A hypervalent pentacoordinate boron compound with an N-B-N three-center four-electron bond

For the purpose of synthesizing and characterizing hypervalent boron compounds with strong hypervalent interaction, we have prepared a boron compound with a tridentate ligand bearing two pyrimidine rings as nitrogen donors. X-ray analysis and molecular orbital calculations suggested that the boron compound was of hypervalent pentacoordinate structure with an N-B-N hypervalent bond. Thus, we have prepared the first hypervalent second row element compound with apical N coordination. A breakdown of energy contributions by DFT calculations revealed that the N-B-N bond energy of the pentacoordinate state ground state (13) was 2.8 kcal mol(-1). Implications were that the conjugation energy difference of 6.6 kcal mol(-1) (14.2-7.6 kcal mol(-1)) with the tetracoordinate state was a crucial factor for shifting stability toward the pentacoordinate structure.     

Separation of lead from high matrix electroless nickel plating waste solution using an ion-selective immobilized macrocycle system

Separation of trace levels of lead from concentrated-matrix electroless nickel plating (ENP) waste solutions is required to meet the increasingly stringent environmental regulations. A solid phase extraction (SPE) system using a molecular recognition technology (MRT) gel was used for the selective separation of trace levels of lead (Pb) from the waste discharge of ENP operations, followed by subsequent analysis with inductively coupled plasma optical emission spectrometry (ICP-OES). Two SPE-MRTs, AnaLig® Pb-01 and AnaLig® Pb-02, packed in 3 mL polypropylene cartridges were used to treat the synthetic metal-waste solutions that were used to simulate the typical metal mixture in ENP bath waste. The fortified solutions contained 100-1000 μg L^− 1 of Pb in an HNO₃ matrix with pre-added Ni, Cu and other interfering elements (1000 mg L^− 1). After the sample treatment, the SPE-MRT cartridges were washed with water and 0.1 M nitric acid, followed by elution with 0.03 M EDTA. The matrix elements (e.g., Ni, Cu) were completely removed at the washing step, while the ‘captured’ Pb was quantitatively eluted, as determined by ICP-OES measurements. The detection limit of the proposed method was 2.6 μg L^− 1. ‘Real’ samples from commercial ENP operations were used to assess the validity of this method, and almost quantitative Pb recovery was observed. The excellent Pb selectivity of the SPE-MRT system indicates the potential of the proposed technique for trace-level Pb separation from the Pb-containing high matrix aqueous waste discharge.     

Prorocentrol, a polyoxy linear carbon chain compound isolated from the toxic dinoflagellate Prorocentrum hoffmannianum

A polyoxy linear carbon chain compound, prorocentrol (1), was isolated from cultured cells of the dinoflagellate Prorocentrum hoffmannianum, which produces a polyether carboxylic acid, okadaic acid. The structure of 1 was elucidated by detailed analyses of 2D NMR spectra. Compound 1 possesses 30 hydroxy groups, 1 ketone, and 8 double bonds on the C65-linear carbon chain. Its partial relative configuration was deduced by the proton-proton and long-range carbon-proton coupling constants, and compound 1 showed moderate cytotoxicity and antidiatom activity.     

Echolocation and flight strategy of Japanese house bats during natural foraging, revealed by a microphone array system

Using only a microphone array system, echolocation pulses and three-dimensional flight paths in the frequency-modulated bat, Pipistrellus abramus, during natural foraging, were simultaneously examined. During the search phase, the inter-pulse interval, pulse duration, and moving distance of the bat between successive emissions were relatively constant at around 89.5 ± 18.7 ms, 6.90 ± 1.31 ms, and 0.50 ± 0.20 m, respectively. The bats started to decrease these acoustical parameters within 2-3 m of the prey capture point. For every emission along a flight path, the distance between a bat and its prey capture point was calculated as both direct distance to capture (DDC), which corresponded to the target distance, and flight distance to capture (FDC) along the flight path. The DDC matched the FDC after the start of the approach phase, indicating that foraging bats followed a straight-ahead path to the target. In addition, the duration of the quasi-constant frequency component of emitted pulses was slightly extended just before the convergence of the DDC with the FDC. These findings suggest that the bats confirm the presence of target prey by extending the duration of the pulse and then select a straight-ahead approach by forecasting the movement of the prey.     

Ultrahigh-resolution laser photoemission study of URu2Si2 across the hidden-order transition

We have studied the electronic structures of URu₂Si₂ employing ultrahigh-resolution laser angle-resolved photoemission spectroscopy. The change of photoemission spectra is investigated across the hidden-order transition, and the emergence of a narrow band is clearly observed near the Fermi level for both (π,0) and (π,π) directions. In addition, it is shown that tuning of light's polarization allows the signal of a hole-like dispersive feature to enhance. These observations prove that laser angle-resolved photoemission spectroscopy is an effective tool for studying the evolution of electronic structures across the hidden-order transition in URu₂Si₂.     

Dendritic, nanosized building block for siloxane-based materials: a spherosilicate dendrimer

A spherosilicate dendrimer ( DMS‐1 ) with closely spaced reaction sites (Si? H groups) on the dendrimer surface has been synthesized by stepwise silylation of double‐four‐ring silicate with chlorotriethoxysilane (ClSi(OEt)₃) and subsequently with chlorodimethylsilane (ClSiHMe₂). DMS‐1 consists of a maximum of 40 Si atoms in the interior frameworks and 24 reactive Si? H groups on the surface. Because DMS‐1 is spherical and about 1.5 nm in diameter, it can be regarded as the smallest well‐defined silica‐based nanoparticle. DMS‐1 also forms molecular crystals and is soluble in typical organic solvents. A molecularly ordered silica‐based hybrid can be prepared by heating a cast film of DMS‐1 at 180 °C for 5 days. The surface of DMS‐1 can be modified by hydrosilylation with 1‐hexadecene, triethoxyvinylsilane, and allylic‐terminated tetraethylene glycol monomethyl ether. More than 20 Si? H groups out of 24 react with these reagents. The solubilities of the products depend on the modification. DMS‐1 is not only a building block for nanohybrids, but also the smallest and most precisely designed siloxane‐based nanoparticle.     

Optimizing the separation of gaseous enantiomers by simulated moving bed and pressure swing adsorption

The resolution of racemic gas mixtures by simulated moving bed (SMB) and pressure swing adsorption (PSA) is investigated by dynamic simulation and optimization. Enantiomer separation of inhalation anesthetics is important because there is evidence that the purified enantiomers may have different pharmacological properties than the racemate. The model parameters reported in an experimental investigation performed elsewhere are used to study the feasibility of this separation using SMB and PSA configurations. Both processes were modeled in gPROMS^® as systems of differential algebraic equations. Operating conditions are optimized such that the feed throughput and product recovery for each process were maximized subject to equal constraints on the pressures and superficial gas velocities. SMB was found to be capable of resolving racemic feed mixtures with purity and recovery exceeding 99%. On the other hand, PSA was also able to provide a single purified enantiomer with low recovery of about 30% which may limit its application to enantiomer separation. Nevertheless, PSA consumes less desorbent, and achieves higher throughput at the sacrifice of lower recovery.     

Bifunctional hydrogen-bond donors that bear a quinazoline or benzothiadiazine skeleton for asymmetric organocatalysis

Hydrogen-bond (HB)-donor catalysts that bear a 2-aminoquinazolin-4-(1H)-one or a 3-aminobenzothiadiazine-1,1-dioxide skeleton have been developed, and it has been shown that these catalyst motifs act similarly to other HB-donor catalysts such as thioureas. The highly enantioselective hydrazination of 1,3-dicarbonyl compounds was realized even at room temperature with up to 96% ee for 2-aminoquinazolin-4-(1H)-one-type catalysts, which were more effective than the corresponding urea and thiourea catalysts. In addition, benzothiadiazine-1,1-dioxide-type catalysts were shown to promote the isomerization of alkynoates to allenoates with high enantioselectivity. To overcome the problem that the products were obtained as mixtures with the starting alkynoates, we developed the tandem isomerization and cycloaddition of alkynoates for the synthesis of advanced chiral compounds such as bicyclo[2.2.1]heptenes and 3-alkylidene pyrrolidine without a significant loss of enantioselectivity.     

Covariance tapering for prediction of large spatial data sets in transformed random fields

The best linear unbiased predictor (BLUP) is called a kriging predictor and has been widely used to interpolate a spatially correlated random process in scientific areas such as geostatistics. However, if an underlying random field is not Gaussian, the optimality of the BLUP in the mean squared error (MSE) sense is unclear because it is not always identical with the conditional expectation. Moreover, in many cases, data sets in spatial problems are often so large that a kriging predictor is impractically time-consuming. To reduce the computational complexity, covariance tapering has been developed for large spatial data sets. In this paper, we consider covariance tapering in a class of transformed Gaussian models for random fields and show that the BLUP using covariance tapering, the BLUP and the optimal predictor are asymptotically equivalent in the MSE sense if the underlying Gaussian random field has the Matérn covariance function.     

A note on skew differential operators on commutative rings

Let A be a commutative integral domain that is a finitely generated algebra over a field k of characteristic 0 and let ø be a k-algebra automorphism of A of finite order m. In this note we study the ring D(A;ø of differential operators introduced by A.D. Bell. We prove that if A is a free module over the fixed sub-ring A ^ø, with a basis containing 1, then D(A;ø) is isomorphic to the matrix ring M_m(D(A ^ø). It follows from Grothendieck's Generic Flatness Theorem that for an arbitrary A there is an element c?Asuch that D(A[c^-1];ø)?M _m(D(A[c^-1]^ø)). As an application, we consider the structure of D(A;ø)when A is a polynomial or Laurent polynomial ring over k and ø is a diagonalizable linear automorphism.