Individual polyphenylene dendrimer 1 and their self-assembled nanostructures, prepared by spincoating and solvent casting on various substrates such as mica, silanized mica, and highly oriented pyrolytic graphite (HOPG), have been investigated by noncontact atomic force microscopy. Besides globular clusters and monolayers, polyphenylene dendrimer 1 self-organizes into micrometer long nanofibers on a HOPG surface. Fibrillar nanostructures have also been visualized on a silanized mica surface, while on a mica surface the dendrimers only aggregate into globular clusters. Two possibilities for the development of dendrimer nanofibers are proposed.
The fluorescence of polyphenylene dendrimers and the intramolecular energy transfer in polyphenylene dendrimers containing a perylenediimide core have been investigated in this paper. Polyphenylene dendrimers composed of tens or hundreds of out-of-plane twisted phenyl units exhibit strong fluorescence, with quantum yields ranging from 0.2 to 0.5 depending on the dendrimer generation and its degree of functionality. The fluorescence of polyphenylene dendrimers can be efficiently quenched by the incorporated perylenediimide core, and consequently, a predominant emission from the core has been observed, indicating a very efficient intramolecular energy transfer.
Novel perylene-3,4,9,10-tetracarboxdiimides (PDI) dyes functionalized with polyphenylene dendrimers attached at the bay region are reported. Derivatives of PDI bearing polyphenylene dendrimers up to the second generation, substituted with an increasing number of triphenylamine (TPA) moieties at the periphery, as well as a related nondendronized model compound were prepared. Intramolecular energy transfer was demonstrated by the observation of PDI emission on excitation of the triphenylamines, and electron transfer was detected by comparing photoluminescence quenching in solvents of different polarity.
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