Localized emitting state and energy transfer properties of quadrupolar chromophores and (multi)branched derivatives.

In order to better understand the nature of intramolecular charge and energy transfer in multibranched molecules, we have synthesized and studied the photophysical properties of a monomer quadrupolar chromophore with donor-acceptor-donor (D-A-D) electronic push-pull structure, together with its V-shaped dimer and star-shaped trimers. The comparison of steady-state absorption spectra and fluorescence excitation anisotropy spectra of these chromophores show evidence of weak interaction (such as charge and energy transfer) among the branches. Moreover, similar fluorescence and solvation behavior of monomer and branched chromophores (dimer and trimer) implies that the interaction among the branches is not strong enough to make a significant distinction between these molecules, due to the weak interaction and intrinsic structural disorder in branched molecules.

A versatile approach to the fabrication of palladium hollow spheres with aluminiumoxide nanoparticles as template.

Palladium hollow nanospheres were prepared by the adsorption of metal nanoparticles onto functionalized gamma-Al2O3 templates. The silanizing agent 3-mercaptopropyl trimethoxysilane was reacted with the surface of the gamma-Al2O3 templates to afford thiol-terminal groups. Metal layers of palladium were coated directly on the gamma-Al2O3 templates by increasing the temperature stepwise.

Solution-processable red-emission organic materials containing triphenylamine and benzothiodiazole units: synthesis and applications in organic light-emitting diodes.

Three solution-processable red-emissive organic materials with a hole-transporting unit triphenylamine (TPA) as the core part and a D-pi-A bipolar structure as the branch part, TPA-BT (single-branched molecule), b-TPA-BT (bibranched molecule), and t-TPA-BT (tribranched molecule), were synthesized by the Heck coupling reaction. Herein, for the D-pi-A push-pull structure, we use TPA as the electron donor, benzothiodiazole (BT) as the electron acceptor, and the vinylene bond as the pi-bridge connecting the TPA and BT units. The compounds exhibit good solubility in common organic solvents, benefited from the three-dimensional spatial configuration of TPA units and the branch structure of the molecules.

Photophysical properties of photoactive molecules with conjugated push-pull structures.

The photophysical properties of two newly synthesized photoactive compounds with asymmetrical D-pi-A structure and symmetrical D-pi-A-pi-D structure are investigated in different aprotic solvents by steady-state and femtosecond fluorescence depletion measurements. It is found that the asymmetrical DA compound has larger dipole moment change than that of the symmetrical DAD compound upon excitation, where the dipole moments of the two compounds have been estimated using the Lippert-Mataga equation. Furthermore, the steady-state spectral results show that increasing solvent polarity results in small solvatochromic shift in the absorption maxima but a large red shift in the fluorescence maxima for them, indicating that the dipole moment changes mainly reflect the changes of dipole moment in excited-state rather than in ground state.

Photophysical processes of a fluorene derivative containing 1,3,4-oxadiazole.

The photophysical processes of 9,9-bis[4'-[2''-phenyl-5''-(3'''-(methacryl-amido)phenyl)]-1'',3'',4''-oxadiazolylphenyl]fluorene (F-MAOP) formed by Heck reaction of 9,9-bis(4'-iodophenyl)fluorene (F-IP) and 2-phenyl-5-[3'-(methacrylamido)phenyl]-1,3,4-oxadiazole (OXD) have been carefully studied. The results show that the compound emits blue and blue-violet light and the emission spectra exhibit obvious solvent effect. With the increase of polarity of solvents, the fluorescence spectra change obviously and appear blue shift at room temperature.

Photophysical processes of a copolymer containing 1,1'-binaphthyl-2,2'-diamino and carbazolyl units.

The photophysical processes of copolymer formed by copolymerization of 2,2'-dimethacrylamido-1,1'-binaphthyl (DMBN) with vinylcarbazole (VCZ) have been carefully studied. The results show that when the solution of copolymer (DMBN-VCZ) in THF located in low concentration range (< 10(-3) mg/ml), the fluorescence emission is in good agreement with that of DMBN monomer and the excimer is formed with gradual increase in concentration of copolymer (DMBN-VCZ). The fluorescence of copolymer (DMBN-VCZ) can be quenched both by electron donors and acceptors where the quenching effects follow the Stern-Volmer equation.

Fluorescence investigation of model compounds for light-emitting alternating copolymers in heterogeneous environments.

In this paper, the fluorescence spectra of the model compounds M(TPA-PPV) and M(TPA-PAV) of novel light-emitting alternating copolymers, were studied and the effect of KNO3 on the interaction between the model compounds and the ionic micelle-water interface was also investigated. The following is found: (i) the fluorescence changes of M(TPA-PPV) are related to the state of cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulfate (SDS) solution: (ii) an aggregated state can be formed in M(TPA-PAV) solution at low concentration of CTAB; (iii) higher concentrations of KNO3 may affect the interaction between the model compounds and the ionic micelle-water interface.