Abstract
This article is focused on the design and photophysical properties of a series of novel porphyrin and metalloporphyrin dendrimers containing cationic η
6
-chloroarene-η
5
-cyclopentadienyliron(II) complexes functionalized with naphthalene and capped with ferrocene. The incorporation of cationic η
6
-chloroarene-η
5
-cyclopentadienyliron moieties into the dendrimer structures enhances solubility, and facilitates nucleophilic aromatic substitution and addition reactions due to the intense electron-withdrawing ability of the iron center. Divergent approaches were employed to yield highly symmetrical branched materials, with interesting and potentially useful properties. The preparation of these dendrimers was achieved via metal-mediated nucleophilic aromatic substitutions and Steglich esterifications. These dendrimers and their precursors were characterized through nuclear magnetic resonance spectroscopy, infrared spectroscopy, and UV–Visible and fluorescence spectroscopy. Substitution on the porphyrin core with various side chains and terminal functional groups and chromophores had little impact on the porphyrin emission properties, allowing for a wide variety of fluorescent macromolecules to be prepared which retain this characteristic emission. Also, the presence or absence of the organopyrene moieties also had little effect on the emission from these compounds. Complexation of a metal cation, such as Zn
2+
, by these compounds, did however result in a significant blue shift in the observed fluorescence; this interesting result has the potential for applications in the development of fluorescent-based cation sensors.