Metal Ion Enhanced Charge Transfer in a Terpyridine-bis-Pyrene System.

The synthesis, electrochemical and photophysical properties of a branched molecule 3,5-bis(pyrene-1-yl)-4'-phenyl-2,2':6',2″-terpyridine are reported. Spectroscopy in different solvents reveals that an optical electron transfer from the pyrene donor to the terpyridyl electron acceptor can occur in polar media, as the system displays both charge transfer (CT) absorption and CT emission. Furthermore, the study of the zinc complex as well as the bis-protonated form shows an enhancement of the electron transfer character of the system, by an increase of the acceptor strength.

Effective two-photon absorption cross section of heteroaromatic quadrupolar dyes: dependence on measurement technique and laser pulse characteristics.

The linear and nonlinear optical properties of the heteroaromatic push-pull-push two-photon absorbing dye N-methyl-2,5-bis[1-(N-methylpyrid-4-yl)ethen-2-yl]-pyrrole ditriflate (PEPEP) are reported. The determination of the two-photon absorption (TPA) cross-section spectrum has been performed with different techniques: femtosecond TPA-white light continuum probe experiments, two-photon-induced fluorescence, and open aperture Z-scan measurements using both nanosecond and femtosecond laser pulses. The measured TPA cross sections and their wavelength dispersion show a marked dependence on the parameters of the laser pulses and on the measurement technique employed.

One- and two-photon absorption and emission properties of a Zn(II) chemosensor.

This paper presents the synthesis and two photon-induced absorption (TPA) properties of a functionalized distyrylbenzene (DSB) 1 containing a tetra-azacyclododecane (cyclen) receptor for Zn(II). The influence of Zn(II) on one- and two-photon absorption characteristics of 1 has been investigated in dimethyl sulfoxide. The experiments show that the TPA action spectrum of uncomplexed 1, at 750 nm employing nanosecond-long excitation pulses, is 5 times more intense than that of the complexed form.

Energy transfer by a hopping mechanism in dinuclear Ir(III)/Ru(II) complexes: a molecular wire?

The synthesis and electrochemical and photophysical properties of a series of heterodinuclear ruthenium-iridium complexes linked by a modular para-phenylene bridge [Ir-ph(n)-Ru]3+ (Ir=Ir(ppyFF)2bpy, Ru=Ru(bpy)3, ppyFF=2-(2,4-difluorophenyl)pyridine), bpy=2,2'-bipyridine, ph=phenylene, n=2, 3, 4, 5) are reported. The use of a high-energy iridium complex, which can act as an energy donor when coupled to the lower energy ruthenium-based component, allows the investigation of photoinduced energy transfer from the excited iridium-centre to the ruthenium fragment (energy acceptor). The rate constants of the energy-transfer processes are determined by time-resolved emission and sub-picosecond transient absorption spectroscopy.