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排序方式: 共有206条查询结果,搜索用时 265 毫秒
1.
Sonoko Kikuchi Kazuteru Kawauchi Sadatsugu Ooki Masaru Kurosawa Hisashi Honjho Teruo Yagishita 《Analytical sciences》2004,20(8):1111-1112
Using Raman spectroscopy without any preparation, we analyzed the brominated flame retardant, polybromodiphenyl ethers (PBDEs), which has been prohibited by the European Union. The typical Raman bands of PBDEs, which are clearly different from those of other brominated flame retardants, are from 100 to 300 cm(-1). In our analysis, the detection limit was about 100 ppm, and the analysis took about 1 min, whereas the usual method of solvent extraction using gas chromatography/mass spectroscopy takes 50 h. 相似文献
2.
The negative chemical ionization mass spectra of representative perfluorinated alkanes, cycloalkanes, ethers and tertiary amines have been examined, using Ar at about 0.5 torr as the reagent gas. The compounds chosen are typical of those under study as components of fluorochemical emulsion blood substitutes. Many such PFC's, particularly those with cyclic or branched structures, give intense molecular ions; most give simple spectra with a few major fragment ions at high mass, in marked contrast to the EI spectra which are dominated by m/e 69 (CF3+) and 131 (C3F5+) of no value for structure elucidation. NCI-GC/MS is more sensitive than conventional EI-GC/MS and promises to be more generally useful for structure determination. Specific examples from the various classes will be presented, and their NCI and EI mass spectra compared. 相似文献
3.
Tsutomu Kagiya Shizuo Narisawa Taizo Ichida Kenichi Fukui Hisao Yokota Masatsune Kondo 《Journal of polymer science. Part A, Polymer chemistry》1966,4(2):293-299
The copolymerization of carbon monoxide and aziridines such as ethylenimine and propylenimine was carried out by γ-ray irradiation. Aziridines and carbon monoxide were allowed to copolymerize under γ-ray irradiation from a Co60 source and gave a crystalline solid copolymer. The yield of the copolymer increased with reaction temperature. The composition of copolymers obtained did not depend on the feed ratio of monomers and was found to be almost equimolar. The copolymer of ethylenimine and carbon monoxide melted at about 322–335°C. with decomposition and has an infrared spectrum identical with that of poly-β-alanine obtained by the hydrogen-migration polymerization of acrylamide. The hydrolyzed product of the ethylenimine–carbon monoxide copolymer was confirmed to be β-alanine by paper chromatography. These results lead to the conclusion that the copolymerization of aziridines and carbon monoxide took place alternatively by γ-ray irradiation, and produced crystalline poly-β-alanines. 相似文献
4.
A systematic study has been carried out on the characteristic changes in the fluorescence spectra of 1-naphthol doped in the
sol-gel-xerogel transition systems comprised of tetraethyl orthosilicate and diisobutoxyaluminium triethylsilicate catalyzed
by a small amount of HCl, NH4OH, as well as under uncatalyzed conditions. In the systems containing large amounts of silicon, the fluorescence of 1-naphthol
shifts to the red (a predominant emission from the 1La state) during the first stage of the reaction. This red shift indicates an increase in the polarity of the matrix surrounding
1-naphthol. In the second stage of the reaction, the spectrum shifts to the blue (a predominant emission from the 1Lb state), reflecting an increase in the micro-viscosity around 1-naphthol. In the systems containing relatively large amounts
of aluminum, however, the spectrum just after mixing shows a larger red shift than that originating from the 1L2 emission. This large red-shifted fluorescence reflects the formation of a complex between 1-naphthol and the −O−Al−O−Si−O-network.
The spectrum then shifted to the blue. The spectral behaviours observed indicate that there is a large and dynamic molecular-level
change in the physicochemical properties of the matrix surrounding the 1-naphthol molecules during the sol-gel-xerogel transitions
of the systems while the gelation phenomenon reflects macroscopic inflexibility although it is completely different from the
restriction of movement at the molecular level. 相似文献
5.
We revealed that in ATX-S10.Na(II)(13,17-bis (1-carboxypropionyl) carbamoylethyl-8-etheny-2-hydroxy-3-hydroxyiminoethylidene-2,7,12,18-tetraethyl porphyrin sodium)-mediated photodynamic therapy using 667 nm nanosecond-pulsed light excitation at a peak intensity of 2.0 MW/cm(2), phototoxicity increased with decreasing pulse repetition rate in the range of 5-30 Hz for A549 cell cultures. To examine the relation between the reaction mechanism and measured phototoxicity, we carefully measured the kinetics of photochemical oxygen consumption and photobleaching during irradiation of ATX-S10.Na(II)-sensitized A549 monolayer cultures. Measurements of oxygen consumption with a microelectrode, which was performed just above the cells, showed that there was no significant difference between the magnitudes of decrease in oxygen at the three repetition rates at the same cumulative fluence. Loss of ATX-S10.Na(II) fluorescence intensity also exhibited little repetition rate dependence when compared at the same cumulative fluence. We investigated the correlation between oxygen consumption and photobleaching during irradiation and obtained "fluorescence-oxygen diagrams." The diagrams showed dynamic changes between oxygen-dependent and oxygen-independent photobleaching at the higher repetition rates of 10 and 30 Hz, whereas such change was not clearly seen over the whole irradiation time at 5 Hz. These results suggest that the reduced phototoxicity at high repetition rates might be due to an oxygen-independent reaction. We presumed that the change in the reaction mechanism was associated with the local concentrations of the photosensitizer and oxygen in cells during irradiation. 相似文献
6.
Otohiko Tsuge Taizo Hatta Hisashi Kojima Nobutaka Miyahara Masafumi Sugaya 《Journal of heterocyclic chemistry》1994,31(5):1283-1287
2-Benzoyl- 5 and 2-acetylacenaphthenone 6 , prepared from the corresponding 1-acyl-2-(1-pyrrolidinyl)-acenaphthylenes 2 and 3 , reacted with arylhydrazines 8 under acidic conditions to give the corresponding 1-arylacenaphtho[1,2-d]pyrazoles 9 and 10 . Novel heteropentalene mesomeric betaines, 5,7-dehydro-5H,7H-benzo[b]acenaphtho[1,2-e]-1,3a,6a-triazapentalenes 13 and 14 were prepared by reductive cyclization of 1-(o-nitrophenyl)acenaphtho[1,2-d]pyrazoles 9d and 10d , respectively. 相似文献
7.
Taizo Sasaki 《Synchrotron Radiation News》2016,29(2):31-32
The Japanese electron synchrotron started operation on December 15, 1961, with energy of 750 MeV at the Institute for Nuclear Study (INS) of the University of Tokyo, Tanashi. It was established as a joint effort of the entire Japanese community of high-energy physicists so that its use was announced as being open to all Japanese users from the start. 相似文献
8.
9.
Akter Sharmin Tanabe Tomoki Maejima Satoshi Kawauchi Satoko Sato Shunichi Hinoki Akinari Aosasa Suefumi Yamamoto Junji Nishidate Izumi 《Optical Review》2016,23(2):354-359
Optical Review - To quantify the changes in optical properties of in vivo rat liver tissue, we applied diffuse reflectance spectroscopy (DRS) system using single-reflectance fiber probe during... 相似文献
10.
Yoshida Keiichiro Ishizuka Tomohiro Mizushima Chiharu Nishidate Izumi Kawauchi Satoko Sato Shunichi Sato Manabu 《Optical Review》2015,22(2):374-384
Optical Review - To evaluate multi-spectral images of the absorption and scattering properties in the cerebral cortex of rat brain, we investigated spectral reflectance images estimated by the... 相似文献