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排序方式: 共有259条查询结果,搜索用时 15 毫秒
1.
Hisao Yoshihara 《manuscripta mathematica》1989,64(2):169-187
We study a plane curve C whose singular points are cusps and the surface which is a triple covering of 2 branched along C. As a result, especially we obtain an inequality for the sum of the Milnor numbers at the singularities of C and new surfaces of general type. 相似文献
2.
Keitaro Yoshihara Yutaka Nagasawa Arkadiy Yartsev Shigeichi Kumazaki Hideki Kandori Alan E. Johnson Keisuke Tominaga 《Journal of photochemistry and photobiology. A, Chemistry》1994,80(1-3):169-175
We have investigated the ultrafast intermolecular electron transfer (ET) from an electron-donating solvent (aniline (AN) or N, N-dimethylaniline (DMA)) to an excited dye molecule (oxazines (Nile blue and oxazine 1) or coumarins). A non-exponential time dependence was observed in AN and can be explained by solvent reorientation and nuclear motion of the reactants. However, in DMA, a single exponential process was observed for Nile blue (160 fs) and oxazine 1 (280 fs), which can be explained by assuming that the rate of ET is limited mainly by ultrafast nuclear motion. A clear substituent effect on intermolecular ET was observed for the 7-aminocoumarins. When the alkyl chain on the 7-amino group is extended and a hexagonal ring with the benzene moiety is formed, the rate of ET is reduced by three orders of magnitude. This effect can be explained by a change in the free energy difference of the reaction and by the vibrational motion of the amino group. 相似文献
3.
A. Miyakawa H. Takeya T. Sekine K. Yoshihara 《Journal of Radioanalytical and Nuclear Chemistry》1989,136(2):151-157
In recoil implantation reaction of51Cr in Cr/acac/3 a polymer component which was sensitive to radiation dose was found. However, a retention type component51Cr/acac/3 was not so sensitive to radiation dose. A remarkable dependence of the yield of51Cr/acac/3 on recoil energy was found in the range 102–106 eV in recoil implantation using a thin film technique. This suggests a special role of implantation reaction in solids. 相似文献
4.
Dobashi T Nobe M Yoshihara H Yamamoto T Konno A 《Langmuir : the ACS journal of surfaces and colloids》2004,20(16):6530-6534
Curdlan dissolved in aqueous sodium hydroxide was dialyzed to aqueous calcium chloride to form a gel. Transparent and turbid concentric layers observed in the gel cross section perpendicular to the long axis of the dialysis tube were identified as liquid crystalline gels with refractive index gradient and amorphous gels, respectively. The thickness of each layer was proportional to the diameter of the dialysis tube, and the gelation proceeded in proportion to the root of time. The unique pattern formation was attributed to the change of curdlan conformation and calcium-induced cross-linking resulting from a diffusion of calcium cations and hydroxide anions through the dialysis tube. It is suggested that the orderedness of the curdlan molecules decreases by the increase of the curvature of the concentric liquid crystal layers as the layer comes toward the center of the dialysis tube. 相似文献
5.
A. Mutalib T. Omori K. Yoshihara 《Journal of Radioanalytical and Nuclear Chemistry》1992,165(1):19-25
A new chemical species of bis(acetonitrile)bis(acetylacetonato)technetium(III), [Tc(acac)2(CH3CN)2]+, has been prepared by the reaction of tris(acetylacetonato)technetium(III) with acetonitrile in the presence of a strong acid, perchloric or hydrochloric acid. The reaction kinetics were followed by observing spectral change of Tc(acac)3 in the UV-visible region. The complex has been characterized by combination of elemental analyses, IR and UV-visible spectrophotometry, ion-exchange chromatography, and paper electrophoresis. Applicability of this substance to synthesize mixed-ligand technetium(III) complexes was discussed based on the solubility of this complex and the ease of substitution of the acetonitrile ligand. 相似文献
6.
Yoshihara T Druzhinin SI Zachariasse KA 《Journal of the American Chemical Society》2004,126(27):8535-8539
The planar rigidized molecule fluorazene (FPP) undergoes fast reversible intramolecular charge transfer (ICT) in the excited state, with a reaction time of 12 ps in the polar solvent ethyl cyanide at -45 degrees C. The ICT state of FPP has a dipole moment mu(e)(ICT) of 13 D, much larger than that of the locally excited state LE (1 D). The ICT behavior of FPP is similar to that of its flexible counterpart N-phenylpyrrole (PP), for which mu(e)(ICT) = 12 D. These results show that intramolecular charge transfer to a planar ICT state can occur efficiently. In designing ICT systems capable of rapid switching, it is therefore important to realize that large amplitude motions such as those necessary for the formation of a twisted intramolecular charge transfer (TICT) state are not required. 相似文献
7.
Hiroki Nakamura Jiro Tanaka Nobuaki Nakashima Keitaro Yoshihara 《Chemical physics letters》1981,77(2):419-421
The photoionization of 8-anilino-1-naphthalenesulfonate in polar solvents occurs through a biphotonic process, as proved by nanosecond flash photolysis. A transient absorption of a charge transfer to solvent (CTTS) state is found with ≈10 ns life-time. The state is shown to be an intermediate of the photoionization process. 相似文献
8.
A. Mutalib T. Sekine T. Omori K. Yoshihara 《Journal of Radioanalytical and Nuclear Chemistry》1994,178(2):311-318
A new convenient method has been proposed to synthesize mixed-ligand -diketonato Tc(III) complexes, using the ligand exchange reaction [Tc(acac)2(CH3CN)2]++L–[Tc(acac)2L]+ +2CH3CN where L is bza, dpm or dbm. The yield was about 30–40%. UV-visible and IR spectra of these complexes were measured. Characteristic features of the compounds were compared with those of the corresponding complexes of ruthenium. 相似文献
9.
M. Hashimoto H. Wada T. Omori K. Yoshihara 《Journal of Radioanalytical and Nuclear Chemistry》1991,153(4):283-291
Tc(III)-EDTA complex has been synthesized by the ligand substitution reaction of hexakis-(thiourea) technetium(III) ion with EDTA. The complex exhibits absorption maxima at 368 and 470 nm. The formation reaction proceeds predominantly as follows:
相似文献
10.
Tetsuo Yamasaki Yuji Yoshihara Yoshinari Okamoto Tadashi Okawara Mitsuru Furukawa 《Journal of heterocyclic chemistry》1992,29(5):1313-1316
The reaction of 5-hydrazinopyridazin-3(2H)-ones 1 with α-keto diester 2 in acetic acid afforded the corresponding 4,6-dihydropyridazino[4,5-c]pyridazin-5(1H)-ones 3 and pyrrolo[2,3-d)pyridazin-4(5H)-ones 4 . Compounds 3 were also obtained from 4-bromo-5-hydrazinopyridazin-3(2H)-ones 8 and 2 under milder conditions. 5-Bromo-4-hydrazinopyridazin-3(2H)-one 9 , the regioisomer of 8b , also reacted readily with 2a to give 4,7-dihydropyridazino[4,5-c]pyridazin-8(1H)-one 10b , the regioisomer of 3b . 相似文献
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