Near-Infrared Electrochemiluminescence from Bistridentate Ruthenium(II) Di(quinoline-8-yl)pyridine Complexes in Aqueous Media.

We report the synthesis, photophysics, electrochemistry and electrochemiluminescence (ECL) of two dqp (dqp=2,6-di(quinoline-8-yl)pyridine) based ruthenium(II) complexes, bearing either a n-butyl ester (1) or the corresponding carboxylic acid functionality (2). The complexes were prepared from [Ru(dqp)(MeCN) ][PF ] by reaction with the dqp precursor using microwave irradiation. In both cases, photoluminescence spectra present strong MLCT-based red/near-infrared (NIR) emissions centred at about 710 nm.

Interactions between an amphipathic di-histidine peptide and a metal affinity chromatographic resin derived from a bis(tacn)butane chelating ligand.

The interactive behavior of an amphipathic peptide with the Cu , Ni , and Zn complexes of 1,4-bis(triazacyclonon-1-yl)butane), bis(tacn) , immobilized onto Sepharose CL-4B, has been investigated. The effects of incubation time, as well as the incubation buffer pH and ionic strength, have been examined. The binding data have been interrogated using Langmuir, Langmuir-Freundlich, bi-Langmuir, and Temkin isothermal models and Scatchard plots.

Molecular Engineering of Zinc-Porphyrin Sensitisers for p-Type Dye-Sensitised Solar Cells.

Invited for this month's cover are the groups of Prof. Dr. Udo Bach, Prof.

Transformation of Indium and Gallium Metal into Mixed Group 11/13 Ternary Sulfide Nanoparticles by Using a Dithioic Acid.

Heterobimetallic Group 11/13 sulfide nanoparticles (AgInS , CuInS , Ag GaS , and CuGaS ) are formed by treatment of [M(S CAr) ] (M=Ga or In) with either AgNO or CuCl under mild conditions. The intermediary gallium or indium tris(aryldithioate) complexes are easily prepared by stirring the appropriate metal and aryldithioc acid at room temperature. Overall, this two-step process is a simple solution-based method for transforming Ga and In metal into valuable ternary metallosulfide nanoparticles at relatively low temperatures.

Molecular Engineering of Zinc-Porphyrin Sensitisers for p-Type Dye-Sensitised Solar Cells.

Design of novel efficient light-harvesters for p-type dye-sensitised solar cells (DSSCs) is indispensable for further advances in this photovoltaic technology. Herein, a novel D-π-A (D=donor, π=π-conjugated linker, A=acceptor) sensitiser, ZnP1, featuring an electron acceptor, perylenemonoimide (PMI), connected to an electron donor, di(p-carboxyphenyl)amine (DCPA), through fluorene and a zinc(II) porphyrin with alkyl chains as a π-conjugated bridge is introduced. Spectroscopic and electrochemical characterisation of this dye along with a newly synthesised PMI-free reference dye ZnP0 has been undertaken to demonstrate strong electron coupling between the DCPA donor and PMI acceptor subunits through the porphyrin ring in ZnP1, which redshifts the light absorption onset to the near-IR region.