Abstract
The fluorescence properties of the dye Rhodamine 590 and Rhodamine 640 intercalated into montmorillonite were studied. All of the intercalation reactions were accomplished in an ethanol solution which contained the corresponding quality of Rhodamine. The TG-DTA and the X-ray diffraction data showed that the immobilization of Rhodamine depended on the amount of ethanol incorporated in the interlayer space of montmorillonite. The 14.8 Å basal spacing of products indicated a conformation of Rhodamine with the xanthene nucleus and the phenyl group positioned parallel and perpendicular to the silicate layer, respectively. Also, the infrared pleochromism, which supported the proposed orientation of the phenyl group, was observed at 1250 and 712 cm −1. The main fluorescence bands of both products were observed near 600 nm when excited by the 514.5 nm line of an argon ion laser. The results indicated that the mesomeric structure determined the fluorescence behavior, which was little different for the two products owing to the environment of the interlayer. These data are briefly discussed relative to the reaction conditions utilized for the synthesis of products. Also, the results support the idea that the products have a high potential for use as a host for a tunable laser.
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