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111.
Masaru Matsuoka Akihiro Iwamoto Takeshi Ouchi Hiroshi Yoshioka Kazumi Nakatsu 《Journal of heterocyclic chemistry》1993,30(1):173-176
The structure of 1,4-dithiines obtained from orthodihalogeno heterocycles with thiocarbonyl compounds was determined by X-ray structure analysis of the intermolecular charge-transfer complex between 5,7,12,14-tetramethoxydibenzo[b,i]thianthrene and TCNQ. The formation of the thiazole ring has already been reported but the products were confirmed to be 1,4-dithiines by X-ray structure analysis and the previously reported results. 相似文献
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114.
Hiroshi Watanabe Takemoto Shin Hiromichi Matsuo Fumio Okuno Tsutomu Tsuji Midori Matsuoka Junichi Fukaura Hisashi Matsunaga 《Journal of voice》1994,8(4):340-346
The current study was carried out with particular emphasis on the association between phonetic function tests and alterations in the appearance of the hypopharyngeal and laryngeal mucosa, such as capillary dilatation, edema, and vocal fold injection after alcohol intake. The results demonstrated the occurrence of previously unrecognized pathophysiological changes associated with synchronous phonetic functions in the vocal pathway after alcohol intake. Serum ethanol and aldehyde concentration levels were evaluated hourly for 2.5 h after ingestion of alcohol. When an electronystagmogram showed the typical pattern of alcohol intake, the study was initiated. Occasionally, rhinography was performed on subjects complaining of a stuffy nose after alcohol intake. 相似文献
115.
Eiji Ihara Shingo Honjyo Tomomichi Itoh Mitsufumi Nodono 《Journal of polymer science. Part A, Polymer chemistry》2007,45(20):4597-4605
Radical copolymerization of alkyl 2‐norbornene‐2‐carboxylates (alkyl = Me 1a , nBu 1b ) with alkyl acrylates (alkyl = ethyl, methyl, and n‐butyl) was investigated. Copolymerization of 1a,b with the alkyl acrylates initiated by 1,1′‐azobis (cyclohexane‐1‐carbonitrile) at 85 °C proceeded to give random copolymers, although the homopolymerization of 1a,b did not proceed efficiently under the same conditions. Typically, bulk copolymerization of 1a with ethyl acrylate in a feed ratio of 1:3 ([ 1a ]:[EA]) afforded a copolymer with Mn = 33,300 containing 19.4 mol % of 1a unit in the composition. An increase of Tg derived from the incorporation of the rigid norbornane framework was observed, although the extent of the temperature rise was rather moderate. The ternary radical copolymerization of 1a,b /alkyl acrylate/N‐phenylmaleimide proceeded to give copolymers with the three repeating units in the main chain. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4597–4605, 2007 相似文献
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Transition moment directions for the double-bond region vibrations of uracil, thymine and cytosine are calculated using the fixed partial charge model approximation. The coupling between the two carbonyl bonds and the carbon—carbon double bond in uracil and thymine is sensitive to the choice of the corresponding stretching force constants. The transition moment directions are correspondingly changed, thus, in principle, enabling the quantitative determination of coupling between the vibrations from linear dichroism measurements. 相似文献
118.
An experimental study of the damage of Si solar cells due to Q-switched ruby laser radiation has been made. Four kinds of specimen with different surface states were used in order to examine how the damage depends on the surface state: (a) chemically etched to a mirror finish, (b) mechanically polished by a 0.5 m Al2O3 powder, (c) chemically etched, but rough, (d) coated with SiO on the (c) surface. The threshold power densities, at which a change in the photo-current occurs, were for the specimens (a) to (d) respectively 60 MW cm–2, 20 MW cm–2, 30 MW cm–2 and 9 MW cm–2. Attenuations of the photo-current of the specimens, a, c and d were observed over the whole range of wavelength 500 to 1000 nm. For the b cell, however, increase of the photo-current was observed mainly in the short wavelength region. 相似文献
119.
Matsuoka H Yamamoto T Harada T Ikeda T 《Langmuir : the ACS journal of surfaces and colloids》2005,21(16):7105-7108
The effect of counterion species on the colloidal crystal structure in a dispersion was carefully investigated as a function of the degree of neutralization (alpha) by the ultra-small-angle X-ray scattering technique. The nearest neighbor interparticle distance (2D(exp)) first increased with decreasing alpha, and then decreased after passing through the maximum. This behavior was confirmed for K(+), Li(+), Ca(2+), TMA(+) (tetramethylammonium) as a counterion, and Na(+) in our previous report (Harada, T.; Matsuoka, H.; Ikeda, T.; Yamaoka, H. Langmuir 2000, 16, 1612). However, the alpha value of the maximum position (alpha(max)) largely depended on the counterion species, and it was in the order K(+) < Na(+) < TMA(+) approximately Li(+). This behavior was well characterized by the specific features of each ion: the alpha(max) map could be well superimposed in the Stokes radius-crystal ion radius relationship of counterions. The alpha(max) dependence on Stokes radius was very similar to that of the B coefficient by Jones and Dole except in the case of Ca(2+). In principle, the smaller the value for B, the smaller alpha(max), indicating that a water structure breaker such as K(+) can more easily destroy the colloidal crystal structure. In other words, the effect of the counterion species on colloidal crystal stability follows the Hofmeister series. Including Ca(2+), the relationship was linear for the alpha(max) values plotted as a function of the limiting equivalent conductivity of small ions. A counterion with larger conductivity would be a stronger breaker for the colloidal crystal structure. 相似文献
120.
Takahashi T Matsuoka K Takimiya K Otsubo T Aso Y 《Journal of the American Chemical Society》2005,127(25):8928-8929
A series of highly extensive quinoidal oligothiophenes carrying a dicyanomethylene group at both terminal positions is synthesized. As the quinoidal structures extend, they have highly amphoteric abilities and show strong electronic absorptions in the visible to near-infrared region. The higher homologues, quinquethiophene and sexithiophene, exist as equilibrium mixtures with the biradical species. 相似文献