Synthesis and photoinduced memory effect of poly[2-N-carbazolylethyl acrylate-co-2-(3,5-dinitrobenzoyloxy) ethyl methacrylate]

Copolymers containing an intramolecular electron donor-acceptor (EDA) complex were synthesized by free radical copolymerization of 2-N-carbazolylethyl acrylate and 2-(3,5-dinitrobenzoyloxy)ethyl methacrylate. Glass transition temperatures show a positive deviation from the weight-average values of copolymers, indicating the presence of the specific EDA interaction in copolymers in the solid state. Photoinduced “memory effect,” which is defined as the percentage of the difference of the surface potential given by corona charging before and after irradiation of light on polymer films, was 30% for the copolymer with 5 mol% of acceptor content. Memory effect increased to 70% for a 8 μm film by doping with 2 wt% of trichloroacetic acid (TCAA), and leveled off at 5 wt% of TCAA content. Memory effect was also enhanced by increasing the thickness of polymer films and irradiation time. The largest value of memory effect (85%) was obtained from the film of the copolymer with 5 mol% acceptor content doped with 1 wt% TCAA and with thickness larger than 14 μm.     

Stereoselective nucleophilic addition reactions to nitro sugars

Nucleophile(s) almost exclusively added from the equatorial side of 2-nitro-β-$\text{D}$-2-enopyranoside and the axial side of 2-nitro-$\text{D}$-$\text{ribo}$-1-enitol. On the other hand, methoxide and $\text{tert}$-butyl peroxide ions approached from the equatorial side of 2-nitro-α-$\text{D}$-2-enopyranoside, whereas methanol and hydrogen peroxide ion from the axial side.     

Amino acid end-group in commercial heparin. III. Determination of the number of amino groups of amino acid and hexosamine residues per heparin molecule

The reactions of heparin with 2,4,6-trinitrobenzenesulfonic acid (TNBS) were studied spectrometrically. Seven different commercial heparins were used in this study. The amino groups react with TNBS to form equimolar amounts of trinitrophenylated (TNP) amino groups and bisulfite ions. The TNP-amino groups further react with bisulfite ions to form the monosubstituted anionic sigma complex. The absorption spectrum with two maxima at approximately 350 nm and approximately 420 nm, characteristic of either the TNP-amino groups or the complex, was analyzed for the reaction of TNBS with heparin. It was shown that the reactivities of TNBS with amino groups from α-amino acid and hexosamine residues are greatly different. By combining the results of the reaction kinetics and the reaction of heparin with Sanger's reagent, the number of the α-amino groups and the free amino groups in hexosamine residues were determined. These data have been performed with a range of heparins from different commercial sources, of different activities and physical characteristics. No correlation was found between the free amino contents of these heparins and biological potency. © 1993 John Wiley & Sons, Inc.     

Water-soluble stilbene dendrimers

The third generation of novel photo-responsive water-soluble stilbene dendrimer (trans- and cis-G3 WSD) undergoes unusual one-way trans-to-cis isomerization to give 100% of cis isomer at the photostationary state on UV irradiation in water.     

Control of methanol oxidation by ionic behavior in supercritical water

In supercritical water the rate of methanol oxidation was controlled by ionic behavior as follows: the oxidation rate of methanol decreased with increasing proton and hydroxide ion concentration, possibly due to stabilization of the reactant, while that of CO was suppressed by added protons and enhanced by added hydroxide ions.     

Stability of porphyrin-calix[4]arene complexes analyzed by electrospray ionization mass spectrometry

The stability of some porphyrin-calix[4]arene sodium-ion complexes were determined by a collision-activated decomposition (CAD) method utilizing electrospray ionization mass spectrometry (ESI-MS). Comparing the values of E(1/2), the collision energy at which the relative intensity of the complex ion is 0.5, we found that the porphyrin-calix[4]arene complex with the higher value of E(1/2) corresponded to that with the larger association constant (Kass), as measured by 1H-NMR in CDCl3. Both our ESI-MS and NMR studies proved that the number of hydrogen bonds and the rigidity of the calix[4]arene stabilized the complex. The ESI-MS technique could be successful in screening the binding affinity in host-guest systems with a small amount of sample.     

Synthesis of new azonia-helicenes with a quaternary nitrogen at the inner helix skeleton

The 16c-azonia[6]helicene salts, in which a carbon atom at the inner helix skeleton of [6]helicene is replaced by a quaternary nitrogen atom, have been synthesized by photo-induced intramolecular quater-nization of 2-[2-(1-chloronaphthyl)vinyl]benzo[h]quinolines in acetonitrile.     

Electron correlations and transport effective mass in narrow-band systems and the Hubbard model

The Hubbard model is rederived from a tight-binding band calculation, showing that, as long as parameters are properly chosen, the model is justified for calculating electronic properties of narrow-band systems. The treatment is extended by including correlations and it was found that bound solutions called dimers exist. The concept of dimers is found to be very powerful for understanding the unusual properties of heavy fermion systems. However, a Mott-Hubbard-like model may be required to calculate properties of high T_c cuprates. © 1994 John Wiley & Sons, Inc.     

A highly diastereoselective pinacol coupling reaction of aldehydes and ketones using low-valence niobium generated from Nb(V)

A simple method for the diastereoselective synthesis of racemic 1,2-diol mediated by low-valence niobium generated in situ is described. A 1,4-dioxane-toluene solvent system was found to be essential to achieve higher selectivities and to prevent other reactions of pinacols, such as deoxygenation and acetal formation. Aromatic aldehydes and ketones were converted to the corresponding pinacols with up to 97 and 85% de, respectively.     

Analysis to obtain precise density fluctuation of supercritical fluids by small-angle X-ray scattering

A procedure of analysis for small-angle X-ray scattering (SAXS) data has been established to obtain density fluctuation of supercritical fluids near the critical point. It is indispensable for the certain analysis to utilize both of high-quality SAXS data measured under stable thermodynamic condition and accurate P–ρ–T data in supercritical region. As a standard example, SAXS measurements have been performed for supercritical CO₂, which is a suitable sample satisfying the condition for both experiment and analysis. The measurements were carried out along four isothermal conditions at reduced temperature of T_r = T/T_c = 1.020, 1.022, 1.043 and 1.064. Comparing the experimental density fluctuation with calculated one from the most reliable equation of state, the differences are within 8% at most.