RESUMEN
The palladium catalyzed cyclotrimerization of ortho-silylaryl triflates as aryne precursors is meanwhile an established method to synthesize polycyclic aromatic hydrocarbons (PAHs) with triphenylene cores. During the palladium-catalyzed reaction of a pyrene with an o-silylaryl triflate moiety in the K-region higher homologues with central eight- and ten-membered rings (the pyrenylenes) were found, besides the expected trimer and a protocol was developed to isolate all members of this series. This unprecedented new class of PAHs was fully investigated by all means, including X-ray diffraction of single-crystals, UV/Vis and fluorescence spectroscopy and theoretical calculations. Supported by density-functional theory (DFT) calculations, a mechanism of all higher cyclooligomers is proposed.
RESUMEN
Ortho substituted octaazaperopyrenes (OAPPs) are a new class of functional dyes characterized by their strong electron-accepting behavior. Herein, the synthesis, as well as the electrochemical and photo physical properties of an OAPP dye, is reported. The OAPP target was prepared via selective nucleophilic substitution at the peri position of a bay chlorinated tetraazaperylene by introduction of four amino-substituents. The resulting tetraminoperylene was reacted with different acyl chlorides and anhydrides to give the twisted bay chlorinated OAPP derivatives which were isolated in their reduced dihydro-form. The OAPP target could be obtained via a palladium catalyzed dehalogenation and a subsequent oxidation. The eightfold isosteric [CHâN] replacement within the peropyrene core structure results in a large decrease of the frontier orbital energies, rendering the target compound a potent oxidant while preserving the planarity of the aromatic core. The radical anion was obtained by reduction of the OAPP with KC8 and characterized by EPR spectroscopy. A general discussion of the number and location of [CHâN] replacements in peropyrene structures and their frontier orbital energies is provided.
RESUMEN
Yttrium oxide (Y2O3) is considered as one of the best host lattices for europium (Eu3+) based red emitting phosphors because of its unit cell and good photo-saturation properties. As a bulk material, it reaches nearly 100% quantum yield. However, providing high quality nanosized materials for the LED industry is still a challenge and not easily accomplished. Within this publication, a simple one pot, non-hydrolytic, solvent-based synthesis method for producing uniform and monodisperse red-emitting europium doped yttrium oxide (Y2O3:Eu) nanoparticles is provided. The synthesis is the cheapest and fastest reported yet, yields up to 80%, and offers good scalability, and the diameter of the produced nanodiscs is tunable from 7 nm to 30 nm. The dispersed nanomaterial shows bright red emission (607 nm) under UV excitation (273 nm) and a higher quantum yield (>30%) compared to other nanosized Y2O3:Eu materials. In order to shift the excitation wavelength towards the visible region we added Tb3+ as the sensitizer. Thereby, it was also possible to tune the emission colour towards orange/yellow. Further, a distorted anisotropic cubic Y2O3 phase is confirmed by XRD analysis, resulting in a distinct change in the intensities of red emission transitions. A calcination step transforms it into a highly crystalline cubic phase, known from the bulk material, and exhibiting a typical emission spectrum.
RESUMEN
BACKGROUND: Attempts to establish a biomarker reflecting individual player load in intermittent sports such as football have failed so far. Increases in circulating DNA (cfDNA) have been demonstrated in various endurance sports settings. While it has been proposed that cfDNA could be a suitable marker for player load in intermittent sports, the effects on cfDNA of repeated sprinting as an essential feature in intermittent sports are unknown. For the first time, we assessed both alterations of cfDNA due to repeated maximal sprints and due to a professional football game. METHODS: Nine participants were subjected to a standardised sprint training session with cross-over design of five maximal sprints of 40 meters with either "short" (1 minute) or "long" pauses (5 minutes). Capillary cfDNA and lactate were measured after every sprint and venous cfDNA before and after each series of sprints. Moreover, capillary cfDNA and lactate values were taken in 23 professional football players before and after incremental exercise testing, during the course of a training week at rest (baseline) and in all 17 enrolled players following a season game. RESULTS: Lactate and venous cfDNA increased more pronounced during "short" compared to "long" (1.4-fold, p = 0.032 and 1.7-fold, p = 0.016) and cfDNA correlated significantly with lactate (r = 0.69; p<0.001). Incremental exercise testing increased cfDNA 7.0-fold (p<0.001). The season game increased cfDNA 22.7-fold (p<0.0001), while lactate showed a 2.0-fold (p = 0.09) increase compared to baseline. Fold-changes in cfDNA correlated with distance covered during game (spearman's r = 0.87, p = 0.0012), while no correlation between lactate and the tracking data could be found. DISCUSSION: We show for the first time that cfDNA could be an objective marker for distance covered in elite intermittent sports. In contrast to the potential of more established blood-based markers like IL-6, CK, or CRP, cfDNA shows by far the strongest fold-change and a high correlation with a particular load related aspect in professional football.