(+)-Apollineanin: a new flavanone from Tephrosia apollinea

Chemical investigation of the leaves of Tephrosia apollinea has yielded a new flavanone named (+)-apollineanin, together with two known flavones: (-)-semiglabrin and (-)-semiglabrinol. The structure of the new compound was determined on the basis of mass, 1D and 2D NMR spectroscopies including NOE difference spectroscopy. The absolute stereochemistry of (+)-apollineanin was determined by Mosher ester methodology and from CD data.     

Numerical schemes for random ODEs with affine noise

Numerical schemes for random ordinary differential equations, abbreviated RODEs, with an affine structure can be derived in a similar way as for affine control systems using Taylor expansions that resemble stochastic Taylor expansions for Stratonovich stochastic differential equations. The driving noise processes can be quite general, such as Wiener processes or fractional Brownian motions with continuous sample paths or compound Poisson processes with piecewise constant sample paths, and even more general noises. Such affine-Taylor schemes of arbitrarily high order are constructed here. It is shown how their structure simplifies when the noise terms are additive or commutative. A derivative free counterpart is given and multi-step schemes are derived too. Numerical comparisons are provided for various explicit one-step and multi-step schemes in the context of a toggle switch model from systems biology.     

Theory of inelastic electric current through single molecules

An electronic structure theory has been developed for an inelastic electric current of electron-intramolecular vibration coupling origin in terms of the Keldysh Green function method and the self-consistent Born approximation. Numerical calculations were made for the benzenedithiol molecule linking the two Au(111) electrodes. The calculations successfully reproduce typical features commonly observed in inelastic tunneling spectroscopy. The vibrational excitation energy due to the inelastic current was estimated. The inelastic electric current is quite important for the structural stability and the switching possibility of the molecular device.     

Structures of bulgecins,bacterial metabolites with bulge-inducing activity

The structure of bulgecin A, a bacterial metabolite with bulge-inducing activity, was determined chemically and spectrometrically to be 4-o-(2'-acetylamino-2'-deoxy-4'-o-hydroxysulfonyl-β-D-glucopyranosyl)-(2S, 4S, 5R -4-hydroxy-5-hydroxymethylprolyltaurine monosodium salt. Bulgecns B and C, the minor components, were found to be analogs of bulgecin A in which the taurine moiety was replaced as shown in Fig, 1.     

On thek-stability ofm-quota games

We consider thek-stability ofm-quota games ofn players. We prove that anm-quota game (N, v), which satisfies the conditionv(S)=0 for allS, ¦S¦ ≤m ?1, is (m ?1)-stable if and only if there is no weak player. Further, some relationships between ak-stable pair and anm-quota are shown. Some ofLuce's results [1955] on Shapley quota games are generalized tom-quota games.     

Proton and Li-7 NMR study on the effect of the OH− anion upon the Li+-ion conduction in the solid solution Li5NI2LiOH

From ¹H and ⁷LiNMR relaxation times T₁, T₂ and T_1ρ in Li₅NI₂ and the solid solution Li₅NI₂?0.77LiOH, the diffusive motion of the Li⁺ ion was studied to make clear the role of the OH^? ion in improving the Li⁺ ionic conduction. At temperatures as low as 140 K, each Li⁺ ion jumps among four available positions. Its activation energies are 9.26 and 11.8 kJ mol^?1 for Li₅NI₂ and Li₅NI₂?0.77LiOH, respectively. Diffusive motion was observed in T₂ and T_1ρ above 240 K. The mode of the cation distribution and the diffusion mechanism are not affected by the presence of the OH^? anion. The most noticeable fact is that the OH^? ion is substituted selectively for the N^3? ion that is the nearest neighbour of the Li⁺ ion. This selective substitution increases the concentration of the Li⁺ vacancy most effectively up to 4.2% of the total Li positions. At the same time it diminishes the strong attractive force of the N^3? anion binding the Li⁺ ion to the position, and thus the activation energy. For the diffusion, an anomalously low attempt frequency of 3̃ × 10⁹Hz was obtained from T_1ρ, while the normal value of 4.8 × 10¹²Hz was obtained from the ionic conductivity. The large discrepancy was attributed to the collective nature of the Li⁺ diffusive motion.     

Suspension of layered particles: an optimum electrorheological fluid for d.c. applications

 A comparison is made between two types of solid particles used in electrorheological fluids: particles with homogeneous electrical properties versus layered particles with a semi-conducting core surrounded by an outer layer of lower conductivity. Rheological measurements of these suspensions under steady shear and d.c. electric field show that the layered particle system produces the same yield stress but with a substantially reduced electric current. X-ray spectroscopic analysis confirms that these particles have a thin layer of SiO_x on the outer surface which causes the reduction in conductivity. Measurement of the dielectric permittivity followed by analysis using the Maxwell-Wagner model of polarization indicates that the conductivity of the outer layer is about 0.62 times that of the core region. Received: 13 January 1999 Accepted: 26 July 1999     

Synthesis of poly(ethynylplatinumporphyrin) and its application as an oxygen pressure-sensitive paint

5-(4-Trimethylsilyethynylphenyl)-10,15,20-triphenylplatinumporphyrin was synthesized and copolymerized with trimethylsilylpropyne to give a new high-molecular-weight porphyrin polymer. The polymer formed a smooth and tough coating on many types of surfaces. The coating showed a strong blue luminescence from the platinumporphyrin residue which was quenched in the presence of oxygen. The relationship of the luminescence intensity vs oxygen pressure displayed a remarkably high pressure sensitivity in the low oxygen pressure area, which was ascribed to the high oxygen permeability of the polymer.