. The absorption spectra of TDC adsorbed onto a DHP film showed only one J-band, whose maximum gradually shifted from an initial value of 646 nm to 637 nm and then to 652 nm. The flexible alkyl sp acer chain between the localized negative charges of the sulfate groups and the nitrogen atoms of the benzthiazole units allows a packing of the THIAT S molecules that is less dependent on the charge distribution in the opposi tely charged lipid film than for TDC. Fluorescence micrographs of THIATS/DO DAB and TDC/AA films reveal different spatial features. They confirm the pr edominant influence of the lipid on the TDC/AA film morphology, as conclude d from the spectral data. The presented study offers substantial informatio n that was still lacking in this field of research: the time-dependence ads orption of the dyes onto charged monolayers as well as an investigation of the influence of the substitution pattern and the role of the packing of th e amphiphiles on the formation of a specific type of aggregate.