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61.
62.
Kazuo Ito Kenichi Yakushijin Shigetaka Yoshina Akira Tanaka Katsumi Yamamoto 《Journal of heterocyclic chemistry》1978,15(2):301-305
2-Methylfuro [2,3-c] isoquinolin-5(4H)one (X) and 1-phenylfuro[2,3-c] isoquinolin-5(4H)one (XI) were prepared from thermal cyelization via the Curtius rearrangement of 5-methyl-3-phenyl-2-furoyl azide (VI) and 3,4-diphenyl-2-furoyl azide (VII), respectively. Stability against acid, alkylation and conversion of the NHCO group to a C=N double bond of X and XI, which were synthesized, are described. Also, 5-substituted furo[2,3-c] isoquinolines (XVIIIa-c) and (XIXa-c) were prepared. 相似文献
63.
Flow injection analysis, with chemiluminescence detection, is used to determine traces of cobalt(II) by means of the gallic acid—hydrogen peroxide—sodium hydroxide system containing a small amount of methanol to increase the sensitivity. This permits the determination of cobalt(II) more selectively than any other chemiluminescent system with a detection limit of 0.04 μg l-1 (continuous sample flow) or 0.04 ng (10-μl sample injection). The linear range is 3 orders of magnitude, the sampling rate is 20 h-1, and the relative standard deviation is 5.9% for 0.06 ng Co(II) (n = 10). Silver(I), the strongest enhancer after cobalt(II), provides a signal 1.3% of that for Co(II). A few precipitants and complexing agents suppress the signal. 相似文献
64.
Screening tests are described for the development of chemiluminescence systems (oxidizing systems) capable of detecting biological organic compounds. The light emission depends strongly on the oxidizing systems employed. Acidic permanganate system gives rise to light emission for many compounds, including catechols, catecholamines, triphenols and indoles. The following oxidizing systems led specifically to chemiluminescence for hydroquinone, adrenaline or phenylpyruvic acid: 10?1 M thiosulphate with 10?1 M sodium hydroxide and 10?4 M Ag (I), 0.3 % hydrogen peroxide with 10?3 M sodium hydroxide/50% acetonitrile and 10?4 M Fe (II), and 0.3% hydrogen peroxide with 10?2 M sodium hydroxide/10?2 M didodecyldimethylammonium bromide and 10?4 M Co(II), respectively. 相似文献
65.
Akira Tanaka Kenichi Yakushijin Shigetaka Yoshina 《Journal of heterocyclic chemistry》1978,15(1):123-125
Monobromination and monoacylation at the 2-position of 4H-furo[3,2-b]indole ring (III) were facilitated by the benzoyl group in the 4-position; subsequent nitration attempts were unsuccessful. 相似文献
66.
Shigetaka Fukuda 《Geometriae Dedicata》2001,85(1-3):183-187
We prove that every log crepant birational morphism between log terminal surfaces can be decomposed into log flopping type divisorial contraction morphisms and log blowdowns. Repeating these two kinds of contractions, we reach a minimal log minimal surface from any log minimal surface. 相似文献
67.
Isamu Maeba Masahiko Ando Shigetaka Yoshina Raymond N. Castle 《Journal of heterocyclic chemistry》1979,16(2):245-247
The reaction of 4,7-diehlorofuro[2,3-d]pyridazine (1) with potassium cyanide in DMSO gave two products, (E)-3,6-diehloro-5-(2-cyanovinyl)-4-hydroxypyridazine (II) and 5,8-dichloro-2-oxo-2H-pyrano[2,3-d]pyridazine (III) as a result of ring opening or ring expansion. A new ring system, 2-oxo-2H-pyrano[2,3-c]pyridazines (IX, XII, XIII) was obtained from 5,8-dichloro-3-methyl-2-oxo-2H-pyrano[2,3-d]pyridazine (VI). 相似文献
68.
Saruwatari K Sato H Idei T Kameda J Yamagishi A Takagaki A Domen K 《The journal of physical chemistry. B》2005,109(25):12410-12416
A hybrid film of layered niobate and an organic amphiphile was prepared by the Langmuir-Blodgett (LB) method. Trimethylammonium-exchanged perovskite-type niobates ((CH(3))(3)NHSr(2)Nb(3)O(10)) were exfoliative to form an aqueous suspension. A monolayer of octadecylamine was produced on such an aqueous dispersion as a template for a hybrid film. A hybrid film was transferred as a Y-type LB film onto a hydrophilic glass plate or an ITO substrate. The structure of a deposited film was investigated with X-ray diffraction (XRD), Fourier transform infrared (FT-IR), and atomic force microscopy (AFM) measurements, indicating a layer-by-layer structure with a single or double sheet of niobate as an inorganic composite. From the cyclic voltammogram on an ITO electrode modified with the Y-type 10 layered film, the lower edge of the conduction band of a niobate layer was determined to be - 0.6 V (vs Ag/AgCl). ac impedance and dc measurements were carried out on 1, 5, and 10-layered LB films (2 mm (electrode spacing) x 8 mm (width)) with aluminum electrodes. The freshly deposited samples behaved as an insulator under the illumination of 280 nm light (2.04 x 10(16) quanta s(-1)). Photoconductivities appeared, however, when they were preirradiated with a 150 W Xe lamp (ca. 2 x 10(18) quanta s(-1)) for 0.5-8.5 h. The process was denoted as photomodification. From the FT-IR and XRD results, it was deduced that the photomodification of LB films caused the decomposition of organic templates (octadecylammonium) accompanied by the collapse of layer-by-layer structures. dc analyses on the 5- and 10-layered films after photomodification also showed that they behaved as a photosemiconductor under UV light illumination. 相似文献
69.
Hydrogen fluoride in a standard or sample gas stream at 200 ml min?1 permeates through a teflon membrane (0.8 μm pore size, 0.08 mm thick) into an absorption solution (citrate/acetate buffer at pH 5.4) flowing at 30 ml min?1. The fluoride produced is measured with the fluoride-selective electrode. The response time is about 12 min. The absorption efficiency of hydrogen fluoride is about 70% between 6.5 and 0.25 ppm by volume (5.2 and 0.2 mg m?3). In this range, the Nernst equation is valid with a relative standard deviation of less than 1.8%. The lower determination limit for hydrogen fluoride is 0.1 ppm (0.08 mg m?3). 相似文献
70.
Fourier analysis, using the atomic trajectory calculated by molecular dynamics simulation at 300 K, is applied to the study of low-frequency phonons of guanine dihydrate. The vibrational modes of guanine bases are analyzed, and the optically active modes associated with the guanine moieties are extracted. There are a few significant peaks in the low-frequency region. A possible assignment of the Raman active mode near 27 cm(-1), whose origin would be common to the S-mode of DNA double helices, is discussed. 相似文献