具有双裂纹的弹性复合材料板承受剪切冲击时的动应力强度因子

本文研究了两个材半限弹性的接合面附近存在与接合面平行的双裂纹，并承受剪切冲击时的瞬态应力，运用付里叶（Ｆｏｕｒｉｅｒ）和拉普拉斯（Ｌａｐｌａｃｅ）变换，将问题归结为求解二元积分方程，求解时将裂纹所在面上，下的位移差展成级数，并让其自动满足裂纹面外的位移差为零的条件，利用裂纹面上的边界条件和施密特（Ｓｃｈｍｉｄｔ）方法求解级数中的待定系数，在拉普拉斯像空间中，求得动应力强度因子，并将其数值地逆变换至     

Heteroatom-guided torquoselective olefination of alpha-oxy and alpha-amino ketones via ynolates

Ynolates were found to react with alpha-alkoxy-, alpha-siloxy-, and alpha-aryloxyketones at room temperature to afford tetrasubstituted olefins with high Z selectivity. Since the geometrical selectivity was determined in the ring opening of the beta-lactone enolate intermediates, the torquoselectivity was controlled by the ethereal oxygen atoms. From experimental and theoretical studies, the high Z selectivity is induced by orbital and steric interactions rather than by chelation. In a similar manner, alpha-dialkylamino ketones provided olefins with excellent Z selectivity. These products can be easily converted into multisubstituted butenolides and gamma-butyrolactams in good yield.     

Competing ferromagnetism and superconductivity on FeAs layers in EuFe2(As0.73P0.27)2

We have measured the spin-polarized electron momentum density distributions of EuFe2(As0.73P0.27)2 by magnetic Compton scattering (MCS) measurements. For the first time, we show direct evidence of competing ferromagnetism and superconductivity (SC) on FeAs layers in this iron pnictide system. The MCS orbitalwise decomposition of the density distributions reveals that between 16 and 19 K, the spin-polarized Fe-3d character is enhanced (as the ferromagnetic character supersedes superconducting character), where the resistivity shows a maximum, reentrant SC-like peak, at 18 K. The spin polarization of the Fe-3d orbital, enhanced by ferromagnetic Eu ions, suppresses the SC around 18 K, while at other temperatures the system indeed exhibits SC where the Fe-3d spin polarization is suppressed or collapses.     

Carbon monoxide ligand-exchange reaction of triruthenium cluster complexes induced by photosensitized electron transfer: a new type of photoactive CO color sensor

Oxo-acetato-bridged triruthenium cluster complexes ([Ru3(mu3-O)(mu-CH3CO2)6(L1)(L2)2](+/0)) show various color changes with variations of the total charge of the cluster complexes and terminal ligands. After photosensitized electron transfer via the triplet excited state of zinc tetraphenylporphyrin, the change of the formal oxidation state of the ruthenium ion allowed coordination with the carbon monoxide ligand accompanying the color changes.     

Observation of a strongly nested Fermi surface in the shape-memory alloy Ni0.62Al0.38

The Fermi surface topology of the shape-memory alloy Ni0.62Al0.38 has been determined using Compton scattering. A large area of this Fermi surface can be made to nest with other areas by translation through a vector of approximately 0.18[1,1,0](2pi/a), which corresponds to the wave vector associated with martensitic precursor phenomena such as phonon softening and diffuse streaking in electron diffraction patterns. This observation is compelling evidence that these phenomena are driven by the enhanced electron-lattice coupling due to the Fermi surface nesting.     

Photoinduced intramolecular electron-transfer processes in [60]fullerene-(Spacer)-N,N-bis(biphenylyl)aniline dyad in solutions

Intramolecular photoinduced charge-separation and charge-recombination processes in a covalently connected C60-(spacer)-N,N-bis(biphenylyl)aniline (C60-spacer-BBA) dyad, in which the center-to-center distance of the electron acceptor and electron donor is 15 A, have been studied by time-resolved fluorescence and transient absorption methods. The observed low fluorescence intensity and the short fluorescence lifetime of the C60 moiety of the dyad in PhCN and THF indicate that charge separation takes place via the excited singlet state of the C60 moiety at a quite fast rate and a high efficiency. The nanosecond transient absorption spectra in PhCN and THF showed the broad absorption bands at 880 and 1100 nm, which were attributed to C60(*-)-spacer-BBA(*+). The charge-separated state decays with a lifetime of 330-360 ns in PhCN and THF at room temperature. From temperature dependence of the charge-recombination rate constants, the reorganization energy was evaluated to be 0.77-0.87 eV, which indicates that the charge-recombination process is in the inverted region of the Marcus parabola. With lowering temperature, the contribution of charge separation via the excited triplet state of the C60 moiety increases due to an increase in solvation of C60(*-)-spacer-BBA(*+).     

Energy transfer followed by electron transfer in a supramolecular triad composed of boron dipyrrin, zinc porphyrin, and fullerene: a model for the photosynthetic antenna-reaction center complex

The first example of a working model of the photosynthetic antenna-reaction center complex, constructed via self-assembled supramolecular methodology, is reported. For this, a supramolecular triad is assembled by axially coordinating imidazole-appended fulleropyrrolidine to the zinc center of a covalently linked zinc porphyrin-boron dipyrrin dyad. Selective excitation of the boron dipyrrin moiety in the boron dipyrrin-zinc porphyrin dyad resulted in efficient energy transfer (k(ENT)(singlet) = 9.2 x 10(9) s(-)(1); Phi(ENT)(singlet) = 0.83) creating singlet excited zinc porphyrin. Upon forming the supramolecular triad, the excited zinc porphyrin resulted in efficient electron transfer to the coordinated fullerenes, resulting in a charge-separated state (k(cs)(singlet) = 4.7 x 10(9) s(-)(1); Phi(CS)(singlet) = 0.9). The observed energy transfer followed by electron transfer in the present supramolecular triad mimics the events of natural photosynthesis. Here, the boron dipyrrin acts as antenna chlorophyll that absorbs light energy and transports spatially to the photosynthetic reaction center, while the electron transfer from the excited zinc porphyrin to fullerene mimics the primary events of the reaction center where conversion of the electronic excitation energy to chemical energy in the form of charge separation takes place. The important feature of the present model system is its relative "simplicity" because of the utilized supramolecular approach to mimic rather complex "combined antenna-reaction center" events of photosynthesis.     

Use of highly energetic (116 keV) synchrotron radiation for X-ray fluorescence analysis of trace rare-earth and heavy elements

This study has revealed the advantages of the use of 116 keV X-rays as an excitation source of X-ray fluorescence (XRF) analyses. This technique is suitable for nondestructive multielemental analyses of heavy elements such as rare-earth elements. The lowest MDL value evaluated for the bulk analysis of a JG-1 standard reference sample (granite rock) was 0.1 ppm for W for a 500 s measurement. The spectrum of standard glass samples of SRM612 demonstrated clearly resolved K-line peaks of more than 30 elements, including all the existing rare-earth elements, at 50 ppm levels. The calibration curve for the determination of a rare-earth element shows a linear relation between the XRF intensity and concentrations from 10 to 0.03 ng. This powerful technique should be useful for nondestructive analyses of rare-earth and heavy elements in geological, geochemical and archaeological samples as well as industrial materials.     

Magnetic-field-induced Mott transition in a quasi-two-dimensional organic conductor

We investigated the effect of magnetic field on the highly correlated metal near the Mott transition in the quasi-two-dimensional layered organic conductor, kappa-(BEDT-TTF)(2)Cu[N(CN)(2)]Cl, by the resistance measurements under control of temperature, pressure, and magnetic field. It was demonstrated that the marginal metallic phase near the Mott transition is susceptible to the field-induced localization transition of the first order, as was predicted theoretically. The thermodynamic consideration of the present results gives a conceptual pressure-field phase diagram of the Mott transition at low temperatures.     

d Orbital doping into pi charge-ordered molecular insulator

A quasi-one-dimensional pi-electron charge-ordered insulator, (DI-DCNQI)2Ag, is metallized by Cu doping into the Ag sites. It is found that with doping the charge gap is diminished and then disorder-induced insulating nature comes up, eventually followed by transition or crossover to a pi-d networked metal. The profile of the charge-gap collapse is consistent with the prediction of the theory highlighting the interplay between electron correlation and disorder. The present doping method is regarded as doping of d orbital, which is different from the conventional charge and/or spin doping developed in cuprates and manganites.