Collisional activation mass spectra of pentene and hexene molecular ions

The collisional activation spectra of the molecular ions from fourteen pentene and hexene isomers show substantial differences, some of which can be rationalized using known ion fragmentation mechanisms. These differences, and their negligible dependence on ion internal energy, are advantageous for the structural characterization of such isomeric ions, including those produced by fragmentation of larger molecules. The decompositions of metastable ions of the pentenes were nearly identical, but those of the hexenes showed some differences useful for structural charactrization.     

Preferential Uniplanar Orientation of Cellulose Microfibrils Reinvestigated by the FTIR Technique

A simple detection method to observe the uniplanar orientation behavior of native cellulose microfibrils to the cell wall surface by using Fourier transform infrared (FTIR) spectroscopy in the transmission mode is reported. Four bands at 1372, 1355, 1337, and 1317 cm⁻¹ (the latter two have been mentioned previously by Liang and Marchessault (1960, J. Polym. Sci. 43: 85–100)) were found to be sensitive to such orientation: the two middle bands at 1355 and 1337 cm⁻¹ increase remarkably when the 0.60–61 nm lattice planes lie parallel to the cell wall surfaces. The reverse was true when the 0.53–54 nm lattice planes oriented preferentially. Polarization of the two bands at 1372 and 1355 cm⁻¹ was parallel, while that of the other two bands at lower wavenumbers, i.e., at 1337 and 1317 cm⁻¹, was perpendicular to the molecular axis of cellulose. These bands were assigned to OH-related motion, probably to in-plane OH bending, as reported by Maréchal and Chanzy (2000, J. Mol. Spectrosc. 523: 183–196).     

Homoleptic cyclometalated iridium complexes with highly efficient red phosphorescence and application to organic light-emitting diode

Phosphorescence studies of a series of facial homoleptic cyclometalated iridium(III) complexes have been carried out. The complexes studied have the general structure Ir(III)(C-N)(3), where (C-N) is a monoanionic cyclometalating ligand: 2-(5-methylthiophen-2-yl)pyridinato, 2-(thiophen-2-yl)-5-trifluoromethylpyridinato, 2,5-di(thiophen-2-yl)pyridinato, 2,5-di(5-methylthiophen-2-yl)pyridinato, 2-(benzo[b]thiophen-2-yl)pyridinato, 2-(9,9-dimethyl-9H-fluoren-2-yl)pyridinato, 1-phenylisoquinolinato, 1-(thiophen-2-yl)isoquinolinato, or 1-(9,9-dimethyl-9H-fluoren-2-yl)isoquinolinato. Luminescence properties of all the complexes at 298 K in toluene are as follows: quantum yields of phosphorescence Phi(p) = 0.08-0.29, emission peaks lambda(max) = 558-652 nm, and emission lifetimes tau = 0.74-4.7 micros. Bathochromic shifts of the Ir(thpy)(3) family [the complexes with 2-(thiophen-2-yl)pyridine derivatives] are observed by introducing appropriate substituents, e.g., methyl, trifluoromethyl, or thiophen-2-yl. However, Phi(p) of the red emissive complexes (lambda(max) > 600 nm) becomes small, caused by a significant decrease of the radiative rate constant, k(r). In contrast, the complexes with the 1-arylisoquinoline ligands are found to have marked red shifts of lambda(max) and very high Phi(p) (0.19-0.26). These complexes are found to possess dominantly (3)MLCT (metal-to-ligand charge transfer) excited states and have k(r) values approximately 1 order of magnitude larger than those of the Ir(thpy)(3) family. An organic light-emitting diode (OLED) device that uses Ir(1-phenylisoquinolinato)(3) as a phosphorescent dopant produces very high efficiency (external quantum efficiency eta(ex) = 10.3% and power efficiency 8.0 lm/W at 100 cd/m(2)) and pure-red emission with 1931 CIE (Commission Internationale de L'Eclairage) chromaticity coordinates (x = 0.68, y = 0.32).     

Determination of trace amounts of vanadium in air samples with 2-(8-quinolylazo)-5-N,N-diethylaminophenol by reversed-phase liquid chromatography

A reversed-phase liquid chromatographic method for the determination of trace amounts of vanadium is described. Metal ions are converted into 2-(8-quinolylazo)-5-N,N-diethylaminophenol chelates in an off-line system. The chelates are injected onto a Zorbax CN column and separated with an aqueous acetonitrile mobile phase containing no chromogenic reagent. Unter these conditions, only vanadium(V) is spectrophotometrically detected at 540 nm among the metal ions Al(III), Ba(II), Ca(II), Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Ga(III), Hg(II), Mg(II), Mn(II), Ni(II), Pb(II), V(V) and Zn(II). Amounts of 8.0–200 pg of vanadium(V) in 100-μl injections can be determined without interference from 10-fold molar excesses of many cations. At 0.001 a.u.f.s., the detection limit (twice the peak-to-peak noise) for vanadium(V) is 8.0 pg in 100 μl of injected solution and the relative standard deviation at 120 pg of vanadium(V) in a 100-μl injection is 3.5%. The proposed method is applied to the determination of vanadium in rain water and airborne particulates.     

Profiling analysis of oligosaccharides in antibody pharmaceuticals by capillary electrophoresis

Carbohydrate chains in glycoprotein pharmaceuticals have important roles for the expression of their biological activities. Therefore, development of an assessment method for the carbohydrate chains is an important parameter for quality control of glycoprotein pharmaceuticals such as newly developed therapeutic antibodies. In this report, we applied capillary electrophoresis with laser-induced fluorescence detection to the analysis of carbohydrate chains after releasing with glycoamidase followed by derivatization with 3-aminobenzoic acid. We found that four major oligosaccharides present in antibody pharmaceuticals were successfully separated with good resolution. The present method showed good precision in both migration times and relative peak areas, and gave comparable accuracy with that using a derivatization method with 8-aminopyrene-1,3,6-trisulfonate.     

NLO‐active maleimide copolymers with ­high glass transition temperatures

We synthesized some novel rigid NLO‐active maleimide copolymers bearing DR‐1 moieties ( PMPD , PHSD and PHND ). All copolymers exhibited high T_g's (190～197 °C), good solubilities for common solvents and excellent film‐forming properties. Dependence of film thickness on the d₃₃ value for the poled copolymer films induced by corona poling was investigated and it was demonstrated that in less than thickness of 0.3 µm decrease of the thickness gives rise to remarkable increase in the d₃₃ value. The poled copolymer films exhibited large d₃₃ values (270 × 10^?9 esu (film thickness 0.13 µm) for PMPD , 290 × 10^?9 esu (0.12 µm) for PHSD and 350 × 10^?9 esu (0.08 µm) for PHND ) as well as large r₃₃ values (51.0 pmV^?1 for PMPD and 60.4 pmV^?1 for PHND ) which are significantly large compared to the value of LiNbO₃ (31 pmV^?1) as a typical EO material. The d₃₃ values of the poled copolymers were kept constant even after standing 1000h at 80 °C, although a small decrease was observed at an initial stage. Further, the d₃₃ values did not change up to ca. 123 °C upon heating at the rate of 10 °C/min in all cases. Copyright © 2002 John Wiley & Sons, Ltd.     

Novel synthesis of 1,3-dienes from 1-alkenes via /ldene/rd reaction with pummerer rearrangement product: a short synthesis of the sex pheromone of the red bollworm moth

A Pummerer rearrangement product, 4-chlorophenylthiomethyl trifluoroacetate (6), obtained from 4-chlorophenyl methyl sulfoxide (5) and trifluoroacetic anhydride, reacted with 1-alkenes in trifluoroacetic acid to give the ene products 8, which were readily converted into the terminal 1,3-dienes 10 by oxidation and subsequent pyrolysis. Using this method, 9,11-dodecadien-1-yl acetate (12), a sex pheromone of the red bollworm moth, was synthesized.     

Synthesis of 2-, 4- and 5-(2-alkylcarbamoyl-1-methylvinyl)-7-alkyloxybenzo[b]furans and their leukotriene B4 receptor antagonistic activity

Variable benzo[b]furan derivatives having (E)- and (Z)-2-alkylcarbamoyl-1-methylvinyl groups at the 2-, 4- and 5-positions and a carboxylpropoxy or (1-phenyl)ethoxy group at the 7-position were prepared to find novel and selective leukotriene B4(LTB4) receptor antagonists. (E)-2-(2-diethylcarbamoyl-1-methylvinyl)-7-(1-phenylethoxy)benzo[b]furan (4v) showed selective inhibition to the human BLT2 receptor (hBLT2). On the other hand, (E)-2-acetyl-4-(2-diethylcarbamoyl-1-methylvinyl)-7-(1-phenylethoxy)benzo[b]furan (7v) inhibited both human BLT(1) receptor (hBLT1) and hBLT2. The (E)-2-(2-diethylcarbamoyl-1-methylvinyl) group lay on approximately the same plane as the benzo[b]furan ring, whereas the (E)-4-(2-diethylcarbamoyl-1-methylvinyl) group had the torsion angle (45.7 degree) from the benzo[b]furan ring plane. However, the (Z)-(2-alkylcarbamoyl-1-methylvinyl)benzo[b]furans were inactive. The inhibitory activity depended on the conformation of the 2-diethylcarbamoyl-1-methylvinyl group.     

Electronic polarizability and crystallization of K2O-TiO2-GeO2 glasses with high TiO2 contents

Some K₂O-TiO₂-GeO₂ glasses with a large amount of TiO₂ contents (15-25 mol%) such as 25K₂O-25TiO₂-50GeO₂ have been prepared, and their electronic polarizability, Raman scattering spectra, and crystallization behavior are examined to clarify thermal properties and structure of the glasses and to develop new nonlinear optical crystallized glasses. It is proposed that the glasses consist of the network of TiO₆ and GeO₄ polyhedra. The glasses show large optical basicities of Λ=0.88-0.92, indicating the high polarizabity of TiO_n (n=4-6) polyhedra in the glasses. K₂TiGe₃O₉ crystals are formed through crystallization in all glasses prepared in the present study. In particular, 20K₂O-20TiO₂-60GeO₂ glass shows bulk crystallization and 18K₂O-18TiO₂-64GeO₂ glass exhibits surface crystallization giving the c-axis orientation. The crystallized glasses show second harmonic generations (SHGs), and it is suggested that the distortion of TiO₆ octahedra in K₂TiGe₃O₉ crystals induces SHGs.     

Ion-pair adsorption film colorimetry — A new simple method for ppb level of aluminum ion in water sample

A new, highly sensitive and simple colorimetric method for trace aluminum(III) with 2,2-dihydroxyazobenzene, H₂L, is described, based on the ion-pair adsorption of the anionic Al chelate, [A1L₂ ^–, with crystal violet cation, CV⁺, on the surface of Polyvinylchloride film plasticized with dioctylphthalate. The blue violet species, CV⁺[A1L₂]^–, is enriched onto the transparent film, leading to a remarkable enhancement of the sensitivity, and the detection limits are 3 ng/ml by spectrophotometry and 5 ng/ml by visual colorimetry, respectively. Using spectrophotometer, a linear calibration curve is obtained over the concentration range of 0 to 50 ng/ml of Al. Further, the color system, consisting of red ([A1L₂]^–), yellow (H₂L), and blue violet (CV⁺), gave clear color changes suitable for visual determination of aluminum with an applicable range of 0 to above 3000 ng/ml. The four different color zones are khaki for 0–5 ng/ml, reddish-brown for 5–200 ng/ml, blue violet for 200 ng/ml-3g/ml, and colorless for more than 3g/ml. The proposed method has been successfully applied for the determination of aluminum in tap waters.