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Yusei Maruyama, Kyoko Machida, Noriko Iwasaki, Satoshi Iwashima
1975 Volume 4 Issue 9 Pages
911-914
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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An annealing effect in the absorption spectrum of an amorphous naphthacene film was investigated. The remarkable effect observed may be explained by assuming the change of the range of order in molecular arrangements. The fluorescence life times of some amorphous organic films were also measured comparing with those of crystalline films. The differences between them were discussed in terms of the localization character of electronic states in the amorphous film.
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Masamitsu Shirai, Taizo Koizumi, Yoshio Iguchi, Makoto Tanaka
1975 Volume 4 Issue 9 Pages
915-918
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Autoxidations of hydroquinone and its derivatives are catalyzed by pyridinium salts positively or negatively depending on the properties of the substituents of the pyridinium rings. Formation of charge–transfer complexes between hydroquinones and pyridinium salts plays an important role.
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Akikazu Kakehi, Suketaka Ito, Takahisa Funahashi, Norio Ogasawara
1975 Volume 4 Issue 9 Pages
919-922
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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The reactions of 1-alkylpyridinium salts carrying a 2- or 4-methyl group with activated β-ethoxymethylene compounds in the presence of alkali gave the corresponding 2- or 4-allylidenedihydropyridine derivatives in good yields.
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Shosuke Yamamura, J. A. Lamberton, Hajime Irikawa, Yasuaki Okumura, Yo ...
1975 Volume 4 Issue 9 Pages
923-926
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Five new alkaloids have been isolated from the plant
Daphniphyllum gracile Gage, and their structures also been elucidated on the basis of their spectral and chemical evidences. Particularly, daphnigraciline methiodide (VI) was directly converted into yuzurine methiodide (VII). Furthermore, application of
13C NMR spectra plays an important role in the structural elucidation.
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Tomihisa Kambara, Junsuke Suzuki, Hiroe Yoshioka, Toshio Nakamura
1975 Volume 4 Issue 9 Pages
927-930
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Redox substoichiometry in the isotope dilution analysis of antimony was studied. As the substoichiometric reaction the oxidation of trivalent antimony to pentavalent with potassium permanganate was used, followed by the BPHA extraction of trivalent antimony. The redox substoichiometry was applied to the determination of antimony content in
124Sb obtained from JAERI. The content determined was 0.481±0.02 μg, which agreed with the certified value.
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Seishi Yajima, Josaburo Hayashi, Mamoru Omori
1975 Volume 4 Issue 9 Pages
931-934
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Continuous silicon carbide fiber of high-tensile strength (about 350 Kg/mm
2) was synthesized by means of the heat-treatment of organosilicon polymer obtained from dodecamethylcyclohexasilane. X-ray analysis and high voltage electron microscopic observations revealed that the obtained continuous fiber is an ultrafine grain structure of β-silicon carbide.
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Yuzo Saeki, Akemi Kato, Ryoko Matsuzaki
1975 Volume 4 Issue 9 Pages
935-938
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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The reaction process between Na
2WO
4 and chlorine can be represented as follows: Na
2WO
4 \xrightarrowabout140°C Na
2W
2O
7 \xrightarrowabout350°C Na
2W
4O
13 \xrightarrowabout480°CWO
3. The WO
3 The reacts with chlorine above about 700°C to form volatile WO
2Cl
2. WOCl
4 obtained together with WO
2Cl
2 above 800°C is probably formed by the reaction between WO
3 and NaCl.
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G. Bennett
1975 Volume 4 Issue 9 Pages
939-942
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Various 3,4,4-trisubstituted-2-buten-4-olides were prepared by the condensation of 2-alkyn-1,4-diols with triethyl orthoacetate in the presence of a catalytic amount of pivalic acid.
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Shun-ichi Meguro, Tsutomu Mizoroki, Atsumu Ozaki
1975 Volume 4 Issue 9 Pages
943-946
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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α-Methyl-cinnamaldehyde, cinnamaldehyde, and croton aldehyde are hydrogenated to the corresponding unsaturated alcohols with a fairly high selectivity by use of RhCl
3·3H
2O or Rh
2(CO)
4Cl
2 catalyst in tertiary amine-benzene solution under an oxo-reaction condition. A catalytic amount of triphenylphosphine to this catalyst system substantially retards the hydrogenation of –CHO giving saturated aldehyde.
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Kenryo Namba, Shuichi Suzuki
1975 Volume 4 Issue 9 Pages
947-950
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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A photochromic α-amylase was prepared by chemical modification with a spiropyran compound and isolated with DEAE-Sephadex chromatography. The modified α-amylase showed the reverse photochromism in water. UV- or VS-light irradiation caused a decrease in enzyme activity of the modified enzyme. The initial activity could be recovered when the modified enzyme irradiated was kept in the dark.
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Kentaro Takagi, Tadashi Okamoto, Yasumasa Sakakibara, Atsuyoshi Ohno, ...
1975 Volume 4 Issue 9 Pages
951-954
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Convenient syntheses of various ketones from acyl halides and organomercury(II) compounds have been achieved by the aid of catalytic amounts of tetrakis(triphenylphosphine)palladium in hexamethylphosphoric triamide. Plausible reaction path is proposed.
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Hiromichi Kono, Naofumi Wakao, Yoichiro Nagai
1975 Volume 4 Issue 9 Pages
955-956
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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[RuX
2(PPh
3)
3] (X = Cl or Br) and [RhCl(PPh
3)
3] were reduced with silicon hydrides in the presence of triethylamine in benzene to give [RuHX(PPh
3)
3·C
6H
6] and [RhH(PPh
3)
4] in high yields.
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Naotake Takaishi, Yoshiaki Fujikura, Yoshiaki Inamoto, Hiroshi Ikeda
1975 Volume 4 Issue 9 Pages
957-960
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Decomposition of 1-(tricyclo[5.3.1.0
3,8]undec-3-yl)-2-diazoethan-1-one (IV) in toluene gave predominantly tetracyclo[7.3.1.0
2,5.0
5,10]tridecan-4-one (V) under silver oxide catalysis, while tetracyclo-[5.4.1.1
1,9.0
5,13]tridecan-11-one (VI) was the major reaction product in the presence of cupric sulfate.
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Ken-ichi Yoshikawa, Isao Morishima, Jun-ichi Kunitomo, Motoharu Ju-Ich ...
1975 Volume 4 Issue 9 Pages
961-964
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Carbon-13 NMR spectra of quaternary protoberberine alkaloids were measured and their preferential conformation was concluded by comparison of the chemical shift.
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Hiroko Sato, Takenori Kusumi, Kiyoto Imaye, Hiroshi Kakisawa
1975 Volume 4 Issue 9 Pages
965-966
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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1,3-Dipolar addition of the nitronic ester
1 to methyl acrylate and methyl crotonate afforded the corresponding adducts,
2 and
6, respectively. These were converted to the 4-amino-2-hydroxybutyric acids,
5 and
8.
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Shigeru Yamashita
1975 Volume 4 Issue 9 Pages
967-970
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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The photolysis of vinyl iodide has been studied using UV light beam of high intensity and a collision-free photochemical reactor incorporated in the ion-source of mass spectrometer. The primary process C
2H
3I + hν → C
2H
3 + I was found predominant and the process C
2H
3I + hν → C
2H
2 + HI minor, and the mass spectrum of vinyl radical was obtained.
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Masao Sakurai, Toshio Nakajima, Tsuyoshi Komatsu, Tsurutaro Nakagawa
1975 Volume 4 Issue 9 Pages
971-976
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Apparent molal adiabatic compressibilities of sodium chloride were measured in water at 5, 25, and 45°C. The Debye–Hückel limiting slopes were estimated experimentally. A convenient equation for the conversion of adiabatic to isothermal compressibilities was derived. The results indicate that the limiting slope for isothermal compressibility is larger by about 10% than that for adiabatic compressibility.
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Tsujiaki Hata, Isamu Yamamoto, Mitsuo Sekine
1975 Volume 4 Issue 9 Pages
977-980
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Azido group was introduced selectively to 5′-position of nucleosides by one-step reaction using carbon tetrabromide, triphenylphosphine, and lithium azide.
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Kiyoshi Iwai, Hiroshi Kosugi, Hisashi Uda
1975 Volume 4 Issue 9 Pages
981-982
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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α-Phenylsulfinyl-Δ
α,β-butenolide reacts more effectively with the enolates of cyclopentanone, 2-ethoxycarbonylcyclohexanone, and ethyl
n-valerate than the phenylthio analog to give the Michael addition products, which, except the cyclopentanone derivative, are transformed into the corresponding β-substituted Δ
α,β-butenolides.
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Atsuyoshi Ohno, Kaoru Nakamura, Misao Uohama, Shinzaburo Oka
1975 Volume 4 Issue 9 Pages
983-984
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Several nucleophilic and electrophilic reactions of di-
t-butyl thioketone are reported.
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Iwao Ojima, Tetsuo Kogure, Yoichiro Nagai
1975 Volume 4 Issue 9 Pages
985-988
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Selective asymmetric reductions of carbonyl functionalities in α,β-unsaturated carbonyl compounds, such as β-ionone, 2-methylcyclohexenone and mesityl oxide, were successfully carried out using dihydrosilane-chiral rhodium(I) complex catalyst combinations.
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Kazuhiko Saigo, Masaaki Osaki, Teruaki Mukaiyama
1975 Volume 4 Issue 9 Pages
989-990
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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In the presence of TiCl
4, ketene alkyl trialkylsilyl acetals, prepared from α-lithio esters and a trialkylsilyl halide, react with aldehydes and ketones at −78°C to afford the corresponding β-hydroxyesters and β-trialkylsiloxyesters in good yields.
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Hiroshi Minato, Kei Yamaguchi, Michio Kobayashi
1975 Volume 4 Issue 9 Pages
991-994
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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An alkoxyaminosulfonium ion is prepared from
N-tetramethylene-
p-toluenesulfinamide and methyl trifluoromethanesulfonate. Its NMR spectrum shows that its two α hydrogens of the pyrrolidine ring are magnetically non-equivalent, and this alkoxyaminosulfonium ion is not planar but pyramidal. It reacts with methyl sulfide, forming the original sulfinamide and trimethylsulfonium ion.
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Yoahihisa Watanabe, Sang Chul Shim, Take-aki Mitsudo, Masakazu Yamashi ...
1975 Volume 4 Issue 9 Pages
995-996
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Glutaraldehyde reacts with primary amines in the presence of tetracarbonylhydridoferrate to give the corresponding N-substituted piperidines.
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Yukio Takahashi, Nobu Tomita, Norihiko Yoneda, Akira Suzuki
1975 Volume 4 Issue 9 Pages
997-1000
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Alcohols with short carbon chains, one to four, which are not carboxylated under the usual Koch conditions, were carboxylated with carbon monoxide in the presence of HF–SbF
5 as a catalyst. This was carried out at temperatures from −20 to 30°C under atmospheric pressure. Except for methanol, such alcohols were found to react readily with carbon monoxide to give corresponding carboxylic acids in high yields.
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Atsuyoshi Saito, Sadayuki Himeno
1975 Volume 4 Issue 9 Pages
1001-1004
Published: September 05, 1975
Released on J-STAGE: March 27, 2006
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Polarographic reduction of nitrate took place in the ascending branch of an Fe(II) reduction wave in an unbuffered solution (pH 4–6) of a supporting electrolyte that contained iodate. In the potential region of reducing nitrate, the current varied periodically of which the period depended on the experimental condition.
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