Syntheses and Crystal Structures of 4,5-Dihydro-2-(2′-hydroxyphenyl)oxazole-Containing Metal Complexes

The synthesis of the complexes 3 of various metals ligated to chiral 4,5-dihydro-2-(2′-oxidophenyl-?O)oxazoles-?N is described (Scheme). Three of them, i.e. 3a , 3e , and 3f containing Cu^II, Zn^II and Ni^II, respectively, were analyzed by X-ray diffraction studies. A series of Cu^II complexes ( 6a – d ) with differently substituted dihydrooxazoles have been synthesized.     

Long-term characteristics of analogical processing in high-school students with high fluid intelligence: an fMRI study

Intelligence is known to predict scholastic achievement and enables high performance in cognitive tasks. Fluid intelligence is strongly related to analogical reasoning abilities, which are fundamental to mathematical thinking. Geometric analogical reasoning is a prototypical measure of fluid intelligence. However, the cerebral correlates of geometric analogical reasoning and their developmental modulation over time are still rarely investigated. We report a 1-year follow-up functional magnetic resonance imaging study of a geometric analogical reasoning task in high fluid intelligence high-school students. This study was designed to characterise the cerebral correlates of geometric analogical reasoning and to improve our knowledge about the impact of general cognitive development on behavioural performance and on cerebral mechanisms underlying geometric analogical reasoning in adolescents. Our data indicate that a fronto-parietal network comprising the left and right parietal lobes and the left middle frontal gyrus was equally modulated by task difficulty at both measuring time points. At the behavioural level, however, participants showed improvements in performance at the second measuring time point. The behavioural improvements point to a more efficient task processing. As this is not accompanied by differential recruitment of fronto-parietal brain regions, the data suggest an increase in neural efficiency for these brain regions.     

Chiral Excitonic Organic Photodiodes for Direct Detection of Circular Polarized Light

A facile route to soft matter self‐powered bulk heterojunction photodiode detectors sensitive to the circular polarization state of light is shown based on the intrinsic excitonic circular dichroism of the photoactive layer blend. As light detecting materials, enantiopure semiconducting small molecular squaraine derivates of opposite handedness are employed. Via Mueller matrix ellipsometry, the circular dichroism is proven to be of H‐type excitonic nature and not originating from mesoscopic structural ordering. Within the green spectral range, the photodiodes convert circular polarized light into a handedness‐dependent photocurrent with a maximum dissymmetry factor of ±0.1 corresponding to 5% overall efficiency for the polarization discrimination under short circuit conditions. On the basis of transfer matrix optical simulations, it is rationalized that the optical dissymmetry fully translates into a photocurrent dissymmetry for ease of device design. Thereby, the photodiode's ability to efficiently distinguish between left and right circularly polarized light without the use of external optical elements and voltage bias is demonstrated. This allows a straightforward and sustainable future design of flexible, lightweight, and compact integrated platforms for chiroptical imaging and sensing.     

Metabolic Tumor Imaging with Rapidly Signal-Enhanced 1-13C-Pyruvate-d3

The metabolism of malignant cells differs significantly from that of healthy cells and thus, it is possible to perform metabolic imaging to reveal not only the exact location of a tumor, but also intratumoral areas of high metabolic activity. Herein, we demonstrate the feasibility of metabolic tumor imaging using signal-enhanced 1-¹³C-pyruvate-d₃, which is rapidly enhanced via para-hydrogen, and thus, the signal is amplified by several orders of magnitudes in less than a minute. Using as a model, human melanoma xenografts injected with signal-enhanced 1-¹³C-pyruvate-d3, we show that the conversion of pyruvate into lactate can be monitored along with its kinetics, which could pave the way for rapidly detecting and monitoring changes in tumor metabolism.     

Kinetics of Hydride Abstractions from 2‐Arylbenzimidazolines

The rates of the hydride abstractions from the 2‐aryl‐1,3‐dimethyl‐benzimidazolines 1a – f by the benzhydrylium tetrafluoroborates 3a – e were determined photometrically by the stopped‐flow method in acetonitrile at 20 °C. The reactions follow second‐order kinetics, and the corresponding rate constants k₂ obey the linear free energy relationship log k₂(20 °C)= s(N+E), from which the nucleophile‐specific parameters N and s of the 2‐arylbenzimidazolines 1a – c have been derived. With nucleophilicity parameters N around 10, they are among the most reactive neutral C? H hydride donors which have so far been parameterized. The poor correlation between the rates of the hydride transfer reactions and the corresponding hydricities (ΔH⁰) indicates variable intrinsic barriers.     

Characterization of self-assembled supramolecular [Ga4L6] host-guest complexes by electrospray ionization mass spectrometry

Self-assembled supramolecular host-guest complexes have been characterized by electrospray ionization mass spectrometry. The spectra obtained by use of a Q-TOF instrument equipped with a Z-spray ion source show primarily the 3- and 4- charge states of the assemblies. The assemblies have the general formula [guest subset Ga4L6]11- where L represents the chelating bidentate catechol ligand 1,5-bis(2',3'-dihydroxy-benzamido)naphthalene and guests are tetramethyl ammonium (Me4N+), tetraethyl ammonium (Et4N+), tetra-n-propyl ammonium (Pr4N+) and decamethylcobaltocenium (Cp*2Co+) cations. For the first time, the mass spectrum of the empty assembly [Ga4L6]12- is reported. This article also reports that provided the electrospray ion source is capable of preserving noncovalent interactions, it is possible to observe host-guest complexes containing both weak binding guests as well as sterically demanding guests in the mass spectra. The present data suggest that electrospray mass spectrometry is a powerful tool for characterization of supramolecular host-guest complexes.     

Improvement of ITO-free inverted polymer-based solar cells by using colloidal zinc oxide nanocrystals as electron-selective buffer layer

In this study, we report on the improvement of ITO-free inverted polymer/fullerene solar cells by introducing a zinc oxide (ZnO) layer between the active layer and the cathode. The ZnO layers are deposited from solution, using colloidal ZnO nanocrystals with a rodlike shape, which are obtained using a wet-chemical synthesis route at low temperature. The nanocrystals are widely characterized with respect to their structural, optical, and electronic properties. In particular, simulations of powder X-ray diffraction data based on Rietveld refinement are shown to be a suitable method to characterize the average crystallite shape and particle size. Cyclic voltammetry reveals that nanocrystalline ZnO is an appropriate choice as electron-selective buffer layer in organic solar cells based on a bulk heterojunction of poly (3-hexylthiophene) (P3HT) and [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM). Using ITO-free inverted solar cells in substrate configuration with an opaque Cr/Al/Cr bottom electrode, we demonstrate that introducing a cathodic interlayer of ZnO nanocrystals leads to a notable enhancement in photovoltaic performance. The magnitude of the effect is found to depend on the solvents used to process the active layer. In case of absorber blends processed from o-dichlorobenzene, we show an almost threefold increase in efficiency from 0.8 to 2.2% at an active area of 1 cm².