Xichen Cai

Carbazole-Based Cyano-Stilbene Highly Fluorescent Microcrystals

Aggregation-induced enhanced emission (AIEE) is reported for 1-cyano-trans-1,2-bis-(4-carbazolyl)phenylethylene (CN-CPE). The weak luminescence of dilute CN-CPE solutions is enhanced upon aggregate formation into 2-3 μm sized crystals. In contrast to general observations, crystal formation of CN-CPE causes a blue-shift in emission and enhances the intensity. X-ray crystallographic analysis revealed that key factors causing high luminescence efficiency in the crystal are a lack of strong cofacial π-π alignment and the existence of the strong supramolecular interactions due to the intermolecular H-bonding. These factors seem to be responsible for the AIEE phenomenon as molecules of CN-CPE are held in a rigid twisted conformation, thereby increasing the fluorescence intensity in the solid or aggregated states. Accordingly, conformational twisting in the crystal packing process may be responsible for the unusual emission blue-shift in the aggregate.

Nonradiative Decay Mechanism of Fluoren-9-ylidene Malononitrile Ambipolar Derivatives

We report recent results on the nonradiative decay (NRD) of fluoren-9-ylidene malononitrile (FM) ambipolar derivatives (FMDs). 2,7- and 3,6-disubstituted FMDs present distinctive photophysics. Charge separation was found dominant for excited state relaxation. The radiative decay (RD) is sensitive to changes in temperature and solvent medium only for the case of 3,6-FMDs. Excited state deactivation of carbazole-containing 3,6-FMD (CPAFM36) was exclusively nonradiative in polar solvents with excited state lifetimes shorter than 10 ps. The charge separation/recombination mechanism of the corresponding FMDs is suggested to fall in the inverted Marcus region of electron transfer. Given the electron-withdrawing properties of the FM unit, its ambipolar derivatives are suggested as potential candidates for air-stable organic thin-film transistors and molecular organic photovoltaics.

Gold nanoparticle photosensitized radical photopolymerization

We report the photopolymerization of an acrylic monomer using thiol-stabilized gold nanoparticles (AuNPs) and [4-[(octyloxy)phenyl] phenyl] iodonium hexafluoroantimonate (OPPI) as photoinitiator and coinitiator, respectively. Polymerization occurred only when the AuNPs, in the presence of the iodonium salt, were irradiated at the particle plasmonic absorption region (lambda>450 nm). The AuNPs activate the coinitiator by intermolecular electron transfer since OPPI has no absorption in the visible region. Fourier transform infrared spectroscopy was used to monitor polymerization. UV-Vis spectroscopy and transmission electron microscopy measurements were used to characterize the NPs.