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排序方式: 共有279条查询结果,搜索用时 15 毫秒
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Takuya Hashimoto Koichi Kitazawa Masaaki Nakabayashi Tadashi Shiraishi Youichi Suemune Takakazu Yamamoto Hideomi Koinuma 《应用有机金属化学》1991,5(4):325-330
For low-temperature deposition of oxide films relating to Bi-Sr-Ca-Cu-O superconductors, photo-absorption and -decomposition properties were examined with respect to copper and alkaline-earth ß-diketonates. It was confirmed that all ß-diketonates examined were promising as source materials for photochemical vapour deposition (photo-CVD) using a low-pressure mercury lamp, in view of their large light absorption coefficients at wavelength 254 nm. The light irradiation was effective for the formation of highly crystalline oxide films at temperatures below 600 °C. By combining two sources, Ca2CuO3 and SrCuO2 films were prepared. Photo-CVD of c-axis oriented Bi2Sr2CuOx film was achieved by the irradiation of ternary sources of Bi(C6H5)3 and strontium and copper ß-diketonates at 500 °C. 相似文献
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Shimazaki Y Tashiro M Motoyama T Iwatsuki S Yajima T Nakabayashi Y Naruta Y Yamauchi O 《Inorganic chemistry》2005,44(17):6044-6051
Synthetic, structural, spectroscopic, and kinetic studies have been carried out on the Pd(II) complexes of new 2N1O-donor ligands containing a pendent indole, 3-(N-2-pyridylmethyl-N-2-hydroxy-5-methoxybenzylamino)ethylindole (HMeO-iepp), 3-(N-2-pyridylmethyl-N-2-hydroxy-5-nitrobenzylamino)ethylindole (HNO2-iepp), and (N-2-pyridylmethyl-3-indolylethylamino)acetic acid (Hiepc) (H denotes a dissociable proton). [Pd(MeO-iepp)Cl] (2), [Pd(NO2-iepp)Cl] (3), and [Pd(iepc)Cl] (4) were prepared and revealed by X-ray analysis to have a pyridine nitrogen, an amine nitrogen, a phenolate or carboxylate oxygen, and a chloride ion in the coordination plane. UV absorption and 1H NMR spectral changes indicated that all the complexes could be converted to the indole-binding complexes where the O donor was replaced by the indole C2 atom by cyclopalladation in DMSO or DMF in the temperature range of 40-60 degrees C. Formation of the indole-binding complex species obeyed the first-order kinetics, from which the activation parameters were estimated. The formation rate was dependent on the properties of the O-donor group, a lower pKa value of its conjugate acid causing faster conversion to the indole-binding species in the order 2 (methoxyphenolate) < 3 (nitrophenolate) < 4 (carboxylate). On the other hand, the ratio of the indole-binding complex to the O-donor complex as a result of the conversion was greater for the complexes with a higher pKa value of the ligand OH group, the order being 2 > 3 > 4. 相似文献
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Takakazu Yamamoto Junichi Ishizu Sanshiro Komiya Yoshiyuki Nakamura Akio Yamamoto 《Journal of organometallic chemistry》1979,171(1):103-112
13C NMR data are given for a series of phosphinenickel(0) complexes of ethyl methacrylate (ema), Ni(PR3)2(CH2=C(CH3)COOC2H5) (PR3 = PPh3 (Ia), PEtPh2 (Ib), PEt2Ph (Ic), PMe2Ph (Id), PEt3 (Ie)). The olefinic carbon signals of ema shift upfield by 71.5–86.5 ppm on coordination, the magnitude of the upfield shift increasing with increase in the bacisity of the phosphine ligand. The effect of the basicity of PR3 is discussed on the basis of the back-bonding from Ni to ema. Variable temperature1H NMR studies reveal that the ema of Id, the complex having the least sterically demanding phosphine ligands, exchanges with free ema in toluene on the NMR time scale. The dependence of the rate of exchange on the concentration of ema shows that the exchange proceeds through anSN2 mechanism. The activation parameters are: ΔH273≠ 2.75 kcal/mol, ΔG273≠ 12.7 kcal/mol, ΔS273≠ ?37 e.u. The31P NMR spectra of the complexes show two doublets when the exchange is frozen out, indicating the inequivalence of the two phosphine ligands in the ema-coordinated complex. The difference in the31P chemical shifts of the two coordinated tertiary phosphines increases with increase in the basicity of the PR3 ligand. 相似文献
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Abstract— Two fluorescence probes, 1-dimethylaminonaphthalene-5-sulfonylchloride and pyrene-1-sulfonylchloride, were conjugated to the protein in purple membrane and fluorescence intensity and anisotropy were measured as a function of temperature. The anisotropy of the 1-dimethyl-aminonaphthalene-5-sulfonate conjugate showed a characteristic temperature dependence, in which, the anisotropy is constant at 0.22 ± 0.01 until 25-30°C and decreases above 30°C. The fluorescence intensity, however, varies linearly with temperature. These results imply that the transition is due to bacteriorhodopsin in the trimer. 相似文献
9.
Gerhard Wegner Nobuo Nakabayashi Harold G. Cassidy 《Journal of polymer science. Part A, Polymer chemistry》1968,6(11):3151-3156
It is possible to prepare polyurethanes from p-benzoquinone-diols and diisocyanates by using dibutyltin diacetate catalyst at room temperature or below, since the benzoquinone group does not react with isocyanate under these conditions. This permits preparation of new redox polymers. In preparing the polyurethanes excess isocyanate groups must be destroyed at the end of the reaction time in order to prevent crosslinking during work-up. These polymers are readily reduced by aqueous hydrosulfite. Good viscosity numbers are obtained; and, in general, upon reduction the viscosity increases over that of the oxidized form. There is no evidence of crosslinking. When oxidized and reduced forms of these polymers are mixed there is no evidence of charge transfer. 相似文献
10.
Motoyama T Shimazaki Y Yajima T Nakabayashi Y Naruta Y Yamauchi O 《Journal of the American Chemical Society》2004,126(23):7378-7385
The Pd(II) complexes of new 2N1O-donor ligands containing a pendent indole, 3-[N-2-pyridylmethyl-N-2-hydroxy-3,5-di(tert-butyl)benzylamino]ethylindole (Htbu-iepp), 1-methyl-3-[N-2-pyridylmethyl-N-2-hydroxy-3,5-di(tert-butyl)benzylamino]ethylindole (Htbu-miepp), 3-[N-2-pyridylmethyl-N-2-hydroxy-3,5-di(tert-butyl)benzylamino]methylindole (Htbu-impp), and 3-(N-2-pyridylmethyl-N-4-hydroxybenzylamino)ethylindole (Hp-iepp) (H denotes a dissociable proton), were synthesized, and the structures of [Pd(tbu-iepp)Cl] (1a), [Pd(tbu-iepp-c)Cl] (1b), [Pd(tbu-miepp)Cl] (3), and [Pd(p-iepp-c)Cl] (4) (tbu-iepp-c and p-iepp-c denote tbu-iepp and p-iepp bound to Pd(II) through a carbon atom, respectively) were determined by X-ray analysis. Complexes 1a prepared in CH(2)Cl(2)/CH(3)CN and 3 prepared in CH(3)CN have a pyridine nitrogen, an amine nitrogen, a phenolate oxygen, and a chloride ion in the coordination plane. Complex 1b prepared in CH(3)CN has the same composition as 1a and was revealed to have the C2 atom of the indole ring bound to Pd(II) with the Pd(II)-C2 distance of 1.973(2) A. The same Pd(II)-indole C2 bonding was revealed for 4. Interconversion between 1a and 1b was observed for their solutions, the equilibrium being dependent on the solvent used. Reaction of 1b and 4 with 1 equiv of Ce(IV) in DMF gave the corresponding one-electron-oxidized species, which exhibited an ESR signal at g = 2.004 and an absorption peak at approximately 550 nm, indicating the formation of the Pd(II)-indole pi-cation radical species. The half-life, t(1/2), of the indole radical species at room temperature was calculated to be 20 s (k(obs) = 3.5 x 10(-)(2) s(-)(1)) for 1b. The cyclic voltammogram for 1b in DMF gave two irreversible oxidation peaks at E(pa) = 0.68 and 0.80 V (vs Ag/AgCl), which were ascribed to the oxidation processes of the coordinated indole and phenolate moieties, respectively. 相似文献