A simple HPLC-fluorescence detection of nitric oxide in cultivated plant cells by in situ derivatization with 2,3-diaminonaphthalene.

An HPLC method with fluorescence detection for the determination of nitric oxide (NO) in cultivated plant cells (Agave pacifica, Agavaceae) was developed. NO was derivatized in situ with 2,3-diaminonaphthalene (DAN) as a labeling reagent and converted to 1(H)-naphthotriazole. The maximum peak height of the derivative was observed by incubation for 3 h at 25 degrees C with 0.2 mM DAN. Excess reagent in cells was removed by washing 3 times with 5 ml of water. The calibration curve for authentic standard of DAN-NO spiked to cultivated plant cells showed a good linearity (r = 0.995) in the range of 5.0 to 50 pmol/g cell. The detection limit at a signal-to-noise ratio of 3 was 3.4 pmol/g cells. The proposed method was successfully applied to the monitoring of NO concentration with cell growth. The effect of thermal treatment on the concentration of NO in plant cells was also examined. The concentration of NO in cells treated at 5 degrees C for 1 h was significantly higher than that treated at 25 degrees C and 35 degrees C for 1 h (n = 3, p < 0.05).     

Affine geometric crystals and limit of perfect crystals

For every non-exceptional affine Lie algebra, we explicitly construct a positive geometric crystal associated with a fundamental representation. We also show that its ultra-discretization is isomorphic to the limit of certain perfect crystals of the Langlands dual affine Lie algebra.

     

Synthesis of 2-azabicyclo[2.1.0]pentanes by the intramolecular nucleophilic substitution of cyclopropylmagnesium carbenoids with magnesium anilide

A variety of 2-azabicyclo[2.1.0]pentanes were synthesized by the intramolecular nucleophilic substitution of cyclopropylmagnesium carbenoids with magnesium anilide. The 1-chlorocyclopropyl p-tolyl sulfoxides possessing an N-aryl-substituted aminomethyl group were prepared from dichloromethyl p-tolyl sulfoxide, α,β-unsaturated carboxylic acid esters, and anilines in four steps. The deprotonation of the amine with t-BuMgCl followed by sulfoxide/magnesium exchange of the sulfoxides with i-PrMgCl led to the generation of the cyclopropylmagnesium carbenoids possessing a magnesium anilide moiety. Subsequent intramolecular nucleophilic substitution of the cyclopropylmagnesium carbenoids occurred in a 4-exo-tet manner to give the 2-azabicyclo[2.1.0]pentanes. The optically active 2-azabicyclo[2.1.0]pentane was synthesized using a p-tolylsulfinyl group as a chiral auxiliary.     

Addition of ArSSAr to carbon-carbon multiple bonds using electrochemistry

ArS(ArSSAr)⁺ (arylbis(arylthio)sulfonium ions), which were generated and accumulated by the electrochemical oxidation of diaryl disulfides (ArSSAr) in CH₂Cl₂ at −78 °C, reacted with alkenes to give the corresponding diarylthio-substituted compounds in a stereospecific manner in good yields, when the reaction was quenched with a soft nucleophile, such as allylsilanes, ketene silyl acetals, and triethylamine. A mechanism involving the initial formation of an episulfonium ion followed by ring-opening by the attack of ArSSAr has been suggested. The reactions of ArS(ArSSAr)⁺ with alkynes also took place to give 1,2-diorganothio-substitued alkenes stereoselectively under similar conditions.     

Hybrid micelle formation from poly(ethylene oxide-b-sodium 2-acrylamido-1-propanesulfonate-b-styrene) and Fe3+ ion in aqueous solution

Organic–inorganic nanohybrid particles are prepared in aqueous solution from poly(ethylene oxide-b-sodium 2-acrylamido-1-propanesulfonate-b-styrene) (PEO-b-PAMPS-b-PS) triblock copolymer and ferric ions. The hybrid micelles were characterized by dynamic light scattering, scanning electron microscopy, transmission electron microscopy, and zeta-potential measurements. The hydrodynamic diameter of the hybrid micelles ranges from 68 to 118 nm depending on the concentration of the polymer and the amount of ferric ions loaded on the polymer. Zeta-potential measurements revealed that the micelles are assembled mainly by electrostatic interaction between the ferric ions and the negatively charged PAMPS block in the PEO-b-PAMPS-b-PS.     

Analysis of Th, U, Pu, and Am in radioactive metal waste using extraction chromatography

In order to analyze actinide elements in radioactive metal waste, the dissolution and chemical separation conditions were optimized. The surfaces of a type 304 stainless steel plate and of pipe waste sampled from the prototype advanced thermal reactor (Fugen) were dissolved in mixed acid solution (HNO₃:HCl:H₂O = 1:1:4). The resulting solution was evaporated to dryness and dissolved with 2 mol/dm³ of HNO₃ to prepare sample solutions. In order to analyze trivalent actinide elements in the sample solution containing a large amount of Fe(III) (>0.1 g) using TRU resin, the effect of Fe(III) concentration on the recovery of Am(III) and reduction effect of Fe(III) to Fe(II) with ascorbic acid were studied. On the basis of results of this study, chemical separation scheme was constructed and Pu and Am in the sample solutions were separated. Thorium and U in the sample solutions were separated with UTEVA resin. High recoveries for all experimented elements were obtained from the analysis of spiked sample solutions, the effectiveness of the method was confirmed.     

Fredholm operators,evolution semigroups,and periodic solutions of nonlinear periodic systems

Let X be a Banach space and L the generator of the evolution semigroup associated with the τ  -periodic evolutionary process _{{U(t,s)}t≥s}${\{U(t,s)\}}_{t\ge s}$ on the space _Pτ(X)$P_{\tau }(X)$ of all τ-periodic continuous X  -valued functions. We give criteria for the existence of periodic solutions to nonlinear systems of the form Lp=−?F(p,?)$Lp=-?F(p,?)$ under the condition that 1 is a normal eigenvalue of the monodromy operator U(τ,0)$U(\tau ,0)$. The proof is based on a new decomposition of the space _Pτ(X)$P_{\tau }(X)$ by constructing a right inverse of L.