Dipicolylglycyl-phenylalanine zinc(II): a metallopeptide with a built-in conformational switch and its homochiral helical coordination polymer

The peptide-zinc complex [(Dpg-Phe)Zn]2+ (Dpg = N,N-dipicolylglycine; Phe = phenylalanine) reversibly forms a homochiral P-helical coordination polymer upon switching the pH from mildly basic to mildly acidic.     

Piezoelectricity of porous polytetrafluoroethylene single- and multiple-film electrets containing high charge densities of both polarities

Single-film bipolar electrets of porous polytetrafluoroethylene are generated by means of a two-step corona-charging process at elevated temperatures. Quasi-static direct piezoelectric coefficients of up to 0.15 nC/N have been observed on these films. In addition, multiple-layer stacks of porous and non-porous polytetrafluoroethylene films with monopolar charge were also investigated. While the piezoelectric responses of the stacks were not as high as those of the single films, the multiple-film arrangements may have other advantages such as better electrical shielding or tunable mechanical properties and adjustable acoustical impedance. Our new results are discussed in the context of the emerging field of porous polymer electrets with many potential device applications.     

The SYM integrable super spin chain

Recently it was established that the one-loop planar dilatation generator of super-Yang–Mills theory may be identified, in some restricted cases, with the Hamiltonians of various integrable quantum spin chains. In particular Minahan and Zarembo established that the restriction to scalar operators leads to an integrable vector chain, while recent work in QCD suggested that restricting to twist operators, containing mostly covariant derivatives, yields certain integrable Heisenberg XXX chains with non-compact spin symmetry . Here we unify and generalize these insights and argue that the complete one-loop planar dilatation generator of is described by an integrable super spin chain. We also write down various forms of the associated Bethe ansatz equations, whose solutions are in one-to-one correspondence with the complete set of all one-loop planar anomalous dimensions in the gauge theory. We finally speculate on the non-perturbative extension of these integrable structures, which appears to involve non-local deformations of the conserved charges.     

On-line electrochemically controlled solid-phase extraction interfaced to electrospray and inductively coupled plasma mass spectrometry

Electrochemically controlled solid-phase extractions of anions were interfaced on-line to electrospray mass spectrometry (ESI-MS) and inductively coupled plasma mass spectrometry (ICP-MS), using polypyrrole coated electrodes and a thin-layer electrochemical (EC) flow cell. The results indicate that electrochemically controlled solid-phase extraction (EC-SPE) can be used as a versatile potential controlled sample preparation technique for a range of anions and that the properties of the polypyrrole coatings can be modified by altering the electrodeposition conditions. In the present study, the influence of interfering anions (i.e., fluoride and sulfate), and the anion used during the electropolymerisation, on the bromide extraction recovery was investigated for EC-SPE interfaced to ICP-MS. The results of these experiments show that the interference due to the presence of similar concentrations of sulfate can be reduced when using a polypyrrole coating electropolymerised in the presence of bromide ions. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) measurements were also used to study the morphology of the coatings, as well as the variations in the film thickness within the coatings. The effect of different desorption techniques on the bromide preconcentration factor in the ICP-MS on-line flow system was also examined. Stopped-flow desorption was found to give rise to significantly increased preconcentration factors in comparison with desorptions in flowing solutions. While the desorption efficiency depends on the type of desorption electrolyte (the electrolyte in which the desorption takes place), due to the competing influx of cations, the influence of the pH on the switching charge of the polypyrrole coating was found to be small, at constant ionic strength. To study the applicability of the EC-SPE technique with respect to real samples, investigations were also made with tap water samples spiked with different bromide concentrations. The results of these experiments, which were carried out using a modified thin-layer EC flow cell allowing in situ polymerisation of polypyrrole yielding a polymer plug covering the cross section of the channel, demonstrate that 3 microM concentrations of bromide could be detected in the tap water sample. This demonstrates that the extraction technique allows extractions of low concentrations of ions in the presence of significantly higher concentrations of other similar ions. The fact that the extraction and desorption steps are electrochemically controlled makes EC-SPE particularly well suited for inclusion in miniaturised lab-on-a-chip systems.     

Discovery of Highly Selective Alkyne Semihydrogenation Catalysts Based on First‐Row Transition‐Metallated Porous Organic Polymers

Five different first‐row transition metal precursors (V^III, Cr^III, Mn^II, Co^II, Ni^II) were successfully incorporated into a catechol porous organic polymer (POP) and characterized using ATR‐IR and XAS analysis. The resulting metallated POPs were then evaluated for catalytic alkyne hydrogenation using high‐throughput screening techniques. All POPs were unexpectedly found to be active and selective catalysts for alkyne semihydrogenation. Three of the metallated POPs (V, Cr, Mn) are the first of their kind to be active single‐site hydrogenation catalysts. These results highlight the advantages of using a POP platform to develop new catalysts which are otherwise difficult to achieve through traditional heterogeneous and homogeneous routes.