Ground-state complex formation of perylene with pyromellitic dianhydride studied by static fluorescence quenching

The association of complex formation with static quenching in CT systems was investigated. Evaluation of the data made evident that the inner filter effect must be allowed for. Time-resolved and temperature-dependent stationary measurements of fluorescence led to the separation of dynamic and static quenching components. The static quenching constant is discussed with respect to the equilibrium constant of complex formation determined by absorption spectroscopy.     

Investigation of the photothermally modulated ferromagnetic resonance signal from magnetostatic modes in yttrium iron garnet films

The conventional and photothermally modulated (PM) ferromagnetic resonance (FMR) of magnetostatic modes (MSM) in yttrium iron garnet (YIG) films have been investigated as a function of temperature. Approaching the ferrimagnetic transition at T _c=560 K a strong enhancement of the PM-FMR signal amplitude is observed which is accompanied by a change of the signal shape. The observations are discussed in the framework of a model that takes into account the temperature derivatives of those quantities that contribute to the high-frequency susceptibility. At temperatures still below T _c a paramagnetic line emerges. The MSM disappear in a state of finite magnetization which is explained on the basis of damping of the MSM being important in the vicinity of the magnetic phase transition. Additionally, frequency and power dependent measurements are presented and the imaging ability of PM-FMR is demonstrated.     

Topochemically Controlled Redox Reactions in the System In/Sn/Cl

The difference in reactivity of the two modifications of InCl in solid state reactions with SnCl₂ is discussed. It is explained on the basis of semi‐empirical and ab initio calculations giving the density of states diagrams of InCl and the energies of possible disproportionation reactions. Their general features are discussed on the basis of a simple bonding picture for open‐packed structures involving inert pair elements. A detailed analysis of the DOS distribution allows to pinpoint the observed redox instability to a specific structural feature of α‐InCl.