Discrete Hf18 Metal-oxo Cluster as a Heterogeneous Nanozyme for Site-Specific Proteolysis

The selective hydrolysis of proteins by non-enzymatic catalysis is difficult to achieve, yet it is crucial for applications in biotechnology and proteomics. Herein, we report that discrete hafnium metal-oxo cluster [Hf₁₈O₁₀(OH)₂₆(SO₄)₁₃⋅(H₂O)₃₃] ( Hf₁₈ ), which is centred by the same hexamer motif found in many MOFs, acts as a heterogeneous catalyst for the efficient hydrolysis of horse heart myoglobin (HHM) in low buffer concentrations. Among 154 amino acids present in the sequence of HHM, strictly selective cleavage at only 6 solvent accessible aspartate residues was observed. Mechanistic experiments suggest that the hydrolytic activity is likely derived from the actuation of Hf^IV Lewis acidic sites and the Brønsted acidic surface of Hf₁₈ . X-ray scattering and ESI-MS revealed that Hf₁₈ is completely insoluble in these conditions, confirming the HHM hydrolysis is caused by a heterogeneous reaction of the solid Hf₁₈ cluster, and not from smaller, soluble Hf species that could leach into solution.     

Pattern replication in blends of semiconducting and insulating polymers casted by horizontal dipping

Pattern replication in solution‐deposited thin films of insulating and conjugated polymer mixtures might provide an alternative to spatially resolved printing techniques for the fabrication of polymer‐based circuitries. Though it has been previously shown that phase separation in the course of spin‐casting leads to the formation of domain structures resembling the chemical patterns pre‐set on the film substrate, finding optimal casting conditions is a tedious process, which requires multiple sample preparations. Here, we have demonstrated pattern replication in a mixture of poly(3,3′′′‐didodecyl quarter thiophene) (PQT‐12) and deuterated poly(styrene‐co?4‐bromostyrene) (dPBrS) deposited by horizontal‐dipping on substrates, patterned with self‐assembling molecules by micro‐contact printing. Moreover, we show that casting conditions for accomplishing pattern replication can be efficiently screened by preparing thickness gradient samples. We have optimized the reconstruction of the substrate pattern in the PQT‐12:dPBrS film. Our results prove that desired structures of semiconducting and insulating polymers can be produced in a simple, high‐throughput technological process. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 1419–1426     

High-frequency EPR applications of open nonradiative resonators

A new class of open single-mode cavities, the nonradiative (NR) resonators, has recently been proposed in order to overcome the limitations of standard cylindrical cavities and Fabry-Perot resonators at millimeter wavelengths. This paper presents the first applications of a NR resonator in W-band pulsed electron paramagnetic resonance spectroscopy. It consists of a cylindrical cavity having a lateral aperture that represents about 35% of its total height. Electron-spin-echo measurements performed on different samples show that the signal-to-noise ratio and the optimal pulse length obtained with the proposed device are comparable to those obtained with the closed cavity used in the commercial W-band spectrometer, at both cryogenic and room temperature. Similar results have been obtained for paramagnetic species optically activated by means of an optical fiber inserted in the aperture of the resonator. The insertion losses estimated for the probe employed with the NR resonator are higher than those of the commercial probe, hence, demonstrating that the proposed cavity holds the promise of improved resonator performance.     

Analysis of chlortetracycline and related substances by capillary zone electrophoresis: Development and validation

Summary A capillary zone electrophoresis method has been developed and validated for the analysis of chlortetracycline and related substances. The influence of the type of buffer, pH and concentration of the buffer were investigated. In all cases 1 mM EDTA was added to prevent metal ion complexation. Instrumental parameters such as capillary temperature and applied voltage were optimised. The following methods is proposed: capillary: fused silica, 44 cm (36 cm effective length), 50 μm i.d.; buffer: 120 mM sodium tetraborate including 1mM EDTA at pH 8.5; voltage: 10 kV; temperature: 25°C; detection wavelength: 280 nm. The robustness of the method has been examined by means of a full-fraction factorial design. The parameters for validation namely relative standard deviation, linearity, precision, limit of detection and limit of quantitation are also reported.     

Molecular orientation and composition at the surface of spin‐coated polyfluorene:Fullerene blend films

The surface composition in spin‐coated films of polyfluorene:fullerene blends was determined quantitatively by near‐edge X‐ray absorption fine structure (NEXAFS) spectroscopy. By comparing partial and total electron yield spectra, we found vertical compositional differences in the surface region. Furthermore, the orientation of the polymer chains was investigated by variable‐angle NEXAFS. Blend films of poly[(9,9‐dioctylfluorenyl‐2,7‐diyl)‐co‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole] with [6,6]‐phenyl‐C61‐butyric acid methyl ester in two different blend ratios were studied. Results showed polymer enrichment of the surfaces for films with a polymer:fullerene weight ratio of 20:80 and of 50:50, spin‐coated from both chlorobenzene and chloroform solutions. The angular dependence of the NEXAFS spectra of the pure polymer films showed a preferential plane‐on orientation, which was slightly stronger in the subsurface region than at the surface. In blend films, this orientational preference was less pronounced and the difference between surface and subsurface vanished. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

The solid-state organization of 'self-doped' PPV oligomers

Using a combination of multi-frequency EPR and NMR spectroscopy and quantum-chemical calculations at the level of Density Functional Theory (DFT), the organization of self-doped PPV oligomers in their solid state is investigated. The analysis of the different spectra shows that the electrochemical procedure used to self-dope these materials produces positive radicals (polarons) in an almost quantitative way, but still magnetically isolated polarons are observed. The difference between chemical and electrochemical oxidation of the oligomers is studied in detail. Furthermore, ageing of the electrochemically oxidized oligomers may be accompanied by a stacking of the oligomers.     

Interlayer exchange coupling,crystalline and magnetic structure in Fe/CsCl–FeSi multilayers grown by molecular beam epitaxy

Crystalline and magnetic structure as well as the interlayer exchange coupling in MBE grown Fe/FeSi multilayers are investigated. From conversion electron Mössbauer spectroscopy and ion beam channeling measurements the spacer FeSi material is found to be stabilized in a crystalline metastable metallic FeSi phase with the CsCl structure. Strong non-oscillatory interlayer exchange coupling is identified with magnetometry and synchrotron Mössbauer reflectometry. From the fits of the time spectrum and the resonant ?—? scans a model for the sublayer magnetization of the multilayer is deduced.

     

Growth and characterization of thin PTCDA films on 3C-SiC(0 0 1)c(2 × 2)

The growth of thin 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA) films on a 3C-SiC(0 0 1)c(2 × 2) substrate has been studied by means of photoelectron spectroscopy (PES) and atomic force microscopy (AFM). In the first monolayer the molecules interact with the substrate mainly through the O atoms in the end groups of the molecule. The O atoms have a higher binding energy in the first molecular layer compared to the following layers. No chemical shifts are observed in the Si 2p spectra or in the C 1s spectra from the perylene core of the molecules. From the VB spectra and LEED pattern we conclude that the substrate remains in the c(2 × 2) reconstruction after PTCDA deposition. For thicker films a Stranski-Krastanov film growth was observed with flat lying molecules relative to the substrate.     

Mössbauer spectroscopy investigation of body centered cubic Co in Co/Fe superlattices prepared with MBE

A new spectrum component is observed in Mössbauer spectra of thin body centered cubic Co layers prepared in Fe/Co superlattices doped with⁵⁷Co. It is characterized by a large magnetic hyperfine field (31.2 T) and an isomer shift nearly equal to that of -Fe. The decrease of the isomer shift in bcc Co with respect to hcp Co is consistent with smaller s to d charge transfer in bcc Co as compared to hcp Co. The cubic structure of the CoFe superlattices is evidenced with X-ray diffraction and ion-channeling measurements. The Fe/Co interface is investigated with conversion electron Mössbauer spectroscopy. It is shown that the interface alloy thickness is about six monolayers for growth temperatures up to 450 K and that increasing alloying occurs for higher growth temperatures.