Double solid twistor spaces: the case of arbitrary signature

In a recent paper ([9]) we constructed a series of new Moishezon twistor spaces which are a kind of variant of the famous LeBrun twistor spaces. In this paper we explicitly give projective models of another series of Moishezon twistor spaces on n CP ² for arbitrary n≥3, which can be regarded as a generalization of the twistor spaces of ‘double solid type’ on 3CP ² studied by Kreußler, Kurke, Poon and the author. Similarly to the twistor spaces of ‘double solid type’ on 3CP ², projective models of the present twistor spaces have a natural structure of double covering of a CP ²-bundle over CP ¹. We explicitly give a defining polynomial of the branch divisor of the double covering, whose restriction to fibers is degree four. If n≥4 these are new twistor spaces, to the best of the author’s knowledge. We also compute the dimension of the moduli space of these twistor spaces. Differently from [9], the present investigation is based on analysis of pluri-(half-)anticanonical systems of the twistor spaces.     

Koshikamide B, a cytotoxic peptide lactone from a marine sponge Theonella sp

Koshikamide B (1) has been isolated from two separate collections of the marine sponge Theonella sp. as the major cytotoxic constituent. Koshikamide B is a 17-residue peptide lactone composed of six proteinogenic amino acids, two D-isomers of proteinogenic amino acids, seven N-methylated amino acids, and two unusual amino acid residues. The unusual amino acids are N(delta)-carbamoylasparagine and 2-(3-amino-2-hydroxy-5-oxopyrrolidin-2-yl)propionic acid (AHPP); the former is first found as the constituent of peptides, whereas the latter is a new amino acid residue. The N-terminus of koshikamide B is blocked by a methoxyacetyl group. The structure of koshikamide B (1) has been determined by interpretation of spectral data and analysis of chemical degradation products. Koshikamide B (1) exhibits cytotoxicity against P388 murine leukemia cells and the human colon tumor (HCT-116) cell line with an IC50 value of 0.45 and 7.5 microg/mL, respectively.     

Preparation of oriented titanium phosphate and tin phosphate/polyaniline hybrid films by electrochemical deposition

The preparation of hybrid films of metal (Ti and Sn) phosphate nanosheets and polyaniline by simultaneous electrophoretic and electrolytic deposition was performed in an acetonitrile solvent. Emeraldine polyaniline was intercalated between the phosphate nanosheets with a monolayer arrangement. The obtained hybrid films were several tens of micrometers in thickness. The ratio of incorporated polyaniline to metal phosphate in the hybrid films reaches to around 0.45 and 0.30 at suitable concentrations of tetrabutylammonium hydroxide (TBAOH). These amounts correspond with occupancy of polyaniline in the interlayer gallery of several tens percent. Fractions of voids in a horizontal direction were around 22 and 1% in titanium phosphate/polyaniline and tin phosphate/polyaniline hybrid films, respectively. Thus, anodic electrodeposition makes it possible to form thick films of intercalation compounds of alpha-titanium and tin phosphates with polyaniline. These hybrid films were examined for redox activity. The cyclic voltammetry results of these films confirmed that the hybrid films have redox activity by polyaniline. For these voltammograms, the maximum current was observed in the tin phosphate/polyaniline hybrid deposited for 15 min. The redox activity of these hybrids possibly depends on the mesoscopic texture of the film, especially on the amount of voids in a horizontal direction.     

Preparation of apatite-type-silicate-supported precious metal catalysts for selective catalytic reduction of NOx

Apatite-type silicate supported precious metal catalysts were prepared and investigated for their catalytic activity in selective catalytic NO reduction. Single-phase La_9.33Si₆O₂₆ and La_8.33ASi₆O_25.5 (A=Ca, Sr, Ba) were obtained by a sol-gel method. Pd/La_9.33Si₆O₂₆ catalyst exhibited high activity for oxidation of C₃H₆, comparable to Pd/Al₂O₃ catalyst, although the specific surface area of La_9.33Si₆O₂₆ was lower than that of Al₂O₃. In addition, Pt/La_9.33Si₆O₂₆ catalyst exhibited higher activity for selective catalytic reduction of NO than Pt/Al₂O₃ catalyst. Substitution of Ba²⁺ for La³⁺ of La_9.33Si₆O₂₆ led to increased catalytic activity at low temperature.     

Matrix-assisted laser desorption/ionization quadrupole ion trap time-of-flight (MALDI-QIT-TOF)-based imaging mass spectrometry reveals a layered distribution of phospholipid molecular species in the mouse retina

We recently developed a matrix-assisted laser desorption/ionization quadrupole ion trap time-of-flight (MALDI-QIT-TOF)-based imaging mass spectrometry (IMS) system. This system enables us to perform structural analyses using tandem mass spectrometry (MS/MS), as well as to visualize phospholipids and peptides in frozen sections. In the retina, phototransduction is regulated by the light-sensitive interaction between visual pigment-coupled receptor proteins, such as rhodopsin, and G proteins, such as transducin. There are some reports that the conformation of rhodopsin is influenced by the composition of phospholipids in the lipid bilayer membrane. However, these results were based on in vitro experiments and have not been analyzed in vivo. In this study, we visualized and identified phospholipids in mouse retinal sections with the MALDI-QIT-TOF-based IMS system. From a spectrum obtained by raster-scanned analysis of the sections, ions with high signal intensities were selected and analyzed by MS/MS. As a result, sixteen ions were identified as being from four diacyl-phosphatidylcholine (PC) species, i.e., PC (16:0/16:0), PC (16:0/18:1), PC (16:0/22:6), and PC (18:0/22:6), with different ion forms. The ion images revealed different distributions on the retinal sections: PC (16:0/18:1) was distributed in the inner nuclear layer and outer plexiform layer, PC (16:0/16:0) in the outer nuclear layer and inner segment, and both PC (16:0/22:6) and PC (18:0/22:6) in the outer segment and pigment epithelium. In conclusion, our in vivo IMS analyses demonstrated a three-zone distribution of PC species on the retinal sections. This approach may be useful for analyzing lipid changes and their contribution to phototransduction in the retina.     

Patterning reactive microdomains inside polydimethylsiloxane microchannels by trapping and melting functional polymer particles

This paper describes a facile technique to pattern reactive microdomains inside polydimethylsiloxane microchannels by utilizing polymer particles as the carrier of functional groups. The air/liquid interface formed in microchannels equipped with microwells exerts lateral force on the particles, trapping particles only inside the wells. We then fix the polymer matrix on the wells by melting the trapped particles to form reactive domains with flexible shapes and high resolution. We employed monodisperse poly(styrene-co-glycidyl methacrylate) microparticles having an epoxy group and patterned various types of microdomains with a resolution of several micrometers. Several tests confirmed the presence of the epoxy group and the flatness of the patterned domain. The presented scheme provides a new way of preparing highly functional microsystems by using simple operations and would be useful for various applications, including local patterning of graft polymers and the site-specific cultivation of cells in a confined space.     

Synthesis and Applications of (ONO Pincer)Ruthenium‐Complex‐Bound Norvalines

Two (ONO pincer)ruthenium‐complex‐bound norvalines, Boc?[Ru(pydc)(terpy)]Nva?OMe ( 1 ; Boc=tert‐butyloxycarbonyl, terpy=terpyridyl, Nva=norvaline) and Boc?[Ru(pydc)(tBu‐terpy)]Nva?OMe ( 5 ), were successfully synthesized and their molecular structures and absolute configurations were unequivocally determined by single‐crystal X‐ray diffraction. The robustness of the pincer Ru complexes and norvaline scaffolds against acidic/basic, oxidizing, and high‐temperature conditions enabled us to perform selective transformations of the N‐Boc and C?OMe termini into various functional groups, such as alkyl amide, alkyl urea, and polyether groups, without the loss of the Ru center or enantiomeric purity. The resulting dialkylated Ru‐bound norvaline, n‐C₁₁H₂₃CO?l ‐[Ru(pydc)(terpy)]Nva?NH‐n‐C₁₁H₂₃ (l ‐ 4 ) was found to have excellent self‐assembly properties in organic solvents, thereby affording the corresponding supramolecular gels. Ru‐bound norvaline l ‐ 1 exhibited a higher catalytic activity for the oxidation of alcohols by H₂O₂ than parent complex [Ru(pydc)(terpy)] ( 11 a ).     

Negatively Charged π‐Electronic Systems by Deprotonation of Hydroxy‐Substituted Dipyrrolyldiketone Boron Complexes

Boron complexes of meso‐hydroxy‐substituted dipyrrolyldiketones, as the precursors of negatively charged π‐electronic systems, were synthesized via the oxidative introduction of an acetoxy unit at the meso position of dipyrrolyldiketones and subsequent hydrolysis. The anionic site formed upon deprotonation was moderately stabilized by hydrogen‐bond‐donating pyrrole NH, generating non‐complexing anionic species.