Preparation and Studies of Ratiometric Fluorescent Chemosenors based on the Attenuation of Excitation on energy Tranfer

Abstract

Molecular devices possessing -electron conjugated scaffold demonstrate unique capabilities as fluorescent chemosensors for the trace detection of analytes in a variety of environments. Important properties of these compounds such as charge transport and exciton migration, emission intensity etc. can be simply attenuated by external stimuli or analyte binding, leading to considerable changes in observable signals. The main goal of this Ph.D. dissertation was to study the possibility to control excitation energy migration in conjugated systems. Towards this goal, we designed surface-immobilized monodispersed oligo(p-phenylene ethynylene)s (OPEs) as a general basis for thin-film ratiometric fluorescent chemosensors. The sensor molecules have been functionalized with a specific analyte receptor at one end and a linkage for the covalent attachment to a glass surface at the opposite end. Upon surface immobilization these sensor molecules form a highly ordered monolayer with the receptors positioned at the monolayer surface. Analyte binding to the receptor causes attenuation of the HOMO–LUMO gap at the receptor terminus leading to the ratiometric change in fluorescent emission. The thin-film sensors for L-cysteine, pH and Zn 2+ were prepared and studied in detail to uncover a number of unusual properties, thus demonstrating the potential of this platform as a universal foundation for designing a broad range of fluorescent ratiometric thin-film chemosensors.