Linear dichroism of Zn(II)-tetrapyridylporphine aggregates formed at the toluene/water interface

The apparent circular dichroism (CD) and the linear dichroism (LD) spectra of the aggregates of achiral zinc(II)-5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine (ZnTPyP), formed at the toluene/water interface in a centrifugal liquid membrane (CLM) cell, were investigated by comparison with the microscopic CD and LD spectra of a single interfacial aggregate of ZnTPyP about 100 mum in length, measured by a microscope-spectropolarimeter. The interfacial ZnTPyP aggregate showed two types of flat trapezoidal shapes, one had a seedlike core at an edge (type I) and another a needlelike core at an edge (type II). The microscopic CD and LD spectra were observed by varying the angle between the parallel axis of the trapezoidal aggregate and the perpendicular axis of a polarized light for LD. The plot of the CD intensity against the LD intensity for a single aggregate, observed at a given wavelength, showed a rotated elliptical shape with a long axis through the origin, when the orientation angle was changed. From these results, it was concluded that the apparent CD spectra observed by the CLM-CD method were mainly due to the large linear dichroism of the aggregate. Both type I and type II structures showed two transition dipole moments, parallel and perpendicular to the long axis of the structure, but suggesting a more developed J-aggregate in type II structure. AFM measurements showed that the interfacial ZnTPyP aggregate had a multilayer structure, in which the unit monolayer thickness was 1.58 +/- 0.23 nm. Finally, the orientation angle of the interfacial aggregate in the CLM cell was estimated as 41 degrees -44 degrees to the rotating axis of the cell.     

Structure of an unsaturated fatty acid with unique vicinal dimethyl branches isolated from the Okinawan soft coral of the genus Sinularia

A new unsaturated fatty acid with unique vicinal dimethyl branches was isolated from the Okinawan soft coral of the genus Sinularia. The structure of the compound was determined based on the results of spectroscopic analysis and chemical conversion. The absolute configuration was deduced by applying the Ohrui-Akasaka method.     

Incoherent quasielastic neutron scattering study on the polymorphism of tristearin: dynamical properties of hydrocarbon chains

Dynamical properties of acyl chains in the three polymorphic phases alpha, beta', and beta of tristearin [C(3)H(5)(OCOC(17)H(35))3] have been studied by means of incoherent quasielastic neutron scattering (IQNS) using selectively deuterated samples. The mean square displacement of hydrogen atoms, , was estimated from the scattering vector Q dependence of the elastic scattering component under the harmonic approximation. It was shown that the temperature dependence of was significantly different between the three phases. There was no marked difference in between these phases up to 193 K, and the value increased linearly with temperature. Although the beta phase remained linear up to 293 K, the alpha and beta' phases started to show a nonlinear increase around 200 K, suggesting an anharmonic nature of molecular motions. The alpha phase exhibited the most conspicuous temperature dependence. These characteristics were ascribable to the difference in the lateral packing of acyl chains. Compared with the beta phase which has a tightly packed T// subcell, the beta' and alpha phases have looser O perpendicular and H subcells, respectively. The molecular motion in the alpha phase was analyzed using the model of uniaxial rotational diffusion in a onefold cosine potential. It has been clarified that the rotational fluctuation about the chain axis in the alpha phase is rather restricted compared with that in the rotator phase of n-alkanes.     

Excited-state structure and dynamics of 1,3,5-tris(phenylethynyl)benzene as studied by Raman and time-resolved fluorescence spectroscopy

Excited-state structure and dynamics of 1,3,5-tris(phenylethynyl)benzene (TPB) have been studied in n-hexane and n-heptane solutions. Time-resolved fluorescence spectra, fluorescence anisotropy, and lifetime of TPB were recorded with femtosecond to nanosecond time resolution. Raman depolarization ratio was also measured to elucidate a nonplanar structure of the ground state. Two fluorescence components, the short-lived component with 150 fs lifetime and the long-lived component with 10 ns lifetime, were observed. The analysis of the fluorescence anisotropy values combined with the Raman depolarization data has led to a conclusion that TPB is primarily excited to a short-lived excited singlet state with a nonplanar structure, and then it relaxes to a long-lived excited singlet state with a 3-fold axis. A rapid structural change from a nonplanar to a planar structure is suggested to take place in the process of relaxation.     

Two Paths Joining Given Vertices in 2k-Edge-Connected Graphs

Let k≥2 be an integer and G = (V(G), E(G)) be a k-edge-connected graph. For X⊆V(G), e(X) denotes the number of edges between X and V(G) − X. Let {s_i, t_i}⊆X_i⊆V(G) (i=1,2) and X₁∩X₂=∅. We here prove that if k is even and e(X_i)≤2k−1 (i=1,2), then there exist paths P₁ and P₂ such that P_i joins s_i and t_i, V(P_i)⊆X_i (i=1,2) and G − E(P₁∪P₂) is (k−2)-edge-connected (for odd k, if e(X₁)≤2k−2 and e(X₂)≤2k−1, then the same result holds [10]), and we give a generalization of this result and some other results about paths not containing given edges.     

Every 4k-edge-connected graph is Weakly 3k-linked

We prove:

1. Fork ≥ 2 andα = 0, 1, every (4k + 2α)-edge-connected graph is weakly (3k + 2α)-linked.
2. IfG is ak-edge-connected graph (k ≥ 2),s, t are vertices andf is an edge, then there exists a pathP betweens andt such thatf ? E(P) andG ? E(P) ? f is (k ? 2)-edge-connected, whereE(P) denotes the edge set ofP.

     

Densities and Viscosities of Tris(acetylacetonato)cobalt(III) Complex Solutions in Various Solvents

The densities and the viscosities of tris(acetylacetonato)cobalt(III) solutions in acetonitrile, dichloromethane, chloroform, tetrachloromethane, benzene, toluene, ethylbenzene, and p-xylene were measured in the dilute concentration regions at several temperatures ranging from 278 to 313 K under ambient pressure. The partial molar volumes of the solvents and solute were calculated. They are independent of concentration and increase slightly as the temperature increases. The viscosity A- and B-coefficients of the Jones-Dole equation were obtained. The A-coefficients were found to be zero within experimental error. The B-coefficients are positive and decrease as the temperature increases. Thermodynamic quantities of activation for viscous flow were calculated on the basis of Eyring’s viscosity equation. From the quantities obtained in this study, along with some information from the literature, it is suggested that structure-making interactions occur between the segments of the complex and the solvent molecules. These interactions include electrostatic interactions between the local charge on the complex and the dipole moment of the solvent in solutions of acetonitrile and dichloromethane, interlocking packing interactions along C ₃-axis of the complex with solvent in solutions of chloroform and tetrachloromethane, and π-electron interactions between the chelate ring of the complex and the solvent in solutions of benzene, toluene, ethylbenzene, and p-xylene.     

Solid‐Phase Synthesis of a Combinatorial Methylated (±)‐Epigallocatechin Gallate Library and the Growth‐Inhibitory Effects of these Compounds on Melanoma B16 Cells

We report on the solid‐phase synthesis of a combinatorial methylated (±)‐epigallocatechin gallate (EGCG) library and its biological evaluation. Epigallocatechin gallate (EGCG) and its methylated derivatives, which are members of the catechin family, exhibit various anti‐cancer effects. The solid‐phase synthesis of methylated EGCG involves the preparation of the α‐acyloxyketone by the coupling of a solid‐supported aldehyde with a ketone and an acid. The subsequent release and reductive etherification reaction of the solid‐supported α‐acyloxyketone provide the protected EGCG in good total yields. Sixty‐four methylated EGCGs were successfully prepared. The growth‐inhibitory effects of the methylated EGCG library were also examined. Although methylation of EGCG generally causes reduced growth inhibition, the growth‐inhibitory effect of 7‐OMe EGCGs was comparable to that of EGCG. The 7‐OMe EGCGs are attractive drug candidates because of their enhanced bioavailability.     

Photoreaction of N-(ω-indol-3-ylalkyl)phthalmides: intramolecular oxetane formation of the aromatic imide system.

Photoreaction of N-(ω-indol-3-ylalkyl)phthalimides ($\text{1a}$ and $\text{1c}$) gave oxeto[2,3-b]indoles ($\text{3a}$ and $\text{3c}$), the first example of oxetane formation of the aromatic imide carbonyl in the Paterno-Buchi reaction.