Primary charge separation in Chloroflexus aurantiacus reaction centers at room temperature: ultrafast transient absorption measurements on Q-depleted preparations with native and chemically modified bacteriopheophytin composition.

The initial electron transfer (ET) processes in reaction centers (RCs) of Chloroflexus (Cfl.) aurantiacus were studied at 295 K using femtosecond transient absorption (TA) difference spectroscopy. Particular attention was paid to the decay kinetics of the primary electron donor excited state (P) and the formation/decay of the absorption band of the monomeric bacteriochlorophyll a anion (B) at ~ 1035 nm, which reflects the dynamics of the charge-separated state PB.

[Chronic epidural spinal cord stimulation for gait impairments in Parkinson's disease and atypical parkinsonism].

Spinal cord stimulation is a well-established, minimally invasive surgical technique that has been effectively utilized for the treatment of chronic pain syndromes. In the past 15 years, there has been a significant increase in reports on the use of spinal stimulation for patients with advanced Parkinson's disease (PD), as well as in isolated cases of atypical parkinsonism. These reports frequently highlight a positive impact of spinal stimulation on gait impairments.

Electronic states bound by repulsive potentials in graphene irradiated by a circularly polarized electromagnetic field.

In the framework of the Floquet theory of periodically driven quantum systems, it is demonstrated that irradiation of graphene by a circularly polarized electromagnetic field induces an attractive area in the core of repulsive potentials. Consequently, the quasi-stationary electron states bound by the repulsive potentials appear. The difference between such field-induced states in graphene and usual systems with the parabolic dispersion of electrons is discussed and possible manifestations of these states in electronic transport and optical spectra of graphene are considered.

6-Fold-Coordinated Beryllium in Calcite-Type Be[CO].

The anhydrous beryllium carbonate Be[CO] with calcite-type crystal structure was obtained by a reaction of BeO with CO in a laser-heated diamond anvil cell at pressures between 30 GPa and 80 GPa and elevated temperatures. Its calcite-type crystal structure (3̅ with = 6) is characterized by 6-fold-coordinated beryllium atoms forming [BeO] octahedra and by trigonal-planar [CO] groups. The crystal structure was determined by synchrotron-based single-crystal X-ray diffraction and confirmed by density-functional-theory-based calculations in combination with experimental Raman spectroscopy.