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91.
A. Yamada Y. Makita H. Asakura T. Iida S. Kimura T. Matsumori S. Uekusa 《Applied Physics A: Materials Science & Processing》1991,53(2):102-108
Mg+ ions were implanted into highly pure InP grown by the liquid encapsulated Czochralski (LEC) method in which the Mg concentration [Mg] was varied between 1×1015 cm–3 and 3×1020 cm–3. Two annealing methods were used: furnace annealing (FA) up to 740° C and flash lamp annealing (rapid thermal annealing, RTA) up to 900° C. For characterization, photoluminescence (PL) spectra were measured between 2K and room temperature together with Raman scattering measurements at room temperature. An emission designated by g, which was attributed to a novel energy state of an isolated acceptor, was found to be produced for a rather low value of [Mg]. In addition, a broad emission denoted by [g–g], which was ascribed to acceptor-acceptor pairs, was observed below bound exciton emissions for moderate values of [Mg]. These features were quite similar to those previously observed in acceptor-doped GaAs when the background concentration of donors is extremely low. Two additional novel emissions located far below the band-to-acceptor emission were also obtained, and each showed a remarkable energy shift towards lower energy with increasing [Mg]. The binding energies of these emissions were estimated from the temperature dependence of PL spectra and the results suggest that they are complex-type radiative recombination centers, presumably donor-acceptor-type centers. A strong broad emission centered near the band-to-acceptor emission was observed for [Mg]=3×1020 cm–3. This observation indicates a formation of a new material between In, P and Mg, which was also attested by the appearance of a new TO-like Raman signal for [Mg] greater than 1×1019 cm–3. A substantial difference of PL and Raman spectra was revealed for the two annealing methods, suggesting that the annealing behaviour of ion-implanted InP should be investigated more extensively in order to establish reliable annealing procedures.Dedicated to H.-J. Queisser on the occasion of his 60th birthday 相似文献
92.
In order to observe the propagation of a conducting zone of a polyaniline film in response to anodic switching, propagation perpendicular to the film surface was simulated by propagation along the film by mounting the film on an insulated plate. A polyaniline film electrochemically deposited on an indium tin oxide (ITO) electrode was reinforced by casting polymethylmethacrylate solution on the film. It was peeled off the ITO, chemically reduced and then potentiostatically oxidized at one end in 1 mol dm−3 H2SO4 solution. Dynamic growth of the conducting zone was observed through an optical microscope. A well-defined boundary between the conducting zone and the insulating zone was seen. The contrast of the boundary did not vary with the electrolysis time, the growth length or the applied potential. The growth rate decreased slightly with the electrolysis time as a result of IR drop across the film. A differential equation for growth rate involving the effect of the IR drop was presented and solved to give more accurate values of the rate. The logarithmic growth ratio exhibited a linear relation with the applied potential, indicating a charge-transfer rate of the Tafel type. The anodic transfer coefficient was 0.2 and the rate constant was 5 × 10−5 m s−1. The propagation on a molecular scale was discussed on the basis of the experimental results. 相似文献
93.
Hideshi Nakamura Houming Wu Junichi Kobayashi Yoichi Nakamura Yasushi Ohizumi Yoshimasa Hirata 《Tetrahedron letters》1985,26(37):4517-4520
Purealin , a novel secondary metabolite, which modurates enzymic reactions of ATPases, has been isolated from the okinawan marine sponge and the structure has been determined by the 1H-1H homonuclear and 1H-13C heteronuclear NMR chemical shift correlations and CD spectra. 相似文献
94.
Koichi Aoki Hiroyasu Kamo Jingyuan Chen Yoshimasa Hoshino 《Journal of Electroanalytical Chemistry》1997,420(1-2)
A new tetranuclear ruthenium complex in which a metal was bridged radially to three identical metals with acetylene links showed a mixed-valence state in cyclic voltammograms. The peak potential difference for the mixed-valence state was twice the potential difference for a mixed-valence state of the corresponding binuclear complex. This fact suggests stabilization of the mixed-valence state twice by configurational modification of redox centers. However, this is inconsistent with the prediction from the additive pair model of the redox interaction. A quantum chemical model of the redox interaction was presented, in which the potential difference was expressed by the overlap integral S and the nearest neighbor interaction energy between the reduced center and the oxidized one. Application of the theory gave a negative value of S, which demonstrated reasonably the stabilization of the mixed-valence state from a quantum chemical viewpoint. 相似文献
95.
Shohei Makita Hiroto Kudo Tadatomi Nishikubo 《Journal of polymer science. Part A, Polymer chemistry》2004,42(15):3697-3707
Hyperbranched polyimides (HBPI)s with high glass‐transition temperatures and excellent thermal stability were synthesized through the reaction of commercially available carboxylic acid dianhydrides with tris[4‐(4‐aminophenoxy)phenyl]ethane (TAPE). In particular, hyperbranched polyimide HBPI(TAPE‐DSDA), prepared through the reaction of TAPE with 3,3′,4,4′‐diphenylsulfonetetracarboxylic dianhydride (DSDA), showed higher thermal stability and good solubility. Furthermore, alkaline‐developable, photosensitive HBPI(TAPE‐DSDA)‐MA‐CA was prepared through the reaction of HBPI(TAPE‐DSDA) with glycidyl methacrylate with tetrabutylammonium bromide as a catalyst in N‐methyl‐2‐pyrrolidinone (NMP) followed by the addition reaction of cis‐1,2,3,6‐tetrahydrophthalic anhydride with triphenylphosphine as a catalyst in NMP. The glass‐transition temperatures of HBPI(TAPE‐DSDA)‐MA‐CA were greater than 300 °C. A resist composed of 74 wt % HBPI(TAPE‐DSDA)‐MA‐CA, 22.2 wt % trimethylpropane triacrylate, and 3.8 wt % Irgacure 907 as a photoinitiator achieved a resolution of a 55‐μm line pattern and a 275‐μm space pattern by UV irradiation (1000 mJ/cm2). © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3697–3707, 2004 相似文献
96.
Four azuleno(2,6)pyridinophanes (1–4) were synthesized and their conformations were found by NMR spectroscopy to be very similar to those of the corresponding azulenometacyclophanes. A transverse conformational change was observed for [2.2](5,7)azuleno(2,6)pyridinophane. 相似文献
97.
Mikio Hoshino Shiro Konishi Shigeyuki Watanabe Yoshimasa Hama 《Chemical physics letters》1984,110(2):205-208
Optical absorption spectra of one-electron reduced species of copper(II) and oxovanadium(IV) tetraphenylporphyrins. Cu(II)TPP and V(IV)OTPP, in 2-methyltetrahydrofuran at 77 K reveal that not the central metal but the porphyrin ligand is reduced by an excess electron. The triplet ESR spectrum resulting from the spin-spin interaction between two odd electrons located on the porphyrin ligand and the central metal is observed for the one-electron reduced species of V(IV)OTPP while not for that of Cu(II)TPP. 相似文献
98.
Mohammad Abul Hossain Mikio Kumita Yoshimasa Michigami Shigeru Mori 《Adsorption》2005,11(5-6):561-568
Dynamic characteristics of Cr(VI) sorption on used black tea leaves (UBTLs) as a low-cost adsorbent are studied. Batch experiments
were conducted to evaluate the effects of Cr(VI) concentration, solution pH and temperature on the removal process. Both of
adsorption and reduction, involved in the process, are affected by the processing parameters. The adsorption kinetics is described
successfully using pseudo-second order rate equation and the rate constant decreases with increasing the initial concentration
of Cr(VI) up to 150 mg/L (for 0.1 g/L UBTLs) then becomes slow. Experimental and calculated kinetic data for equilibrium are
well expressed by Langmuir isotherm. The solution pH has a profound effect on the adsorption rate. The rate constant increases
linearly with an increase in temperature, and the low value of activation energy of adsorption, 16.3 kJ/mol, indicates that
Cr(VI) is easily adsorbed on UBTLs. The maximum Cr(VI) adsorptive conditions, with a minimum reduction, were achieved from
the dynamics of operational parameters: the initial Cr(VI) concentration < 150 mg/L (for 0.1 g/L UBTLs); the initial solution
pH = 1.54–2.00 and the processing temperature < 50 ∘C, for the possibility of its practical application. 相似文献
99.
Koiwa T Masuda Y Shono J Kawamoto Y Hoshino Y Hashimoto T Natarajan K Shimizu K 《Inorganic chemistry》2004,43(20):6215-6223
Binuclear beta-diketonatoruthenium(III) complexes [[Ru(acac)(2)](2)(tae)], [[Ru(phpa)(2)](2)(tae)], and [(acac)(2)Ru(tae)Ru(phpa)(2)] and binuclear and mononuclear bipyridine complexes [[Ru(bpy)(2)](2)(tae)](PF(6))(2) and [Ru(bpy)(2)(Htae)]PF(6) (acac = 2,4-pentanedionate ion, phpa = 2,2,6,6-tetramethyl-3,5-heptanedionate ion, tae = 1,1,2,2-tetraacetylethanate dianion, and bpy = 2,2'-bipyridine) were synthesized. The new complexes have been characterized by (1)H NMR, MS, and electronic spectral data. Crystal and molecular structures of [[Ru(acac)(2)](2)(tae)] have been solved by single-crystal X-ray diffraction studies. Crystal data for the meso isomer of [[Ru(acac)(2)](2)(tae)] have been confirmed by the dihedral angle result that two acetylacetone units of the bridging tae ligand are almost perpendicular to one another. A detailed investigation on the electrochemistry of the binuclear complexes has been carried out. The electrochemical behavior details of the binuclear complexes have been compared with those of the mononuclear complexes obtained from the half-structures of the corresponding binuclear complexes. Studies on the effects of solvents on the mixed-valence states of Ru(II)-Ru(III) and Ru(III)-Ru(IV) complexes have been carried out by various voltammetric and electrospectroscopic techniques. A correlation between the comproportionation constant (K(c)) and the donor number of the solvent has been obtained. The K(c) values for the binuclear complexes have been found to be low because of the fact that two acetylacetone units of the bridging tae ligand are not in the same plane, as revealed by the crystal structure of [[Ru(acac)(2)](2)(tae)]. 相似文献
100.
A new simple model of porphyrin ring current effect was proposed based on a line current approximation. It can reproduce the porphyrin-induced shifts for several Sn(IV)(tpp) and Sn(IV)(oep) dicarboxylate complexes quite satisfactorily. Perpendicular arrangement of the aromatic rings in the diaromatic-carboxylate complexes of Sn(IV)(tpp) and Sn(IV)(oep) was clarified with this porphyrin ring current effect model. There are two structures, exo and endo, in solution in dinaphthalene-1- and 2- carboxylate complexes of Sn(IV)(tpp) and Sn(IV)(oep). The exo conformer is in dynamic equilibrium with the endo form in solution. Thermodynamic data of these conformational equilibria are given. 相似文献