A new synthesis of 7-substituted 2,3-bis(alkylthio)naphth[1,8-bc]-azepines using the tris(alkylthio)cyclopropenyl cation

7-Substituted 2,3-bis(isopropylthio)naphth[1,8-bc]azepines 3a-c were synthesized in good yields by the reactions of 5-substituted 1-naphthylamines 2a-c with tris(isopropylthio)cyclopropenylium perchlorate ( 1 ) in acetonitrile under reflux. This reaction proceeds through the facile ring opening of 1 , followed by the intermediary formation of iminium salts 5a-c and then intramolecular cyclization.     

Cytotoxicity of asymmetric platinum complexes against L-1210 cells. Effect of bulky substituents

The asymmetric platinum complexes cis-Pt(LL')Cl2 (L = NH3, L' = CH3NH2, (CH3)2NH, C2H5NH2 and (C2H5)2NH and LL' = N,N-dimethylethylenediamine),--one of the NH3 groups of cis-Pt(NH3)2Cl2 was substituted by alkylamine--, were synthesized and their cytotoxic effects have been measured using L-1210 cells. The IC50 values of the asymmetric platinum complexes,--being obtained after 24 h exposure of L-1210 cells to the platinum complexes--, are almost comparable to the corresponding value of cis-Pt(NH3)2Cl2. In 2 h exposure, however, the IC50 values of the platinum complexes were dramatically changed, i.e., a marked difference was observed between those of L' = RNH2 and L' = R2NH. On the other hand, the amounts of platinum taken into the L-1210 cells is little affected by the alkylamino substitution. The results suggest that the bifunctional platinum binding to the target molecule may be responsible for the cytotoxicity.     

Electrical conductivity of cytochrome c anhydrous film

Electrical conducitivities of both ferricytochrome c and ferrocytochrome c anhydrous films were measured at physiological temperatures. A film-casting method was applied to prepare the films. Rather low values of resistivities (55°C) of 6.5 × 10¹⁰ Ω cm for ferrocytochrome c in comparison with the previously reported value of 10¹¹ Ω cm (127°C) were obtained. Apparent activation energies for the above conductivities, 0.6 eV, were the same in both samples.     

Electroproduction of π from C leading to low-lying residual states in B

Energy distributions of π⁺ produced from ¹²C by electrons of total energy 195 MeV were measured at various angles. The results show large contributions from transitions leaving the residual nucleus in the ground (1⁺), first (2⁺) excited state and states at around 4.5 MeV. The angular distributions of ¹²C(γ, π⁺)¹²B leading to these residual states are deduced from the energy distributions by the unfolding method with the virtual photon theory. Theoretical results with the Helm model and the shell model are compared with the experimental results. Their relative shapes are in good agreement. A better agreement in the absolute value is found for the theoretical results which include the final-state interaction estimated with a pion optical potential. The surface production model shows better agreement with the experimental (γ, π⁺) cross sections than the volume production model.     

Application of hydride generation to the determination of trace concentrations of arsenic by inductively-coupled plasma atomic emission spectrometry

A method is described for the determination of traces of arsenic, based on sodium tetrahydroborate reduction of arsenic and introduction of the arsine formed to a relatively low-powered (1.6 kW) inductively-coupled plasma where the arsenic atomic emission is generated, Inter-element interference effects are described; many can be eliminated by addition of potassium iodide to the sample solutions, but the standard additions method is recommended for accurate arsenic determination. Potassium iodide is also used for prereducing arsenic(V) to arsenic(III). The method has a detection limit of 0.1 ng As ml^-1 and the linear calibration range spans nearly four orders of magnitude. The proposed method is applied to the determination of ng ml^-1 levels of arsenic in waste waters.     

121Sb Mössbauer spectroscopic study on electronic states of pentavalent organoantimony compounds

A systematic study of pentavalent organoantimony compounds, (RC₆H₄)₃SbX₂ (R=H,p-CH₃,p-F,p-Cl,p-CF₃,o-CH₃; X=Cl, Br), was carried out to examine the effect on Mössbauer parameters of the substituent on the aromatic ring. The Mössbauer parameters obtained in polycrystalline form reflected the steric effect caused by the position of the substituent on the aromatic ring. On the other hand, measurements in frozen organic solutions revealed that the electron density and electric field gradient at and around the antimony nucleus became smaller when the more electron-attractive group was introduced into thepara position.     

High-performance gel filtration of water-soluble samples on polyvinyl alcohol columns

The chromatographic behaviour in aqueous solution of pullulans, polyethylene glycols, peptides and proteins with different molecular weights on newly developed polyvinyl alcohol columns (Asahipak GS column series: GS-310, GS-320, GS-510 and GS-520) has been investigated. Pullulans and polyethylene glycols eluted according to the gel filtration mode, so both series of compounds produced almost equal calibration curves for GS-310 and GS-320 and for GS-510 and GS-520; the exclusion limits on GS-310 and GS-320 and on GS-510 and GS-520 were found to be ca. 40,000 and 300,000, respectively. Peptides and proteins were found to adsorb slightly on the columns. However, the plots of the elution volumes against the logarithm of the molecular weights for many of the substrates tested gave rise to the linear calibration curves. Recovery of several crude proteins was also studied for the columns and high values were obtained (81–100%). The effects of changes in the flow-rate, temperature and concentration of electrolytes added to the eluents, on the retention of all four types of compound are also reported.     

Immobilization of histidine-tagged recombinant proteins onto micropatterned surfaces for cell-based functional assays

This letter describes a method for preparing protein microarrays that allow the functional analysis of proteins at a cellular level. This method involves the utilization of recombinant proteins genetically engineered to carry a fusion tag that has an affinity for metal ions. A micropatterned alkanethiol monolayer was used to prepare a microarray having multiple spots with immobilized metal ions. The fusion protein was chelated to the spots under physiological conditions. The feasibility of the method was demonstrated by culturing neural stem cells on the microarray that displayed oligohistidine-tagged epidermal growth factor.