MIP sensors – the electrochemical approach

This review highlights the importance of coupling molecular imprinting technology with methodology based on electrochemical techniques for the development of advanced sensing devices. In recent years, growing interest in molecularly imprinted polymers (MIPs) in the preparation of recognition elements has led researchers to design novel formats for improvement of MIP sensors. Among possible approaches proposed in the literature on this topic, we will focus on the electrosynthesis of MIPs and on less common hybrid technology (e.g. based on electrochemistry and classical MIPs, or nanotechnology). Starting from the early work reported in this field, an overview of the most innovative and successful examples will be reviewed.     

Phonon dynamics and electron-phonon coupling in pristine picene

The paper reports a complete analysis of the phonon structure of crystalline picene, a recently announced organic semiconductor. Both lattice and intramolecular vibrations are investigated. An exhaustive assignment of lattice phonons is obtained through polarized Raman spectra assisted by lattice dynamics calculations based on a well tested atom-atom potential model. Raman, infrared spectra and density functional (DFT) calculations are used for the characterization of intramolecular modes. Coupling between low-frequency molecular vibrations and lattice phonons is accounted for. Molecule-to-molecule transfer integrals, as well as the Peierls and Holstein (non-local and local) coupling constants, are evaluated through the semiempirical method INDO/S (Intermediate Neglect of Differential Overlap with Spectroscopic parametrization).     

NIR emitting ytterbium chelates for colourless luminescent solar concentrators

A new oxyiminopyrazole-based ytterbium chelate enables NIR emission upon UV excitation in colorless single layer luminescent solar concentrators for building integrated photovoltaics.     

Transient photothermal spectra of plasmonic nanobubbles

The photothermal efficacy of near-infrared gold nanoparticles (NP), nanoshells, and nanorods was studied under pulsed high-energy optical excitation in plasmonic nanobubble (PNB) mode as a function of the wavelength and duration of the excitation laser pulse. PNBs, transient vapor nanobubbles, were generated around individual and clustered overheated NPs in water and living cells. Transient PNBs showed two photothermal features not previously observed for NPs: the narrowing of the spectral peaks to 1 nm and the strong dependence of the photothermal efficacy upon the duration of the laser pulse. Narrow red-shifted (relative to those of NPs) near-infrared spectral peaks were observed for 70 ps excitation laser pulses, while longer sub- and nanosecond pulses completely suppressed near-infrared peaks and blue shifted the PNB generation to the visual range. Thus, PNBs can provide superior spectral selectivity over gold NPs under specific optical excitation conditions.     

Reconfigurable silicon filter with continuous bandwidth tunability

We present the design and the fabrication of compact tunable silicon-on-insulator bandpass filters based on the integration of a Mach-Zehnder interferometer with ring resonators and activated via thermo-optic phase shifters. The proposed architecture provides wide filter bandwidth tunability from 10% to 90% of the free spectral range preserving the filter off-band rejection. Possible applications are channel subset selection in wavelength division multiplexing optical systems, adaptive filtering to signal bandwidth, and reconfigurable filters for gridless networking.     

Captured at last: a catalyst-substrate adduct and a Rh-dihydride solvate in the asymmetric hydrogenation by a Rh-monophosphine catalyst

The mechanism of asymmetric hydrogenation catalyzed by [Rh(NBD)((R)-PhenylBinepine)(2)]SbF(6)1 has been studied by NMR experiments and DFT computations. Either the low-temperature hydrogenation of the catalyst-substrate adduct 4 or the reaction of solvate dihydride 6 with MAC produced the hydrogenation product with over 99% ee (S).     

Development of a chemiluminescence-based quantitative lateral flow immunoassay for on-field detection of 2,4,6-trinitrotoluene

Simple, rapid and highly sensitive assays, possibly allowing on-site analysis, are required in the security and forensic fields or to obtain early signs of environmental pollution. Several bioanalytical methods and biosensors based on portable devices have been developed for this purpose. Among them, Lateral Flow ImmunoAssays (LFIAs) offer the advantages of rapidity and ease of use and, thanks to the high specificity of antigen–antibody binding, allow greatly simplifying and reducing sample pre-analytical treatments. However, LFIAs usually employ colloidal gold or latex beads as labels and they rely on the formation of colored bands visible by the naked eye. With this assay format, only qualitative or semi-quantitative information can be obtained and low sensitivity is achieved. Recently, the use of enzyme-catalyzed chemiluminescence detection in LFIA has been proposed to overcome these problems. In this work, we describe the development of a quantitative CL-LFIA assay for the detection of 2,4,6-trinitrotoluene (TNT) in real samples. Thanks to the use of a portable imaging device for CL signal measurement based on a thermoelectrically cooled CCD camera, the analysis could be performed directly on-field. A limit of detection of 0.2 μg mL⁻¹ TNT was obtained, which is five times lower than that obtained with a previously described colloidal gold-based LFIA developed employing the same immunoreagents. The dynamic range of the assay extended up to 5 μg mL⁻¹ TNT and recoveries ranging from 97% to 111% were obtained in the analysis of real samples (post blast residues obtained from controlled explosion).     

Phase transitions for random walk asymptotics on free products of groups

Suppose we are given finitely generated groups Γ₁,…,Γ_m equipped with irreducible random walks. Thereby we assume that the expansions of the corresponding Green functions at their radii of convergence contain only logarithmic or algebraic terms as singular terms up to sufficiently large order (except for some degenerate cases). We consider transient random walks on the free product Γ₁* … *Γ_m and give a complete classification of the possible asymptotic behaviour of the corresponding n‐step return probabilities. They either inherit a law of the form ?^nδn log n from one of the free factors Γ_i or obey a ?^nδn^?3/2‐law, where ? < 1 is the corresponding spectral radius and δ is the period of the random walk. In addition, we determine the full range of the asymptotic behaviour in the case of nearest neighbour random walks on free products of the form $\mathbb{Z}^{d_1}\ast \ldots \ast \mathbb{Z}^{d_m}Suppose we are given finitely generated groups Γ₁,…,Γ_m equipped with irreducible random walks. Thereby we assume that the expansions of the corresponding Green functions at their radii of convergence contain only logarithmic or algebraic terms as singular terms up to sufficiently large order (except for some degenerate cases). We consider transient random walks on the free product Γ₁* … *Γ_m and give a complete classification of the possible asymptotic behaviour of the corresponding n‐step return probabilities. They either inherit a law of the form ?^nδn log n from one of the free factors Γ_i or obey a ?^nδn^?3/2‐law, where ? < 1 is the corresponding spectral radius and δ is the period of the random walk. In addition, we determine the full range of the asymptotic behaviour in the case of nearest neighbour random walks on free products of the form $\mathbb{Z}^{d_1}\ast \ldots \ast \mathbb{Z}^{d_m}$. Moreover, we characterize the possible phase transitions of the non‐exponential types n log n in the case Γ₁ * Γ₂. © 2011 Wiley Periodicals, Inc. Random Struct. Alg., 2012