Electrochemical wettability control on conductive TiO2 nanotube surfaces modified with a ferrocene redox system

This work reports on an electrochemical system which allows the control of surface wettability properties by voltage induced changes in contact angle (Θ) of ΔΘ  50°. For this we used conductive TiO₂ nanotubular layers that were modified with ferrocene coupled to the TiO₂ surface via triethoxysilane. To enhance the hydrophobic character of the nanotubular TiO₂ surface, also mixed organic monolayers namely perfluorotriethoxysilane, were explored. Formation of the ferrocene and mixed organic monolayer was confirmed by X-ray-photoelectron-spectroscopy (XPS). Contact angle combined with electrochemical measurements show that ferrocene in these monolayers can successfully be switched from Fe²⁺ to Fe³⁺ and that this change in the redox state considerably alters the wetting properties. Using a conductive nanotube substrate allows us to amplify this change by a factor of more than 10, and thus this surface can be used to trigger significant wetting alterations.     

Raman and ATR FTIR spectroscopy in reactive crystallization: Simultaneous monitoring of solute concentration and polymorphic state of the crystals

Batch-reactive crystallization of the two polymorphs of l-glutamic acid was studied using in-line Raman and ATR FTIR spectroscopy. It was observed that the barrier to the nucleation of the stable β-form was higher, and thus the occurrence of β-form nucleation requires a higher supersaturation level. The local supersaturation level inside the reactive crystallizer is significantly affected by the feeding manner of the reactant. When the reactant was fed to a poorly mixed zone, such as the surface of the liquid, a high local supersaturation level was generated near the feeding point. This high local supersaturation level drastically increased with the increase in the concentrations of the reactants. As a consequence, the fraction of the β-form increased with the increase in reactants concentrations. On the other hand, feeding the reactant to a well-mixed zone near the impeller can avoid the occurrence of high local supersaturation, and therefore the dependence of the polymorphic composition of the final product on the concentration of the reactants can be reduced. The information obtained from the spectroscopy leads to improved understanding of the precipitation process and offers great potential for process optimization and control of crystalline quality.     

Bulky Phosphinines: From a Molecular Design to an Application in Homogeneous Catalysis

The design and preparation of an asymmetrically substituted and bulky phosphinine was achieved by introducing sterically demanding substituents into specific positions of a rigid phosphorus‐heterocyclic framework. Compound 5 shows, at the same time, axial chirality and a sufficiently high energy barrier for internal rotation to prevent enantiomerization. Both enantiomers of 5 were isolated by means of chiral analytical HPLC, and their absolute configurations could be assigned by combining experimental data and DFT calculations. Despite its substitution pattern, 5 can still coordinate to transition‐metal centers through the lone pair of electrons on the phosphorus atom. Rapid C? H activation on the adjacent aryl substituent at the 2‐position of the phosphorus heterocycle was achieved by using [{Cp*IrCl₂}₂] (Cp*=1,2,3,4,5‐pentamethylcyclopentadienyl) as a metal precursor. A racemic mixture of 5 was applied as a π‐accepting low‐coordinate phosphorus ligand in the Rh‐catalyzed hydroformylation of trans‐2‐octene, which showed a clear preference for the formation of 2‐methyloctanal.     

Utilising thermoporometry to obtain new insights into nanostructured materials

Thermoporometry is a relatively new method of characterising porous properties of nanostructured materials based on observation of solid–liquid phase transitions of materials confined in pores. It provides several advantages over the conventional characterisation methods, mercury porosimetry and gas sorption. The advantages include possibility of using short measurement times, non-toxic chemicals and wet samples. In addition, complicated sample preparation and specialised instruments are not required. Therefore, it has a great potential of becoming a widely utilised characterisation method, although its potential has not yet been widely realised. In recent years, there has been a significant increase in research activities regarding the method. In the second part of the review, results and conclusions of the recent studies about thermoporometry are surveyed and discussed focusing on the application of thermoporometry in extracting various structural information from the porous materials.     

Note on multidimensional Breeden–Litzenberger representation for state price densities

In this note, we consider European options of type $h(X^1_T, X^2_T,\ldots , X^n_T)$ depending on several underlying assets. We give a multidimensional version of the result of Breeden and Litzenberger (J Bus 51:621–651, 1978) on the relation between derivatives of the call price and the risk-neutral density of the underlying asset. The pricing measure is assumed to be absolutely continuous with respect to the Lebesgue measure on the state space.     

Development of a GPU-based high-performance radiative transfer model for the Infrared Atmospheric Sounding Interferometer (IASI)

Satellite-observed radiance is a nonlinear functional of surface properties and atmospheric temperature and absorbing gas profiles as described by the radiative transfer equation (RTE). In the era of hyperspectral sounders with thousands of high-resolution channels, the computation of the radiative transfer model becomes more time-consuming. The radiative transfer model performance in operational numerical weather prediction systems still limits the number of channels we can use in hyperspectral sounders to only a few hundreds. To take the full advantage of such high-resolution infrared observations, a computationally efficient radiative transfer model is needed to facilitate satellite data assimilation. In recent years the programmable commodity graphics processing unit (GPU) has evolved into a highly parallel, multi-threaded, many-core processor with tremendous computational speed and very high memory bandwidth. The radiative transfer model is very suitable for the GPU implementation to take advantage of the hardware’s efficiency and parallelism where radiances of many channels can be calculated in parallel in GPUs.In this paper, we develop a GPU-based high-performance radiative transfer model for the Infrared Atmospheric Sounding Interferometer (IASI) launched in 2006 onboard the first European meteorological polar-orbiting satellites, METOP-A. Each IASI spectrum has 8461 spectral channels. The IASI radiative transfer model consists of three modules. The first module for computing the regression predictors takes less than 0.004% of CPU time, while the second module for transmittance computation and the third module for radiance computation take approximately 92.5% and 7.5%, respectively. Our GPU-based IASI radiative transfer model is developed to run on a low-cost personal supercomputer with four GPUs with total 960 compute cores, delivering near 4 TFlops theoretical peak performance. By massively parallelizing the second and third modules, we reached 364× speedup for 1 GPU and 1455× speedup for all 4 GPUs, both with respect to the original CPU-based single-threaded Fortran code with the –O₂ compiling optimization. The significant 1455× speedup using a computer with four GPUs means that the proposed GPU-based high-performance forward model is able to compute one day’s amount of 1,296,000 IASI spectra within nearly 10 min, whereas the original single CPU-based version will impractically take more than 10 days. This model runs over 80% of the theoretical memory bandwidth with asynchronous data transfer. A novel CPU–GPU pipeline implementation of the IASI radiative transfer model is proposed. The GPU-based high-performance IASI radiative transfer model is suitable for the assimilation of the IASI radiance observations into the operational numerical weather forecast model.     

Lindelöf type of generalization of separability in Banach spaces

We will introduce the countable separation property (CSP) of Banach spaces X, which is defined as follows: X has CSP if each family E of closed linear subspaces of X whose intersection is the zero space contains a countable subfamily E₀ with the same intersection. All separable Banach spaces have CSP and plenty of examples of non-separable CSP spaces are provided. Connections of CSP with Marku?evi?-bases, Corson property and related geometric issues are discussed.     

Hydrolytic reactions of thymidine 5'-o-phenyl-N-alkylphosphoramidates, models of nucleoside 5'-monophosphate prodrugs

To obtain detailed data on the kinetics of hydrolytic reactions of triester-like nucleoside 5'-O-aryl-N-alkylphosphoramidates, potential prodrugs of antiviral nucleoside monophosphates, the hydrolysis of diastereomeric (Rp/Sp) thymidine 5'-{O-phenyl-N-[(1S)-2-oxo-2-methoxy-1-methylethyl]phosphoramidate} (3), a phosphoramidate derived from the methyl ester of L-alanine, has been followed by reversed-phase HPLC over the range from Ho=0 to pH 8 at 90 degrees C. According to the time-dependent product distributions, the hydrolysis of 3 proceeds at pH<4 by two parallel routes, namely by nucleophilic displacement of the alaninyl ester moiety by a water molecule and by hydrolysis of the carboxylic ester linkage that allows intramolecular attack of the carboxy group on the phosphorus atom, thereby resulting in the departure of either thymidine or phenol without marked accumulation of any intermediates. Both routes represent about half of the overall disappearance of 3. The departure of phenol eventually leads to the formation of thymidine 5'-phosphate. At pH>5, the predominant reaction is hydrolysis of the carboxylic ester linkage followed by intramolecular displacement of a phenoxide ion by the carboxylate ion and hydrolysis of the resulting cyclic mixed anhydride into an acyclic diester-like thymidine 5'-phosphoramidate. The latter product accumulated quantitatively without any indication of further decomposition. Hydroxide-ion-catalyzed P--OPh bond cleavage of the starting material 3 occurred as a side reaction. Comparative measurements with thymidine 5'-{N-[(1S)-2-oxo-2-methoxy-1-methylethyl]phosphoramidate} (4) revealed that, under acidic conditions, this diester-like compound is hydrolyzed by P--N bond cleavage three orders of magnitude more rapidly than the triester-like 3. At pH>5, the stability order is reversed, with 3 being hydrolyzed six times as rapidly as 4. Mechanisms of the partial reactions are discussed.