共查询到20条相似文献,搜索用时 31 毫秒
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Yu Xin LI Zheng Ming LI Wei Guang ZHAO Wen Li DONG Su Hua WANG State Key Laboratory of Elemento-Organic Chemistry Nankai University Tianjin 《中国化学快报》2006,17(2)
Some 1-arylsulfonylthiosemicarbazides have been reported as fungicides1 and bacterio-static agents2. Recently, it is well documented that thiosemicarbazide is a novel class ofnon-peptide antagonists for bradykinin B2 , which is beneficial in the symptomat… 相似文献
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《Tetrahedron: Asymmetry》1998,9(2):285-292
The title compound 3, an intermediate in the synthesis of fluorocarbapenems, is obtained with high stereocontrol by the condensation of (R)-(+)-ethyl 4,4,4-trifluoro-3-hydroxybutanoate with N-trimethylsilyl cinnamylidenimine. X-Ray diffraction analysis of the condensation product and chemical correlations allowed the unambiguous determination of the absolute configuration. 相似文献
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A general method has been proposed for synthesizing 3-(3-acetyl-5-aroyl-1,3,4-oxadiazolyl-2)-chromones that has been based on conversion of 3-formylchromones to acylhydrazones and of theacylhydrazones into the heterocyclic chromones. 相似文献
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Construction of new effective photovoltaic devices based on organic dyes has important implications for modern and future technologies. In this article, we studied the equilibrium, the rate, and the spectral manifestation of the reaction of [(2,3,7,8,12,18-hexamethyl,13,17-diethyl,5-(2-pyridyl)porphyrinato)cobalt(II)]–[2′-(pyridin-4-yl)-5′-(pyridin-2-yl)-1′-(pyridin-2-ylmethyl)-2′,4′-dihydro-1′H-pyrrolo[3′,4′ : 1,2](C60-Ih)[5,6]fullerene] triad formation as well as its spectral properties and photo electrochemical behavior. The cobalt porphyrin–pyridyl-substituted fullerene mixtures in toluene are self-assembling systems due to axial donor–acceptor binding between Co of the porphyrin complex and N-pyridyl of the substituted fullerene. The formation rate constant, k298K, and the stability constant, K298K, of donor–acceptor triad formed by coordination of two substituted fullerene molecules to Co porphyrin are (44.4 ± 0.8) mol L?1 s?1 and (56 ± 16)×107 L2 mol?2, respectively. Modification of the titanium electrode coated with the natural oxide film was carried out using the porphyrin–fullerene triad and its individual components. Photopotential and photocurrent density of the system with modified electrode were studied. The obtained results are of interest for creating porphyrin-based donor–acceptor systems as components in organic photovoltaics. 相似文献
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V. Yu. Gusev A. V. Radushev L. S. Shabalina V. I. Karmanov 《Russian Journal of Inorganic Chemistry》2011,56(4):639-643
Acid-base properties of 2′,2′-diethylheptanohydrazide (DEHH) and its complex formation with copper(II) ions in water-isopropanol
solutions were studied. Cationic complexes with [Cu2+] : [DEHH] ratios of 1 : 1 and 1 : 2 were found to be formed in weak acid media, and an uncharged complex with a [Cu2+] : [DEHH] ratio of 1 : 2 was found to be formed in a basic medium. log K
st values were determined. The data obtained were compared with the stability constants of copper(II) 2′,2′-diethylbenzohydrazide
complexes. 相似文献
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The crystal of the title compound (C36H29N3O,Mr = 519.62) has been prepared and structurally determined by X-ray single-crystal diffraction. It crystallizes in triclinic P ī space group with the crystal cell parameters: a = 12.544(4), b = 14.112(4), c = 17.770(5)A, α = 96.150(6), β = 106.112(5), γ = 107.156(5)°, V = 2825.7(14) ?3, Z = 4, Dc = 1.221g/cm3, μ(MoKα) = 0.074 mm-1 , F(000) = 1096,the final R = 0.0747 and wR = 0.1632 for 4713 observed reflections with I >2σ(I). The E-stereochemistry of the title compound can be confirmed by the result of the X-ray diffraction analysis. 相似文献
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《Microchemical Journal》1986,34(2):174-179
A fluorometric method for the determination of aluminum through complexation with 1-isonicotinoyl-2-(2′,4′-dihydroxy)benzylidene hydrazine is presented. The dependence of fluorescence efficiency on pH and ethanol/water ratios as well as the kinetics of complex formation are discussed. The detection limit at 20% RSD was observed to be 0.5 ppb (ng/ ml). 相似文献
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Peng Song Shi-guo Sun Pan-wang Zhou Jian-yong Liu Yong-qian Xu Xiao-jun Peng 《化学物理学报(中文版)》2010,23(5):558-564
Spectral and photophysical investigations of 4′-(p-aminophenyl)-2,2′:6′,2′′-terpyridine (APT) have been performed in various solvents with different polarity and hydrogen-bonding ability.The emission spectra of APT are found to exhibit dual fluorescence in polar solvents, which attributes to the local excited and intramolecular charge transfer states, respectively. The two-state model is proven out for APT in polar solvent by the time-correlated single photon counting emission decay measurement. Interestingly, the linear relationships of different emission maxima and solvent polarity parameter are found for APT in protic and aprotic solvents, because of the hydrogen bond formation between APT and alcohols at the amino nitrogen N25. Furthermore, the effects of the complexation of the metal ion with tpy group of APT and the hydrogen bond formation between APT with methanol at the terpyridinenitrogen N4—N8—N14 are also presented. The appearance of new long-wave absorption and fluorescence bands indicates that a new ground state of the complexes is formed. 相似文献
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A. V. Aksenov O. N. Nadein I. V. Borovlev Yu. I. Smushkevich 《Chemistry of Heterocyclic Compounds》1998,34(3):316-320
A method was developed for the synthesis of 2-alkyl(aryl)-1,2-dihydro-2,3-biquinolines, based on the addition of organolithium compounds to 2,3-biquinoline in the presence of tetramethylethylenediamine. Their oxidation with manganese dioxide led to 2-alkyl(aryl)-2,3-biquinolines.For Communication 2, see [1].Stavropol State University, Stavropol 355009, Russia. Russian Chemical-Technology University, Moscow 125190. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 350–354, March, 1998. 相似文献
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Julian Mirek Janusz Moskal Krzysztof Nagraba 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2)
Abstract Some authors have shown that tetrahydropyrimidine-2-thiones are hydrated in acidic solution and then isomerise to the 2-imino-or 2-enamino-1,3-thiazine. 相似文献
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A. A. Volod’kin L. N. Kurkovskaya G. E. Zaikov S. M. Lomakin 《Russian Chemical Bulletin》2013,62(10):2265-2265
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The first example of fused phosphorus heterocyclic 4-[ l′-(β-bromoethyl)-4'-oxo-3'-prop yl-1′, 2′, 3′, 4-tetrahydro-1, 3, 2-benzodiazaphosphorin-2′-sulfide]-1, 2, 3, 4, 4a, 4b, 5, 6-octahydro -6-oxo-5-propyl-3, 4b, 4a-thiazphosphaphenanthridine 4a, 2′-dioxide was synthesized in excellent yield by refluxing a mixture of 1-(2-bromoethyt)-2, 3-dihydro-3-propyl-l, 3, 2-benzodiazaphos phorin-4(1H)-one 2-oxide with carbon disulfide in benzene in the presence of triethylamine. 相似文献
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Steroidal ketone thiosemicarbazones (4–6), obtained from the corresponding ketones(1–3), on oxidative cyclization with H2O2 at 0°C provide title compounds (7–9), respectively. The structures of these compounds have been established on the basis of their elemental analytical and spectral data. 相似文献
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P. A. Slepukhin N. S. Boltacheva V. I. Filyakova V. N. Charushin 《Journal of Structural Chemistry》2011,52(2):443-444
Specific features of the molecular and crystal structures of 1,5-bis-(4′,4′,4′-trifluoro-1′-methyl-3′-oxo-but-1′-enylamino)-3-oxapentane are determined by single crystal XRD. 相似文献
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《Tetrahedron letters》1987,28(23):2623-2626
2′-5′,3′-5′ Linked triadenylates have been synthesized by direct bisadenylylation of adenosine 2′ and 3′ hydroxyls with an adenosine 5′-phosphorochloridite followed by oxidation. 相似文献
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Pavla Perlíková Neus Jornet Martínez Lenka Slavětínská Michal Hocek 《Tetrahedron》2012,68(39):8300-8310
A series of novel sugar-modified derivatives of cytostatic 6-hetaryl-7-deazapurine ribonucleosides (2′-deoxy-2′-fluororibo- and 2′-deoxy-2′,2-difluororibonucleosides) bearing an aryl or hetaryl group in position 6, was prepared and screened for biological activity. The fluororibo derivatives were prepared by aqueous palladium catalyzed cross-coupling reactions of the corresponding 6-chloro-7-deazapurine 2′-deoxy-2′-fluororibonucleoside 11 with (het)arylboronic acids. The key intermediate 11 was prepared by a six-step sequence from the corresponding arabinonucleoside by selective protection of 3′- and 5′-hydroxyls by acid-labile groups followed by stereoselective SN2 fluorination and deprotection. The difluororibo-series was prepared by non-stereoselective glycosidation of 6-chloro-7-deazapurine with benzoyl-protected 2-deoxy-2,2-difluoro-d-erythro-pentofuranosyl-1-mesylate followed by cross-couplings, separation of anomers and deprotection. The title nucleosides did not show considerable cytostatic or antiviral activity. 相似文献