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Akira Takase, Sakumitsu Akagami, Minoru Nakamizo
1975 Volume 4 Issue 8 Pages
797-802
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Raman spectra of the smectic H phase and two unidentified phases of terephthal-bis-butylaniline are studied in the 0–400cm
−1 region. Observation of the Raman peaks due to lattice vibrations suggests that the latter two phases are closer to the crystalline solid phase rather than the smectic H phase.
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Katsuyuki Ogura, Ikuo Yoshimura, Nobuko Katoh, Gen-ichi Tsuchihashi
1975 Volume 4 Issue 8 Pages
803-804
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Methyl ester of
N-lauroylvaline, as well as its α-methylthio and α-methoxy derivatives, was synthesized, starting from 1-methylsulfinyl-1-methylthio-2-amino-3-methyl-1-butene (
2, R
1 = i-Pr) which was obtained by the reaction of isobutyronitrile and methyl methylthiomethyl sulfoxide (
1).
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Yoshio Ikefuji, Norihiko Yoshioka, Hisayuki Noumi, Susumu Tsuchiya
1975 Volume 4 Issue 8 Pages
805-806
Published: August 05, 1975
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The isomerization of 1-butene takes place over potassium;
trans-2-butene and
cis-2-butene are formed. The ratio,
trans/
cis, was 0.1–0.2 in the temperature range 20–40°C, and was about unity in the range 90–140°C.
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Hideaki Imai, Takeshi Nishiguchi, Kazuo Fukuzumi
1975 Volume 4 Issue 8 Pages
807-808
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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In the hydrogen transfer reaction catalyzed by dihydridotetrakis(triphenylphosphine)ruthenium(II), aldehydes and ketones are reduced to corresponding alcohols by ethers, hydroaromatic compounds, a
tert-amine and alcohols under mild conditions.
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Shigeaki Muto, Hajime Ogata, Yoshio Kamiya
1975 Volume 4 Issue 8 Pages
809-812
Published: August 05, 1975
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Oxidative addition reactions of organic acids to dioxygen complexes are investigated. In the case of Pt(PPh
3)
2O
2, hydrogen peroxide is obtained in as much as 70% yield with a platinum carboxylato complex, Pt( PPh
3)
2(OCOCH
2Cl)
2. The effect of pKa of the substrates on the oxidative addition of the dioxygen complexes is also examined.
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Tadashi Endo, Hidetoshi Tasai, Tatsuzo Ishigami
1975 Volume 4 Issue 8 Pages
813-814
Published: August 05, 1975
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Unsymmetrical disulfides were readily prepared in high yields by successive treatment of silver thiolates initially with 2,4-dinitrobenzenesulfenyl chloride in acetonitrile at 0 °C and then with the second thiols and silver acetate in DMF at room temperature.
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Masahiko Iyoda, Masazumi Nakagawa
1975 Volume 4 Issue 8 Pages
815-818
Published: August 05, 1975
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Dinaphtho-di-
t-butyltetradehydro[18]annulene (X) was prepared in order to clarify the effect of annelation on the diatropicity of dehydroannulenes containing formal acetylene and cumulene in the cyclic system. It was found that the diatropicity of X is strongly suppressed by fusion with two naphthalene nuclei in contrast to strongly diatropic dinaphtho-di-
t-butyldidehydro[l4]annulene (III). The result indicates that equivalent Kekule structures exert prominent effect on the delocalization of π-electrons in annelated annulene. The preparation of bis(dihydronaphtho)- (VIII) and naphtho-dihydronaphtho- (XII) analogues as reference compounds was also described.
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Syun-ichi Ishikawa, Hirochika Sakuragi, Masayuki Yoshida, Naoki Inamot ...
1975 Volume 4 Issue 8 Pages
819-822
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Irradiation of benzophenone
O-acyloximes (I) in benzene or toluene effects aromatic substitution on the solvents by diphenylmethaniminyl radicals (IV) to give
N-diphenylmethyleneaniline (II) or
N-diphenylmethylenetoluidines (VIII) unless concurrently formed acyloxyl radicals facilely decarboxylate. A mechanism involving a participation of sufficiently lived acyloxyl radicals is proposed for the above substitution reactions.
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Yoshio Nakamura, Hidefumi Hirai
1975 Volume 4 Issue 8 Pages
823-828
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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A polymer–rhodium complex prepared from rhodium(III) chloride and styrene-divinylbenzene copolymer with iminodiacetic acid groups is found to catalyze the heterogeneous hydrogenation of alkenes in polar solvents at 30°C under an atmospheric hydrogen pressure. The polymer complex hydrogenates selectively the ethylenic double bonds in the alkenes with carbonyl and aromatic groups. The rates of hydrogenation of alkenes by the polymer complex are found to be markedly affected by the steric hindrance of the substrates.
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Mamoru Ohashi, Kazuo Tsujimoto
1975 Volume 4 Issue 8 Pages
829-830
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Irradiation of 1,2,4,5-tetracyanobenzene in tetrahydrofuran underwent photosubstitution to give tetrahydro-2-(2,4,5-tricyanophenyl)furan. The reaction is scarecely affected by trifluoroacetic acid and hence it appears to belong to a novel class of photoelectrophilic substitution.
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Ushio Sakaguchi, Hayami Yoneda
1975 Volume 4 Issue 8 Pages
831-832
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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The proton spin-lattice relaxation times have been measured on diamminebis(acetylacetone)ethylenediimino-cobalt(III) ion in D
2O using the pulsed Fourier transform method at 100 MHz. The shorter relaxation time of the methyl resonating at lower magnetic field indicates that this methyl signal should be assigned to the methyl groups adjacent to the diimine bridge.
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Akira Itaya, Ken-ichi Okamoto, Shigekazu Kusabayashi
1975 Volume 4 Issue 8 Pages
833-836
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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The triplet energy transfer in poly-
N-vinylcarbazole (PVCz) films has been investigated by measuring the delayed emission spectra at 77 K. By doping of a triplet quencher such as naphthalene and fluorene, the PVCz phosphorescence decreased significantly and was replaced by the sensitized dopant phosphorescence. On the contrary, the PVCz delayed fluorescence rather increased with increasing concentration of triplet quenchers. This phenomenon suggests the presence of a heterogeneous triplet–triplet annihilation in PVCz films.
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Teruo Umemoto, Toshihide Kawashima, Yoshiteru Sakata, Soichi Misumi
1975 Volume 4 Issue 8 Pages
837-840
Published: August 05, 1975
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[2.2] (1,3)Pyrenophane (
5) and a triple-layered metacyclopyrenophane (
10) were synthesized successfully via transannular reaction of 4,6-bisbromomethyl[2.2]metacyclophane with bromine as a key step and finally by dehydrogenation with DDQ.
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Kyoichi Sekine
1975 Volume 4 Issue 8 Pages
841-846
Published: August 05, 1975
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A new electrochemical method for the study of the diffusion process of hydrogen in metal foils is proposed. In the bielectrode system when hydrogen charging direct current is overlapped with sinusoidal current, there appears a phase lag in permeation current. This phase lag is related mathematically to the diffusion coefficient D of hydrogen in metal. The values of D obtained by this method are in good agreement with those by other methods in α-phase palladium-hydrogen system.
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Toschitake Iwamoto, Mamoru Kiyoki, Niro Matsuura
1975 Volume 4 Issue 8 Pages
847-848
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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The cyclohexadienyl radicals in the γ-irradiated benzene clathrates Cd(diam)M(CN)
4·2C
6H
6 (diam = (NH
3)
2, NH
2(CH
2)
2NH
2, or NH
2(CH
2)
3NH
2; M = Cd or Hg) are stable up to 423 K.
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Teizo Kitagawa, Tetsutaro Iizuka, Masao Saito, Yoshimasa Kyogoku
1975 Volume 4 Issue 8 Pages
849-852
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Classification of the Raman spectra of various hemoproteins including HbNO and HbCNC
2H
5 suggests that there are two kinds of ferrous low spin states. They are specified by the binding nature of the sixth ligand (L) to heme iron. The Fe–L bond in HbNO and HbCNC
2H
5 as well as in HbCO and HbO
2 is of π type while that in ferrous cytochromes
b5 and
c is of σ type.
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Takeo Taguchi, Hisashi Okamura, Hisashi Takei
1975 Volume 4 Issue 8 Pages
853-854
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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A convenient method for the preparations of 3-alkylfuran and 2,4-dialkylfuran has been established via three step-procedures starting from α-(alkylthio)carbonyl compounds.
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Mikio Watanabe, Kozo Shirai, Takanobu Kumamoto
1975 Volume 4 Issue 8 Pages
855-858
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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The reaction of γ-butyrolactone with
N-phenylthiophthalimide in the presence of lithium diisopropylamide afforded α,α-bis (phenylthio)-γ-butyrolactone
1 in high yield. Further, a convenient method for the preparation of 3-substituted 2-buten-4-olide was established by the use of
1.
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Katsuo Ohkata, Yasuo Kubo, Akira Tamaru, Terukiyo Hanafusa
1975 Volume 4 Issue 8 Pages
859-862
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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1,1,2,2-Tetraacylcyclopropanes (
1a,
1b) were rearranged into nine-membered enol lactones (
2a,
2b) by tertiary amines, while primary arylamines brought about retro-Mannich reaction to give bisdimedone (
4) and Schiff base.
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Akitami Ichihara, Hideo Kaibuchi, Makio Kobayashi, Kengo Oda, Sadao Sa ...
1975 Volume 4 Issue 8 Pages
863-866
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Novel cage-shaped compounds were obtained by the reduction of
r-2,3-epoxy-2,3,4,
c-4
a,5,8,
c-8
a-hexahydro-
c-5,8-isobutylidene-1,4-naphthoquinones (
1) and assigned the structure
2 on the basis of the spectral data and X-ray crystallography. The compounds have an oxygen-containing strained cage structure hitherto unknown.
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Takashi Kawamura, Masaji Matsunaga, Teijiro Yonezawa
1975 Volume 4 Issue 8 Pages
867-870
Published: August 05, 1975
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Correlations between coupling constants in electron spin resonance and nuclear magnetic resonance are examined. Plots of proton hyper-fine splitting constants of HR
· against the corresponding proton–proton coupling constants of the parent hydrocarbons HRH are shown to fit one curve.
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Yutaka Watanabe, Manzo Shiono, Teruaki Mukaiyama
1975 Volume 4 Issue 8 Pages
871-872
Published: August 05, 1975
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2-(Phenylthio)ethanols readily accessible from carbonyl compounds and phenylthiomethyllithium were converted into terminal olefins in high yields by way of the reductive β-elimination on treatment with TiCl
4 and LiAlH
4 in the presence of tertiary amine such as 1,8-bis(dimethylamino)naphthalene or tri-
n-butylamine.
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Hiroshi Takaku, Yoshifusa Shimada, Tsujiaki Hata
1975 Volume 4 Issue 8 Pages
873-874
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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8-Hydroxyquinolyl group was used as a new protecting group on phosphates in the synthesis of oligonucleotides. This group was easily removed by treatment with cupric chloride in a mixture of dimethyl sulfoxide and water.
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Masayoshi Muraki, Teruaki Mukaiyama
1975 Volume 4 Issue 8 Pages
875-878
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Bis(4-methyl-1-piperazinyl)aluminum hydride was found to be a useful reagent for reduction of various
N,
N-disubstituted carboxamides, such as
N-acylmorpholines and
N,
N-dimethylcarboxamides, to provide the corresponding aldehydes in fairly good yields.
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Khurshid A. Khan
1975 Volume 4 Issue 8 Pages
879-882
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Primary processes in photolysis of 1-nitropropane in gas phase are analogous to those of nitroethane and 2-nitropropane. Ethylene, propylene and methyl nitrite are the major photolysis products,while minor products are methane, methyl nitrate, ethylene oxide, ethyl nitrite, propyl nitrite, formaldehyde, propionaldehyde, water, nitric oxide and nitrogen dioxide. Quantum yields of formation of photoproducts ethylene and propylene at 22°C are 0.074 and 0.042; and at 56°C these are 0.039 and 0.01. A mechanism of the photolysis is suggested.
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Yoshihiro Nakato, Toshihiro Ohnishi, Hiroshi Tsubomura
1975 Volume 4 Issue 8 Pages
883-886
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Contrary to most ordinary semiconductor electrodes, metal-coated semiconductor electrodes have been found to cause photocurrents in aqueous solutions without dissolution into or reaction with the solution, and will be useful as solar-energy convertors.
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Hideki Sakurai, Yoshiyasu Kamiyama, Yasuhiro Nakadaira
1975 Volume 4 Issue 8 Pages
887-890
Published: August 05, 1975
Released on J-STAGE: March 27, 2006
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Organodisilanes undergo a novel 1:2 cycloaddition reaction with butadiene or isoprene in the presence of a palladium complex. For example, the reaction of 1,1,2,2-tetramethy1-1,2-disilacyclopentane with isoprene gave 1,1,5,5,8,11-hexamethyl-l,5-disilacyclotrideca-7,11-diene in 76% yield.
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Hideki Sakurai, Takafumi Imai
1975 Volume 4 Issue 8 Pages
891-894
Published: August 05, 1975
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In the presence of a palladium complex, 1,1-dimethyl-1-silacyclobutane reacts smoothly with dimethyl acetylenedicarboxylate to give 1,1-dimethyl-2,3-bis(methoxycarbonyl)-1-silacyclohex-2-ene in quantitative yield. Other silacyclobutanes react similarly with various acetylenes to give silacyclohexene derivatives.
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Tadashi Masamune, Hajime Matsue
1975 Volume 4 Issue 8 Pages
895-898
Published: August 05, 1975
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The synthesis of the titled hydrooxocinone (
2) is described. Hydride reduction of a mixture of methyl 5-ethyl-2,5-dihydro-2-furoates (
3) followed by ozonization afforded a dialdehyde mixture, which was submitted to the Robinson-Schöpf condensation to give, after acetylation, three 9-aza-3-oxabicyclo[3. 3 .1]nonanones (
5 ∼
7).
cis-Bicyclononanone (
5) was further transformed by a modification of the Paquette procedure (
5 →
8 →
9 →
10a →
11) to give
cis-2-ethyl-8-hydroxymethyl-7, 8-dihydro-2
H oxocin-3 (4
H)-one (
11), which was converted smoothly into the aldehyde (
2), one of the most important intermediates for synthesis of laurencin (
1).
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Akihiko Yamagishi
1975 Volume 4 Issue 8 Pages
899-902
Published: August 05, 1975
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The rates of the electron-transfer reaction between 7,7,8,8-tetracyanoquinodimethane anion radical and 2,3-dichloro-5,6-dicyano-
p-benzoquinone in acetonitrile have been determined with a temperature-jump apparatus. The forward and backward rate constants are (4±1) ×10
9M
−1s
−1 and (1±0.5) ×10
4M
−1s
−1 at 15°C, respectively. Addition of 10 per cent water to acetonitrile decreases the forward rate constant by a factor of 100.
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Kiyoshi Kawakami, Tsutomu Mizoroki, Atsumu Ozaki
1975 Volume 4 Issue 8 Pages
903-904
Published: August 05, 1975
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Dimerization of ethylene is very selectively catalyzed by halogenotris(triphenylphosphine)cobalt(I) in the presence of Lewis acid in halobenzene. The catalytic activity is significantly affected by the solvent, bromobenzene being most effective.
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Shin Sato, Kiyoshi Okazaki
1975 Volume 4 Issue 8 Pages
905-908
Published: August 05, 1975
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The apparatus for the measurement of the efficiency of the conversion of γ-rays into UV-light has been devised. The conversion system consists of helium gas with a drop of mercury. The G-value of UV-light-photons at 253.7 nm produced in this system by γ-irradiation was estimated both experimentally and theoretically. The mercury photosensitized decomposition of nitrous oxide at 0°C was used as the actinometer. The efficiency of the conversion of
60Co γ-rays into UV-light at 253.7 nm was found to be 80 %.
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Yoshio Takasu, Shun-ichi Maru, Yoshiharu Matsuda
1975 Volume 4 Issue 8 Pages
909-910
Published: August 05, 1975
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Oxidation of iron plates in nitric oxide was examined. The oxidation rate was higher than that in oxygen in a certain temperature range, 450–580°C, however, it had a minimum at 550°C in regard to its temperature dependencies. The scales formed in nitric oxide was found to be consisted of only Fe
3O
4.
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