Current topics of the structure, spectroscopic properties, excitation dynamics and photochemistry of dye aggregates have been reviewed. Five typical cyanine dyes and merocyanine dyes have been taken up; those having long-alkyl chains: oxacyanine (S9) and thiacyanine (S11), merocyanine (MC), and those without long-alkyl chains: pseudoisocyanine (PIC), benzimidazolocarbocyanine (BIC, TDBC), meso-ethyl-thiacarbocyanine (TDC, THIATS). The J-aggregate (JA) of PIC was first reported by Jelley and Scheibe in 1936. Since then, JA of PIC, BIC, TDBC, TDC, THIATS in aqueous solutions, in lowtemperature glassy matrices, in adsorbed layers has been successfully prepared. Kuhn's group discovered the JA of S9, 511, MC in LB films, which open up the research field of photophysics, photochemistry and molecular architecture of organized molecular assemblies. Nowadays, the J-aggregate of many cyanine dyes without long-alkyl chains can be easily incorporated into organic thin films (LB films, SA films), and polymer films by LB technique, alternate adsorption technique, and spincoating method, which enhances the exploration of linear-and nonlinear optical materials composed of organic dyes. Rapid progress of new techniques; cryo-TEM, confocal fluorescence microscopy, SNOM and AFM has enabled us to visualize complex supramolecular structures of JA. Particularly, suprastructures of PIC and TDBC in aqueous solutions as visualized by cryo-TEM are striking. The application of ultrafast spectroscopy and non-linear spectroscopy to the JA in low-temperature glassy matrices combined with theoretical analysis has revealed special features as well as a common feature of the J-aggregate derived from different dyes. A beautiful ring structure of bacteriochlorophyll (BChl) molecules in the antenna system of photosynthetic bacteria has been mentioned in connection with the JA of organic dye molecules.
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