Ultraviolet photoinduced weak bonds in aryl-substituted polysilanes.

The susceptibility of aryl-substituted polysilylenes to photodegradation by ultraviolet (UV) radiation is examined on the prototypical materials poly[methyl(phenyl)silylene] (PMPSi) and poly[(biphenyl-4-yl)methylsilylene] (PBMSi). We extend the scope of our last paper (Schauer et al 2004 Polym. Degrad. Stabil. 84 383) with the elucidation of the degradation mechanisms for two different degradation wavelengths: 266 and 355 nm. The main purpose of this paper was to study photoluminescence (PL) after major degradation, predominantly in long-wavelength range 400-600 nm, studying the disorder, dangling bonds (DBs) and weak bonds (WBs) created by the degradation process. We claim that the PL of the 500-600 nm band is related to the existence of WBs on the Si chain and originates in the σ(*)-σ exciton migration at room temperature by diffusion, free electron-hole formation, trapping in WBs and subsequent radiative recombination by tunnelling. Increase of the normalized PL 520-540 nm band after UV degradation can be then evaluated as the increase of the density of states (DOS) of WBs. The efficiency of the WB creation in PMPSi is greater for 266 nm irradiation, supporting the notion of the suppressed exciton transport compared to the less energetical photon of 355 nm, where the WB creation is lowered due to the exciton migration to longer segments and/or already existing defects. For PBMSi the WB creation kinetics for 355 nm degradation is similar to that of PMPSi. The 266 nm degradation results then support the model calculations of DB and WB reconstruction in the more rigid Si skeleton.

Kinetics of photochromic reactions in condensed phases.

A review of kinetic data reported for a few organic photochromic systems is given. The kinetics of processes taking place in solid matrices and in crystals was briefly discussed. The effect of solid matrices manifests itself in the kinetics being controlled by distributions rather than by discrete rate constants. The photochromic reactions often require a substantial free volume to occur, hence they seldom take place in crystals without a destruction of the crystal lattice. The activation energies of thermally driven reactions are in this case related rather to crystal parameters than to the reactions themselves.

Molecular optical memories and switches based on photochromic dihydropyridines.

Photochromic behavior of dihydropyridines and the mechanism of the photochromism based on phenyl transfer is described. Formation of polar coloured species, changes in optical absorption and in the tau electron character of the molecular skeleton allow for the fabrication of molecular optical memories and switches.