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101.
102.
Tae-Ho Kim Masakazu Saito Masaya Matsuoka Shinya Tsukada Kiyohisa Wada Masakazu Anpo 《Research on Chemical Intermediates》2010,36(5):453-461
It was found that the photoelectrochemical performance and photocatalytic activity of rod-type TiO2 electrodes were affected by various post-calcination treatments, for example, calcination in NH3 or under vacuum. Post-calcination treatment in NH3 at 773 K was particularly effective in increasing the photoelectrochemical performance and photocatalytic activity of rod-type TiO2 electrodes. A unique photoelectrochemical circuit was constructed by connecting a rod-type TiO2 electrode to a Pt electrode through a silicon solar cell in which the negative bias was applied on the rod-type TiO2 electrode. It was found that the photoelectrochemical circuit can effectively oxidize ethanethiol in water into CO2. 相似文献
103.
Daisuke Saito Dr. Tomasz Galica Prof. Dr. Eiji Nishibori Dr. Masaki Yoshida Dr. Atsushi Kobayashi Prof. Dr. Masako Kato 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(32):e202200703
The vapochromic single-crystal-to-single-crystal (SCSC) transformation of a highly luminescent PtII complex bearing an N-heterocyclic carbene [Pt(CN)2(tBu-impy)] (tBu-impyH+=1-tert-butyl-3-(2-pyridyl)-1H-imidazolium) is reported. The trihydrate form of the complex, which exhibits blue 3MMLCT emission owing to weak Pt⋅⋅⋅Pt interactions, changed its luminescence color from blue to yellowish-green upon the desorption of water molecules while keeping the high emission quantum yield of more than 0.45. Variable-temperature and continuous in-situ tracking of single-crystal X-ray diffraction measurements revealed that the SCSC transformation proceeds reversibly by the release and reabsorption of water molecules, thereby changing the stacked structure slightly. As a result, the dynamics of vapor-induced SCSC transformation were elucidated: that the anhydrous form returned to the original trihydrate form in a two-step process under a water vapor atmosphere. In addition, the PtII complex exhibited a similar SCSC response accompanied by a luminescence color change in the presence of methanol vapor, while being inactive toward ethanol vapor. 相似文献
104.
Oxidation of substituted thioanisoles by chemically generated singlet oxygen was investigated in polar aqueous media. The formation of the superoxide ion was observed during sulphoxidation of 4-hydroxythioanisole (4) in phosphate buffer at pH 7.5. Control experiments indicated that the superoxide ion was formed by a direct reaction between singlet oxygen and 4. The kinetics of the trapping reaction by diphenylsulphoxide indicated the involvement of a single intermediate. The overall rate constants of the reaction of thioanisoles with singlet oxygen in methanol-water (1:1) are one order of magnitude larger than those in benzene. On the basis of these results, a mechanism involving a charge-transfer complex has been proposed for the reaction of electron-rich thioanisoles with singlet oxygen, whereby the charge-transfer complex would produce persulphoxide directly or dissociate to the cation radical and superoxide ion in polar aqueous media. 相似文献
105.
Isao Saito Shigeru Muramatsu Hiroshi Sugiyama Akihiro Yamamoto Teruo Matsuura 《Tetrahedron letters》1985,26(48):5891-5894
Photochemical hydrogen-deuterium exchange reaction of biologically important indoles is reported. The regioselectivity of the photodeuteration was found to be controlled by the ammonium group of the side chain. 相似文献
106.
Irradiation of 5-iodouridine or 6-iodo-1,3-dimethyluracil in aq. acetonitrile in the presence of allyltrimethylsilane provided the corresponding 5- or 6-allylated product. 相似文献
107.
Theoretical equations were proposed to adequately simulate the electrical conductivity behavior of aqueous solutions of both
charged and uncharged polymers. The theory, based on the mixture equation of Boned and Peyrelasse, was experimentally verified
on poly(acrylic acid) (PAA) in water and poly(ethylene oxide) (PEO) in aqueous electrolyte solutions. The data analysis suggested
that both the polymer coils may be depicted as oblate ellipsoids. Subsequently, the semiaxes values of the polymer coils were
determined, and they were in good agreement with the results reported in the literature.
Received: 25 June 1996 Accepted: 2 October 1996 相似文献
108.
Morimasa Saito 《Analytical and bioanalytical chemistry》1997,357(1):18-21
In dc glow discharge mass spectrometry, the addition of small amounts of H2 to pure Ar as discharge gas has greatly increased the ion intensities of elements compared with the conventional method using
pure Ar. This phenomenon was also observed for the addition of H2 to pure Kr. The reason for the increase of the ion intensities of elements was studied by using a Kr gas mixture containing
0.2% (v/v) H2. The ion intensities of the elements P, Se and As (whose first ionization potentials are higher than the energy levels of
the excited state of Kr) did not increase even if the Kr/H2 gas mixture was used. The results show that the addition of H2 significantly contributed to increasing the number of metastable argon or krypton atoms (Penning ionization).
Received: 4 November 1995/Revised: 5 January 1996/Accepted: 10 January 1996 相似文献
109.
Some organogermanium oligomers with different side groups were synthesized via li-gand substitution polymerization from 1, 4-dioxane complex of germanium dichloride withdifferent organolithitum compounds. The oligomers were isolated through either precipi-tation from methanol or extraction using toluene with a yield of no less than 50%. Theweiglit average molecular weight (M_w) of the oligomers is ranging from 1.4×10~3 to 5.9×10~3depending on the type and alkyl length of the organolithium compounds used. 相似文献
110.
Morimasa Saito 《Fresenius' Journal of Analytical Chemistry》1997,357(1):18-21
In dc glow discharge mass spectrometry, the addition of small amounts of H2 to pure Ar as discharge gas has greatly increased the ion intensities of elements compared with the conventional method using
pure Ar. This phenomenon was also observed for the addition of H2 to pure Kr. The reason for the increase of the ion intensities of elements was studied by using a Kr gas mixture containing
0.2% (v/v) H2. The ion intensities of the elements P, Se and As (whose first ionization potentials are higher than the energy levels of
the excited state of Kr) did not increase even if the Kr/H2 gas mixture was used. The results show that the addition of H2 significantly contributed to increasing the number of metastable argon or krypton atoms (Penning ionization).
Received: 4 November 1995/Revised: 5 January 1996/Accepted: 10 January 1996 相似文献