Photoinduced hole transfer forming polymer quantum dot nanocomposites.

The study of hole transfer from CdSe QD core to ligands under visible light irradiation and conductive polymer-QD composites formation without conventional photoinitiator.

Isomer restriction on a nanoparticle surface and enhanced blue emission.

5-Mercapto-2,2'-bithiophene (BTSH) functionalized copper (Cu), silver (Ag), and gold (Au) nanoparticles (NPs) of various diameters have been synthesized. Emission with a peak around 455 nm is detected on irradiation with UV light. This emission, however, disappears upon photopolymerization of the NPs.

Solvent dependent optical switching in carbazole-based fluorescent nanoparticles.

Suitably substituted ethynylphenyl carbazoles (PBM and PPM) form stable fluorescent organic nanoparticles. The emission of the nanoparticles can be reversibly switched on/off in the blue-green and orange-red regions by a change in the ratio of the tetrahydrofuran/water system used in their preparation. The size of the nanoparticles was found to be dependent on the solvent ratio, and the emissions were significantly red-shifted compared to those of dilute solutions of PBM and PPM in tetrahydrofuran.

Carbazole-based donor-acceptor compounds: highly fluorescent organic nanoparticles.

Carbazole-based donor-acceptor compounds 1,2-dicyano-trans-1,2-bis-4-(carbazolyl)phenylethylene (1) and 1,2-dicyano-trans-1,2-bis-4-(3,6-di-tert-butylcarbazolyl)phenylethylene (2) were synthesized. 1 and 2 show negative solvatochromic absorption behavior, but show both positive and negative solvatochromic behavior in the fluorescence spectra. In a water/THF mixture, 1 as well as 2 aggregate into 50-150 nm nanoparticles.

Synthesis of highly soluble and oxidatively stable tetraceno[2,3-b]thiophenes and pentacenes.

A comparative study of suitably functionalized, highly soluble tetraceno[2,3-b]thiophenes (1-3) and pentacenes (4-6) that show higher photoxidative stability than that of unfunctionalized corresponding acenes is reported. The absorption and emission of 1-3 (Amax = 624-656 nm, lambda max = 634-672 nm, PhiF approximately 10%) and 4-6 (Amax = 672-704 nm, lambda max = 682-718 nm, PhiF approximately 10%) were found to be systematically red-shifted by the substitution in the order of the tert-butylethynyl < triisopropylsilylethynyl < phenylethynyl groups. The oxidation potentials of these compounds were similar (E1/2 approximately 0.