Schiek Manuela, Balzer Frank, Al-Shamery Katharina, Lützen Arne, Rubahn Horst-Günter
Mads Clausen Institute, NanoSYD, University of Southern Denmark, Alsion 2, DK-6400, Sønderborg, Denmark.
University of Oldenburg, Institute of Pure and Applied Chemistry, PO Box 2503, D-26111, Oldenburg, Germany.
Soft Matter. 2008 Jan 22;4(2):277-285. doi: 10.1039/b713295f.
Functionalized para-phenylenes are versatile building blocks for generating aligned fiber-like nanostructures by a self-assembly growth process on muscovite mica substrates upon controlled vapor deposition (molecule epitaxy). Functional groups were implemented at the 1,4‴-para-positions of p-quaterphenylenes (p4P) using a Suzuki cross-coupling strategy. The nanoaggregates possess outstanding optical properties, which can be modified in a controlled manner by functionalization. Functionalization allows the fluorescence peak emission frequency to shift within the blue spectral range, and the nanoaggregates' three-dimensional shape alters depending on the substitution. In the case of asymmetrically functionalized phenylenes due to the intrinsic non-zero hyperpolarizability of push-pull functionalized oligomers and non-centrosymmetry of the respective nanofibers, they act as frequency doublers.